EP1948773A1

EP1948773A1 - Fragrant consumer products comprising oxidizing agents

Info

Publication number: EP1948773A1
Application number: EP06806237A
Authority: EP
Inventors: Peter Schmiedel; Wolfgang Von Rybinski; Andreas Bauer; Sören HÖLSKEN
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 2005-11-14
Filing date: 2006-09-30
Publication date: 2008-07-30
Anticipated expiration: 2026-09-30
Also published as: DE102005054565A1; JP2009516034A; ES2572178T3; US20090081755A1; WO2007054177A1; EP1948773B1

Abstract

Fragrant consumer products comprising oxidizing agents are described, which may be, for example, detergents or cleaners or, for example, also cosmetics. These consumer products comprise certain minimum amounts of fragrances of certain classes of substances. They are characterized by very good (storage) stability, both with regard to the fragrance of the product, and also with regard to the potency of the oxidizing agent.

Description

"Oxidizing agent-containing, fragrant consumable products"

The present invention relates to a consumable product containing oxidizing agent, which comprises a fragrance composition, said fragrance composition containing a certain minimum amount of fragrances of certain classes. The consumer products are, for example, washing or cleaning agents or, for example, also cosmetics

The use of fragrances in typical consumer products such as detergents usually serves two different purposes. On the one hand, the products should be scented as such, on the other hand, the objects on which the products are to be scented. or detergent should give the freshly cleaned surfaces or freshly washed laundry a "freshly cleaned" olfactory impression that should last as long as possible, on the other hand, the sometimes very strong odor of detergents and cleaners should be covered

For many consumers, the fragrance of the consumer product, eg a washing or cleaning agent, ultimately also provides a welcome opportunity for differentiation in the face of an ever more confusing supply of products, for example in the field of detergents and cleaners

The consumer therefore usually wants to acquire a product which not only works well, but also appeals to its aesthetic sensibility, for example by the product as such or objects treated with it developing a fragrance. For example, the consumer expects stains on textiles or cosmetics Moreover, it expects that at least the product, but also the treated object will smell pleasant at all. This expectation on the part of the consumer is even so pronounced that, for example, in the case of a cleaned object appropriate fragrance expected missing this fragrance (eg "Citrusfπsche" in toilet cleaners), the consumer even doubts the actual active power of the product

Nachteihgerweise is a suitable perfuming of products, especially with a view to the perfuming of low-cost mass products such as detergents or cleaners but not only costly, but partially, for example, due to incompatibilities of ingredients with the fragrances sensitive, only in very inadequate manner feasible As far as the odor quality of the scented products is concerned

A particular problem in this case is a perfuming of products with an ability to oxidize. Here, in many cases even completely dispensed with a perfume, because a perfume Such products often, especially after storage, leads to significant product instabilities, so that, for example, an originally fragrant perfumed product after a few weeks of storage odorously changed in a dramatic negative way, so that it is not even neutral, but even repugnant. The product thus becomes unusable or unsaleable as a result of perfuming.

Against this background, it was the object of the present invention to provide a way to alleviate problems in perfuming products with oxidizing power.

This object is achieved by a consumable product containing oxidizing agents, preferably washing or cleaning agent or cosmetic product comprising a fragrance composition, wherein at least 50 wt .-%, preferably at least 60 wt .-%, advantageously at least 65 wt .-%, in a more advantageous manner at least 70 wt .-%, more preferably at least 75 wt .-%, in turn advantageously at least 80 wt .-%, in a particularly advantageous manner at least 85 wt .-%, in particular at least 90 wt .-% of the fragrances contained are selected from those fragrances which are at least one of the following classes of substances attributable saturated alcohols, preferably primary, secondary, and / or tertiary saturated, optionally branched or optionally cyclic alcohols, saturated esters, optionally branched or cyclic saturated esters saturated ethers, optionally branched or cyclic saturated ether aromatics with saturated substituents, optionally branched en, saturated substituents nitriles, optionally unsaturated in conjugation with the nitrile group saturated acetals, optionally branched or cyclic saturated acetals saturated hemiacetals, wherein the wt .-% - refers to the total amount of fragrance.

The consumption product according to the invention, the terms "consumable product", "product" and "agent" being used interchangeably hereinafter, is preferably a washing or cleaning agent or a cosmetic agent but they can also be used for industrial, institutional or commercial purposes.

The detergents or cleaners are, in particular, liquid detergents or cleaners, also in spray form, but solid detergents or cleaners, in particular also in tablet form, piece form or powder form, are preferred. Agents which are particularly preferred for the purposes of the invention are detergents and cleansing preparations, preferably for cleaning, treatment and / or care of fibers or textile articles, ie textile washing, textile care, textile treatment, textile aftertreatment agents and conditioners of all kinds. These also include separate bleaching agents, such as stain salts, liquid bleaches, detergency boosters. They can be used both as a detergent additive as well as for pretreatment. These include hygiene rinse, which are preferably added to the last rinse and contain an antimicrobial agent or oxidants and preferably nonionic surfactants. These include curtain detergents and special detergents for white laundry.

Dishwashing agents, in particular those for automatic dishwashing and hard surface cleaners, are among the preferred cleaning agents. Particularly preferred cleaning agents, which include the care agents for the purposes of this application, are e.g. in particular also all-purpose cleaners or special cleaners such as preferably car care or cleaner, oven cleaner, bathroom cleaner, decalcifier, facade cleaner, window cleaner, stain remover, floor care products, floor cleaner, glass ceramic hob cleaner, (hand) dishwashing detergent, stove cleaner or care products, leather cleaners or care products, metal cleaning agents , Furniture cleaner or care products, pipe cleaner, sanitary cleaner, scouring agent, carpet cleaner or care products, toilet cleaner, toilet flush cleaner for hanging in the toilet bowl or the cistern, the aforementioned each in solid or liquid form.

The most preferred cleaning agents include, in particular, the machine dishwashing detergents.

Among the preferred cleaning agents include i.a. also the toilet cleaner or toilet cleaner, ie products for cleaning toilet bowls and urinals, which are preferably as powder, tablets, shaped bodies or liquids, preferably gels offered. In addition to oxidizing agents and fragrances, as well as other common ingredients such as preferably surfactants, they may preferably contain organic acids (e.g., citric acid and / or lactic acid) or, preferably, sodium bisulfate, amidosulfuric acid, or phosphoric acid to remove lime deposits or so-called urine stones. For hanging in the toilet bowl or cistern flushing detergents are used, these preferably give small amounts of acid, surfactant, oxidizing agent and / or fragrance and thereby slow down the preparation of soiling.

Typical constituents, in particular of a solid toilet cleaner, preferably powder, may, for example, preferably be selected from the following: anionic surfactants, preferably 0-40 wt.%, Advantageously 0.1-30 wt.%, In particular 15-20 wt. % nonionic surfactants, preferably 0-10% by weight

organic acids or acid salts, preferably 3-50% by weight, preferably 5-10% by weight

inorganic acids or acid salts, preferably 3-95% by weight, in particular 25-90% by weight

Alkalis, preferably 0-10% by weight, in particular up to 5% by weight

Sodium hydrogencarbonate, preferably 0-30% by weight

Neutral salts, preferably 0-30% by weight

Sodium carbonate, preferably 0-10% by weight

Cellulose, preferably 0-5% by weight, in particular 1-2% by weight,

- complexing agent, preferably 0-10 wt .-%, in particular 0.1 to 5 wt .-%

Dye, preferably <1% by weight

Perfume, preferably 0.01-10% by weight

- Oxidizing agent, preferably 0.01-25 wt .-%, in particular 0.1-20 wt .-%, wherein the wt .-% - in each case based on the total average.

Typical constituents of a particularly liquid WC cleaner may be e.g. preferably be selected from the following: anionic surfactants, preferably 0-30 wt .-%, advantageously 0.1-20 wt .-%, in particular 1-10 wt -.% Nonionic surfactants, preferably 0-20 wt .-%, in particular 1 -10% by weight of organic acids or acid salts, preferably 0-50% by weight, advantageously 4-40

% By weight, in particular 3-30% by weight of inorganic acids or acid salts, preferably 0-5% by weight, in particular 0-2% by weight

Sodium hydrogencarbonate, preferably 0-10% by weight

Neutral salts, preferably 0-10% by weight

Cellulose, preferably 0-5% by weight

Dye, preferably <1% by weight

Perfume, preferably 0.01-10% by weight, in particular 0.05-5% by weight

Thickening agents, e.g. Xanthan, preferably 0-5% by weight

Water, preferably 0-99% by weight

Oxidizing agent, preferably 0.01-25 wt .-%, in particular 0, 1-20 wt .-%, wherein the wt .-% indication in each case based on the total mean.

Typical components of a rinsing cleaner (solid) for hanging in the toilet bowl or the cistern may preferably be selected from the following: Surfactants, for example APG, fatty alcohol ethoxylates, fatty alkyl sulfates, fatty alkyl ether sulfates, linear alkylbenzenesulfonates, alkanesulfonates etc., preferably in amounts of 0-40% by weight, in particular 15-30% by weight,

Acids or acidic salts, for example formic acid, acetic acid, citric acid, amidosulfonic acid, sodium hydrogensulfate, coconut fatty acids, etc., preferably in amounts of 0-20% by weight, in particular 0.1-15% by weight,

Complexing agents, for example sodium citrate, sodium phosphonate, preferably in amounts of 0-10% by weight, in particular 0.1-5% by weight,

Fillers, for example sodium sulphate, preferably in amounts of 0-60% by weight, in particular 0.1-30% by weight,

Dye, preferably <1% by weight

Perfume, preferably 0.01-10% by weight, in particular 0.05-5% by weight of oxidizing agent, preferably 0.01-25% by weight, in particular 0.1-20% by weight, the percent by weight indicating in each case based on the total mean

Typical components of a rinsing cleaner (liquid) for hanging in the toilet bowl or the

Winding boxes may preferably be selected from the following

Surfactants, for example APG, fatty alcohol ethoxylates, fatty alkyl sulfates, fatty alkyl ether sulfates, linear alkylbenzenesulfonates, alkanesulfonates etc., preferably in amounts of 0-30% by weight, in particular 5-20% by weight,

Acids or acidic salts, for example formic acid, acetic acid, citric acid, amidosulfonic acid, sodium hydrogensulfate, coconut fatty acids, etc., preferably in amounts of 0-10% by weight, in particular 0.1-5% by weight,

Complexing agent, for example sodium citrate, sodium phosphonate, preferably in amounts of 0-10% by weight, in particular 0.1-5% by weight, water, solvent, preferably 0-99% by weight, dye, preferably <1% by weight fragrance , preferably 0.01-10% by weight of oxidizing agent, preferably 0.01-25% by weight, in particular 0.1-20% by weight, the percentage by weight in each case being based on the total agent

The preferred cleaning agents include, inter alia, the pipe cleaning agents or Abflußremi- ger These are preferably strong alkaline preparations, which are usually the elimination of pipe blockages of organic materials - such as hair, fat, food residues, soaps deposits etc - serve Zur Formation of H ₂ -GaS with a sparkling effect can serve as additives of AI or Zn powder. Possible ingredients, in addition to oxidizing agents and fragrances, are preferably alkalis, alkaline salts and neutral salts. In powdered formulations, preferably sodium nitrate and sodium chloride are also contained in pipe cleaners flussi- ger form may preferably contain hypochlorite. In addition, there are also drain cleaner on Enzymbasis. Acid preparations are also possible. Oxidizing agent is preferably present in amounts of 0.01 to 60 wt .-%, in particular in amounts up to 40 wt .-%, fragrances preferably in amounts of 0.01-10 wt .-%, wherein the wt .-% statement in each case based on the total mean.

Among the preferred cleaning agents pay u.a. also the universal or all-purpose cleaner or all-purpose cleaner. These are universally applicable cleaners for all hard surfaces in household and commercial, which are wet or damp wipeable. As a rule, these are neutral or weakly alkaline or weakly acidic products, in particular liquid products. In particular, all-purpose cleaners may contain ingredients selected from the following: surfactants [e.g. Alkanesulfonates (SAS), alkylbenzenesulfonates (LAS), alkylpolyglucosides (APG), fatty alcohol polyglycol ether sulfates (FAES), fatty alcohol polyglycol ethers (FAE, FAEO), preferably 0-25% by weight, in particular 0.1 to 20% by weight

Builders [e.g. Trisodium citrate, sodium nitrilotriacetic acid salt, sodium phosphonate, pentasodium triphosphate] preferably 0-10% by weight, especially 0.1 to 5% by weight, of solvent and hydrotrope [e.g. Ethanol, propylene glycol ether, sodium toluene or cumene sulfonate], preferably 0-10% by weight, in particular 0.1 to 5% by weight of dyes, preferably <1% by weight

Perfume, preferably 0.01-10% by weight, in particular 0.05-5% by weight preservative,

Oxidizing agent, preferably 0.01-30% by weight, especially 0.1-20% by weight of acids, e.g. Acetic acid, citric acid, maleic acid, preferably 0.1-10% by weight, in particular 0.1-5% by weight in the case of weakly alkaline all-purpose cleaners, also alkalis, e.g. Sodium hydroxide solution, soda, preferably 0-5 wt .-% water, preferably 0-99 wt .-%, wherein the wt .-% - in each case based on the total mean.

There are also special disinfecting all-purpose cleaners. These additionally contain antimicrobial agents (e.g., alcohols, quaternary ammonium compounds, amphoteric surfactants, triclosan) or more oxidizing agents, e.g. preferably> 1% by weight, the percentage by weight being based on the total agent.

The preferred cleaning agents include, among others, the sanitary cleaners. These are products for cleaning in the bathroom and toilet. The alkaline sanitary cleaners are preferably used to remove grease, while the acidic sanitary cleaners are used primarily for the removal of limescale. Sanitary cleaners have advantageous wise also a significant disinfecting effect, especially the strong alkaline, chlorine-containing sanitary cleaner.

In particular, the components of alkaline sanitary cleaners may contain ingredients, selectable from the following: anionic surfactants, preferably 0-10 wt .-%, in particular 1-5 wt .-% of nonionic surfactants, preferably 0-5 wt .-%, in particular 1-3 wt .-% sodium hydroxide, preferably 0-10 wt .-%, in particular 1-5 wt .-% oxidizing agent, for example Sodium hypochlorite or calcium hypochlorite or hydrogen peroxide, preferably 0.01-10% by weight, in particular 1-5% by weight of perfume, preferably 0.01-10% by weight, in particular 0.05-5% by weight, of water, preferably 0-99 wt .-%, wherein the wt .-% - is in each case based on the total average.

Acid sanitary cleaners preferably contain no alkalis, but acid or acid salts, preferably in amounts of 0.01-30 wt .-%, wherein the wt .-% - refers to the total average.

Among the preferred cleaning agents include i.a. also the oven cleaner or grill cleaner, which are advantageously offered in the form of gels or foam sprays. These are usually used to remove burnt or charred food particles. Preferably, oven cleaners are e.g. strongly alkaline with sodium hydroxide, sodium metasilicate, 2-aminoethanol. In general, they also preferably contain anionic and / or nonionic surfactants, preferably water-soluble solvents and preferably thickeners such as polycarboxylates, carboxymethylcellulose, as well as oxidizing agents and fragrances.

The preferred cleaning agents include, inter alia, the metal cleaning agents. These are cleaners for certain metal types such as stainless steel or silver. Stainless steel cleaners preferably contain not only acids (preferably up to 3% by weight, eg citric acid, lactic acid), surfactants (in particular up to 5% by weight, preferably nonionic and / or anionic surfactants), water also solvents (preferably up to 15% by weight). %) to eliminate greasy soiling and other substances such. As thickeners and preservatives. Very fine polishing bodies are also contained in products for preferably glossy stainless steel surfaces. Silver cleaning agents, in turn, are preferably acidified. They contain, in particular for removing black deposits of silver sulfide, preferably complexing agents (eg thiourea, sodium thiosulfate). Typical offer forms are cleaning cloths, dip baths, pastes, liquids. To remove dark discolorations (oxide layers), copper and non-ferrous metal cleaners (eg for brass and bronze) are used. These are usually adjusted to weakly alkaline (preferably with ammonia) and usually contain polishing agents and preferably also ammonium soaps and / or complexing agents. Among the preferred cleaning agents include the glass cleaner or window cleaner. These are preferably used to eliminate in particular fatty greasy soil from glass surfaces. They preferably contain substances which are advantageously selectable from the following: anionic and / or nonionic surfactants (in particular up to 5% by weight),

Ammonia and / or ethanolamine (in particular up to 1% by weight),

Ethanol and / or 2-propanol, glycol ether (in particular 10-30% by weight),

Water,

Preservatives,

dyes,

fragrances,

Oxidant

Anti-fogging agent etc, wherein the wt .-% indication in each case based on the total mean.

Among the preferred cleaning agents include i.a. also all special cleaning agents, e.g. such as ceramic hobs, as well as carpet and upholstery cleaners and stain removers.

Products preferred according to the invention are also car care products. Among the preferred car care products include u.a. Paint preservatives, paint polishes, paint cleaners, washing preservatives, shampoos for car wash, car wash and wax products, polishes for decorative metals, protective films for decorative metals, plastic cleaner, tar remover, window cleaner, engine cleaner etc.

The cleaners of the invention can be used in general for cleaning surfaces such as glass, porcelain, plastic, textiles, leather, paints or wood.

The institutional or commercial cleaners, which are usually made available in the form of large containers, are preferably for the operational cleaning and hygiene, e.g. designed in public buildings, schools, office buildings, hotels, restaurants and hospitals, such products are preferably designed so that preferably a safe surface disinfection can be guaranteed. Thus, e.g. greater amounts of oxidizing agent, e.g. > 1 wt .-% or> 3 wt .-% or> 5 wt .-%, wherein the wt .-% indication in each case based on the total mean.

Technical cleaners are generally used in industry, namely in particular in the beverage, metal, food, cosmetic and pharmaceutical industries used, for example as a cleaner for car washes, Tankwagen- u. Aircraft cleaner. Advantageously, in particular technical cleaners with particularly low-foaming surfactants (for example special nonionic surfactants, such as ethylene oxide-propylene oxide block copolymers and so-called end-capped alkyl ethoxylates) may be formulated in order to achieve a possibly required productivity

Here, for example, larger amounts of oxidizing agent may be contained, for example,> 1% by weight or> 3% by weight or> 5% by weight, the weight percentage being based in each case on the total agent

The inventively preferred cosmetic agents include in particular

(a) those for skin care, such as, preferably, bath preparations, skin cleansers, skin care products, ocular cosmetics, lip care products, nail care products, personal care products, foot care products

(b) those having a specific action, such as, preferably, depigmenting agents, deodorants, antihidrotic agents, hair removing agents, shaving agents, fragrances

(c) dentifrice and oral care such as, preferably, oral and oral care products, dentifrices, denture cleaners, denture adhesives

(D) those for hair care, such as, preferably, shampoos, hair care preparations, hair hardening agents, hair treatment agents, hair lotions, hair styling agents, hair dyes, bleaching agents

Preferred ingredients of the consumer products according to the invention, in particular of the cosmetic agents, can be defined by their function. Of course, some ingredients may also be multifunctional

Preferred ingredients of the consumer products of the invention, preferably cosmetic products, may be selected from the following: a) Absorbents

These preferably have the task of absorbing water and / or oil-soluble dissolved or finely divided substances b) antimicrobial substances

These may be added to the products to generally reduce the activities of microorganisms, eg on the skin and in the oral cavity. C) Antioxidants, preferably present in a separate form from the oxidizing agent

These are intended to prevent oxygen-triggered reactions such as oxidation and thus extend the shelf life of the products, ie the quality of the products obtained d) antiperspirants

These are preferably used in cosmetics and reduce the sweat e) antifoam These may be added, for example, to remove foam during manufacture or to reduce the tendency of finished products to over foam, f) anti-dandruff actives

These are used primarily in hair care products because they can counteract dandruff. g) antistatics

These are e.g. Combability aids in hair care products. They generally reduce the electrostatic charge on objects, such as the hair surface. Hair can be combed much easier, h) binders

They ensure e.g. the cohesion of powdered and powdered products, e.g. cosmetic preparations, (i) substances of biological origin

These are e.g. certain plant ingredients, e.g. Green tea extract. They are intended to give certain desired properties to a product, which are related to the corresponding biological material, or to further improve existing properties or to suppress undesirable properties or reduce them as much as possible, k) chelating agents

These are e.g. added to cosmetic agents to form complexes with metal ions, for example, to manipulate the stability and / or the appearance of the agents. I) Deodorants / antiperspirants

These can help to prevent or reduce the development of unpleasant body odors. You can cover such odors and possibly the formation of perspiration. Reduce m) emollients

These have e.g. In the cosmetic field, the task of making the skin supple and smooth. n) emulsifiers

These are surface-active substances which are preferably capable of stably dispersing immiscible liquids such as oil and water, o) emulsion stabilizers

These can further support the process of emulsification (see emulsifiers) and thus further improve the stability and shelf life of the product, p) depilatories

These are used for preferably selective removal of body hair, q) moisturizers

These can contribute to the maintenance or restoration of the skin moisture and counteract the drying out of the skin, r) film former These are capable of producing, for example, in cosmetics, a protective, stabilizing film on surfaces, preferably skin, hair or nails

These are, for example, also added to cosmetic products in order to produce a product coloration or else to bring about an indirect object coloration, for example hair colorant t) preservatives

These are added, for example, to cosmetic products in order to protect them from the harmful action of microorganisms (bacteria, fungi, yeasts) and thus to prevent their spoilage u) anticorrosive agents

These can serve, for example, to prevent the corrosion of the packaging, for example of a cosmetic agent, or else the corrosion of parts which otherwise come into contact with the agent. V) Solvent

They may, for example, be the basis for, for example, liquid cosmetic preparations or else be part of solid products w) oral care substances

These can serve the care of teeth and gums y) pH regulator / buffer substances

These can be used, for example, in cosmetics to adjust or stabilize a desired pH. Z) Reducing agent, preferably present in a separate form from the oxidizing agent

These are able to change the chemical composition of another substance by redox processes aa) abrasives

These can be used to remove materials from various (body) surfaces, for example, to assist the mechanical cleaning of the teeth or to improve tooth gloss. B) Surfactants / wash-active substances

These are surface-active compounds used for cleaning purposes cc) propellants

These are gaseous substances with which products, for example cosmetic agents, can be placed under pressure in pressure-resistant containers in order to produce the contents when pressure is released dd) turbidity agent

These can be added preferably transparent or translucent products to make them more impenetrable to visible light or near-light radiation ee) UV absorber / light filter substances They are able to filter certain UV rays and can thus protect the skin, for example, from premature light-induced aging as well as from sunburn. ff) denaturant

For example, these are added to cosmetics containing ethanol to render them inedible. gg) viscosity regulator

These are able to increase or decrease the viscosity of a product.

The aforementioned ingredients can be contained according to a preferred embodiment in the products according to the invention, preferably cosmetic agents.

For example, creams, pastes, tinctures, lotions, solutions, waters, emulsions such as W / O, O / W, PIT emulsions (emulsions according to US Pat Phase inversion theory called PIT), microemulsions and multiple emulsions, coarse, unstable, single or multi-phase shaking mixtures, gels, sprays, pouches, aerosols and foam aerosols.

The products according to the invention, such as preferably detergents or cleaners, are advantageously able, in particular in comparison with oxidant-free compositions, improved performances, in particular cleaning performances, e.g. with regard to the removal of stains, in particular colored stains. Furthermore, they are advantageously able to achieve more effective hygiene performance in the material to be treated (eg textiles, dishes, hard surfaces, etc.), in particular in comparison with oxidant-free compositions, by improving the destruction of bacteria and other microorganisms, in particular with regard to one significant reduction in germ count. Furthermore, the fragrance composition according to the invention contributes to a pleasant odor of the entire composition, in particular washing or cleaning agent or cosmetic and thus increases its acceptance by the consumer.

Another advantage of the invention is that such a product is stable on storage, in particular as regards the stability of the oxidizing agent as well as the perfuming of the product. The scent impression of the perfumed composition according to the invention advantageously does not change even during prolonged storage over several weeks. Likewise, the activity of the oxidizing agent advantageously does not diminish significantly more than in the absence of perfuming even after prolonged storage for several weeks. Both advantageously also apply to liquid funds.

According to a preferred embodiment, the perfume composition contained in the agent according to the invention contains at least 91% by weight, preferably at least 92% by weight, advantageously at least 94% by weight, more preferably at least 96% by weight, even more preferably at least 98% by weight, more preferably at least 99% by weight, in particular even 100% by weight of such fragrances, which at least one of saturated alcohols, preferably primary, secondary, and / or tertiary saturated, optionally branched or optionally cyclic alcohols, saturated esters, optionally branched or cyclic saturated esters saturated ethers, optionally branched or cyclic saturated ether - aromatics with saturated substituents, if necessary with branched, saturated substituents

Nitriles, optionally unsaturated in conjugation with the nitrile group, saturated acetals, optionally branched or cyclic saturated acetals, saturated hemiacetals, the percentages by weight being based on the total amount of fragrance

According to a further preferred embodiment, the perfume composition contained in the agent according to the invention contains at least 50% by weight, at least 60% by weight, at least 70% by weight, at least 80% by weight, at least 90% by weight or at least 91% by weight, preferably at least 92% by weight, advantageously at least 94% by weight, more preferably at least 96% by weight, even more preferably at least 98% by weight, more preferably at least 99% by weight, in particular even 100% by weight of fragrances, selected from citronitrile, ortho-tert-butylcyclohexyl acetate, cyclohexylsahcylate, (+) - (1 ^l R, 3S, 6S) -1- (2 ^l , 2 ^l , 6'-tri-methyl-1'-cyclohexyl) -3- hexanol, (-) - (1 ¹ S ₁ SR ¹ R) -I - (2 \ 2 \ 6'-tri-methyl-r-cyclohexyl) -3-hexanol, (+) - (r R, ³ R, 6'S) - 1- (2 ^l , 2 ^l , 6 ^l -trimethyl-1 ^l -cyclohexyl) -3-hexanol, (-) - (1'S, 3S, 6 ^l R) -1- (2 ^l , 2 ^{l of} _I 6 ^l - trimethyl-1'-cyclohexyl) -3-hexanol, phenylethyl alcohol, 2-cyclohexyl-2-phenylacetone, decahydro-b-naphthol acetate, kresylac eta (para), methyl phenylacetate, allylamyl glycolate, benzyl acetate, cyclohexyl ethyl acetate, ethyl 2-cyclohexyl propionate, phenylethyl acetate, cyclopentylidene-acetic acid methyl ester [CAS No. 0040203-73-4), allyl (cyclohexyloxy) acetate, 2,4-dimethylethyl 1, 3-dιoxolan-2-ethyl acetate, 3,12-Trιdecadιen-nιtπl, amyl acetate, isoamyl acetate, ethyl phenylacetate, 2-Propenylphenoxyacetat, Isobornylacetat, Dimethylbenzylcarbinylacetat, hexyl acetate, cresyl acetate (para), Isobutylphenyl- acetate, Butylcyclohexylacetat- cis-para-tert , Butylcyclohexylacetate trans-para-tert, hydroxymethyl alcohol, 2,6-dimethylheptan-2-ol, decanol, octanol, 2,6-dimethylcyclo [4 4 0] decan-1-ol (0 1% in di- propylene glycol), tetrahydrouguol [= tetrahydro-naph- ol (3,7-dimethyl-octan-3-ol) / tetrahydromyr- nol (2-octanol, 2,6-dimethyl) mixture (11)], dihydroterpmeol, alpha 3,3-t-methylcyclohexylmethyl format , Octanol-3, hexanol, 2,2,6-Trιmethy! -Alpha-propylcyc (ohexanpropanol, Decahydro-b-naphtolformiat, (1 ¹ S , 1 "S, 2'S, 3" R, 5 ¹¹ R) - [I-methyl-2- (1,2,2-tri-methyl-bicyclic [3 1 0] hex-3-ylmethyl) -cyclopropyl-1-methanol , (1 ^L R, 1 "R, 2'R, 3" S, 5 "S) - [1-methyl-2- (1,2,2-t-methyl-bicyclic [3 1 0] hex-3-ylme - methyl) -cyclopropyl] -methanol, (1 ^{l of} R, 1 "S, 2 ^{l of} R, 3" R, 5 "R) - [1-methyl-2- (1, 2,2-tπmethyl-bιcyclo [3 1 0] hex-3-ylmethyl) -cyclopropyl] -methanol, (1'S, 1 "R, 2'S, 3" S, 5 "S) - [1-methyl-2- (1,2,2-tri-methyl-bicycl - [3 l] Olhex-S-ylmethoxy-cyclopropyl-methanol, borneol, dipropylene glycol, tetrahydrogeraniol, tetrahydrolyn-olool, 2,2,6-tri-methyl-alpha-propylcyclohexanepropanol (Timberolforte), alpha-methyl-4- (1-methylethylcyclohexanemethanol, Isocyclogeraniol, fenchyl alcohol, (-) - (2R, 4S) -2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, (+) - (2S, 4R) -2-isobutyl-4-methyltetrahydro-2H- pyran-4-ol, (+) - (2S, 4S) -2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, (-) - (2R, 4R) -2-isobutyl-4-methyltetrahydro- 2H-pyran-4-ol, methyl benzoate, ethyl benzoate, methyl salicylate, amyl propionate, ethyl 2,6,6-tri-methyl-1,3-cyclohexadiene-1-carboxylate, benzyl propionate, ethyl salicylate, 2-methoxy-4-formyl-phenyl isobutyrate (isobutane) , Ethyl caprylate, allyl caproate, 2-methyl-2-butenoic acid 2-methylpropyl ester, 2-ethyl-ethylhexanoate (Irotyl), 2-methylpentanoic acid 2-methylpentyl ester, jasmacycate, 2,5-dimethyl-4,6-dihydroxybenzoic acid methyl ester, Ethyl 2-methylvalerate, heptanoic acid 2-propenyl ester (allylheptanoate - al lyloenanthate), methyl anthranilate, phenylacetic acid, allylcyclohexyl propionate, 2-nonynoic acid methyl ester, cyclohexyl salicylate, 2-tert-butylcyclohexylethyl carbonate, 2,2,4-trimethylcaproic acid ethyl ester, ethyl ester labdanum extract (ambrarome), styrolyl acetate, hydroquinone dimethyl ether, diphenyl ether, cresyl methyl ether (para) , Cymene (para), phenylethyl isoamyl ether, phenylethyl methyl ether, 4-isopropyl-5,5-dimethyl-1,3-dicanoan, 2,2,5,5-tetramethyl-4-isopropyl-1,3-dicoxan, 5-methyl-5-propyl-2 (1-methylbutyl) -1,3-dinoxane, anethole, 2-phenylpropionaldehyde dimethyl acetal, frambomethyl ether, coumarin, isocumarin, acetophenone, 1,1,3,3-pentamethylene ethyl 6,7-dihydro-4 (5H) -indanone, octalactone gamma, ethylamyl ketone, camphor synth, oxacycloheptadec-8-en-2-one, 2-heptylcyclopentanone, 2- (1-methylpropyl) cyclohexanone, 4 tert-butyl-2,6-dimethylacetophenone, cyclopentadecanolides, 3-methylcyclopentadecanone, dihydrojasmon, dihydro-iso-jasmon, decalactone gamma, methyl octalactone, 1,4-Dicoxacyclohexadecane-5,16-dιone, 4- (2-butenylidene) -3,5,5-trimethyl-2-cyclohexen-1-one, ethyl ^^, δ-methylcyclohexanecarboxylate, cinnamic acid nitrate, lactonitrile , Hydrocitronitπl, 2-benzyl-2-methyl-3-butennιtrιl, 3-Methyldodecanonι- tπl, Citronitπl, Trιdecen-2-nιtrιl, ^* 3 (4,7,7-Trιmethylbιcyclo <4 1 0> hept-3-yl) -2-propenylnιtrιl, Irolene p, 8-alpha-12-Oxιdo-13,14,15,16-tetranorlabdane, 3,3,5-Trιmethylcyclohexylethylether, Inval (70% 4-tert-pentylcyclohexanone, 10% white mineral oil, 10 % Non-2-enenetrile, 10% dibutyl sebacate), isobutylquinoline, 5-ethylbendenebicyclo [2 2 1] -2-heptene-2-methoxyphenol adduct, methylbutyl-2-propionate, indeno [1,2-d] -tetrahydro 1,3-dioxan, dodecahydro-3a, 6,6,9a-tetramethyl-naphthio (2,1-b) furan, 2,4-dimethyl-4-phenyl-tetrahydrofuran, spiroti .s-dioxolane ^ .S ' ^ '^'. δ'.δ'-tetramethyl-hexahydro-S'.'-methanonaphthalene)], methyl dihydrojasmonate, methyl S-oxo-pentylcyclopentane acetate, O- (allyloxy) anil sol, dihydromyrcenol, 9-decene 1-ol, Tetrahydromyrcenol, hexahydro-4,7-methyl-6-yl acetate, 2-Phenoxyethylιsobutyrat, 2-Methylpropensaure-1, 3-dιmethyl-3-butenylester, methylace- tophenone para, 4-phenyl-2-butanone, Hδ.δ- Dimethyl-i-cyclohexen-i-ylM-pentene-i-one, 3-hydroxy-1-methyl-4-isopropylbenzene [CAS No. 89-83-8], wherein the Gew -Ngabe on the total amount of the fragrances refers

These aforementioned fragrances can be used in particular in liquid agents with great success in the context of the invention Corresponding fragrance compositions, even with highly reactive oxidizing agents such as peroxycarboxylic acids, which may advantageously be selected from mono- and diperoxycarboxylic acids, in particular dodecanediperoxyacid or preferably imidoperoxycarboxylic acids, more preferably 6-phthalimidoperoxycaproic acid (6-phthalimidoperoxyhexanoic acid, PAP), provide exceptional stability results, in particular Look at PAP. The potency of the oxidizing agent remains very well preserved even after prolonged storage, advantageously also in liquid agents. The fragrance of the fragrance composition remains very well preserved even after prolonged storage, advantageously also in liquid agents.

In a preferred embodiment, the product contains certain minimum values of fragrances, namely at least 0.01% by weight or 0.05% by weight, advantageously at least 0.1% by weight, in a considerably advantageous manner at least 0.15% by weight. -%, more preferably at least 0.2 wt .-%, in a further advantageous manner at least 0.25 wt .-%, more preferably at least 0.3 wt .-%, in a very advantageous manner at least 0.35 Wt .-%, in a particularly advantageous manner at least 0.4 wt .-%, in a particularly advantageous manner at least 0.45 wt .-%, in a significantly advantageous manner at least 0.5 wt .-%, in a very significantly advantageous manner at least 0.55 wt .-%, in an extremely advantageous manner at least 0.6 wt .-%, most advantageously at least 0.65 wt .-%, in an extremely advantageous manner at least 0.7 wt .-%, in exceptionally advantageous manner at least 0.75 wt .-%, in an exceptionally advantageous manner at least 0.8 wt .-%, in extremely vorteilha at least 0.85 wt .-%, in particular at least 0.9 wt .-% of fragrances, based on the total product.

In a preferred embodiment, however, the product contains larger amounts of fragrances, namely at least 1 wt .-%, advantageously at least 2 wt .-%, in a considerably advantageous manner at least 5 wt .-%, more preferably at least 10 wt .-%, in a further advantageous manner at least 13 wt .-%, more preferably at least 14 wt .-%, in a very advantageous manner at least 15 wt .-%, in a particularly advantageous manner at least 16 wt .-%, in a particularly advantageous manner at least 17% by weight, in a significantly advantageous manner at least 18% by weight, in a very advantageous manner at least 19% by weight, in particular at least 20% by weight, of perfumes, based on the total product.

However, it is rather uncommon in consumer products to achieve very high fragrance levels in order to prevent the product from smelling too intrusive. Rather, it is often desirable that the amount of fragrance contained is limited. In a preferred embodiment, the product therefore contains certain maximum values of perfume oil, namely, for example, not more than 30% by weight, 25% by weight, 20% by weight or 15% by weight, advantageously not more than 10% by weight. %, in a considerably advantageous manner not more than 9% by weight, more advantageously not more than 8% by weight, more advantageously not more than 7% by weight, even more advantageously not more than 6% by weight %, most preferably not more than 5% by weight, in particular Advantageously, not more than 4.5 wt .-%, in a particularly advantageous manner not more than 4 wt .-%, in a significantly advantageous manner not more than 3.5 wt .-%, in particular not more than 3 wt .-% or 2 wt .-% of fragrances, based on the total product. It should be noted at this point for the entire text that the statement Gew .-% refers in each case to the entire product, unless it is concretely stated otherwise, or it emerges from the concrete context in a clear way another Reference.

The general concept of the fragrance within the meaning of the invention is in accordance with the usual definition, i. they are usually substances that are perceptible by their smell, especially pleasant smell. These preferably also include the flavorings. The fragrances used today are above all essential oils, flower oils, extracts from plant and animal drugs, from natural products, isolated components (isolates) as well as semi-synthetic and fully synthetic uniform fragrances.

As the oxidizing agent, any conceivable oxidizing agent may be used, e.g. Perborates, percarbonates, hydrogen peroxide, sodium hypochlorite, dichromate, dithionite, permanganate, chlorine, concentrated sulfuric acid, organic peracids, chlorine, hypochlorite, chlorine dioxide, peroxides, etc. A number of advantageously usable bleaching agents are mentioned below.

The oxidizing agents, preferably bleaching agents, may preferably be coated. The coating can serve to reduce the interaction with other ingredients, but this is not completely successful.

According to a further preferred embodiment, the oxidizing agent is an oxidative bleaching agent, preferably based on oxygen, with particular preference being given to peroxycarboxylic acids.

According to a further preferred embodiment, the agent according to the invention contains a peroxycarboxylic acid, which is advantageously selected from mono- and diperoxycarboxylic acids, in particular dodecanediperoxyacid or preferably imidoperoxycarboxylic acids, more preferably 6-phthalimidoperoxycaproic acid (6-phthalimidoperoxyhexanoic acid, PAP) and / or wherein the Peroxycarboxylic acid at atmospheric pressure has a melting point above 25 ° C, in particular above 35 ° C, preferably above 45 ⁰ C, preferably above 50 ° C, more preferably above 100 ⁰ C.

According to a further preferred embodiment, the oxidizing agent, in particular the peroxycarboxylic acid, is present in granular form, preferably coated, the mass of the coating advantageously being from 0.1 to 30% by weight, based on the total of the particles containing the oxidizing agent, preferably Granules. "Essentially" means here that, preferably in the case of a freshly prepared product, advantageously at least 50, 55, 60, 65, 70, 75% by weight of the oxidizing agent are present in granular form, the statement wt% here referring to the total amount of oxidizing agent Means, in particular after a storage period, also present a proportion of the oxidizing agent in dissolved form

According to a preferred embodiment, the agent according to the invention contains at least 0.01% by weight of surfactants

In this case, the surfactant content of the entire composition z B is 0.1-60% by weight, preferably 1-50% by weight, advantageously 5-45% by weight, more preferably 10-40% by weight, in particular 15-30% by weight However, according to another preferred embodiment, the lower limit of the surfactant content may also be at a value of preferably 1% by weight, 2% by weight, 3% by weight, 4% by weight, 5% by weight, 6 % By weight, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, % By weight, 17% by weight, 18% by weight, 19% by weight, 20% by weight, 21% by weight, 22% by weight, 23% by weight, 24% by weight, 25% by weight, 26 % By weight, 27% by weight, 28% by weight, 29% by weight or 30% by weight, based on the total agent The lower limit of surfactant may in particular even be even higher values, for example at a value of preferably 35% by weight, 40% by weight, 45% by weight, 50% by weight, 55% by weight or 60% by weight, based on the total agent

The upper limit of surfactant can also be used, for example, at a value of preferably 65% by weight, 60% by weight, 55% by weight, 50% by weight, 45% by weight, 40% by weight, 35% by weight, 30% by weight. % or 25% by weight or even only at values such as 20% by weight, 19% by weight, 18% by weight, 17% by weight, 16% by weight, 15% by weight, 14% by weight, 13% by weight %, 12% by weight, 11% by weight or 10% by weight It is, for example, also possible to suitably combine the stated lower limit and upper limits from the abovementioned data, for example to represent a surfactant content of 4-18% by weight It is also possible that 0% by weight of surfactant is included

Particularly preferred according to the invention are anionic surfactants, such as, for example, (linear) alkylbenzenesulfonates, fatty alcohol sulfates or alkanesulfonates etc., preferably in amounts of from 0.1 to 30% by weight, and / or nonionic surfactants, for example alkylpolyglycol ethers, alkylpolygluco - side or amine oxides, etc., preferably in amounts of, for example, from 0.1 to 30% by weight, in each case based on the total agent

The agent according to the invention may also contain cationic surfactants, for example in amounts of 0.01% by weight or 0.05% by weight to 30% by weight. However, it corresponds to a preferred embodiment if the agent according to the invention is cationic surfactant-free, which means the agent is less than 10% by weight, preferably less than 5% by weight, advantageously less than 3% by weight, more preferably less than 1% by weight, even more preferably less than 0.5% by weight, in particular 0% by weight of cationic surfactant According to a preferred embodiment, the agent according to the invention contains electrolytes, in particular inorganic and / or organic salts, in particular phosphate, citrate and / or sulfate, more preferably sodium sulfate, preferably in amounts of at least 0.1% by weight, advantageously at least 3% by weight. %, in particular in amounts of 5 to 30 wt .-%, each based on the total agent. It is also possible that 0 wt .-% electrolyte is included.

When the agent of the invention contains complexing agents, e.g. Nitrilotriacetic acid, ethylenediaminetetraacetic acid or phosphonate etc., preferably in amounts of up to 30% by weight or up to 20% by weight, in particular 0 to 10% by weight, advantageously from 0.1 to 5% by weight , based on the total agent, so is a further preferred embodiment of the invention. Particularly advantageous are

(a) nitrogen-free chelating agents such as e.g. preferably alkali metal polyphosphonates, mono- or polyphosphonic acids, in particular 1-hydroxyethylidene-1,1-diphosphonic acid (HEDP), citrate and / or short-chain dicarboxylic acids. and or

(b) complexing agents from the group quinoline and / or its salts, picolinic acid and dipicolinic acid (ethylenediaminetetraacetic acid (EDTA), diethylenetriamine penta (methylenephosphonic acid) (DTPMP), azacycloheptane diphosphonate (AHP), nitrilotriacetic acid (NTA), aminopolycarboxylic acids, aminohydroxypolycarboxylic acids, polyphosphonic acids and aminopolyphosphonic acids ,

Here, 1-hydroxyethylidene-1, 1-diphosphonic acid is most preferred. It is also possible that 0 wt .-% complexing agent is included.

These complexing agents can be used according to the invention to preferably inactivate or bind heavy metal ions, which in particular can act as catalysts of oxidation processes and thus lead to degradation of oxidizing agent, e.g. Peroxycarboxylic acids, such as PAP, and which, for example, via water pipes or metallic components of the production plants or via raw materials or ingredients in the agent according to the invention, e.g. Detergents or cleaners, can be registered.

According to a preferred embodiment of the invention, the agent according to the invention also contains enzymes, in particular e.g. Proteases, amylases, catalases, peroxidases, cellulases and / or lipases, and / or enzyme stabilizers, preferably in amounts of from 0 to 10% by weight, based in each case on the total agent. It is also possible that 0 wt .-% enzyme is included.

According to a preferred embodiment, the agent according to the invention contains builders (builders). According to a further preferred embodiment of the invention, the builder content of the agent is, for example, 0-99% by weight, preferably 1-60% by weight, advantageously 2-50% by weight. even more advantageously 3-60% by weight, more preferably 5-50% by weight, in particular 6-40% by weight. According to another preferred embodiment, the lower limit of the builder content but also at a value of preferably 7 wt .-%, 8 wt .-%, 9 wt .-%, 10 wt .-%, 11 wt .-%, 12 wt. %, 13 wt%, 14 wt%, 15 wt%, 16 wt%, 17 wt%, 18 wt%, 19 wt%, 20 wt% , 21 wt%, 22 wt%, 23 wt%, 24 wt%, 25 wt%, 26 wt%, 27 wt%, 28 wt%, 29 Wt .-% or 30 wt .-% are. The lower limit may in particular even be at even higher values, for example at a value of preferably 35% by weight, 40% by weight, 45% by weight, 50% by weight, 55% by weight or 60% by weight. -%.

According to a further preferred embodiment, the upper limit of the builder content may also be at a value of preferably 70% by weight, 71% by weight, 72% by weight, 73% by weight, 74% by weight, 75% by weight. %, 76 wt%, 77 wt%, 78 wt%, 79 wt%, 80 wt%, 81 wt%, 82 wt%, 83 wt%, 84 wt.%, 85 wt.%, 86 wt.%, 87 wt.%, 88 wt.%, 89 wt.%, 90 wt.%, 91 wt.%, 92 wt .-%, 93 wt .-%, 94 wt .-% or 95 wt .-% are. In particular, the upper limit can also be at lower values, e.g. at a value of preferably 65 wt .-%, 45 wt .-%, 35 wt .-%, 30 wt .-%, 25 wt .-%, 20 wt .-%, 15 wt .-%, 10 wt. -% or 5 wt .-%. It may also be possible within the meaning of another embodiment that no builder, ie 0% by weight, is contained.

In particular, in the case of liquid detergents, according to a preferred embodiment, preferably also very little builder may be present, e.g. more than 0.1 wt .-%, more than 0.5 wt .-% or more than 1 wt .-%, but advantageously less than 30 wt .-%, preferably less than 20 wt .-%, in particular less than 10 wt .-%.

According to a further preferred embodiment, the inventive composition contains as builder in particular fatty acids, preferably saturated and / or branched fatty acids, especially having a melting point below 4O ⁰ C _{1 is} preferably less than 30 ⁰ C, and / or citric nensäure and / or citrate, preferably in amounts of, for example, from 0 to 15% by weight, and / or polyacrylates, preferably in amounts of, for example, from 0 to 15% by weight, and / or phosphonates, where the term% by weight refers in each case to the total Means relates.

If the agent according to the invention has at least substantially no halide ions, in particular no chloride ions, the amount of halide ions, in particular chloride ions, advantageously being at most 500 ppm, preferably at most 100 ppm, in particular at most 30 ppm, then a preferred embodiment is present. Because the Applicant has surprisingly found that a high halide, in particular chloride ion concentration, as may be common in conventional detergents and cleaners due to contamination of some raw materials or ingredients, especially in liquid agents to increased degradation of oxidizing agents, such as For example, peroxycarboxylic acids can lead. Thus, a reduction of the halide concentration, in particular the chloride ion concentration, lead to a reduced degradation of the oxidizing agent, for example the peroxycarboxylic acid. A low chloride ion concentration can be achieved according to the invention, for example, by the use of methylsulfate, phosphate, tosylate or cumene sulfonate compounds or by the use of low-chloride raw materials or ingredients (eg use of essentially halide-free components, eg halide-free surfactants, halide-free phosphates). phonates etc.).

In a further preferred embodiment less than 30% by weight, preferably less than 20% by weight, advantageously less than 15% by weight, more preferably less than 10% by weight, more preferably less than 5% % By weight, more preferably less than 3% by weight, more preferably less than 2% by weight, even more advantageously less than 1% by weight, most preferably less than 0, 5% by weight, in particular 0% by weight, of the fragrance substances contained are selected from those fragrances which have an aldehyde function (RCH = O) and / or a keto group (RR ¹ C = O), the wording Gew.- % refers to the total amount of fragrances contained in the middle.

If the agent is in liquid form, preferably in aqueous or nonaqueous form, which is advantageously a dispersion, preferably an emulsion or suspension, then a preferred embodiment is present. The agent may also be present as a pouch.

The invention can be e.g. liquid heavy-duty detergents with outstanding washing performance, especially in the area of bleachable stains in connection with a very appealing perfuming both in the product and on the laundry realize. The fragrance impression in the product is subject to no change even during prolonged storage and the perfuming does not show a destabilizing effect on the bleaching agent.

The agent, which is present in particular in liquid form, according to a further preferred embodiment has a pH of advantageously at most 7, in particular a pH of 3.5 to 7, preferably from 4.0 to 6.5, particularly preferably from From 4.5 to 6, very particularly preferably from about 5 to, and / or, if it is a liquid agent, it may preferably be at least one water-miscible solvent having a low dissolving power, preferably glycerol, for the peroxycarboxylic acid, in particular imidoperoxycarboxylic acid. contain.

Bleaching agents, in particular those based on peroxycarboxylic acids, such as PAP, can be stabilized relatively effectively in an acid environment, in particular at a pH of around 6. The According to a preferred embodiment possible reduction of the pH in the inventive dungsgemaßen means, preferably liquid agents, in particular liquid detergents and cleaners can be carried out for example by adding acids or acidic salts According to the invention are preferred bisulfates, bicarbonates and organic polycarboxylic acids, for example It is also possible to use the phosphonates or citrates which can be used as complexing agents as phosphonic acids or citric acid and then to adjust the desired pH by adding alkalis. The addition of ionic surfactant, for example LAS, is also possible as acid , wherein the pH can be adjusted by subsequent addition of sodium hydroxide solution

The agents of the invention, preferably (LIQUID) washing or cleaning agent, can, in a preferred embodiment contain at least one fatty acid this case are saturated and / or branched fatty acids, especially having a melting point below 3O ⁰ C, preferable in the invention In the present invention, for example Isocarb- 16 ^® Sasol be used in the inventive washing or cleaning agents

The agents according to the invention, preferably (liquid) washing or cleaning agents, may advantageously have a citric acid or citrate content. Citric acid or citrate may, for example, lead to a degradation of peroxycarboxylic acids, especially PAP. Nevertheless, it may be advantageous to use citric acid or citrates in the agent according to the invention, for example the detergent or cleaning agent (for example as builder and / or as complexing agent)

The composition according to the invention may also be of gel-like or paste-like consistency. According to a preferred embodiment, the agent is pourable, preferably it has a viscosity between 100 and 10000 mPas at a shear rate of 30 s ^-1 and a temperature of 25 ° C.

According to another preferred embodiment, the agent is present in solid form, preferably as a powder

According to a preferred embodiment of the invention, the powder is predominantly (for example, in amounts of> 50% by weight,> 60% by weight,> 70% by weight,> 80% by weight,> 90% by weight or> 95% by weight). based on the total powder) of uniform, preferably almost spherical or elliptical particles formed. The ellipsoid is similar to the ball, but longitudinal axis and transverse Axes are different. However, the powder can also consist of other embodiments of particles, the majority as well

(a) cubic (cube-shaped) or at least approximately cubic-shaped or

(b) shaped parallelepiped (e.g., cuboid) or at least approximately parallelepiped shaped or

(c) lamellar (platy and the like) or at least approximately lamellar or

(d) needle-like or fibrous-shaped, or at least approximately needle-like or fibrous, or

(e) cylindrically shaped or

(f) are strand-like or at least approximately strand-like.

According to another preferred embodiment of the invention, the inventive

In the case of solid compositions, bulk densities in the range of 200-1500 g / L.

The lower limit for the bulk density can also be set at a value of preferably 250, 300,

350, 400, 450, 500, 550, 600, 650, 700 or even 750 g / L. It is also possible that the lower limit is even higher, e.g. at 800g / L.

The upper limit for the bulk density may be at a value of preferably 1450, 1400, 1350,

1300, 1250, 1200, 1150, 1100, 1050, 1000, 950, 900, 850, 800 or 750 g / L.

It is also possible that the upper limit is even lower, e.g. at a value of preferably 700, 650, 600, 550 or 500 g / L.

When the solid agent is a compactate, available e.g. by operations such as pressing, rolling, briquetting, pelletizing, extruding, agglomerating or related compaction processes, this is a further preferred embodiment.

According to a further preferred embodiment, the agent in solid form is a shaped body, preferably a tablet or a block or a strand. In this case, multiphase or multilayer shaped bodies may be preferred. Also possible are solid pouches, e.g. Powder in the pouch.

In the case of the liquid agents, in particular liquid detergents or cleaners, according to a preferred embodiment, the content of inorganic salt, particularly preferably sodium sulfate, in the dispersion (of the liquid agent) can be selected such that at a temperature which is around 5 ^° C. , in particular to 1O ⁰ C, preferably around 15 ° C, is less than the warehouse or storage temperature (about 2O ⁰ C) of the dispersion, substantially there is a dispersion in which the aqueous phase is saturated with the inorganic salt. In this embodiment can the content of organic salt, particularly preferably sodium sulfate, are chosen such that at about O ⁰ C to 15 ⁰ C, in particular O ⁰ C to 10 ⁰ C, preferably ^{0 0} C to 5 ⁰ C, essentially one with the inorganic salt saturated dispersion is obtained. In this case, the content of inorganic salt, particularly preferably sodium sulfate, in the dispersion, 5 to 30 wt .-%, in particular 10 to 30 wt .-%, preferably 15 to 30 wt .-%, based on the total formulation.

Furthermore, according to a further preferred embodiment, the content of inorganic salt, more preferably sodium sulfate, in the agent according to the invention, preferably liquid agent, in particular liquid detergent or cleaning agent, be chosen such that the surfactants are at least substantially inactivated in the agent, in particular by salting out, ie Inducing a phase separation in a low-surfactant, continuous phase and a preferably lamellar, generally highly viscous, crystalline or liquid-crystalline surfactant-rich phase, preferably by introducing at least one sulfate compound, particularly preferably sodium sulfate. In such an embodiment, in the formulation, preferably washing or cleaning agent formulation, in particular dissolution of the organic peroxycarboxylic acid is at least substantially prevented or at least reduced. According to the invention, the term "continuous phase" is understood to mean the dispersant with the constituents or ingredients dissolved therein (for example salts, surfactants, etc.). According to the invention, the dispersant is preferably water.

The addition of, for example, sulfate according to a preferred embodiment, the surfactants, which may possibly lead to a deactivation of the oxidizing agent, are at least partially inactivated, which can be done in particular by salting out, the surfactants from the particular micellar, active form can be converted into a preferably lamellar, crystalline or liquid-crystalline form (crystal or liquid crystal formation), which is dispersed in a nearly surfactant-free continuous phase. The dispersed liquid crystal itself, which can be separated, for example, by centrifugation, should be as highly viscous as possible. The content of free or active surfactants, ie present in micellar form in the liquid agents, preferably liquid detergents and cleaners formulations or in the continuous phase of the liquid detergent formulations according to the invention may therefore according to a preferred embodiment preferably be very low, advantageously not more than 1%. According to a preferred embodiment, the concentration of an inorganic salt, particularly preferably sodium sulfate, in the agent according to the invention, preferably liquid agent, in particular liquid detergent or cleaning agent should be chosen so that in the continuous phase of the undiluted washing or cleaning agent advantageously less than 1% dissolved surfactant is present and when the temperature is lowered, especially at temperature drops to ^{0 0} C, no crystallization of the salt, preferably sulfate, takes place.

Since, in particular, nonionic surfactants can be problematic with regard to the stability of peroxycarboxylic acid in the agent according to the invention, preferably liquid agent, in particular liquid detergent or cleaning agent, the agents according to the invention may preferably have a correspondingly adapted or optimized surfactant ratio. The content of alkyl polyglycol ethers may preferably be as low as possible. In a preferred embodiment, the content of nonionic surfactants even approaches zero. Corresponding formulations may be used as surfactants, e.g. contain only (linear) alkylbenzenesulfonates and / or (secondary) alkanesulfonates and can show excellent stability of the bleaching agent. According to a further preferred embodiment, the product according to the invention, in particular washing, care or cleaning agent, at least one, preferably more, active components, in particular washing, care and / or cleaning active components, advantageously selected from the group comprising anionic surfactants, cationic surfactants, amphoteric surfactants, nonionic surfactants, acidifiers, alkalizing agents, anti-wrinkle compounds, antibacterial agents, antioxidants, anti redeposition agents, antistatics, builders, bleaches, bleach activators, bleach stabilizers, bleach catalysts, ironing aids, cobuilders, anti-shrinkage agents, electrolytes, Enzymes, colorants, colorants, dyes, color transfer inhibitors, fluorescers, fungicides, germicides, odor-complexing substances, adjuvants, hydrotropes, rinse aids, complexing agents, preservatives, corrosion inhibitors, optical brighteners , Perfume carriers, pearlescers, pH adjusters, repellents and impregnating agents, polymers, swelling and anti-slip agents, foam inhibitors, phyllosilicates, dirt repellents, silver protectants, silicone oils, UV protectants, viscosity regulators, thickeners, discoloration inhibitors, grayness inhibitors, vitamins and / or Fabric softener. In a further preferred embodiment, the agent according to the invention contains one or more skin-care and / or skin-protecting and / or skin-healing active substances.

Skin-care active substances are all those active substances which give the skin a sensory and / or cosmetic advantage. Skin-care active substances are preferably selected from the following substances: a) waxes such as, for example, carnauba, spermaceti, beeswax, lanolin and / or derivatives thereof and others. b) Hydrophobic plant extracts c) Hydrocarbons such as squalene and / or squalane d) Higher fatty acids, preferably those having at least 12 carbon atoms, for example lauric acid, stearic acid, behenic acid, myristic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid, isostearic acid and / or multiple times unsaturated fatty acids and others. e) Higher fatty alcohols, preferably those having at least 12 carbon atoms, for example lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol, cholesterol and / or 2-hexadecanol and other f) esters, preferably such as Cetyloctanoat, lauryl lactate, Myπstyllactat, Cetyllactat, Isopropylmynstat , Myπstyl myristate, isopropyl palmitate, isopropyl adipate, butyl stearate, decyl oleate, cholesterol isoleostearate, glycerol monostearate, glyceryl distearate, glycerol stearate, alkyl lactate, alkyl citrate and / or alkyl tartrate and other g) lipids such as cholesterol, ceramides and / or sucrose esters and other h) vitamins such as for example, vitamins A and E, vitamin VI esters, including vitamin C.

Alkyl esters and other ι) sunscreens j) phospholipids k) derivatives of alpha-hydroxy acids I) fragrances m) germicides for cosmetic use, both synthetic and, for example, salicylic acid and / or other as well as natural ones such as neem oil and / or other n) Silicones o) and mixtures of any of the aforementioned components

Preferred ingredients of the compositions according to the invention are described in more detail below. Anionic surfactants are preferably present in the products according to the invention. Suitable anionic surfactants are, for example, those of the sulfonate and sulfates type. The surfactants of the sulfonate type are preferably C ₉ . _13- Alkylbenzolsulfonate, olefinsulfonates, ie mixtures of alkene and hydroxyalkanesulfonates and disulfonates, as obtained for example from C ₁₂ -i ₈ -Monoolefιnen with terminal or internal double bond by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation Also suitable are alkanesulfonates which are obtained from C ₁₂ .i ₈ -alkanes, for example by sulfochlorination or sulfoxidation with subsequent hydrolysis or neutralization. Likewise, the esters of α-sulfofatty acids (ester sulfonates), for example the α-sulfonated methyl esters of hydrogenated coconut, palm kernel or Taigfettsäuren suitable

Other suitable anionic surfactants are sulfonated fatty acid glycine esters. Fatty acid glycylesters are understood as meaning the mono-, di- and diesters and mixtures thereof, as in the preparation by esterification of a monoglycerine with 1 to 3 moles of fatty acid or in the transesterification of triglycerides with 0.3 to 2 mol of glycene are obtained. Preferred sulfated fatty acid glycine esters are the sulfonation products of saturated fatty acids having 6 to 22 carbon atoms, for example caproic acid, caprylic acid, capnic acid, myristic acid, lauric acid, palmitic acid, stearic acid or behenic acid Alk (en) ylsulfates are the alkali metal salts and in particular the sodium salts of the sulfuric monoesters of C ₁₂ -C ₁₈ fatty alcohols, for example coconut fatty alcohol, tallow fatty alcohol, lauryl, myriphenyl, cetyl or stearyl alcohol or the C ₁₀ -C ₂₀ Oxyalcohols and those half-esters of secondary alcohols of these chain lengths are also preferred. Alk (en) ylsulfates of said chain length which contain a synthetic, petrochemical-based straight-chain alkyl radical which has an analogous degradation behavior as the adequate compounds based on oleochemicals Raw Materials Of washing technology interest, the C ₁₂ -C ₁₆ alkyl sulfates and C ₁₂ -C ₁₅ alkyl sulfates and C ₄ -C ₁ s alkyl sulfates are preferred. Also 2,3-alkyl sulfates, as commercial products of the Shell Oil Company under the name DAN ^® can be obtained, are suitable anionic surfactants

Also, the sulfuric acid monoesters of straight-chain or branched C ₇ ethoxylated with 1 to 6 moles of ethylene oxide. ₂₁ -alcohols, such as 2-methyl-branched C _{9 11} alcohols having an average of 3.5 moles of ethylene oxide (EO) or C ₁₂ . _18- fatty alcohols with 1 to 4 EO, are suitable They are particularly in detergents due to their high foaming behavior preferably only in relatively small amounts, for example in amounts of 1 to 5 wt -%, used

Another class of anionic surfactants is the class of ether carboxylic acids obtainable by reaction of fatty alcohol ethoxylates with sodium chloroacetate in the presence of basic catalysts. They have the general formula R ¹⁰ O- (CH ₂ -CH ₂ -O) _P -CH ₂ -COOH with R ¹⁰ = C 1 -C ₁₈ and p = 0.1 to 20 ether carboxylic acids are water hardness insensitive and have excellent surfactant properties

Suitable anionic surfactants are, for example, the partial esters of di- or polyhydroxyalkanes, mono- and disaccharides, polyethylene glycols with the ene adducts of maleic anhydride and at least monounsaturated carboxylic acids having a chain length of from 10 to 25 carbon atoms with an acid number of from 10 to 140

Preferred anionic surfactants have, in addition to an unbranched or branched, saturated or unsaturated, aliphatic or aromatic, acyclic or cyan, optionally alkoxylated alkyl radical having 4 to 28, preferably 6 to 20, especially 8 to 18, particularly preferably 10 to 16, extremely preferred 12 to 14 carbon atoms, two or more anionic, especially two, acid groups, preferably carboxylate, sulfonate and / or sulfate groups, in particular a carboxylate and a sulfate group, examples of these compounds are the α-sulfo fatty acid salts, the acylglutamates, the Monoglycene disulfates and the alkyl ethers of Glycenndisul- fats and in particular the below-described monoester sulfosuccinates Particularly preferred anionic surfactants are the sulfosuccinates, sulfosuccinamates and sulfosuccinamides, especially sulfosuccinates and sulfosuccinamates, most preferably sulfosuccinates. The sulfosuccinates are the salts of the mono- and di-esters of sulfosuccinic acid HOOCCH (SO ₃ H) CH ₂ COOH, while the sulfosuccinamates include the salts of the monoamides of sulfosuccinic acid and the sulfosuccinamides the salts of the diamides of Sulfosuccinic acid understands.

The salts are preferably alkali metal salts, ammonium salts and mono-, di- or trialkanolammonium salts, for example mono-, di- or triethanolammonium salts, in particular lithium, sodium, potassium or ammonium salts, particularly preferably sodium or ammonium salts , most preferably sodium salts.

In the sulfosuccinates, one or both carboxyl groups of the sulfosuccinic acid is preferably with one or two identical or different unbranched or branched, saturated or unsaturated, acyclic or cyclic, optionally alkoxylated alcohols having 4 to 22, preferably 6 to 20, in particular 8 to 18 , more preferably 10 to 16, most preferably 12 to 14 carbon atoms esterified. Particularly preferred are the esters of unbranched and / or saturated and / or acyclic and / or alkoxylated alcohols, in particular unbranched, saturated fatty alcohols and / or unbranched, saturated, with ethylene and / or propylene oxide, preferably ethylene oxide, alkoxylated fatty alcohols having a degree of alkoxylation of 1 to 20, preferably 1 to 15, in particular 1 to 10, more preferably 1 to 6, most preferably 1 to 4. The monoesters are preferred in the context of the present invention over the diesters. A particularly preferred sulfosuccinate is Sulfobernsteinsäurelaurylpolyglykolester-di-Na- trium salt (lauryl EO sulfosuccinate, di-sodium salt; INCI Disodium Laureth Sulfosuccinate), for example, as Tego ^® sulfosuccinate F 30 (Goldschmidt) with a sulfosuccinate of 30 weight .-% is commercially available.

In the sulfosuccinamates or sulfosuccinamides, one or both carboxyl groups of the sulfosuccinic acid forms preferably with a primary or secondary amine having one or two identical or different, unbranched or branched, saturated or unsaturated, acyclic or cyclic, optionally alkoxylated alkyl radicals with 4 to 22, preferably 6 to 20, in particular 8 to 18, more preferably 10 to 16, most preferably 12 to 14 carbon atoms carries, a carboxylic acid amide. Particular preference is given to unbranched and / or saturated and / or acyclic alkyl radicals, in particular unbranched, saturated fatty alkyl radicals.

Also suitable are, for example, the following sulfosuccinates and sulfosuccinamates designated according to INCI, which are described in more detail in the International Cosmetic Ingredient Dictionary and Handbook: Ammonium Dinonyl Sulfosuccinates, Ammonium Lauryl Sulfosuccinates, Diammo- Dimethicone Copolyol Sulfosuccinate, Diammonium Lauramido-MEA Sulfosuccinate, Diamonium Lauryl Sulfosuccinate, Diammonium Oleamido PEG-2 Sulfosuccinate, Diamyl Sodium Sulfosuccinate, Dicapryl Sodium Sulfosuccinate, Dicyclohexyl Sodium Sulfosuccinate, Diheptyl Sodium Sulfosuccinate, Dihexyl Sodium Sulfosuccinate, Diisobutyl Sodium Sulfosuccinate, Dioctyl Sodium Sulfosuccinates, disodium cetearyl sulfosuccinates, disodium cocamido MEA sulfosuccinates, disodium cocamido glucosides sulfosuccinates, disodium cocoyl butyl gluceth-10 sulfosuccinates, disodium C 12-15 pareth sulfosuccinates, disodium deceth-5 sulfosuccinates, disodium deceth-6 sulfosuccinates, disodium dihydroxyethyl Sulfosuccinyl undecylenates, disodium dimethicone copolyol sulfosuccinates, disodium hydrogenated cottonseed glycerides sulfosuccinates, disodium isodecyl sulfosuccinates, disodium isostearamido MEA sulfosuccinates, disodium isostearamido MIPA sulfosuccinates, disodium isostearyl sulfosuccinates, disodium laneth-5 sulfos uccinate, disodium lauramido MEA sulfosuccinates, disodium lauramido PEG-2 sulfosuccinates, disodium lauramido PEG-5 sulfosuccinates, disodium laureth-6 sulfosuccinates, disodium laureth-9 sulfosuccinates, disodium laureth-12 sulfosuccinates, disodium lauryl sulfosuccinates, disodium myristic amido MEA- Sulfosuccinates, disodium nonoxynol-10 sulfosuccinates, disodium oleamido MEA sulfosuccinates, disodium oleamido MIPA sulfosuccinates, disodium oleamido PEG-2 sulfosuccinates, disodium oleth-3 sulfosuccinates, disodium oleyl sulfosuccinates, disodium palmitamido PEG-2 sulfosuccinates, disodium palmitoleamido PEG-2 sulfosuccinates , Disodium PEG-4 Cocamido MIPA Sulfosuccinate, Disodium PEG-5 Lauryl Citrate Sulfosuccinate, Disodium PEG-8 Palm Glycerides Sulfosuccinate, Disodium Ricinoleamido MEA Sulfosuccinate, Disodium Sitostereth-14 Sulfosuccinate, Disodium Stearamido MEA Sulfosuccinate, Disodium Stearyl Sulfosuccinamate, Disodium Stearyl Sulfosuccinate , Disodium Tallamido MEA Sulfosuccinate, Disodium Valley lowamido MEA sulfosuccinates, disodium tallow sulfosuccinamates, disodium tridecyl sulfosuccinates, disodium undecylenamido MEA sulfosuccinates, disodium undecylenamido PEG-2 sulfosuccinates, disodium wheat germamido MEA sulfosuccinates, disodium wheat germamido PEG-2 sulfosuccinates, di-TEA-Ole-amido PEG -2 Sulfosuccinates, Ditridecyl Sodium Sulfosuccinate, Sodium Bisglycol Ricinosulfosuccinate, Sodium / MEA Laureth-2 Sulfosuccinate and Tetrasodium Dicarboxyethyl Stearyl Sulfosuccinamate. Yet another suitable sulfosuccinamate is disodium C ₁₆ -i ₈ -alkoxy-propylene sulfosuccinamate.

The content of anionic surfactants in the composition according to the invention, preferably of the anionic surfactants mentioned, can vary within wide ranges, depending on the purpose of the agent in question. Thus, an agent according to the invention may contain very large amounts of anionic surfactant, preferably up to an order of magnitude of up to 40, 50 or 60% by weight or more. Likewise, an agent according to the invention may contain only very small amounts of anionic surfactant, for example less than 15 or 10% by weight or less than 5% by weight or even less. However, anionic surfactants may advantageously be present in the compositions according to the invention in amounts of from 2 to 35% by weight and in particular from 5 to 30% by weight, with concentrations above 10% by weight and even above 15% by weight may find particular preference. According to a preferred embodiment, the product according to the invention contains anionic surfactants, preferably in amounts of at least 0.1% by weight.

In addition to the anionic surfactants mentioned, but also independently of these, soaps may be present in the compositions according to the invention. Particularly suitable are saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid, and in particular of natural fatty acids, e.g. Coconut, palm kernel or tallow fatty acids, derived soap mixtures. The content of the soap soaps, independently of other anionic surfactants, is preferably not more than 3% by weight, and more preferably 0.5 to 2.5% by weight.

The anionic surfactants and soaps may be in the form of their sodium, potassium or ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine. Preferably, they are in the form of their sodium or potassium salts, especially in the form of the sodium salts. Anionic surfactants and soaps may also be prepared in situ by incorporating into the spray-dried composition the anionic surfactant acids and optionally fatty acids which are then neutralized by the alkali carriers in the spray-dried composition.

Advantageously, nonionic surfactants may also be included in the compositions of the invention, both in solid and in liquid compositions. For example, their content may be up to 2 or 3 or 5 wt .-%. It may also contain greater amounts of nonionic surfactant, for example, up to 5 wt% or 10 wt% or 15 wt% or 20 wt% or 30 wt% or even more if it is is appropriate. Useful lower limits may be at values of 1, 2, 3 or 4 wt .-%.

Preferably, however, the nonionic surfactants are in relatively large amounts, ie up to 50% by weight, advantageously from 0.1 to 40% by weight, particularly preferably from 0.5 to 30 and in particular from 2 to 25% by weight, in each case based on the total agent included. According to a preferred embodiment, the product according to the invention contains nonionic surfactants, preferably in amounts of at least 0.1% by weight.

Advantageously, all known from the prior art nonionic surfactants may be included in the inventive compositions. Preferred nonionic surfactants are presented below.

The agents according to the invention, in particular cleaning, care and washing agents, can preferably also contain cationic surfactants. Suitable cationic surfactants are, for example, surface-active quaternary compounds, in particular having an ammonium, sulfonium, phosphonium, iodonium or arsonium group. Through the use of quaternary surface-active compounds with antimicrobial action, the agent can be designed with an antimicrobial effect or its possibly existing antimicrobial effect due to other ingredients can be improved.

Particularly preferred cationic surfactants are the quaternary, partially antimicrobial ammonium compounds (QAV, INCI quaternary ammonium compounds) according to the general formula (R ') (R ") (R"') (R ^IV ) N ⁺ X ^" , in which R ¹ to R ^ιv identical or different dz _Σ- alkyl radicals ¹ C _7-28 - aralkyl radicals or heterocyclic radicals, wherein two or in the case of an aromatic inclusion as in pyridine even three radicals together with the nitrogen atom, the heterocycle, for example a pyridinium or Imidazoliniumverbindung , form, represent and X ^"are halide ions, sulfate ions, hydroxide ions or similar anions. For optimum antimicrobial activity, preferably at least one of the radicals has a chain length of 8 to 18, in particular 12 to 16, carbon atoms.

QACs are prepared by reacting tertiary amines with alkylating agents, e.g. Methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also ethylene oxide produced. The alkylation of tertiary amines with a long alkyl radical and two methyl groups succeeds particularly easily, and the quaternization of tertiary amines with two long radicals and one methyl group can be carried out with the aid of methyl chloride under mild conditions. Amines which have three long alkyl radicals or hydroxy-substituted alkyl radicals are less reactive and are preferably quaternized with dimethyl sulfate.

Suitable QACs are, for example, benzalkonium chloride (N-alkyl-N, N-dimethylbenzylammonium chloride, CAS No. 8001-54-5), benzalkone B (mp-dichlorobenzyl-dimethyl-C 1-4 -alkylammonium chloride, CAS No. 58390-78 -6), benzoxonium chloride (benzyldodecyl-bis- (2-hydroxyethyl) -ammonium chloride), cetrimonium bromide (N-hexadecyl-N, N-trimethyl-ammonium bromide, CAS No. 57-09-0), benzotrium chloride (N, N-dimethyl-N- [2- [2- [p- (1,1,3,3-tetramethylbutyl) phenoxy] ethoxy] ethyl] benzylammonium chloride, CAS No. 121-54-0), Dialkyldimethylammonium chlorides such as di-n-decyldimethylammonium chloride (CAS No. 7173-51-5-5), didecyldimethylammonium bromide (CAS No. 2390-68-3), dioctyldimethylammoniumchloric, 1-cetylpyridinium chloride (CAS No 123-03-5) and thiazoline iodide (CAS No. 15764-48-1) and mixtures thereof. Preferred QACs are the benzalkonium chlorides having C ₈ -C ₁₈ -alkyl radicals, in particular C 1 -C -acyl-benzyl-dimethylammonium chloride. A particularly preferred QAC Kokospentaethoxymethylammoniummethosulfat (INCI PEG-5 Cocomonium Methosulfate; Rewoquat CPEM ^®). In order to avoid possible incompatibilities of the antimicrobial cationic surfactants with anionic surfactants optionally present in the composition according to the invention, as far as possible anionic surfactant-compatible and / or optionally cationic surfactant are used or, in a particular embodiment of the invention, cationic surfactants are completely dispensed with

Further below, in particular in connection with conditioning agents and plasticizers, further cationic surfactants, including quaternary ammonium compounds, are described. These too may preferably be present in the compositions according to the invention

The compositions according to the invention, such as preferably cleaning, care and washing agents, may contain one or more cationic surfactants, advantageously in amounts, based on the total composition, of from 0 to 30% by weight, more preferably from 0 to 20% by weight, preferably 0.01 to 10% by weight, in particular 0.1 to 5% by weight Suitable minimum values may also be present at 0.5, 1, 2 or 3% by weight. According to a preferred embodiment, the product according to the invention contains cationic surfactants, preferably in quantities of at least 0.1% by weight

Likewise, the agents according to the invention, such as, preferably, cleaning agents, care agents and detergents, may also contain amphoteric surfactants. These will be described in more detail below, in particular in connection with conditioning agents and plasticizers

The agents according to the invention, such as cleansing, care and washing agents, may contain one or more amphoteric surfactants, advantageously in amounts, based on the total composition, of from 0 to 30% by weight, more preferably greater than 0 to 20% by weight, preferably 0 , 01 to 10% by weight, in particular 0.1 to 5% by weight

Further ingredients of the compositions according to the invention may be inorganic and organic builders. The inorganic builders include water-insoluble or non-water-soluble ingredients, such as aluminosilicates and, in particular, zeolites

In a preferred embodiment, the agent according to the invention contains no phosphate and / or no zeolite. However, it is also possible for the agent to comprise Zeohth. It may then be preferred that this zeohth content, based on the total weight of the agent, is less than 5% by weight, preferably not more than 4% by weight, not more than 3% by weight or not more than 2% by weight

However, it can also advantageously be provided that the agent according to the invention has a zeolite content of at least 10% by weight, for example at least 15% by weight or at least 20% by weight or at least 30% by weight or even beyond, for example at least 50% by weight. % having.

Soluble builders may preferably contain the agent according to the invention in amounts of 10% by weight to 30% by weight, preferably 15% by weight to 25% by weight and particularly preferably 18% by weight to 20% by weight on the total weight of the agent, with sodium carbonate as the soluble builder being particularly preferred. However, it can also be advantageously provided that the agent according to the invention contains less than 10% by weight, for example less than 5% by weight, of soluble builder.

Useful finely crystalline, synthetic and bound water-containing zeolite is preferably zeolite A and / or P. As zeolite P, for example, zeolite MAP ^(R) (commercial product of Crosfield) is particularly preferred. Also suitable however are zeolite X and mixtures of A, X and / or P. Of particular interest is a co-crystallized sodium / potassium aluminum silicate of zeolite A and zeolite X, which as VEGOBOND AX ^® (a product of Condea Augusta SpA) Trade is available. This product is described below. The zeolite can be used as a spray-dried powder or else as undried, still moist, stabilized suspension of its preparation. In the event that the zeolite is used as a suspension, it may contain minor additions of nonionic surfactants as stabilizers, for example 1 to 3 wt .-%, based on zeolite, of ethoxylated C ₁₂ -C ₁₈ -FeK- alcohols with 2 to 5 ethylene oxide groups, C ₁₂ -C ₁₄ fatty alcohols having 4 to 5 ethylene oxide groups or ethoxylated isotridecanols. Suitable zeolites have an average particle size of preferably less than 10 μm (volume distribution, measuring method: Coulter Counter) and preferably contain 18 to 22% by weight, in particular 20 to 22% by weight, of bound water.

Other particularly suitable zeolites are faujasite-type zeolites. Together with the zeolites X and Y, the mineral faujasite belongs to the faujasite types within the zeolite structure group 4, which are characterized by the double-six-membered subunit D6R. In addition to the faujasite types mentioned, the zeolite structural group 4 also includes the minerals chabazite and gmelinite as well as the synthetic zeolites R (chabazite type), S (gmelinite type), L and ZK-5. The latter two synthetic zeolites have no mineral analogs.

Faujasite-type zeolites are composed of β-cages linked by tetrahedral D6R subunits, with the β-cages resembling the carbon atoms in the diamond. The three-dimensional network of the faujasite-type zeolites suitable according to the invention has pores of 2.2 and 7.4 Å, and the unit cell also contains 8 cavities with a diameter of approximately 13 A and can be represented by the formula Na ₈₆ [(Al ₂ O) ₈₆ (SiO 2) ₁ o6] 264 H ₂ O describe. The network of zeolite X contains a void volume of about 50%, based on the dehydrated crystal, which represents the largest void space of all known zeolites (zeolite Y: approx. 48% void volume, faujasite: approx. 47% void volume).

In the context of the present invention, the term "faujasite type zeolite" denotes all three zeolites which form the faujasite subgroup of the zeolite structure group 4. In addition to zeolite X, zeolite Y and faujasite and mixtures of these compounds are also suitable according to the invention, with pure zeolite X being preferred.

Mixtures or cocrystallizates of faujasite-type zeolites with other zeolites, which need not necessarily belong to the zeolite structure group 4, are also suitable according to the invention, with preferably at least 50% by weight of the faujasite-type zeolites being suitable.

The suitable aluminum silicates are commercially available and the methods for their preparation are described in standard monographs.

Examples of commercially available X-type zeolites can be described by the following formulas:

Na ₈₆ [(AIO ₂ ) 86 (SiO ₂ ) i06] ^" x H ₂ O, Kββ1 (Alθ2) Bβ (SiO ₂ ) ₁₀ β] ^' x H ₂ O, Ca 4oNa 6 [(AlO ₂ ) 8 ₆ (SiO ₂ ) ₁₀ 6] x H ₂ O, Sr ₂₁ Ba ₂₂ [(AIO ₂ ) 86 (SiO ₂ ) ₁₀ 6] ^' x H ₂ O, in which x can assume values of greater than 0 to 276. These zeolites have pore sizes of 8, 0 to 8.4 A on.

Also suitable, for example, is zeolite A-LSX, which corresponds to a cocrystal of zeolite X and zeolite A and in its anhydrous form has the formula (M _{2 / n} O + M'2 _{/ n} O) Al ₂ O ₃ zSiO ₂ , wherein M and M 'may be alkali or alkaline earth metals and z is a number from 2.1 to 2.6. Commercially available this product is under the brand name VEGOBOND AX by the company CONDEA Augusta SpA

Y-type zeolites are also commercially available and can be obtained, for example, by the formulas

Na ₅₆ [(AIO ₂ ) ₅₆ (SiO ₂ ) ₁₃₆ ] ^• x H ₂ O, K ₅₆ [(AIO ₂ ) ₅₆ (SiO ₂ ) ₁₃₆ ] ^• x H ₂ O, where x is numbers greater than 0 to 276 stands, describe. These zeolites have pore sizes of 8.0 Å.

The particle sizes of the suitable zeolites are advantageously in the range from 0.1 μm to 100 μm, preferably from 0.5 μm to 50 μm and in particular from 1 μm to 30 μm, in each case measured by standard particle size determination methods. In a preferred embodiment of the invention, all of the inorganic constituents contained should preferably be water-soluble. Therefore, builders other than the zeolites mentioned are used in these embodiments.

Further suitable builder substances are polyacetals which can be obtained by reacting dialdehydes with polyolcarboxylic acids which have 5 to 7 C atoms and at least 3 hydroxyl groups. Preferred polyacetals are obtained from dialdehydes such as glyoxal, glutaraldehyde, terephthalaldehyde and mixtures thereof and from polyol carboxylic acids such as gluconic acid and / or glucoheptonic acid.

Further suitable organic builder substances are dextrins, for example oligomers or polymers of carbohydrates, which can be obtained by partial hydrolysis of starches. The hydrolysis can be carried out by customary, for example acid or enzyme catalyzed processes. Preferably, it is hydrolysis products having average molecular weights in the range of 400 to 500,000 g / mol. In this case, a polysaccharide with a dextrose equivalent (DE) in the range from 0.5 to 40, in particular from 2 to 30 is preferred, DE being a common measure of the reducing action of a polysaccharide compared to dextrose, which has a DE of 100 , is. Usable are both maltodextrins with a DE between 3 and 20 and dry glucose syrups with a DE between 20 and 37 and so-called yellow dextrins and white dextrins with higher molecular weights in the range from 2000 to 30,000 g / mol. A preferred dextrin is described in British Patent Application 94 19 091. The oxidized derivatives of such dextrins are their reaction products with oxidizing agents which are capable of oxidizing at least one alcohol function of the saccharide ring to the carboxylic acid function.

Oxydisuccinates and other derivatives of disuccinates, preferably ethylenediamine disuccinate, are further suitable co-builders. Ethylenediamine-N, N ^{'-di-succinate} (EDDS) is preferably in the form of its sodium or magnesium salts. Also preferred in this context are glycerol disuccinates and glycerol trisuccinates. Suitable amounts are, for example, 3 to 15 wt .-%, based on the total agent.

Other useful organic cobuilders are, for example, acetylated hydroxycarboxylic acids or their salts, which may optionally also be present in lactone form and which contain at least 4 carbon atoms and at least one hydroxyl group and a maximum of two acid groups.

Another substance class with co-builder properties are the phosphonates. these are in particular hydroxyalkane or aminoalkanephosphonates. Among the hydroxyalkane phosphonates, 1-hydroxyethane-1,1-diphosphonate (HEDP) is of particular importance as a co-builder. It is preferably used as the sodium salt, the disodium salt neutral and the tetrasodium salt alkaline (pH 9). Preferred aminoalkane phosphonates are ethylenediamine tetramethylene phosphonate (EDTMP), diethylene triamine pentamethylene phosphonate (DTPMP) and their higher homologs. They are preferably used in the form of the neutral-reacting sodium salts, for example as the hexasodium salt of EDTMP or as the hepta- and octa-sodium salt of DTPMP. The builder used here is preferably HEDP from the class of phosphonates. The aminoalkanephosphonates also have a pronounced heavy metal binding capacity. Accordingly, in particular if the agents also contain bleach, it may be preferable to use aminoalkanephosphonates, in particular DTPMP, or to use mixtures of the phosphonates mentioned.

In cases in which a phosphate content is tolerated, it is also possible to use phosphates, in particular pentasodium triphosphate, optionally also pyrophosphates and orthophosphates, which act primarily as precipitants for calcium salts. Phosphates are predominantly used in automatic dishwasher detergents, but in some cases also in detergents. Alkali metal phosphates is the summary term for the alkali metal (especially sodium and potassium) salts of various phosphoric acids, in which one can distinguish metaphosphoric acids (HPO ₃ ), and orthophosphoric H ₃ PO _{4 in} addition to high molecular weight representatives. The phosphates combine several advantages: they act as alkali carriers, prevent lime deposits on machine parts or lime incrustations in fabrics and also contribute to the cleaning performance.

Sodium dihydrogen phosphate, NaH ₂ PO ₄ , exists as a dihydrate (density 1, 91 like ^'3 , melting point 60 °) and monohydrate (density 2.04 like ^{' 3} ). Both salts are white powders which are very soluble in water and which lose the water of crystallization on heating and at 200 ° C into the weak acid diphosphate (disodium hydrogen diphosphate, Na ₂ H ₂ PaO ₇ ), at higher temperature in sodium trimetaphosphate (Na ₃ P ₃ O ₉ ) and Maddrell's salt (see below). NaH ₂ PO _{4 is} acidic; It arises when phosphoric acid is adjusted to a pH of 4.5 with sodium hydroxide solution and the mash is sprayed. Potassium dihydrogen phosphate (potassium phosphate primary or monobasic, potassium bisphosphate, KDP), KH ₂ PO ₄ , is a white salt of density 2.33 ^"3 , has a melting point of 253 ° [decomposition to form potassium polyphosphate (KPO ₃ ) _X ] and is easily soluble in water.

Disodium hydrogen phosphate (secondary sodium phosphate), Na ₂ HPO ₄ , is a colorless, very slightly water-soluble crystalline salt. It exists anhydrous and with 2 mol. (Density 2.066 like ^"3 , water loss at 95 °), 7 mol. (Density 1, 68 like ^'3 , melting point 48 ° with loss of 5 H ₂ O) and 12 mol. Water (density 1, 52 like ^'3 , melting point 35 ° with loss of 5 H ₂ O), becomes anhydrous at 100 ° and on more intense heating in the diphosphate Na ₄ P ₂ O ₇ over. Disodium hydrogen phos- phate is prepared by neutralization of phosphoric acid with soda solution using phenolphthalein as an indicator. Di-potassium hydrogen phosphate (secondary or dibasic potassium phosphate), K ₂ HPO ₄ , is an amorphous, white salt that is readily soluble in water.

Trisodium phosphate, tertiary sodium phosphate, Na ₃ PO _4, colorless crystals, as a hydrate Dodecahy- a density of 1.62 liked ^"3 and a melting point of 73-76 ⁰ C (decomposition), Decahy- hydrate (corresponding to 19-20 % P ₂ O ₅ ) has a melting point of 10O ⁰ C and in anhydrous form (corresponding to 39-40% P ₂ O ₅ ) has a density of 2.536 like ^"3 . Trisodium phosphate is readily soluble in water under alkaline reaction and is prepared by evaporation of a solution of exactly 1 mole of disodium phosphate and 1 mole of NaOH. Tripotassium phosphate (tertiary or tribasic potassium phosphate), K ₃ PO ₄ , is a white, deliquescent, granular powder with a density of 2.56 ^'3 , has a melting point of 1340 ° and is readily soluble in water with an alkaline reaction. It arises, for example, when heating Thomasschlacke with coal and potassium sulfate. Despite the higher price, the more soluble, therefore highly effective, potassium phosphates are often preferred over the corresponding sodium compounds in the detergent industry.

Tetrasodium diphosphate (sodium pyrophosphate), Na ₄ P ₂ O ₇ , exists in anhydrous form (density 2.534 ^'3 , melting point 988 °, also indicated 880 °) and as decahydrate (density 1, 815-1, 836 like ^{' 3} , melting point 94 ° with loss of water). Both substances are colorless crystals which are soluble in water with an alkaline reaction. Na ₄ P ₂ O ₇ is formed on heating of disodium phosphate to> 200 ° or by reacting phosphoric acid with soda in a stoichiometric ratio and dewatering the solution by spraying. The decahydrate complexes heavy metal salts and hardness agents and therefore reduces the hardness of the water. Potassium diphosphate (potassium pyrophosphate), K ₄ P ₂ O ₇ , exists in the form of the trihydrate and is a colorless, hygroscopic powder with a density of 2.33% ^'3 , which is soluble in water, the pH being 1% Solution at 25 ° 10.4.

Condensation of the NaH ₂ PO ₄ or of the KH ₂ PO ₄ gives rise to relatively high molecular weight sodium and potassium phosphates, in which cyclic representatives, the sodium or potassium metaphosphates and chain-type, the sodium or potassium polyphosphates, can be distinguished. In particular, for the latter are a variety of names in use: melting or annealing phosphates, Graham's salt, Kurrolsches and Maddrell's salt. All higher sodium and potassium phosphates are collectively referred to as condensed phosphates.

The technically important pentasodium triphosphate, Na ₅ P ₃ Oi ₀ (sodium tripolyphosphate), is an anhydrous or with 6 H ₂ O crystallizing, non-hygroscopic, white, water-soluble salt of general formula NaO- [P (O) (ONa) -O] _n -Na where n = 3. In 10O g of water dissolve at room temperature about 17 g, at 60 ° about 20 g, at 100 ° about 32 g of the salt water-free salt; after two hours of heating the solution to 100 ° caused by hydrolysis about 8% orthophosphate and 15% diphosphate. In the preparation of pentasodium triphosphate, phosphoric acid is reacted with soda solution or sodium hydroxide solution in a stoichiometric ratio and the solution is dehydrated by spraying. Similar to Graham's salt and sodium diphosphate, pentasodium triphosphate dissolves many insoluble metal compounds (including lime soaps, etc.). Pentakaliumtriphos-phat, K ₅ P ₃ O ₁₀ (potassium tripolyphosphate), for example, in the form of a 50% by weight solution (> 23% P ₂ O ₅ , 25% K ₂ O) in the trade. The potassium polyphosphates are widely used in the washing and cleaning industry. Furthermore, there are also sodium potassium tripolyphosphates, which can also be used in the context of the present invention. These arise, for example, when hydrolyzed sodium trimetaphosphate with KOH:

(NaPO ₃ ) ₃ + 2 KOH -> Na ₃ K ₂ P ₃ O ₁₀ + H ₂ O

These are used according to the invention exactly as sodium tripolyphosphate, potassium tripolyphosphate or mixtures of these two; Mixtures of sodium tripolyphosphate and sodium potassium tripolyphosphate or mixtures of potassium tripolyphosphate and sodium potassium tripolyphosphate or mixtures of sodium tripolyphosphate and potassium tripolyphosphate and sodium potassium tripolyphosphate can also be used according to the invention.

In a preferred embodiment of the invention, in particular carbonates and silicates are used as inorganic builder substances.

Particularly noteworthy here are crystalline, layered sodium silicates of the general formula NaMSi _x 0 _{2x + 1} yH ₂ O, where M is sodium or hydrogen, x is a number from 1, 6 to 4, preferably 1, 9 to 4.0 and y is one Number is from 0 to 20 and preferred values for x are 2, 3 or 4. However, since such crystalline silicates at least partially lose their crystalline structure in a spray-drying process, crystalline silicates are preferably subsequently added to the direct or post-treated spray-drying product. Preferred crystalline layer silicates of the formula given are those in which M is sodium and x is 2 or

3 accepts. In particular, both β- and δ-sodium disilicates Na ₂ Si ₂ O ₅ yH ₂ O are preferred. Such compounds are commercially available, for example, under the name ^SKS® (from Clariant). Thus, it is mainly SKS-6 ^® is a δ-sodium di-silicate having the formula

Na ₂ Si ₂ O _S yH ₂ O, SKS-7 ^® is predominantly a beta-sodium disilicate. Reaction with acids (eg citric acid or carbonic acid) produces kanemite from the δ-sodium disilicate

NaHSi ₂ O ₅ yH ₂ O, commercially available under the names SKS- ^9® or SKS- ^10® (from Clariant). It may also be advantageous to use chemical modifications of these phyllosilicates. So can For example, the alkalinity of the layered silicates are suitably influenced. Phyllosilicates doped with phosphate or with carbonate have altered crystal morphologies in comparison with the δ-sodium disilicate, dissolve more rapidly and show an increased calcium binding capacity in comparison to δ-sodium disilicate. Thus, phyllosilicates of the general empirical formula x Na ₂ O • y SiO ₂ • z P ₂ O ₅ in which the ratio x to y is a number 0.35 to 0.6, the ratio x to z a number of 1.75 to 1200 and the ratio y to z of a number of 4 to 2800 is known. The solubility of the layered silicates can also be increased by using particularly finely divided layered silicates. Also compounds from the crystalline layer silicates with other ingredients can be used. In particular, compounds with cellulose derivatives which have advantages in the disintegrating action, as well as compounds with polycarboxylates, for example citric acid, or polymeric polycarboxylates, for example copolymers of acrylic acid, may be mentioned.

The preferred builder substances also include amorphous sodium silicates having a modulus Na ₂ O: SiO _{2 of} from 1: 2 to 1: 3.3, preferably from 1: 2 to 1: 2.8 and in particular from 1: 2 to 1: 2, 6, which have secondary washing properties. In the context of this invention, the term "amorphous" is also understood to mean "X-ray amorphous". This means that the silicates in X-ray diffraction experiments do not give sharp X-ray reflections typical of crystalline substances, but at best one or more maxima of the scattered X-radiation, which have a width of several degrees of diffraction angle. However, it may well even lead to particularly good builder properties if the silicate particles provide blurred or even sharp diffraction maxima in electron diffraction experiments. This is to be interpreted as meaning that the products have microcrystalline regions of size 10 to a few hundred nm, with values of up to max. 50 nm and in particular up to max. 20 nm are preferred. Such so-called X-ray amorphous silicates, which also have a dissolution delay compared with conventional water glasses, are known. Particularly preferred are compacted / compacted amorphous silicates, compounded amorphous silicates and overdried X-ray amorphous silicates. The content of the (X-ray) amorphous silicates in particular zeolite-free compositions is preferably 1 to 10 wt .-%, which corresponds to a preferred embodiment of the invention.

Particularly preferred inorganic water-soluble builders are alkali metal carbonates and alkali metal bicarbonates, with sodium and potassium carbonate and especially sodium carbonate being among the preferred embodiments. The content of alkali metal carbonates in particular zeolite-free compositions can vary within a very broad range and is preferably from 5 to 40% by weight, in particular from 8 to 30% by weight, the content of alkali metal carbonates usually being higher than (X-ray). ) amorphous silicates. Useful organic builders are, for example, usable in the form of their alkali and especially sodium polycarboxylic acids, such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids, aminocarboxylic acids, nitrilotriacetic acid (NTA), if such use is not objectionable for environmental reasons , as well as mixtures of these. Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures thereof. The acids themselves can also be used. In addition to their builder action, the acids typically also have the property of an acidifying component and thus also serve, for example in the granules according to the invention, for setting a lower and milder pH of detergents and cleaners. In particular, citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any desired mixtures of these can be mentioned here.

Further suitable organic builders are polymeric polycarboxylates, for example the alkali metal salts of polyacrylic acid or of polymethacrylic acid, for example those having a relative molecular mass of 500 to 70,000 g / mol. For the purposes of this document, the molecular weights stated for polymeric polycarboxylates are weight-average molar masses M _{w of} the particular acid form, which were determined in principle by means of gel permeation chromatography (GPC), a UV detector being used. The measurement was carried out against an external polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship with the polymers investigated. These data differ significantly from the molecular weight data, in which polystyrene sulfonic acids are used as standard. The molar masses measured against polystyrenesulfonic acids are generally significantly higher than the molecular weights specified in this document.

The compositions according to the invention may also contain polymers, in particular as carriers for the perfume oils (fragrances). Suitable polymers which can also be used as carriers in combination with perfume include, in particular, polyacrylates which preferably have a molecular weight of 2,000 to 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates, which have molar masses of from 2000 to 10000 g / mol, and particularly preferably from 3000 to 5000 g / mol, may again be preferred from this group.

Also suitable are copolymeric polycarboxylates, in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid. Copolymers of acrylic acid with maleic acid which contain 50 to 90% by weight of acrylic acid and 50 to 10% by weight of maleic acid have proven to be particularly suitable. Their relative molecular weight, based on free acids, is generally from 2000 to 70000 g / mol, preferably from 20,000 to 50,000 g / mol and in particular from 30,000 to 40,000 g / mol. The content of the organic builder substances may vary within a broad range. Preference is given to contents of from 2 to 20% by weight, in particular contents of not more than 10% by weight being particularly preferred

The agents according to the invention may contain components from the classes of the grayness inhibitors (soil carriers), the neutral salts and / or the fabric softening auxiliaries (for example cationic surfactants), which is preferred

Graying inhibitors have the task to keep suspended from the fiber debris suspended in the fleet and so prevent the re-accumulation of dirt For this purpose, water-soluble colloids are mostly organic nature suitable, for example, the water-soluble salts of polymeric carboxylic acids, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or cellulose or salts of acidic sulfuric acid esters of cellulose or starch. Also water-soluble polyamides containing acidic groups are suitable for this purpose. Furthermore, soluble starch preparations and starch products other than those mentioned above can be used, eg degraded starch, aldehyde starches, etc Polyvinylpyrrolidone is also useful. However, preference is given to cellulose ethers, such as carboxymethylcellulose (Na salt), ₁ -methylcellulose, hydroxyalkylcellulose and mixed ethers, such as methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcarboxymethylcellulose and the like d their mixtures, and polyvinylpyrrolidone, for example, in amounts of preferably 0.1 to 5% by weight, based on the means used

A typical example of a suitable representative of the neutral salts is sodium sulfate. It can be used in amounts of, for example, from 0 to 60% by weight, preferably from 2 to 45% by weight

Suitable plasticizers, which are described in more detail below, are, for example, swellable phyllosilicates of the type of corresponding montmorillonites, for example bentonite, as well as cationic surfactants

The content of water on average depends, inter alia, on whether the composition is in liquid or solid form, and is therefore preferably 0 to less than 100% by weight and in particular 0.5 to 95% by weight, with values of not more than 5% by weight. Particular preference is given in particular to solid or non-aqueous liquid agents Not included in the case of the solid compositions is the water adhering to any aluminosilicates such as zeolite

In the case of liquid agents, the composition according to the invention according to a preferred embodiment contains water in an amount of more than 20% by weight, advantageously more than 30% by weight, in more advantageously more than 40 wt .-%, more preferably more than 50 wt .-%, in particular 60 to 95 wt .-%, particularly preferably 70 to 93 wt .-% and most preferably 80 to 90 wt .-%.

The agent according to the invention can, if it is a solid, have an excellent trickling behavior. According to a preferred embodiment, the agent according to the invention is substantially solid, preferably in powdery, pressed or granular form.

If the agent is in particulate form, the particles can be post-treated, for example, by rounding the particles of the agent. The rounding can be done in a standard roundabout. Preferably, the rounding time is not longer than 4 minutes, especially not longer than 3.5 minutes. Rounding times of a maximum of 1.5 minutes or less are particularly preferred. By rounding a further standardization of the grain spectrum is achieved as any resulting agglomerates are crushed.

An inventive agent in particulate form can in particular with nonionic surfactants, perfume oil (fragrances) and / or foam inhibitors or formulations containing these ingredients, preferably with amounts up to 20 wt .-% of active ingredient, in particular with amounts of 2 to 18 wt. -% active substance, in each case based on the aftertreated product, in a conventional manner, preferably in a mixer or optionally a fluidized bed, post-treatment.

In particular, an agent according to the invention may also be post-treated or powdered with solids, preferably in amounts of up to 15% by weight, in particular in amounts of from 2 to 15% by weight, based in each case on the total weight of the post-treated agent.

Bicarbonate, carbonate, zeolite, silica, citrate, urea or mixtures thereof, in particular in amounts of from 2 to 15% by weight, based on the total weight of the aftertreated product, can preferably be used as solids for the aftertreatment. The aftertreatment can be carried out in an advantageous manner in a mixer and / or by means of Verrunder.

In a preferred embodiment of the invention, an agent according to the invention is aftertreated with nonionic surfactants, which may also contain, for example, optical brighteners and / or hydrotropes, perfume (fragrances), and / or a solution of optical brightener and / or foam inhibitors or preparation forms containing same May contain ingredients. These ingredients or preparation forms containing these ingredients are preferably applied in liquid, molten or pasty form to the particulate agent, which is to be acted upon.

It is preferred that the aftertreatment with the substances mentioned here in a conventional mixer, only for example in a 2-wave mixer within a maximum of 1 minute, preferably within 30 seconds and for example within 20 seconds, the time information for Addition and mixing time is done.

In the following, the nonionic surfactants are described in more detail. These nonionic surfactants can be applied to the particulate agents in an aftertreatment step. Of course, all nonionic surfactants but can advantageously be directly in the composition according to the invention, liquid or solid, foaming or gel may be included.

The nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and an average of 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol residue can be linear or preferably methyl-branched in the 2-position or linear and methyl-branched radicals in the mixture may contain, as they are usually present in Oxoalkoholresten. In particular, however, alcohol ethoxylates with linear radicals of alcohols of natural origin having 12 to 18 carbon atoms, for example of coconut, palm, palm kernel, tallow or oleyl alcohol, and on average 2 to 8 EO per mole of alcohol are preferred. The preferred ethoxylated alcohols include, for example, C ₁₂ -C ₁₄ -alcohols with 3 EO or 4 EO, C ₉ -C ₁₁ -alkyl with 7 EO, C ₁₃ -C ₁₅ -alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C ₁₂ -C ₁₈ -alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures of C ₁₂ -C ₁₄ -AlkOhOl with 3 EO and C ₁₂ -C ₁₈ -alcohol with 7 EO. The stated degrees of ethoxylation represent statistical averages, which may be an integer or a fractional number for a particular product.

Preferred alcohol ethoxylates have a narrow homolog distribution (narrow rank ethoxylates, NRE). In addition to these nonionic surfactants, fatty alcohols with more than 12 EO can also be used. Examples of these are (TaIg) fatty alcohols with 14 EO ₁ 16 EO, 20 EO, 25 EO, 30 EO or 40 EO.

Preferred nonionic surfactants are one or more ethylene oxide (EO) and / or propylene oxide (PO) alkoxylated, unbranched or branched, saturated or unsaturated C ₁₀ . ₂₂ alcohols having a degree of alkoxylation of up to 30, preferably ethoxylated C _10-18 fatty alcohols having an ethoxylation degree of less than 30, preferably 1 to 20, in particular 1 to 12, more preferably 1 to 8, most preferably 2 to 5, for example C ₁₂ . ₁₄ fatty alcohol ethoxylates with 2, 3 or 4 EO or a mixture of the C _12-14 fatty alcohol ethoxylates with 3 and 4 EO in a weight ratio of 1 to 1 or isotridecyl alcohol ethoxylate with 5, 8 or 12 EO. In addition, as further nonionic surfactants and alkyl glycosides of the general formula RO (G) _x can be used in which R is a primary straight-chain or methyl-branched, especially in the 2-position methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol which represents a glycose unit having 5 or 6 C atoms, preferably glucose. The degree of oligomerization x, which indicates the distribution of monoglycosides and oligoglycosides, is any number from 1 to 10; preferably x is 1, 1 to 1, 4.

Another class of preferred nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants, in particular together with alkoxylated fatty alcohols and / or alkyl glycosides, are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably with 1 to 4 carbon atoms in the alkyl chain, in particular fatty acid methyl esters, as described for example in Japanese Patent Application JP 58/217598 or which are preferably prepared according to the method described in International Patent Application WO-A-90/13533. Particularly preferred are C ₁₂ -C ₈ fatty acid methyl esters with an average of 3 to 15 EO, in particular with an average of 5 to 12 EO.

Nonionic surfactants of the amine oxide type, for example N-cocoalkyl-N, N-dimethylamine oxide and N-tallowalkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides may also be suitable. The amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, especially not more than half thereof.

Also suitable are alkoxylated amines, advantageously ethoxylated and / or propoxylated, in particular primary and secondary amines having preferably 1 to 18 carbon atoms per alkyl chain and an average of 1 to 12 MoI ethylene oxide (EO) and / or 1 to 10 MoI propylene oxide (PO) per Mole of amine.

In the case of compositions according to the invention which are particularly suitable for automatic dishwashing, in particular dishwashing compositions in the form of tablet tablets, such as tabs, all surfactants are suitable in principle as surfactants. However, the nonionic surfactants described above and especially the low-foaming nonionic surfactants are particularly preferred for this purpose. Particularly preferred are the alkoxylated alcohols, especially the ethoxylated and / or propoxylated alcohols. The person skilled in the art generally means, under alkoxylated alcohols, the reaction products of alkylene oxide, preferably ethylene oxide, with alcohols, preferably in the context of the present invention, the longer-chain alcohols C ₁₀ to C ₁₈ , preferably C ₁₂ to C ₁₆ , such as C ₁₁ -, C ₁₂ - , C ₁₃ , C ₁₄ , C ₁₅ , C ₁₆ , C ₁₇ and C ₁₈ alcohols. In As a rule, n moles of ethylene oxide and one mole of alcohol give rise to a complex mixture of addition products of varying degrees of ethoxylation, depending on the reaction conditions. A further embodiment consists in the use of mixtures of the alkylene oxides, preferably the mixture of ethylene oxide and propylene oxide. If desired, it is also possible, by a conclusive etherification with short-chain alkyl groups, such as preferably the butyl group, to obtain the class of "closed" Al koholethoxy, which can likewise be used in the context of the invention. Very particularly preferred for the purposes of the present invention are highly ethoxylated fatty alcohols or mixtures thereof with end-group-capped fatty alcohol ethoxylates.

Advantageously, the compositions according to the invention may also contain foam inhibitors, for example foam-inhibiting paraffin oil or foam-inhibiting silicone oil, for example dimethylpolysiloxane. The use of mixtures of these agents is possible. As additives which are solid at room temperature, paraffin waxes, silicic acids, which may also be rendered hydrophobic in a known manner, and of C ₂ , in particular in the case of the abovementioned foam-inhibiting active ingredients. ₇ diamines and C ₁₂ . ₂₂ -carboxylic acids derived bisamides in question.

Foam-inhibiting paraffin oils which are suitable for use and which may also be present in admixture with paraffin waxes are generally complex mixtures without a sharp melting point. For characterization, the melting range is usually determined by differential thermal analysis (DTA) and / or the solidification point. This is the temperature at which the paraffin passes from the liquid to the solid state by slow cooling. Paraffins with less than 17 carbon atoms are not useful according to the invention, their proportion in the paraffin oil mixture should therefore be as low as possible and is preferably below the limit significantly measurable by conventional analytical methods, for example gas chromatography. Preferably, paraffins are used, which solidify in the range of 2O ⁰ C to 70 ⁰ C. It should be noted that even at room temperature appearing paraffin wax mixtures may contain different proportions of liquid paraffin oils. In the case of the paraffin waxes which can be used according to the invention, the liquid fraction at 40 ^° C. is as high as possible, even without being 100% at this temperature. Preferred paraffin wax mixtures have at 4O ⁰ C a liquid content of at least 50 wt .-%, in particular from 55 wt .-% to 80 wt .-%, and at 6O ⁰ C, a liquid content of at least 90 wt .-%. This has the consequence that the paraffins at temperatures down to at least 7O ⁰ C, preferably down to at least 60 ⁰ C are flowable and pumpable. It should also be ensured that the paraffins contain as far as possible no volatile components. Preferred paraffin waxes contain less than 1 wt .-%, in particular less than 0.5 wt .-% at 11O ⁰ C and atmospheric pressure vaporizable fractions. Paraffins which can be used according to the invention can be obtained, for example, under the trade names Lunaflex® from Füller and Deawax® from DEA Mineralöl AG. The paraffin oils may contain at room temperature solid bisamides derived from saturated fatty acids containing 12 to 22, preferably 14 to 18, carbon atoms and alkylenediamines having 2 to 7 carbon atoms. Suitable fatty acids are lauric, myristic, stearic, arachic and behenic acids and mixtures thereof, such as are obtainable from natural fats or hardened oils, such as tallow or hydrogenated palm oil. Suitable diamines are, for example, ethylenediamine 1, 3-propylenediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine, p-phenylenediamine and toluenediamine. Preferred diamines are ethylenediamine and hexamethylenediamine. Particularly preferred bisamides are bis-myristoyl-ethylenediamine, bispalmitoyl-ethylenediamine, bis-stearoyl-ethylenediamine and mixtures thereof and the corresponding derivatives of hexamethylenediamine.

The products according to the invention can preferably be mixed with further constituents, in particular detergents, care and / or cleaning agents or cosmetic ingredients. From the broad state of the art is generally known which ingredients of detergents and cleaners and which raw materials can usually be added. These are, for example, substances such as bleaching agents, bleach activators and / or bleach catalysts, enzymes, temperature-sensitive dyes, etc., which of course may also be contained directly in the composition.

Preferably, the agent may comprise UV absorbers, which are advantageously applied to the treated fabrics and improve the lightfastness of the fibers and / or the lightfastness of other formulation ingredients. Under UV absorber are organic substances (sunscreen) to understand, which are able to absorb ultraviolet rays and the absorbed energy in the form of longer-wave radiation, eg heat to give back. Compounds having these desired properties include, for example, the non-radiative deactivating compounds and derivatives of benzophenone having substituents in the 2- and / or 4-position. Also suitable are substituted benzotriazoles, phenyl-substituted acrylates (cinnamic acid derivatives) in the 3-position, optionally with cyano groups in the 2-position, salicylates, organic Ni complexes and natural substances such as umbelliferone and the endogenous urocanic acid. The biphenyl and especially stilbene derivatives, commercially available as Tinosorb ^® FD or Tinosorb ^® FR ex Ciba. As UV-B absorbers there may be mentioned 3-benzylidene camphor or 3-benzylidene norcamphor and its derivatives, eg 3- (4-methylbenzylidene) camphor; 4-aminobenzoic acid derivatives, preferably 2-ethylhexyl 4- (dimethylamino) benzoate, 2-octyl 4- (dimethylamino) benzoate and 4-dimethylaminobenzoic acid amide; Esters of cinnamic acid, preferably 2-ethylhexyl 4-methoxycinnamate, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid iso-amyl ester, 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene); Esters of salicylic acid, preferably 2-ethylhexyl salicylate, 4-salicylic acid isopropylbenzyl ester, salicylic acid homomenthyl ester; Derivatives of benzophenone, preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone; Esters of benzalmalonic acid, preferably di-2-ethylhexyl 4-methoxybenzmalonate; Triazine derivatives such as 2,4,6-trianilino (p-carbo-2'-ethyl-1'-hexyloxy) -1,3,5-triazine and octyl triazone, or dioctyl butamido triazone (Uvasorb® HEB); Propane-1,3-diones such as 1- (4-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1,3-dione; Ketotricyclo (5.2.1.0) decane derivatives. Also suitable are 2-phenylbenzimidazole-5-sulfonic acid and its alkali metal, alkaline earth metal, ammonium, alkylammonium, alkanolammonium and glucammonium salts; Sulfonic acid derivatives of benzophenones, preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts; Sulfonic acid derivatives of 3-Benzylidencamphers, such as 4- (2-oxo-3-boryl-nylidenemethyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bomylidene) sulfonic acid and salts thereof.

As a typical UV-A filter, in particular derivatives of benzoylmethane come into question, such as 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propane-1, 3-dione, 4-tert-butyl 4'-methoxydibenzoylmethane (Parsol 1789), 1-phenyl-3- (4'-isopropylphenyl) -propane-1,3-dione and enamine compounds. Of course, the UV-A and UV-B filters can also be used in mixtures. In addition to the soluble substances mentioned, insoluble photoprotective pigments, namely finely dispersed, preferably nano-metal oxides or salts, are also suitable for this purpose. Examples of suitable metal oxides are in particular zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof. As salts silicates (talc), barium sulfate or zinc stearate can be used. The oxides and salts are already used in the form of the pigments for skin-care and skin-protecting emulsions and decorative cosmetics. The particles should have an average diameter of less than 100 nm, preferably from 5 to 50 nm and in particular from 15 to 30 nm. They may have a spherical shape, but it is also possible to use those particles which have an ellipsoidal or otherwise deviating shape from the spherical shape. The pigments can also be surface treated, i. hydrophilized or hydrophobized. Typical examples are coated titanium dioxides, e.g. Titanium dioxide T 805 (Degussa) or Eusolex® T2000 (Merck). Suitable hydrophobic coating agents are in particular silicones and in particular trialkoxyoctylsilanes or simethicones. Micronized zinc oxide is preferably used. Further suitable UV light protection filters can be found in the relevant prior art.

The UV absorbers are advantageously contained in amounts of from 0.01% to 5% by weight, preferably from 0.03% to 1% by weight, in the composition. They can also be added to the product later, for example together with other substances. Preferably, the agents according to the invention, if they are solid, can also be in the form of a tablet or shaped article, as has already been shown. For the purposes of the present application, "tablet" or "shaped bodies" are dimensionally stable, solid bodies, irrespective of the manner of their preparation. Such bodies can be produced, for example, by crystallization, molding, injection molding, reactive or thermal sintering, (co) extrusion, powdering, pastillation or compacting processes such as calendering or tableting. The preparation of the "tablets" or "shaped bodies" by tabletting is particularly preferred in the context of the present application. The tablet is thus preferably made of compressed, particulate material.

Solid compositions according to the invention, preferably in the form of tablets or moldings, may preferably contain disintegration aids. Suitable swellable disintegration aids are, for example, bentonites or other swellable silicates. It is also possible to use synthetic polymers, in particular the superabsorbents or cross-linked polyvinylpyrrolidone used in the hygiene sector.

With particular advantage, polymers based on starch and / or cellulose are used as swellable disintegration aids. These base substances can be processed alone or in mixture with other natural and / or synthetic polymers to swellable disintegrating agents. In the simplest case, a cellulosic material or pure cellulose can be converted by pressure transfer into secondary particles by granulation, compaction or other application, which swell on contact with water and thus serve as a disintegrant. Wood pulp which has been obtained by thermal or chemical-thermal processes from wood or wood chips (sawdust, sawmill waste) has proven to be suitable as a cellulosic material. This cellulose material from the TMP process (thermomechanical pulp) or the CTMP process (chemothermomechanical pulp) can then be compacted by application of pressure, preferably roller compacted and converted into particle form. Of course, pure cellulose can also be used in a completely analogous manner, although it is more expensive from the raw material base. Here, both microcrystalline and amorphous finely divided cellulose and mixtures thereof can be used.

Another way is to granulate the cellulose-containing material with the addition of granulation aids. For example, solutions of synthetic polymers or nonionic surfactants have proven useful as granulating aids. In order to avoid residues on textiles washed with the agents according to the invention, the primary fiber length of the cellulose or cellulose used in the cellulosic material should be less than 200 .mu.m, preference being given to primary fiber lengths of less than 100 .mu.m, in particular less than 50 .mu.m. The secondary particles ideally have a particle size distribution in which preferably more than 90 wt .-% of the particles have sizes above 200 microns. A certain proportion of dust can contribute to an improved storage stability of the tablets produced therewith. Shares of a fine dust content of less than 0.1 mm up to 10 wt .-%, preferably up to 8 wt .-% may be present in the agents used in the invention with disintegrant granules.

Furthermore, the agents according to the invention can be present in the form of a conditioning agent and / or conditioner substrate and contain the appropriate components. For the purposes of this invention, the term conditioning is preferably to be understood as meaning the avivating treatment of textiles, fabrics and fabrics. Conditioning gives the textiles positive properties, such as improved softness, increased gloss and color brilliance, improved fragrance impression, reduction of felting, ironing relief by reducing the sliding properties, reducing the creasing behavior and the static charge and a color transfer inhibition in dyed textiles ,

To improve the softness and the reviving properties, the compositions according to the invention may comprise plasticizer components. Examples of such compounds are quaternary ammonium compounds, cationic polymers and emulsifiers, as are used in hair care products and also in agents for Textilavivage. These softening compounds, which will also be described in more detail below, can be present in all inventive compositions, but especially in the conditioners or in compositions with the desired softening effect.

Suitable examples are quaternary ammonium compounds of the formulas (III) and (IV),

wherein in (III) R and R ^{1 is} an acyclic alkyl radical having 12 to 24 carbon atoms, R ^{2 is} a saturated C ₁ -C ₄ alkyl or hydroxyalkyl radical, R ^{3 is} either R, R ¹ or R ² or is a aromatic residue stands. X ^" represents either a halide, methosulfate, methophosphate or phosphate ion and mixtures of these Examples of cationic compounds of the formula (III) are didecyldimethylammonium chloride, ditallowdimethylammonium chloride or dihexadecylammonium chloride.

Compounds of formula (IV) are so-called ester quats. Esterquats are characterized by excellent biodegradability. Here, R ^{4 is} an aliphatic alkyl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds; R ⁵ is H, OH or O (CO) R ⁷ , R ⁶ is, independently of R ^5, H, OH or O (CO) R ⁸ , where R ⁷ and R ^{8 are} independently of each represents an aliphatic alk (en) yl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds, m, n and p can each independently of one another have the value 1, 2 or 3. X ^" can be either a halide, methosulfate, methophosphate or phosphate ion and mixtures thereof Preferred compounds are those for R ^5, the group 0 (CO) R ⁷ and for R ⁴ and R ^{7 are} alkyl radicals having 16 to 18 carbon atoms included. Especially preferred are compounds in which R ⁶ is also OH. Examples of compounds of formula (IV) are methyl-N- (2-hydroxyethyl) -N, N-di (tallow-acyl-oxyethyl) ammonium methosulfate , Bis (palmitoyl) -ethyl-hydroxyethyl-methyl-ammonium-methosulfate or methyl-N, N-bis (acyl-oxy-ethyl) -N- (2-hydroxy-ethyl) -ammonium-methosulphate are quaternized compounds of the formula (IV) having unsaturated alkyl chains, the acyl groups are preferred whose corresponding fatty acids have an iodine value between 5 and 80, preferably between 10 and 60 and in particular between 15 and 45 and which have a cis / trans isomer ratio (in parts by weight). %) of greater than 30: 70, preferably greater than 50: 50 and in particular re greater than 70: 30. Commercial examples are sold by Stepan under the tradename Stepantex ^® Methylhy- droxyalkyldi-alkoyloxyalkylammoniummethosulfate or those known under Dehyquart ^® Cognis products known under or Rewoquat ^® manufactured by Goldschmidt-Witco. Further preferred compounds are the diester quats of the formula (V) ₁ which are obtainable under the name Rewoquat® W 222 LM or CR 3099 and, in addition to the softness, also provide stability and color protection.

R ²¹ and R ²² are each independently an aliphatic radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds.

In addition to the quaternary compounds described above, other known compounds may also be used. are used, such as, for example, quaternary imidazolinium compounds of the formula (VI),

where R ^{s is} H or a saturated alkyl radical having 1 to 4 carbon atoms, R ' ^υ and R "are each independently an aliphatic, saturated or unsaturated alkyl radical having 12 to 18 carbon atoms, R ¹⁰ alternatively also O (CO) R ²⁰ wherein R ^{20 is} an aliphatic, saturated or unsaturated alkyl radical having 12 to 18 carbon atoms, and Z is an NH group or oxygen and X ^"is an anion. q can take integer values between 1 and 4. Further suitable quaternary compounds are described by formula (VII)

R13 H

R12 - N- (CH ₂₎ _r - CO (CO) R15 X ^'(VII);

R14 CH ₂ - O (CO) R 16 wherein R ^12, R ¹³ and R ¹⁴ independently are a C ₄ -Atkyl-, alkenyl or hydroxyalkyl group is of one another, R ¹⁵ and R ¹⁶ are each independently selected a C ₈ _2 ₈ -Alkyl group and r is a number between 0 and 5.

In addition to the compounds of the formulas (III) and (IV) it is also possible to use short-chain, water-soluble, quaternary ammonium compounds, such as trihydroxyethylmethylammonium methosulfate or the alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, e.g. Cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride.

Also protonated alkylamine compounds which have plasticizing effect, as well as the non-quaternized, protonated precursors of cationic emulsifiers are suitable.

Further cationic compounds which can be used according to the invention are the quaternized protein hydrolysates.

Suitable cationic polymers include the polyquaternium polymers as referred to in the CTFA Cosmetic Ingredient Dictionary (The Cosmetic, Toiletry and Fragrance, Inc., 1997), in particular the Polyquaternium-6, Polyquaternium-7, also referred to as Merquats, Polyquaternium-10 polymers (Ucare Polymer IR 400, Amerchol), polyquaternium-4 copolymers such as graft copolymers having a cellulose backbone and quaternary ammonium groups attached via allyldimethylammonium chloride, cationic cellulose derivatives such as cationic guar such as guar hydroxypropyl triammonium chloride, and similar quaternized guar derivatives (eg Cosmedia Guar, manufacturer: Cognis GmbH), cationic quaternary sugar derivatives (cationic alkyl polyglucosides), eg. , The commercial product Glucquat ^® 100, a "Lauryl Methyl Gluceth-10 Hydroxypropyl Dimonium Chloride", copolymers of PVP and Dimethylaminometh- acrylate according to CTFA nomenclature, copolymers of vinylimidazole and vinylpyrrolidone, aminosilicone polymers and copolymers.

Polyquaternized polymers (for example Luviquat Care from BASF) and also cationic biopolymers based on chitin and derivatives thereof, for example, under the trade designation chitosan ^® (manufacturer: Cognis) polymer obtainable. Also useful in the present invention are cationic silicone oils such as the commercially available products Q2-7224 (manufactured by Dow Corning, a stabilized trimethylsilyl-modimeth-icon), Dow Corning 929 emulsion (containing a hydroxylamino-modified silicone, also referred to as amodimethicones is SM-2059 (manufacturer): General Electric), SLM-55067 (manufacturer: Wacker) Abil ^® -Quat 3270 and 3272 (manufacturer: Goldschmidt-Rewo; diquaternary polydimethylsiloxanes, quaternium-80), and Silicone quat Rewoquat ^® SQ 1 ( Tegopren® ^® 6922, manufacturer: Goldschmidt-Rewo).

It is likewise possible to use compounds of the formula (VIII)

the alkylamidoamines may be in their quaternized or, as shown, their quaternized form. R ¹⁷ can be an aliphatic alk (en) yl radical having 12 to 22 carbon atoms with 0, 1, 2 or 3 double bonds, s can assume values between 0 and 5. R ¹⁸ and R ¹⁹ are each independently H ₁ C 1-4 alkyl or hydroxyalkyl. Preferred compounds are fatty acid amidoamines, such as the propyldimethylamine Stearylamido- obtainable under the name Tego Amid ^® S 18 or the 3-9124 available Talgamido- propyl-trimethylammo-nium methosulfate under the name Stepantex ^® X, which is a good conditioning effect by dye transfer-inhibiting Effect and especially characterized by their good biodegradability.

Particularly preferred are alkylated quaternary ammonium compounds, of which at least one alkyl chain is interrupted by an ester group and / or amido group, in particular N-methyl-N (2-hydroxyethyl) -N, N- (ditalgacyloxyethyl) ammonium methosulfate.

Suitable nonionic plasticizers are, in particular, polyoxyalkylene glycol alkanoates, polybutylenes, long-chain fatty acids, ethoxylated fatty acid ethanolamides, alkyl polyglycosides, in particular sorbitan mono-, di- and triester and fatty acid esters of polycarboxylic acids.

In an agent according to the invention, preferably conditioning agents, plasticizers may be used in amounts of from 0.1 to 80% by weight, usually from 0.1 to 70% by weight, preferably from 0.2 to 60% by weight and in particular from 0.5 to 40 Wt .-%, in each case based on the total agent to be included.

Conditioners according to the invention may preferably contain one or more anionic surfactants, in particular those which have already been described above. Conditioners according to the invention may preferably contain one or more nonionic surfactants, in particular those which have already been described above.

As further surfactants for all agents according to the invention, in particular for the conditioning agents, so-called gemini surfactants come into consideration. These are generally understood as meaning those compounds which have two hydrophilic groups and two hydrophobic groups per molecule. These groups are usually separated by a so-called "spacer". This spacer is typically a carbon chain that should be long enough for the hydrophilic groups to be spaced sufficiently apart for them to act independently of each other. Such surfactants are generally characterized by an unusually low critical micelle concentration and the ability to greatly reduce the surface tension of the water. In exceptional cases, however, the term gemini surfactants is understood to mean not only dimeric but also trimeric surfactants.

Suitable gemini surfactants are, for example, sulfated hydroxy mixed ethers or dimer alcohol bis- and trimer tris sulfates and ether sulfates. End-capped dimeric and trimeric mixed ethers are characterized in particular by their bi- and multi-functionality. Thus, the end-capped surfactants mentioned have good wetting properties and are low foaming, so that they are particularly suitable for use in machine washing or cleaning processes.

However, it is also possible to use gemini-polyhydroxy fatty acid amides or poly-polyhydroxy fatty acid amides, as described in the relevant prior art.

Further suitable surfactants are polyhydroxy fatty acid amides of the following formula

R ²³

I R-CO-N- [Z] in the RCO for an aliphatic acyl radical having 6 to 22 carbon atoms, R ²³ for hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms and [Z] for a linear or branched polyhydroxyalkyl radical with 3 to 10 carbon atoms and 3 to 10 hydroxyl groups. The polyhydroxy fatty acid amides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.

The group of polyhydroxy fatty acid amides also includes compounds of the following formula R ²⁴ -OR ²⁵

I R-CO-N- [Z] in the R is a linear or branched alkyl or alkenyl radical having 7 to 12 carbon atoms, R ^{24 is} a linear, branched or cyclic alkyl radical or an aryl radical having 2 to 8 carbon atoms and R ^{25 is} a linear, branched or cyclic alkyl radical or an aryl radical or an oxyalkyl radical having 1 to 8 carbon atoms, wherein C _1-4 alkyl or phenyl radicals are preferred and [Z] is a linear polyhydroxyalkyl radical whose alkyl chain having at least two hydroxyl groups substituted, or alkoxylated, preferably ethoxylated or propoxylated derivatives of this radical.

[Z] is preferably obtained by reductive amination of a reduced sugar, for example glucose, fructose, maltose, lactose, galactose, mannose or xylose. The N-alkoxy- or N-aryloxy-substituted compounds can then be converted into the desired polyhydroxy fatty acid amides, for example, by reaction with fatty acid methyl esters in the presence of an alkoxide as catalyst.

The agents according to the invention preferably also contain amphoteric surfactants. In addition to numerous mono- to tri-alkylated amine oxides, the betaines represent an important class.

Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation of aminic compounds. Preferably, the starting materials are condensed with halocarboxylic acids or their salts, in particular with sodium chloroacetate, wherein one mole of salt is formed per mole of betaine. Furthermore, the addition of unsaturated carboxylic acids, such as acrylic acid is possible. As regards the nomenclature and, in particular, the distinction between betaines and 'true' amphoteric surfactants, reference should be made to the relevant literature. Examples of suitable betaines are the carboxyalkylation products of secondary and in particular tertiary amines which follow the formula (IX),

R ²⁷

R ²⁶ -N- (CH ₂ ) _n COOX ¹ (IX)

R ²⁸ in the R ^{26 is} alkyl and / or alkenyl radicals having 6 to 22 carbon atoms, R ^{27 is} hydrogen or alkyl radicals having 1 to 4 carbon atoms, R ^{28 is} alkyl radicals having 1 to 4 carbon atoms, n is from 1 to 6 and X ^{1 is} an alkali and / or alkaline earth metal or ammonium. Typical examples are the carboxymethylation products of hexylmethylamine, hexyldimethylamine, octyldimethylamine, decyldimethylamine, dodecylmethylamine, dodecyldimethylamine, dodecylethylmethylamine amine, C ^ m cocoalkyldimethylamine, myristyldimethylamine, cetyldimethylamine, stearyldimethylamine, stearylethyl-methylamine, oleyldimethylamine, C _16/ _8- tallowalkyldimethylamine and technical mixtures thereof.

Also suitable are carboxyalkylation products of amidoamines which follow the formula (X),

R ²⁹ R ³¹ CO-NH- (CH ₂ ) _m -N- (CH ₂ ) _n COOX ² (X)

A- in which R ^{31 is} CO for an aliphatic acyl radical having 6 to 22 carbon atoms and 0 or 1 to 3 double bonds, m is a number from 1 to 3 and R ²⁹ , R ³⁰ , n and X ² are as defined above. Typical examples are reaction products of fatty acids having 6 to 22 carbon atoms, namely caproic, caprylic, capric, lauric, myristic, palmitic, palmitic, stearic, isostearic, oleic, elaidic, petro-, linoleic acid gadoleic, behenic, and, which are condensed with sodium chloroacetate erucic acid and technical mixtures with N, N-dimethylaminoethylamine, N ₁ N- dimethylaminopropylamine, N, N-diethylaminoethylamine and N, N-diethylaminopropylamine. Preference is given to the use of a condensation product of C _{8 /} i ₈ coconut fatty acid N, N-dimethylaminopropylamide with sodium chloroacetate.

Furthermore, suitable starting materials for the betaines usable in the context of the invention are imidazolines which follow the formula (XI),

in which R ^{32 is} an alkyl radical having 5 to 21 carbon atoms, R ^{33 is} a hydroxyl group, an OCOR ³² or NHCOR ³² radical and m is 2 or 3. These substances are also known substances which can be obtained, for example, by cyclizing condensation of 1 or 2 moles of fatty acid with polyfunctional amines, such as, for example, aminoethyl-ethanolamine (AEEA) or diethylenetriamine. The corresponding carboxyalkylation products are mixtures of different open-chain betaines. Typical examples are condensation products of the above mentioned fatty acids with AEEA, preferably imidazolines based on lauric acid or C, in turn, _{12 /,} which are then betainized with sodium coconut oil fatty acid ₄ i. In a preferred embodiment, as already shown, the compositions according to the invention are in liquid form, for example in the form of conditioning agents or liquid detergents etc. To achieve a liquid consistency, the use of both liquid organic solvents and water can be indicated. The agents according to the invention therefore optionally contain solvents.

Solvents that can be used in the compositions according to the invention originate, for example, from the group of monohydric or polyhydric alcohols, alkanolamines or glycol ethers, provided they are miscible with water in the concentration range indicated. The solvents are preferably selected from ethanol, n- or i-propanol, butanols, glycol, propane- or butanediol, glycerol, diglycol, propyl- or butyldiglycol, hexylene glycol, ethylene glycol methyl ether, ethylene glycol ethyl ether, ethylene glycol propyl ether, ethylene glycol mono-n-butyl ether, diethylene glycol methyl ether , Diethylene glycol ethyl ether, propylene glycol methyl, ethyl or propyl ether, butoxy propoxy-propanol (BPP), dipropylene glycol monomethyl, or ethyl ether, di-isopropylene glycol monomethyl, or ethyl ether, methoxy, ethoxy or Butoxytriglycol, 1-butoxyethoxy-2-propanol, 3-methyl-3-methoxybutanol, propylene glycol t-butyl ether and mixtures of these solvents.

Some glycol ethers are available under the trade names Arcosolv ^® (Arco Chemical Co.) or Cellosolve ^®, carbitol ^® or Propasol ^® (Union Carbide Corp.); this includes for example ButylCarbitol® ^®, hexyl carbitol ^®, MethylCarbitol® ^®, and carbitol ^® itself, (2- (2-ethoxy) ethoxy) ethanol. The choice of glycol ether can be readily made by one skilled in the art on the basis of its volatility, water solubility, weight percent of total dispersion, and the like. Pyrrolidone solvents, such as N-alkyl-pyrrolidones, for example N-methyl-2-pyrrolidone or NC ₈ - C ₁₂ -alkyl-pyrrolidone, or 2-pyrrolidone, can also be used. Also preferred as the sole solvent or as a component of a solvent mixture are glycerol derivatives, in particular glycerol carbonate.

Alcohols which may be preferably used as cosolvents in the present invention include low molecular weight liquid polyethylene glycols, for example, polyethylene glycols having a molecular weight of 200, 300, 400 or 600. Further suitable cosolvents are other alcohols, for example (a) lower alcohols such as ethanol, propanol, isopropanol and n-butanol, (b) ketones such as acetone and methyl ethyl ketone, (c) C ₂ -C ₄ polyols such as a diol or a triol, for example ethylene glycol, propylene glycol, glycerol or mixtures thereof. Particularly preferred is from the class of diols 1, 2-octanediol.

In a preferred embodiment, the inventive composition contains one or more solvents from the group comprising C ₁ - to C ₄ -Monoalko-hole, C ₂ - to C ₆ glycols, C ₃ - to C ₂ glycol ethers and glycerol, in particular ethanol , The inventive C ₃ - to C ₁₂ glycol ethers contain alkyl or alkenyl groups having less than 10 carbon atoms, preferably up to 8, especially up to 6, more preferably 1 to 4 and most preferably 2 to 3 carbon atoms.

Preferred C 1 to C ₄ monoalcohols are ethanol, n-propanol, isopropanol and tert-butanol. Preferred C ₂ -C ₆ -glycols are ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,5-pentanediol, neopentyl glycol and 1,6-hexanediol, in particular ethylene glycol and 1,2-propylene glycol. Preferred C ₃ - to C ₂ glycol ethers are di-, tri-, tetra- and pentaethylene glycol, di-, tri- and tetrapropylammonium pylenglykol, Propylenglykolmonotertiärbutylether and propylene glycol monoethyl ether as well as pursuant propanol INCI designated solvent Butoxydiglycol, butoxyethanol, butoxyisopropanol, butoxy, Butyloctanol, ethoxydiglycol, ethoxyethanol, ethyl hexanediol, isobutoxypropanol, isopentyldiol, 3-methoxybutanol, methoxyethanol, methoxyisopropanol and methoxymethylbutanol.

The agent according to the invention, preferably conditioning agent or liquid detergent, may contain one or more solvents in an amount of usually up to 40% by weight, preferably 0.1 to 30% by weight, in particular 2 to 20% by weight, more preferably 3 to 15 wt .-%, most preferably 5 to 12 wt .-%, for example, 5.3 or 10.6 wt .-%, each based on the total agent included.

In a preferred embodiment, the agent according to the invention, in particular the conditioning agent, may optionally contain one or more complexing agents.

Chelating agents (INCI), also called sequestering agents, are ingredients that are capable of complexing and inactivating metal ions, for example, to prevent their adverse effects on the stability or appearance of the agents, for example clouding. On the one hand, it is important to complex the incompatible with numerous ingredients calcium and magnesium ions of water hardness. The complexation of the ions of heavy metals such as iron or copper retards the oxidative decomposition of the finished agents.

For example, the following complexing agents designated according to INCI are suitable: Aminotrimethylene Phosphonic Acid, Beta-Alanine Diacetic Acid, Calcium Disodium EDTA, Citric Acid, Cyclodextrin, Cyclohexanediamine Tetraacetic Acid, Diammonium Citrate, Diammonium EDTA, Diethylenetriamine Pentamethylene Phosphonic Acid, Dipotassium EDTA, Disodium Azacyloheptane Diphosphonate, Disodium EDTA, Disodium Pyrophosphate, EDTA, Etidronic Acid, Galactic Acid, Gluconic Acid, Glucuronic Acid, HEDTA ₁ Hydroxypropyl Cyclodextrin, Methyl Cyclodextrin, Pentapotassium Triphosphate, Pentasodium Aminotrimethylene Phosphonates, Pentasodiene, Ethylenediamines, Tetramethylene Phosphonates, Pentasodium Pentetates, Pentasodium Tri- Phosphates, Pentetic Acid, Phytic Acid, Potassium Citrate, Potassium EDTMP, Potassium Gluconate, Potassium Polyphosphate, Potassium Trisphosphonomethylamine Oxides, Ribonic Acid, So- dium Chitosan Methylene Phosphonates, Sodium Citrate, Sodium Diethylenetriamine, Penta- methylene Phosphonates, Sodium Dihydroxyethyl Glycinate, Sodium EDTMP, Sodium Gluceptate, Sodium Gluconate, Sodium Glycereth-1 Polyphosphate, Sodium Hexametaphosphate, Sodium Metaphosphate, Sodium Metasilicate, Sodium Phytate, Sodium Polydimethylglycinophenolsulfonate, Sodium Trimetaphosphate, TEA-EDTA, TEA Polyphosphate, Tetrahydroxyethyl Ethylenediamine, Tetrahy - droxypropyl Ethylenediamine, Tetrapotassium Etidronate, Tetrapotassium Pyrophosphate, Tetrasodium EDTA, Tetrasodium Etidronate, Tetrasodium Pyrophosphate, Tripotassium EDTA, Trisodium Dicarboxymethyl Alaninate, Trisodium EDTA ₁ Trisodium HEDTA, Trisodium NTA and Trisodium Phosphate.

Preferred complexing agents are tertiary amines, in particular tertiary alkanolamines (aminoalkanol). The alkanolamines have both amino and hydroxy and / or ether groups as functional groups. Particularly preferred tertiary alkanolamines are tri-ethanolamine and tetra-2-hydroxypropyl-ethylenediamine (N, N, N ', N'-tetrakis (2-hydroxy-propyl) ethylenediamine). Particularly preferred combinations of tertiary amines with Zinkricinoleat and one or more ethoxylated fatty alcohols as nonionic solubilizers and optionally solvents are described in the prior art.

A particularly preferred complexing agent is etidronic acid (1-hydroxyethylidene-1, 1-diphosphonous acid, 1-hydroxyethyl-1, 1-diphosphonic acid, HEDP, acetophosphonic acid, INCI Etidronic Acid) including their salts. In a preferred embodiment, the agent according to the invention accordingly contains etidronic acid and / or one or more of its salts as complexing agent.

In a particular embodiment, the agent according to the invention contains a complexing agent combination of one or more tertiary amines and one or more other complexing agents, preferably one or more complexing acids or their salts, in particular triethanolamine and / or tetra-2-hydroxypropylethylenediamine and etidronic acid and / or one or more of their salts.

In a further embodiment, the agent according to the invention, in particular conditioner, optionally contains one or more viscosity regulators, which preferably act as thickener.

The viscosity of the agent may be measured using standard methods (e.g., Brookfield viscometer RVD-VII at 20 U / min and 2O ⁰ C ₁ spindle 3) are measured. Preferred liquid to gel compositions may have viscosities of 20 to 4000 mPas, with values between 40 and 40 mPas and 2000 mPas may be particularly preferred.

Suitable thickeners are inorganic or polymeric organic compounds. It is also possible to use mixtures of several thickeners.

The inorganic thickeners include, for example, polysilicic acids, clay minerals such as montmorillonites, zeolites, silicas, aluminum silicates, phyllosilicates and bentonites.

The organic thickeners are derived from the groups of natural polymers, modified natural polymers and fully synthetic polymers.

Naturally derived polymers which are used as thickeners are, for example, xanthan gum, agar agar, carrageenan, tragacanth, gum arabic, alginates, pectins, polyoses, guar gum, gellan gum, locust bean gum, starch, dextrins, gelatin and casein.

Modified natural substances are derived primarily from the group of modified starches and celluloses, examples being carboxymethylcellulose and other cellulose ethers, hydroxyethyl and propylcellulose, highly etherified methylhydroxyethylcellulose and core flour ethers.

A large group of thickeners, which find wide use in a variety of applications, are the fully synthetic polymers such as polyacrylic and polymethacrylic compounds, which may be crosslinked or uncrosslinked and optionally cationically modified, vinyl polymers, polycarboxylic acids, polyethers, activated Polyamide derivatives, castor oil derivatives, polyimines, polyamides and polyurethanes. Examples of such polymers are acrylic resins, ethyl acrylate-acrylamide copolymers, acrylic ester-methacrylic acid-ester copolymers, ethyl acrylate-acrylic acid-methacrylic acid copolymers, N-methylolmeth-acrylamide, maleic anhydride-methyl vinyl ether copolymers, polyether-polyol copoly -mere as well as butadiene-styrene copolymers.

Further suitable thickeners are derivatives of organic acids and their alkoxide adducts, for example aryl polyglycol ethers, carboxylated nonylphenol ethoxylate derivatives, sodium alginate, diglycerol monoisostearate, nonionic ethylene oxide adducts, coconut fatty acid diethanolamide, isododecenemene succinic anhydride and galactomannan. Thickeners from the mentioned classes of substances are commercially available and are described, for example, under the trade names Acusol®-820 (methacrylic acid (stearyl alcohol-20-EO) ester-acrylic acid copolymer, 30% in water, Rohm & Haas), Da-pral®-GT -282-S (alkyl polyglycol ether, Akzo), Deuterol® polymer-11 (dicarboxylic acid co-polymer, Schöner GmbH), Deuteron®-XG (anionic heteropolysaccharide based on β-D-glucose, D-manose, D -Glucuronic acid, Schöner GmbH), Deuteron®-XN (nonionic polysaccharide, Schöner GmbH), Dicrylan®-thickener-0 (ethylene oxide adduct, 50% in water). ser / isopropanol, Pfersse Chemie), EMA®-81 and EMA®-91 (ethylene-maleic anhydride copolymer, Monsanto), thickener QR-1001 (polyurethane emulsion, 19-21% in water / diglycol ether , Rohm & Haas), Mirox® AM (anionic acrylic acid-acrylic acid ester copolymer dispersion, 25% in water, Stockhausen), SER-AD-FX-1100 (hydrophobic urethane polymer, Servo Delden), Shellflo®-S (high Molecular polysaccharide stabilized with formaldehyde, Shell), Shellflo®-XA (xanthan biopolymer stabilized with formaldehyde, Shell), Kelzan, Keltrol T (Kelco).

In a further preferred embodiment, the agent according to the invention, in particular conditioning agent, optionally contains one or more enzymes.

Suitable enzymes are, in particular, those from the classes of the hydrolases, such as the proteases, esterases, lipases or lipolytic enzymes, amylases, cellulases or other glycosyl hydrolases and mixtures of said enzymes. All of these hydrolases in the wash contribute to the removal of stains such as proteinaceous, greasy or starchy stains and graying. In addition, cellulases and other glycosyl hydrolases may contribute to color retention and to enhancing the softness of the fabric by removing pilling and microfibrils. Oxireductases can also be used for bleaching or inhibiting color transfer.

Particularly suitable are enzymatic agents obtained from bacterial strains or fungi such as Bacillus subtilis, Bacillus ichicheniformis, Streptomyceus griseus and Humicola insolens. Preferably, subtilisin-type proteases and in particular proteases derived from Bacillus lentus are used. Enzyme mixtures, for example from protease and amylase or protease and lipase or lipolytic enzymes or protease and cellulase or from cellulase and Lipasebzw. lipolytic enzymes or from protease, amylase and lipase or lipolytic enzymes or protease, lipase or lipolytic enzymes and cellulase, but in particular protease and / or lipase-containing mixtures or mixtures with lipolytic enzymes of particular interest. Examples of such lipolytic enzymes are the known cutinases. Peroxidases or oxidases have also proved suitable in some cases. Suitable amylases include in particular α-amylases, iso-amylases, pullulanases and pectinases. As cellulases are preferably cellobiohydrolases, endoglucanases and ß-Glucosi-denen, which are also called cellobiases, or mixtures thereof used. Since different cellulase types differ by their CMCase and avicelase activities, the desired activities can be set by targeted mixtures of the cellulases.

The enzymes may be adsorbed as a shaped body to carriers or embedded coated to protect against premature decomposition. The proportion of enzymes, enzyme mixtures or enzymes For example, zymgranulate may be about 0.1 to 5% by weight, preferably 0.12 to about 2% by weight, based on the total agent.

The agents according to the invention, in particular washing and cleaning agents, conditioners or conditioning agents, may contain bleaching agents. Among the compounds serving as bleaches in water H ₂ O ₂ , sodium percarbonate, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance. Other useful bleaching agents are, for example, peroxopyrophosphates, citrate perhydrates and H ₂ O ₂ -producing peracidic salts or peracids, such as persulfates or persulfuric acid. The urea peroxohydrate percarbamide, which can be described by the formula H ₂ N-CO-NH ₂ H ₂ O ₂ , is also useful. In particular, when using the means for cleaning hard surfaces, for example in automatic dishwashing, they can, if desired, also contain bleaching agents from the group of organic bleaches, although their use is in principle also possible with detergents for textile laundry. Typical organic bleaching agents are the diacyl peroxides, such as, for example, dibenzoyl peroxide. Other typical organic bleaches are the peroxyacids, examples of which include the alkyl peroxyacids and the aryl peroxyacids. Preferred representatives are the peroxybenzoic acid and its ring-substituted derivatives, such as alkylperoxybenzoic acids, but also peroxy-α-naphthoic acid and magnesium monoperphthalate, the aliphatic or substituted aliphatic peroxy acids, such as peroxylauric acid, peroxystearic acid, ε-phthalimidoperacycaproic acid (phthalimidoperoxyhexanoic acid, PAP), O-carboxybenzamidoperoxycaproic acid, N -nonylamidoperadipic acid and N-nonenylamidopersuccinates, and aliphatic and araliphatic peroxydicarboxylic acids, such as 1,12-diperoxycarboxylic acid, 1,9-diperoxyazelic acid, diperoxysebacic acid, diperoxybrassic acid, the diperoxyphthalic acids, 2-decyldiperoxy- butane-1,4-diacid, N, N-terephthaloyl-di (6-aminopercaproic acid) can be used.

Dyes can be used in the composition according to the invention, wherein the amount of one or more dyes is to be chosen so low that remain after application of the agent no visible residues. Preferably, the agent according to the invention is free of dyes.

The agent according to the invention may preferably contain one or more antimicrobial agents or preservatives in an amount of usually 0.0001 to 3 wt.%, Preferably 0.0001 to 2 wt.%, In particular 0.0002 to 1 wt. more preferably 0.0002 to 0.2% by weight, most preferably 0.0003 to 0.1% by weight.

Antimicrobial agents or preservatives are distinguished depending on the antimicrobial spectrum and mechanism of action between bacteriostats and bactericides, fungistats and fungicides, etc. Important substances from these groups are, for example, benzalkonium chlorides, alkylarylsulfonates, halophenols and phenol mercuriacetate. The terms antimicrobial effect and antimicrobial agent in the context of the teaching of the invention have the usual meaning. Suitable antimicrobial agents are preferably selected from the groups of the alcohols, amines, aldehydes, antimicrobial acids or their salts, carboxylic acid esters, acid amides, phenols, phenol derivatives, diphenyls, diphenylalkanes, urea derivatives, oxygen, nitrogen acetals and formals , Benzamidines, isothiazolines, phthalimide derivatives, pyridine derivatives, antimicrobial surface-active compounds, guanidines, antimicrobial amphoteric compounds, quinolines, 1,2-dibromo-2,4-di-cyanobutane, iodo-2-propyl-butyl-carbamate, iodine, iodophores, Per - oxo compounds, halogen compounds and any mixtures of the above.

The antimicrobial agent may be selected from ethanol, n-propanol, i-propanol, 1,3-butanediol, phenoxyethanol, 1,2-propylene glycol, glycerol, undecylenic acid, benzoic acid, salicylic acid, dihydracetic acid, o-phenylphenol, N-methylmorpholine-acetonitrile (MMA), 2-benzyl-4-chlorophenol, 2,2'-methylenebis (6-bromo-4-chlorophenol), 4,4'-di-chloro-2 'hydroxydiphenyl ether (dichlorosilane), 2,4,4'-trichloro-2'-hydroxydiphenyl ether (trichlosan), chlorhexidine, N- (4-chlorophenyl) -N- (3,4-dichlorophenyl) -urea, N, N '- (1, 10-decanediyldi-1-pyridinyl-4-ylidene) bis (1-octanamine) dihydrochloride, N, N'-bis (4-chlorophenyl) -3,12- diimino-2,4,11,13-tetraaza-tetradecandiimidamide, glucopro- tamines, antimicrobial quaternary surface active compounds, guanidines including the bi- and polyguanidine, such as 1,6-bis- (2-ethylhexyl-biguanido-hexane ) -dihydrochloride, 1,6-di- (N ₁ , N ₁ '-phenyldiguanido-N ₅ , N ₅ ') -hexane-tetrahydrochloride, 1,6-di- (N _{1 l} N ₁ '-phenyl-N ₁ , N ₁ -methyldiguanido-N ₅ , N ₅ ') -hexane dihydrochloride, 1,6-di- (N ₁ , N ₂ -o-chlorophenyl-diguanido- N ₅ , N ₅ ') -hexane dihydrochloride , 1, 6-di- (N ₁ , N ^ .e-dichlorophenyldiguanido-Ns.Ns'Jhexaπ dihydrochloride, 1, 6-di- [N ^ N ^ -beta ^ p-methoxyphenyl) diguanido-N ₅ , N ₅ '] -hexane-dihydrochloride, 1,6-di- (N ₁ , N 1 -α-alpha-methyl-beta-phenyldiguanido-N ₅ , N ₅ ') -hexane dihydrochloride, 1 , 6-di- (N ₁ , N ₂ -p-nitrophenyl-diguanido- N ₅ , N ₅ ') hexane-dihydrochloride, omega: omega-di- (N _L N 1 -phenyl-diguanido-N s, N s ^ -di-n- propylether- dihydrochloride, omega.omega'-di -. ^ N _T '-p-chlorophe-nyldiguanido-Ns.Ns'J-di-n-propyl-tetra hydrochloride, 1, 6-di- (N _1, N / -2, 4-dichlorophenyldiguanido-N _5, N ₅ ') hexane tetrahydrochloride, 1, 6-di- (N _L N ^ -p-methylphe-nyldiguanido-Ns.Ns'Jhexan dihydrochloride, i ^ ^ -DKN N, 1-AS-trichlorophenyl-di-guanido-N ₅ , N ₅ ') hexane-tetrahydrochloride, 1,6-di- [N ₁ , N ₁ ' -alpha- (p-chlorophenyl) ethyl-diguanido- N ₅₁ N ₅ '] hexane dihydrochloride, OmBgBiOmBgS-di- (N _1, N ₁ '-p-chlo rophe-nyldiguanido-N ₅ , N ₅ ') m-xylenedihydrochloride, 1, 12-di- (N ₁ , N 1 -p-chlorophenyldiguanido-N, N ₅ ') dodecane dihydrochloride, 1, 10 Di- (N, N'-phenyldiguanido- N ₅ , N ₅ ') -decane-tetrahydrochloride, 1, 12-di (N ₁ , N 1 -phenyl-diguanido- N ₅₁ N ₅ ') dodecane-tetrahydrochloride, 1, 6 Di- (N ₁ , N 1 -o-chlorophenyl-guanido- N ₅₁ N ₅ ') hexane dihydrochloride, 1,6-di- (N ₁ , N 1 -o-chloro-phenyldiguanido-N ₅₁ N ₅ ') hexane tetrahydrochloride, ethylene bis (1-tolyl biguanide), ethylene bis (p-tolyl biguanide), ethylene bis (3,5-dimethylphenyl biguanide), ethylene bis (p-tert-amylphenyl biguanide) , Ethylene-bis- (nonylphenylbiguanide), ethylene-bis (phenylbi-guanide), ethylene-bis- (N-butylphenyl-biurid), ethylene-bis (2,5-diethoxyphenylbiguanide), ethylene-bis (2,4-) dimethylphenyl biguanide), ethylene bis (o-diphenylbiguanide), ethylene bis (mixed amyl naphthyl biguanide), N-butyl ethylene bis (phenylbiguanide), trimethylene bis (o-tolylbiguanide), N-butyl trimethyl bis- (phenyl biguanides) and the corresponding salts, such as acetates, gluconates, hydrochlorides, hydrobromides, citrates, bisulfites, fluorides, polymaleates, N-cocoalkyl sarcosinates, phosphites, hypophosphites, perfluorooctanoates, silicates, sorbates, salicylates, maleates, tartrates, fumarates, ethylenediamine tetraacetates , Iminodiacetates, cinnamates, thiocyanates, arginates, pyromellitates, tetracarboxybutyrates, benzoates, glutarates, monofluorophosphates, perfluoropropionates and any mixtures thereof. Also suitable are halogenated xylene and cresol derivatives, such as p-chlorometacresol or p-chloro-meta-xylene, and natural antimicrobial agents of plant origin (for example, from spices or herbs), of animal and microbial origin. Preferably, antimicrobial surface-active quaternary compounds, a natural antimicrobial agent of plant origin and / or a natural antimicrobial agent of animal origin, most preferably at least one natural antimicrobial agent of plant origin from the group comprising caffeine, theobromine and theophylline and essential oils such as eugenol, thymol and geraniol, and / or at least one natural antimicrobial agent of animal origin from the group, comprising enzymes such as protein from milk, lysozyme and lactoperoxidase, and / or at least one antimicrobial surface-active quaternary compound with an ammonium, sulfonium, phosphonium, iodonium - or Arsoniumgruppe, peroxo compounds and chlorine compounds are used. Substances of microbial origin, so-called bacteriocins, can also be used. Glycine, glycine derivatives, formaldehyde, compounds which readily split off formaldehyde, formic acid and peroxides are preferably used.

The suitable as antimicrobial agents quaternary ammonium compounds (QAV) have been described above. Particularly suitable is, for example, benzalkonium chloride, etc. Benzalkonium halides and / or substituted benzalkonium halides are for example commercially available as Barquat ^® ex Lonza, Marquat® ^® ex Mason Variquat ^® ex Witco / Sherex and Hyamine, ^® ex Lonza and as Bardac ^® ex Lonza. Other commercially obtainable antimicrobial agents are N- (3-chloroallyl) hexaminium chloride such as Dowicide and Dowicil ^® ^® ex Dow, Benzethonium- chloride such as Hyamine ^® 1622 ex Rohm & Haas, methylbenzethonium as Hyamine ^® 1ox ex Rohm & Haas, cetylpyridinium chloride such as Cepacol ex Merrell Labs.

Furthermore, the agents according to the invention, in particular detergents and cleaners, conditioners or conditioners, may optionally contain ironing aids for improving the water absorbency, the rewettability of the treated textiles and for ease of ironing the treated textiles. For example, silicone derivatives can be used in the formulations. These additionally improve the rinsing out of the wash-active formulations by their foam-inhibiting properties. Preferred silicone derivatives are, for example, polydialkyl or alkylaryl siloxanes in which the alkyl groups have one to five carbon atoms and are completely or partially fluorinated. Preferred silicones are polydimethylsiloxanes, which may optionally be derivatized and then amino-functional or quaternized or Si-OH, Si-H and / or Si-Cl bonds. The viscosities of the preferred silicones at 25 ⁰ C in the range between 100 and 100,000 mPas, wherein the silicones in amounts between 0.2 and 5 wt .-%, based on the total composition can be used.

The agents according to the invention, in particular conditioning agents, can be obtained by all known techniques known to the person skilled in the art. The agents can be obtained, for example, by mixing directly from their raw materials, optionally with the use of high-shear mixing equipment. For liquid formulations, in particular conditioning agents, it is recommended to melt, where appropriate, any plasticizer components present and to subsequently disperse the melt in a solvent, preferably water. The polymerizable betaine esters of the formula (I) which can be used according to the invention or polymers which can be prepared from them according to the invention can be incorporated into the conditioning agents by simple admixing.

The conditioning agents are preferably present as fabric softeners. They are usually introduced into the rinse cycle of an automatic washing machine.

Another object of the invention is a substrate, in particular conditioning substrate, which is impregnated and / or coated with an agent according to the invention, which thus contains the fragrance composition according to the invention and oxidizing agent.

Conditioning substrates according to the invention are mainly used in textile treatment and in particular in textile drying processes. The substrate material is preferably made of porous sheet-like cloths. They may consist of a fibrous or cellular flexible material which has sufficient thermal stability for use in the dryer and which can retain sufficient quantities of impregnating or coating agent to effectively condition fabrics without significant bleeding or bleeding during storage By means of done. These wipes include cloths of woven and non-woven synthetic and natural fibers, felt, paper or foam, such as hydrophilic polyurethane foam.

Preferably, conventional cloths of nonwoven material (nonwovens) are used here. Nonwovens are generally defined as adhesively bonded fibrous products having a mat or layered fibrous structure, or those comprising fibrous mats in which the fibers are randomly or randomly distributed. The fibers may be natural such as wool, silk, jute, hemp, cotton, flax, sisal or ramie; or synthetically, such as rayon, cellulose esters, polyvinyl derivatives, polyolefins, polyamides or polyesters. In general, any fiber diameter or titer is suitable for the present invention. The non-woven used here Fabrics do not tend to rupture or disintegrate due to the random or random arrangement of fibers in the nonwoven material that impart excellent strength in all directions, for example, when used in a household tumble dryer. Examples of nonwoven fabrics suitable as substrates in the present invention are known, for example, from WO 93/23603. Preferred porous and flat cleaning cloths consist of one or different fiber materials, in particular of cotton, refined cotton, polyamide, polyester or mixtures of these. The cleaning substrates in fabric form preferably have an area of from 10 to 5000 cm ² , preferably from 50 to 2000 cm ² , in particular from 100 to 1500 cm ² and particularly preferably from 200 to 1000 cm ² . The grammage of the material is usually between 20 and 1000 g / m ² , preferably from 30 to 500 g / m ² and in particular from 50 to 150 g / m ² . Conditioning substrates can be obtained by impregnation or impregnation or else by melting the agents or conditioners according to the invention onto a substrate.

The invention further provides for the use of a conditioning agent or a conditioning substrate according to the invention in a textile conditioning process, such as, for example, a final rinse, a textile drying process and a textile drying process or textile drying process.

Preferred agents according to the invention are liquid detergents, preferably containing surfactant (s) and other customary ingredients of detergents and cleaners. For example, according to the invention suitable liquid detergent as a thickening system, based in each case on the total agent a) 0, 1 to 5 wt .-% of a polymeric thickener, b) 0.5 to 7 wt .-% of a boron compound and c) 1 to 8 wt. -% of a complexing agent, included.

In the context of the present invention, preference is given to aqueous, higher-viscosity liquid detergents whose content of surfactant (s) is above 35% by weight.

Suitable thickening agents, also called swelling agents, e.g. Alginates or agar-agar have been described above. Preferred aqueous liquid detergents contain as thickening system 0.2 to 4 wt .-%, preferably 0.3 to 3 wt .-% and in particular 0, 4 to 1, 5 wt .-%, of a polysaccharide.

A preferred polymeric thickener is xanthan gum, a microbial anionic heteropolysaccharide produced by Xanthomonas campestris and some other species under aerobic conditions and having a molecular weight of from 2 to 15 million daltons. Xanthan is formed from a chain of β-1,4-linked glucose (cellulose) with side chains. The structure of the subgroups consists of glucose, mannose, glucuronic acid, acetate and Pyruvate, where the number of pyruvate units determines the viscosity of xanthan gum.

Liquid detergents of the invention may preferably contain a boron compound which is used in amounts of from 0.5 to 7% by weight. Examples of boron compounds useful in the present invention are boric acid, boric oxide, alkali borates such as ammonium, sodium and potassium ortho-, meta- and pyroborates, borax in its various stages of hydration and polyborates such as alkali metal pentaborates.

Organic boron compounds such as esters of boric acid can also be used.

Preferred liquid detergents contain 0.5 to 4 wt .-%, preferably 0.75 to 3 wt .-% and in particular 1 to 2 wt .-% boric acid and / or sodium tetraborate.

Furthermore, liquid detergents according to the invention may contain 1 to 8% by weight of a complexing agent. Particularly preferred liquid detergents contain citric acid or sodium citrate, preference being given to liquid detergents which contain from 2.0 to 7.5% by weight, preferably from 3.0 to 6.0% by weight and in particular from 4.0 to 5.0 Wt .-% sodium citrate.

Among other constituents, the liquid detergents according to the invention preferably contain surfactant (s), wherein anionic, nonionic, cationic and / or amphoteric surfactants are used. From an application point of view, preference is given to mixtures of anionic and nonionic surfactants, wherein the proportion of nonionic surfactants may preferably be greater than the proportion of anionic surfactants. The use of sugars and / or sugar derivatives such as alkyl polyglucosides or cyclodextrins can also be done.

Of course, liquid detergents according to the invention contain oxidizing agents and fragrances in accordance with the invention. This applies to all means which have been designated as being according to the invention in the context of this description.

Examples

Example 1 :

There was prepared a liquid detergent of the following composition, wt .-% each based on the total average 16.5 wt .-% linear alkylbenzenesulfonate 10 wt .-% C12-18-fatty alcohol + 7-ethoxy units 1 wt .-% 1-hydroxyethane -1, 1-diphosphonic acid 3 wt .-% sodium citrate 8 wt .-% sodium sulfate

3 wt .-% PAP granules based on the active substance 0.25 wt .-% xanthan gum

1, 3 wt .-% fragrance mixture (see Example 2 or 3) ad 100 wt .-%: water The pH was adjusted to 5.0 by addition of 50% NaOH.

Example 2 (according to the invention):

The formulation of Example 1 was perfumed with a perfume oil I, which included fragrances according to the invention, so that more than 50 wt .-% of the fragrances contained were selected from such fragrances, which at least one of the following classes were attributable saturated alcohols saturated saturated esters ether

Aromatics with saturated substituents - Nitriles saturated acetals saturated hemiacetals, wherein the wt .-% - refers to the total amount of fragrance.

Example 3 (Comparative Example)

The formulation of Example 1 was perfumed with a conventional perfume oil II typical for washing-things, i.a. including:

14.7% by weight of Iso E Super (2-acetyl-1,2,3,4,6,7,8,8A-octahydro-2,3,8,8-tetramethylnaphthalene)

12.5% by weight PTBCA 25 ice (68% trans-4-tert-butylcyclohexyl acetate / 32% cis-4-tert-butyl)

butylcyclohexyl)

8.0% by weight of dihydromyrcenol

6.0% by weight of habanolide (oxacyclohexadecen-2-one) 5.0% by weight of phenylethyl alcohol

3.0% by weight OTBCA (85% cis-2-tert-butylcyclohexyl acetate / 15% trans-2-tert-butylcyclohexyl acetate)

2.0% by weight of Vertofix Coeur (juniper, Juniperus mexicana, extract, acetylated, [3R]

(. 3.alpha, 3a.beta, 7.beta, 8a.alpha...)] - 1- (2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl- 1H-3a, 7-methano-azulene-5-yl) ethan-1-one)

1, 5 wt .-% citronitrile

4.0% by weight of aldehyde C14 so-called (gamma undecalactone) 16.8% by weight of dipropylene glycol

12.4% by weight of Lilial (2-methyl-3 (4-tert-butylphenyl) propionaldehyde)

4.3% by weight hexyl cinnamaldehyde

2.3% by weight of bacdanol (2-ethyl-4 (2,2,3-trimethyl-3-cyclopenten-1-yl) -2-buten-1-ol)

2.1% by weight of lyral (4 (4-methyl-4-hydroxypentyl) cyclohexene-1-carbaldehyde) 1, 9% by weight of isoeugenol (2-methoxy-4-propenylphenol)

0.5% by weight of aldehyde C08 (octanal)

% By weight, in each case based on the total perfume oil II

Example 4 (Evaluation of the temporal evolution of the fragrance impression):

The development over time of the fragrance impression was evaluated over 4 weeks at 25 ⁰ C by abrasion by three perfumers. It turned out that the composition according to the invention, ie the liquid detergent according to Example 1 with the perfume from Example 2, does not change in odor over this period. However, the comparative composition, ie the liquid detergent according to Example 1 with the conventional detergent perfume from Example 3, however, assumed such a very unpleasant odor, so that it would have been no longer suitable for laundry washing or sale solely for reasons of odor.

Example 5 (determination of bleach stability):

The degree of preservation of the bleach PAP was at weekly intervals during storage at 25 ° C over a period of 4 weeks for the composition of the invention, ie the liquid detergent according to Example 1 with the perfume of Example 2 (corresponds to "detergent A according to the invention"), and the comparative composition thus the liquid detergent according to Example 1 with that with the conventional detergent perfume from Example 3 (equivalent to Comparative detergent B) assessed.

For this purpose, the content of bleach was determined by iodometric titration. The initial content (3% absolute) was set as 100%. The following table shows the bleach contents (in%) after the respective storage times (in weeks) at 25 ° C:

Storage time 0 1 2 3 4

Detergent A (according to the invention) 100 99 96 93 89

Comparative detergent B 100 90 75 55 30 It was thus observed in the comparison detergent B a drastic loss of the bleaching agent in the presence of the conventional perfume of Example 3. In the detergent A (according to the invention) containing the perfume of the invention, found an unexpectedly good stability.

Claims

claims

1. A consumable product containing oxidizing agent, comprising a fragrance composition, characterized in that at least 50 wt .-% of the fragrances contained are selected from such fragrances, which are attributable to at least one of the following classes saturated alcohols saturated esters saturated ethers

2. Composition according to claim 1, characterized in that it is the oxidizing agent is an oxidative bleaching agent, preferably based on oxygen, in particular Peroxycar- bonsäuren are preferred.

3. Composition according to claim 2, characterized in that a peroxycarboxylic acid is contained, wherein the peroxycarboxylic acid is advantageously selected from mono- and diperoxycarboxylic acids, in particular dodecanediperoxyacid or preferably imidoperoxycarboxylic acids, more preferably 6-phthalimidoperoxycaproic acid (6-phthalimidoperoxyhexanoic acid, PAP), and / or wherein the peroxycarboxylic acid at atmospheric pressure has a melting point above 25 ⁰ C, in particular above 35 ° C, preferably above 45 ° C, preferably above 50 ⁰ C, particularly preferably above 100 ⁰ C.

4. Composition according to claim 1 to 3, characterized in that the oxidizing agent, in particular the peroxycarboxylic acid, is present in granular form and is preferably coated, wherein the mass of the coating is advantageously 0.1 to 30 wt .-%, based on the whole of the oxidant-containing particles, preferably granules.

5. Composition according to one of claims 1 to 4, characterized in that it contains at least 0.01 wt .-% surfactants, in particular anionic surfactants, preferably in amounts of 0.1 to 30 wt .-%, and / or nonionic surfactants , preferably in amounts of 0.1 to 30 wt .-%, each based on the total agent.

6. Composition according to one of claims 1 to 5, characterized in that it contains electrolytes, in particular inorganic and / or organic salts, in particular phosphate, citrate and / or sulfate, more preferably sodium sulfate, preferably in amounts of at least 0.1 wt. -% advantageously at least 3 wt .-%, in particular in amounts of 5 to 30 wt .-%, each based on the total agent.

7. Composition according to one of claims 1 to 6, characterized in that it contains complexing agents, preferably in amounts of up to 30 wt .-%, in particular 0 to 10 wt .-%, based on the total agent, in particular

(a) nitrogen-free chelating agents such as e.g. preferably alkali metal polyphosphonates, mono- or polyphosphonic acids, in particular 1-hydroxyethylidene-1, 1-diphosphonic acid (HEDP), citrate and / or short-chain dicarboxylic acids and / or

(b) complexing agents from the group quinoline and / or its salts, picolinic acid and dipicolinic acid, ethylenediaminetetraacetic acid (EDTA), diethylenetriamine penta (methylenephosphonic acid) (DTPMP), azacycloheptane diphosphonate (AHP), nitrilotriacetic acid (NTA), aminopolycarboxylic acids, aminohydroxypolycarboxylic acids, polyphosphonic acids and aminopolyphosphonic acids.

8. Composition according to one of claims 1 to 7, characterized in that it contains enzymes, preferably in amounts of 0 to 10 wt .-%, each based on the total agent.

9. Composition according to one of claims 1 to 8, characterized in that it contains builders, in particular fatty acids, preferably saturated and / or branched fatty acids, in particular having a melting point below 30 ⁰ C, and / or citric acid and / or citrate, preferably in amounts of from 0 to 15% by weight, and / or polyacrylates, preferably in amounts of from 0 to 15% by weight, and / or phosphonates, the percentage by weight being based on the total agent.

10. Composition according to one of claims 1 to 9, characterized in that it comprises at least substantially no halide ions, in particular no chloride ions, wherein the amount of halide ions, in particular chloride ions, advantageously at most 500 ppm, preferably at most 100 ppm, in particular at most 30 ppm, is.

11. Composition according to one of claims 1-10, characterized in that less than 30 wt .-%, preferably less than 20 wt .-%, advantageously less than 15 wt .-%, more preferably less than 10 wt. %, more preferably less than 5% by weight, more preferably less than 3% by weight, more preferably less than 2% by weight, even more advantageously less than 1% by weight. , in a particularly advantageous manner less than 0.5 wt .-%, in particular 0 wt .-% of the fragrances contained in such fragrances are selected which an aldehyde function (RCH = O) and / or a keto group (RR ¹ C = O ) wear, wherein the indication Gew .-% refers to the total amount of fragrances contained in the middle.

12. Composition according to one of claims 1-11, characterized in that the agent is in liquid form, preferably in aqueous or non-aqueous form, which is advantageously a dispersion, preferably an emulsion or suspension.

13. Composition according to claim 12, characterized in that it is pourable, preferably has a viscosity between 100 and 10,000 mPas at a shear rate of 30 s ^{' 1} and a temperature of 25 ⁰ C.

14. Composition according to one of claims 1 to 13, characterized in that a pH of at most 7, in particular a pH of 3.5 to 7, preferably from 4.0 to 6.5, particularly preferably from 4, 5 to 6, most preferably from about 5, has.

15. Composition according to one of claims 1-11, characterized in that the agent is in solid form, preferably as a powder.

16. Composition according to claim 15, characterized in that it is a Kompaktat, available for. by processes such as pressing, rolling, briquetting, pelletizing, extruding, agglomerating or related compacting processes.

17. Composition according to one of claims 15 or 16, characterized in that it is a molding, preferably a tablet or a block or a strand.

18. Composition according to one of claims 1 to 17, characterized in that the perfume composition contained in the agent according to the invention at least 50 wt .-%, at least 60% by weight or at least 70 wt .-% or at least 80 wt .-% or at least 90% by weight or at least 91% by weight, preferably at least 92% by weight, advantageously at least 94% by weight, more preferably at least 96% by weight, more preferably at least 98% by weight, in a further advantageous manner, at least 99% by weight, in particular even 100% by weight, of odorants selected from citronitrile, ortho-tert-butylcyclohexyl acetate, cyclohexyl salicylate, (+) - (1'R, 3S, 6'S) -1- (2 ', 2 ^l , 6 ^l -trimethyl-1'-cyclohexyl) -3-hexanol, (-) - (1 ^l S, 3R, 6'R) -1- (2', 2 ^l , 6 ') trimethyl-1 ^l -hydroxyl) -3-hexanol, (+) - (1 ^l R, 3R, 6'S) -1- (2 ^l , 2 ', 6'-trimethyl-1 ^l -cyclohexyl) -3- hexanol, (-) - (1'S, 3S, 6'R) -1- (2 ^L , 2 ^L , 6 ^L -trimethyl-1'-cyclohexyl) -3-hexanol, phenylethyl alcohol, 2-cyclohexylidenes-2- phenylacetonitrile, decahydr o-b-naphthol acetate, cresyl acetate (para), methyl phenylacetate, allylamyl glycolate, benzyl acetate, cyclohexyl ethyl acetate, ethyl 2-cyclohexyl-propionate, phenylethyl acetate, cyclopentylidene-acetic acid methyl ester [CAS-No. 0040203-73-4), allyl (cyclohexyloxy) acetate, 2,4-dimethyl-1,3-dioxolane-2-acetic acid ethyl ester, 3,12-tridecadienitrile, amyl acetate, isoamyl acetate, ethyl phenylacetate, 2-propenylphenoxyacetate, isobornyl acetate, Dimethylbenzylcarbinylacetate, hexylacetate, cresylacetate (para), isobutylphenylacetate, butylcyclohexylacetate-cis-para-tert., Butylcyclohexylacetate-trans. para-tert, hydrocinnamyl alcohol, 2,6-dimethylheptan-2-ol, decanol, octanol, 2,6-dimethylbicyclo [4.4.0] decan-1-ol (0.1% in dipropylene glycol), tetrahydrouguol [= tetrahydrolinalool (3, 7-dimethyl-octan-3-ol) / tetrahydromyrcenol (2-octanol, 2,6-dimethyl) mixture (1: 1)], dihydroterpineol, alpha 3,3-trimethylcyclohexylmethyl formate, octanol-3, hexanol, 2,2, 6-trimethyl-alpha-propylcyclohexanopropanol, decahydro-b-naphtholformate, (1'S, 1 "S, 2'S, 3" R, 5 "R) - [1-methyl-2- (1,2,2-trimethyl- bicyclo [3.1.0] hex-3-ylmethyl) -cyclopropyl] -methanol, (1'R, 1 "R, 2'R, 3" S, 5 "S) - [1-methyl-2 ( 1, 2,2-trimethyl-bicyclo [3.1.0] hex-3-ylmethyl) -cyclopropyl] -methanol, (1'R, 1 "S, 2'R, 3" R, 5 "R) - [1-Methyl-2- (1,2,2-trimethyl-bicyclo [3.1.0] hex-3-ylmethyl) -cyclopropyl] -methanol, (1'S, 1 "R, 2'S, 3" S, 5 "S ) - [1-Methyl-2- (1,2,2-trimethyl-bicyclo [3.1.0] hex-3-ylmethyl) -cyclopropyl] -methanol, borneol, dipropylene glycol, tetrahydrogeraniol, tetrahydrolinalool, 2,2,6- Trimethyl-alpha-propylcyclohexanepropanol (Timberol forte), alpha-methyl -4- (1-methylethyl) cyclohexanemethanol, isocyclogeraniol, fenchyl alcohol, (-) - (2R, 4S) -2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, (+) - (2S, 4R) - 2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, (+) - (2S, 4S) -2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, (-) - (2R, 4R ) -2-isobutyl-4-methyltetrahydro-2H-pyran-4-ol, methyl benzoate, ethyl benzoate, methyl salicylate, amyl propionate, ethyl 2,6,6-trimethyl-1S-cyclohexadiene-i-carboxylate, benzyl propionate, ethyl salicylate, 2- Methoxy-4-formylphenyl isobutyrate (isobutane), ethyl caprylate, allyl caproate, 2-methyl-2-butenoic acid 2-methylpropyl ester, 2-ethyl-ethylhexanoate (irotyl), 2-methylpentanoic acid 2-methylpentyl ester, jasmacycline, 2, Methyl 5-dimethyl-4,6-dihydroxybenzoate, ethyl 2-methylvalerate, heptanoic acid 2-propenyl ester (allylheptanoate-allyloenanthat), methyl anthranilate, phenylacetic acid, allylcyclohexylpropionate, 2-nonynoic acid methyl ester, cyclohexyl salicylate, 2-tert-butylcyclohexylethyl carbonate, 2 , 2,4-Trimethylcapronsaureethylester, Ethyl ester Labdanum Extract (Ambra- rome), styrolyl acetate, hydroquinone dimethyl ether, diphenyl ether, cresyl methyl ether (para), cymene (para), phenylethyl isoamyl ether, phenylethyl methyl ether, 4-isopropyl-5,5-dimethyl-1,3-dioxane, 2,2,5 , 5-Tetramethyl-4-isopropyl-1,3-dioxane, 5-methyl-5-propyl-2 (1-methylbutyl) -1,3-dioxane, anethole, 2-phenylpropionaldehyde dimethyl acetal, frambinone methyl ether, coumarin , isocoumarin, acetophenone, 1,1,2,3,3-pentamethyl-6 _I 7-dihydro-4 (5H) -indanon, octalactone gamma, ethyl amyl ketone, camphor synth., -oxacycloheptadec-δ-en-2-on , 2-heptylcyclopentanone, 2- (1-methylpropyl) -cyclohexanone, 4-tert-butyl-2,6-dimethylacetophenone, cyclopentadecanolides, 3-methyl-cyclopentadecane, dihydrojasmon, dihydro-iso-jasmon, decalactone gamma, Methyloctalactone, 1,4-dioxacyclohexadecane-5,16-dione, 4- (2-butenylidene) -3,5,5-trimethyl-2-cyclohexen-1-one, ethyl-2,2,6, -trimethylcy - clohexanecarboxylate, cinnamonitrile, lauric acid nitrile, hydrocitronitrile, 2-benzyl-2-methyl-3-butene nitrile, 3-methyldodecanonitrile, citronitrile, tridecen-2-nitrile, * 3 (4,7,7-trimethylbicyclo <4.1.0> hept-3-yl) -2-propenylnitrile, Irolene p, 8-alpha-12-oxido -13,14,15,16-tetranorlabdane, 3,3,5-trimethylcyclohexylethyl ether, Irival (70% 4-tert-pentylcyclohexanone, 10% white mineral oil, 10% non-2-enenetrile, 10% dibutyl sebacate) , Isobutylquinoline, 5-ethylidenebicyclo [2.2.1] -2-heptene-2-methoxyphenol adduct, methylbutyl 2-propionate, indeno [1,2-d] -tetrahydro-1,3-dioxane, dodecahydro-3a, 6,6,9a-tetra- methyl-naphtho (2,1-b) furan, 2,4-dimethyl-4-phenyl-tetrahydrofuran, spiro [1,3-dioxolane-2,5'- (4 ', 4'')',8',8'-tetramethyl-hexahydro-3',9'-methanonaphthalene)], methyl dihydrojasmonate, methyl 3-oxo 2-pentylcyclopentane acetate, o- (allyloxy) anisole, dihydromyrcenol, 9-decen-1-ol, tetrahydromyrocene, hexahydro-4,7-methanoinden-6-yl acetate, 2-phenoxyethyl isobutyrate, 2-methylpropenoic acid 1, 3 dimethyl 3-butenyl ester, methylacetophenone para, 4-phenyl-2-butanone, 1- (5,5-dimethyl-1-cyclohexyl-1-yl) -4-penten-1-one, 3-hydroxy-1 Methyl-4-isopropylbenzene [CAS No .: 89-83-8] contains, wherein the Gew.-indication refers to the total amount of the fragrances.