EP3941427A1

EP3941427A1 - Method for dyeing keratinous material, comprising the application of an organosilicon compound, an effect pigment and a sealing reagent vi

Info

Publication number: EP3941427A1
Application number: EP20711867.0A
Authority: EP
Inventors: Torsten LECHNER; Gabriele Weser; Claudia Kolonko; Caroline KRIENER; Ulrike Schumacher; Marc NOWOTTNY; Juergen Schoepgens; Phillip Jaiser; Carsten MATHIASZYK
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 2019-03-19
Filing date: 2020-03-13
Publication date: 2022-01-26
Also published as: US20240207160A1; US11992546B2; JP2022526312A; WO2020187735A1; US20220151904A1; CN113613621A; DE102019203668A1

Abstract

The present invention relates to a method for dyeing keratinous material, in particular human hair, comprising the following steps: - applying an agent (a) to the keratinous material, said agent (a) containing: (a1) at least one organic silicon compound from the group of silanes, said compound having one, two or three silicon atoms; and (a2) at least one chromophoric compound comprising at least one pigment based on a substrate plate which comprises a vacuum-metallised pigment and applying an agent (b) to the keratinous material, said agent (b) containing: (b1) at least one sealing reagent.

Description

Method for coloring keratinic material, comprising the use of an organosilicon compound, an effect pigment and a sealing reagent VI

The present application relates to a method for treating keratinous material, in particular human hair, which comprises the use of two agents (a) and (b). The agent (a) is characterized by its content of at least one organic silicon compound (a1) and at least one selected coloring compound (a2). The means (b) contains at least one sealing reagent.

Another subject of this application is a multi-component packaging unit (kit-of-parts) for coloring keratinous material, in particular human hair, which comprises at least four means (a), (a ”) and (b) separately made up. The means (a) used in the method described above can be prepared from means (a ‘) and (a“).

The change in the shape and color of keratinic fibers, in particular hair, represents an important area of modern cosmetics. The person skilled in the art knows various coloring systems for changing the hair color, depending on the coloring requirements. Oxidation dyes are usually used for permanent, intense dyeings with good fastness properties and good gray coverage. Such colorants usually contain

Oxidation dye precursors, so-called developer components and coupler components, which, under the influence of oxidizing agents such as hydrogen peroxide, form the actual dyes with one another. Oxidation dyes are characterized by very long-lasting coloring results.

If substantive dyes are used, dyes that have already been developed diffuse from the dye into the hair fiber. Compared to oxidative hair coloring, the coloring obtained with substantive dyes is less durable and can be washed out more quickly. Colorations with substantive dyes usually remain on the hair for a period of between 5 and 20 washes.

For short-term color changes on the hair and / or the skin, the use of

Color pigments known. Color pigments are generally understood to mean insoluble, coloring substances. These are present undissolved in the form of small particles in the coloring formulation and are only deposited on the outside of the hair fibers and / or the skin surface. Therefore, they can usually be removed without residue by a few washes with detergents containing surfactants. Various products of this type are available on the market under the name of hair mascara. If the user wants particularly long-lasting coloring, the use of oxidative coloring agents has so far been his only option. However, despite multiple attempts at optimization, an unpleasant smell of ammonia or amine cannot be completely avoided with oxidative hair coloring. The hair damage still associated with the use of oxidative coloring agents also has an adverse effect on the user's hair.

EP 2168633 B1 deals with the problem of producing long-lasting hair colorations using pigments. The document teaches that when the combination of a pigment, an organic silicon compound, a film-forming polymer and a solvent is used, the hair can be colored which is particularly resistant to shampooing.

Metallic luster pigments or metallic effect pigments are widely used in many areas of technology. They are used, for example, for coloring paints, printing inks, inks,

Plastics, glasses, ceramic products and preparations of decorative cosmetics such as nail polish are used. They are characterized above all by their delightful angle-dependent

Color impression (goniochromy) and their metallic-like sheen.

Hair with a metallic finish or metallic reflections are trendy. The metallic shade makes the hair appear thicker and shinier.

There is a need to provide hair colorations with effect pigments which, on the one hand, have high wash and rub fastness and, on the other hand, do not adversely affect hair properties such as handling and haptics. For this purpose it would be desirable if the effect pigments used had a high covering power and could be applied to the hair in thin layers.

Accordingly, the object of the present invention was to provide a coloring system with effect pigments which has fastness properties that are comparable to oxidative coloring.

In particular, the wash fastness should be outstanding, but the use of the oxidation dye precursors usually used for this purpose should be dispensed with.

Surprisingly, it has now been found that the aforementioned object can be achieved excellently if keratinic materials, in particular human hair, are colored using a method in which at least two agents (a) and (b) are applied to the keratinic materials (hair) . The first agent (a) here contains at least one organic

Silicon compound from the group of the silanes with one, two or three silicon atoms, and furthermore at least one selected coloring compound. The mean (a) is thus the organic silicon compound and the coloring compound assembled together. The second means (b) contains at least one sealing reagent.

When using the two means (a) and (b) in one dyeing process, keratinic material could be dyed with a particularly high color intensity.

A first object of the present invention is a method for coloring keratinic material, in particular human hair, comprising the following steps:

Application of an agent (a) to the keratinic material, the agent (a) comprising:

(a1) at least one organic silicon compound from the group of the silanes with one, two or three silicon atoms, and

(a2) at least one coloring compound, comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, and

Application of an agent (b) to the keratinic material, the agent (b) containing:

(b1) at least one sealing reagent.

In the work leading to this invention it has been found that the preferably successive application of means (a) and (b) enables the production of very stable and washfast colorations on the keratinic materials. Without being restricted to this theory, it is assumed in this context that the joint use of organic silicon compound (a1) and coloring compound (a2) leads to the formation of a particularly resistant first film on the keratinic material. The first layer is sealed with the application of the second agent (b). For example, a film-forming polymer is now deposited on this first layer as a sealing reagent (b1) in the form of a further film.

This special type of packaging - i.e. the joint application of silane (a1) and coloring compound (a2) and separate application of the sealing reagent (b1) - the film system produced in this way showed an improved resistance to external influences. The coloring compounds (a2) were permanently fixed on the keratin material in this way, so that extremely washfast coloring with good resistance to shampooing could be obtained.

Keratinic material

Keratinic material is understood to mean hair, skin, and nails (such as fingernails and / or toenails, for example). Furthermore, wool, furs and feathers also fall under the definition of keratinic material. Keratinic material is preferably understood to mean human hair, human skin and human nails, in particular fingernails and toenails. Keratinic material is very particularly preferably understood to mean human hair.

Middle (a) and (bl

In the context of the method according to the invention, agents (a) and (b) are applied to the keratinic material, in particular the human hair. The two means (a) and (b) are different from each other.

In other words, a first object of the present invention is a method for

Treating keratinic material, especially human hair, comprising the following steps:

(b1) at least one sealing reagent.

Medium (a)

The agent (a) preferably contains the ingredients (a1) and (a2) essential to the invention in a cosmetic carrier, particularly preferably in an aqueous or aqueous-alcoholic cosmetic carrier. This cosmetic carrier can be liquid, gel-like or cream-like. Pasty, solid or powdery cosmetic carriers can also be used for the production of the agent (a). For the purpose of hair treatment, especially hair coloring, such carriers are, for example, creams, emulsions, gels or surfactant-containing foaming solutions, such as shampoos, foam aerosols, foam formulations or other preparations which are suitable for use on the hair.

The cosmetic carrier preferably contains - based on its weight - at least 2% by weight of water. The water content is more preferably above 10% by weight, even more preferably above 20% by weight and particularly preferably above 40% by weight. The cosmetic carrier can also be aqueous-alcoholic. In the context of the present invention, aqueous-alcoholic solutions are to be understood as meaning aqueous solutions containing 2 to 70% by weight of a Ci-C ₄ alcohol, in particular ethanol or isopropanol. The agents according to the invention can additionally contain further organic solvents, such as methoxybutanol, benzyl alcohol, ethyl diglycol or 1,2-propylene glycol. All water-soluble organic solvents are preferred. Organic silicon compounds from the group of silanes (a1)

As an essential ingredient (a1) for the invention, the agent (a) contains at least one organic silicon compound from the group of the silanes with one, two or three silicon atoms.

The agent (a) particularly preferably contains at least one organic silicon compound (a1) which is selected from silanes having one, two or three silicon atoms, the organic

Silicon compound comprises one or more hydroxyl groups and / or hydrolyzable groups per molecule.

These organic silicon compounds (a1) or organic silanes contained in the agent (a) are reactive compounds.

Organic silicon compounds, which are alternatively referred to as organosilicon compounds, are compounds that either have a direct silicon-carbon bond (Si-C) or in which the carbon is attached to the silicon via an oxygen, nitrogen or sulfur atom. Atom is linked. The organic silicon compounds of the present invention are compounds containing one to three silicon atoms. Particularly preferably contain the organic

Silicon compounds one or two silicon atoms.

According to the IUPAC rules, the term silane stands for a group of chemical compounds based on a silicon backbone and hydrogen. In the case of organic silanes, the hydrogen atoms have been completely or partially replaced by organic groups such as, for example, (substituted) alkyl groups and / or alkoxy groups. In the organic silanes, some of the hydrogen atoms can also be replaced by hydroxyl groups.

In a particularly preferred embodiment, a method according to the invention is characterized by the use of an agent (a) on the keratinous material, the agent (a) containing at least one organic silicon compound (a1) selected from silanes with one, two or three silicon atoms wherein the organic silicon compound further comprises one or more hydroxyl groups or hydrolyzable groups per molecule.

In the context of a very particularly preferred embodiment, an inventive

Process characterized by the application of an agent (a) on the keratinic material, the agent (a) containing at least one organic silicon compound (a1) selected from silanes having one, two or three silicon atoms, the organic silicon compound also having one or several basic chemical functions and one or more

Includes hydroxyl groups or hydrolyzable groups per molecule. This basic group or basic chemical function can be, for example, an amino group, an alkylamino group or a dialkylamino group, which is preferably connected to a silicon atom via a linker. The basic group is preferably an amino group, a Ci-C6-alkylamino group or a di (Ci-C6) alkylamino group.

The hydrolyzable group (s) is preferably a Ci-C6-alkoxy group, in particular an ethoxy group or a methoxy group. It is preferred if the hydrolyzable group is bonded directly to the silicon atom. If, for example, the hydrolyzable group is an ethoxy group, the organic silicon compound preferably contains a structural unit R’R “R“ ‘Si-0-CH2-CH3. The radicals R ‘, R“ and R “‘ represent the three remaining free valences of the silicon atom.

A very particularly preferred method according to the invention is characterized in that the agent (a) contains at least one organic silicon compound selected from silanes with one, two or three silicon atoms, the organic silicon compound preferably having one or more basic chemical functions and one or more Includes hydroxyl groups or hydrolyzable groups per molecule.

Very particularly good results could be obtained when the agent (a) contains at least one organic silicon compound (a1) of the formula (I) and / or (II).

The compounds of the formulas (I) and (II) are organic silicon compounds which are selected from silanes having one, two or three silicon atoms, the organic silicon compound comprising one or more hydroxyl groups and / or hydrolyzable groups per molecule.

In a further very particularly preferred embodiment, the method is characterized in that an agent is applied to the keratinous material (or the human hair), the agent (a) at least one organic silicon compound (a) of the formula (I) and / or (II) contains,

RiR ₂ NL-Si (OR ₃ ) a (R4) b (I),

in which

- Ri, R ₂ independently represent a hydrogen atom or a Ci-C6-alkyl group,

- L stands for a linear or branched, divalent Ci-C2o-alkylene group,

- R3 stands for a hydrogen atom or a Ci-C6-alkyl group,

- R4 stands for a Ci-C6-alkyl group

- a, stands for an integer from 1 to 3, and - b stands for the whole number 3 - a,

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] _h -Si (R6 ^, ) d (OR5 ^, ) c • (II), where

- R5, R5 ‘, R5“ independently of one another represent a hydrogen atom or a C1-C6 alkyl group,

- R6, R6 ‘and R6“ independently represent a Ci-C6-alkyl group,

- A, A ‘, A“, A “‘ and A ““ independently of one another represent a linear or branched, divalent Ci-C2o-alkylene group,

- R7 and Re independently of one another represent a hydrogen atom, a Ci-C6-alkyl group, a hydroxy-Ci-C6-alkyl group, a C2-C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the formula (III ) stand

- (A "") - Si (R ₆ ") d" (OR ₅ "(III),

- c, stands for an integer from 1 to 3,

- d stands for the whole number 3 - c,

- c ‘stands for an integer from 1 to 3,

- d ‘stands for the integer 3 - c‘,

- c "stands for an integer from 1 to 3,

- d "stands for the whole number 3 - c" stands,

- e stands for 0 or 1,

- f stands for 0 or 1,

- g stands for 0 or 1,

- h stands for 0 or 1,

- With the proviso that at least one of the radicals from e, f, g and h is different from 0.

The substituents Ri, R2, R3, R4, Rs, Rs ', Rs ", R6, R6', Re", R7, Rs, L, A, A ', A ", A"' and A "" in the compounds of formula (I) and (II) are exemplified below:

Examples of a Ci-C6-alkyl group are the groups methyl, ethyl, propyl, isopropyl, n-butyl, s-butyl and t-butyl, n-pentyl and n-hexyl. Propyl, ethyl and methyl are preferred alkyl radicals. Examples of a C2-C6-alkenyl group are vinyl, allyl, but-2-enyl, but-3-enyl and isobutenyl, preferred C2-C6-alkenyl radicals are vinyl and allyl. Preferred examples of a hydroxy-Ci-C6-alkyl group are a hydroxymethyl, a 2-hydroxyethyl, a 2-hydroxypropyl, a 3-hydroxypropyl, a 4-hydroxybutyl group, a 5-hydroxypentyl and a 6-hydroxyhexyl group; a 2-hydroxyethyl group is particularly preferred. Examples of an amino-Ci-C6-alkyl group are the aminomethyl group, the 2-aminoethyl group and the 3-aminopropyl group. The 2-aminoethyl group is particularly preferred. Examples of a linear divalent Ci-C2o-alkylene group are for example the methylene group (-CH2-), the ethylene group (-CH2-CH2-), the propylene group (-CH2-CH2-CH2-) and the butylene group (-CH2-CH2-CH2-CH2-). The propylene group (-CH2-CH2-CH2-) is particularly preferred. From a chain length of 3 carbon atoms, divalent alkylene groups can also be branched. Examples of branched, divalent C3-C2o-alkylene groups are (-CH2-CH (CH3) -) and (-CH2-CH (CH ₃ ) -CH ₂ -).

In the organic silicon compounds of the formula (I)

RiR ₂ NL-Si (OR ₃ ) a (R4) b (I), the radicals Ri and R ₂ independently of one another represent a hydrogen atom or a C ₁ -C 6 -alkyl group. The radicals Ri and R ₂ are very particularly preferably both a hydrogen atom.

In the middle part of the organic silicon compound is the structural unit or the linker -L- which stands for a linear or branched, divalent Ci-C ₂ o-alkylene group.

A divalent Ci-C ₂ o -alkylene group can alternatively also be referred to as a divalent or double-bonded C ₁ -C ₂ o-alkylene group, which means that each group L can form two bonds. One bond is from the amino group R1 R2N to the linker L, and the second bond is between the linker L and the silicon atom.

-L- is preferably a linear, divalent (ie divalent) Ci-C ₂ o-alkylene group. More preferably -L- stands for a linear divalent Ci-C6-alkylene group. -L- particularly preferably stands for a methylene group (-CH2-), an ethylene group (-CH2-CH2-), a propylene group (-CH2-CH2- CH2-) or a butylene group (-CH2-CH2-CH2-CH2-) . L very particularly preferably represents a propylene group (-CH2-CH2-CH2-).

The linear propylene group (-CH ₂ -CH ₂ -CH ₂ -) can alternatively also be referred to as propane-1,3-diyl group.

The organic silicon compounds of the formula (I) according to the invention

RiR ₂ NL-Si (OR ₃ ) a (R4) b (I), each have the silicon-containing grouping -Si (OR3) a (R ₄ ) b at one end

In the terminal structural unit -Si (OR3) a (R ₄ ) b, the radical R3 stands for a hydrogen atom or a Ci-C6-alkyl group, and the radical R ₄ stands for a Ci-C6-alkyl group. Particularly preferably, R3 and _R4 independently represent a methyl group or an ethyl group. Here a stands for an integer from 1 to 3, and b stands for the integer 3 - a. If a is 3, then b is 0. If a is 2, b is 1. If a is 1, b is 2.

Particularly resistant films could be produced if the agent (a) contains at least one organic silicon compound (a1) of the formula (I) in which the radicals R3, R4 independently of one another represent a methyl group or an ethyl group.

When using the method according to the invention for dyeing keratinic material, dyeings with the best wash fastness could be obtained if the agent (a) contains at least one organic silicon compound of the formula (I) in which the radicals R3, R4 independently represent a methyl group or represent an ethyl group.

In addition, dyeings with the best wash fastness properties could be obtained if the agent (a) contains at least one organic silicon compound of the formula (I) in which the radical a stands for the number 3. In this case, the remainder b stands for the number 0.

In a further preferred embodiment, the agent (a) used in the process is characterized in that it contains at least one organic silicon compound (a1) of the formula (I), where

- R3, R4 independently of one another represent a methyl group or an ethyl group and

- a stands for the number 3 and

- b stands for the number 0.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (I),

RiR ₂ NL-Si (OR ₃ ) a (R4) b (I),

in which

- Ri, R2 both stand for a hydrogen atom, and

- L stands for a linear, divalent Ci-C6-alkylene group, preferably for a propylene group (-CH2- CH2-CH2-) or for an ethylene group (-CH2-CH2-),

- R3 represents a hydrogen atom, an ethyl group or a methyl group,

- R4 stands for a methyl group or for an ethyl group,

- a stands for the number 3 and

- b stands for the number 0. Organic silicon compounds of the formula (I) which are particularly suitable for achieving the object of the invention are

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

-1 - (2-aminoethyl) silanetriol - (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane

-1 - (3-dimethylaminopropyl) silanetriol

- (2-Dimethylaminoethyl) triethoxysilane.

- (2-dimethylaminoethyl) trimethoxysilane and

-1 - (2-dimethylaminoethyl) silanetriol

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least one organic silicon compound (a1) which is selected from the group of

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

-1 - (3-aminopropyl) silanetriol

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

-1 - (2-aminoethyl) silanetriol

- (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane

-1 - (3-dimethylaminopropyl) silanetriol

- (2-Dimethylaminoethyl) triethoxysilane.

- (2-Dimethylaminoethyl) trimethoxysilane and / or

-1 - (2-dimethylaminoethyl) silanetriol.

The aforementioned organic silicon compounds of the formula (I) are commercially available. (3-Aminopropyl) trimethoxysilane can be purchased from Sigma-Aldrich, for example. (3-Aminopropyl) triethoxysilane is also commercially available from Sigma-Aldrich.

In a further embodiment, the agent according to the invention contains at least one organic silicon compound (a1) of the formula (II)

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] h-Si (R6> ( 0R5 ') c * (II). The organosilicon compounds of the formula (II) according to the invention each have the silicon-containing groups (R50) _c (R6) dSi and -Si (R6 ') d' (OR5 ') c at their two ends

In the middle part of the molecule of the formula (II) there are the groupings - (A) _e - and - [NR7- (A ')] _f and - [0- (A ”)] _g - and - [NR8- (A' ”)] _H - Here, each of the radicals e, f, g and h can independently represent the number 0 or 1, with the proviso that at least one of the radicals e, f, g and h is different from 0. In other words, contains an organic according to the invention

Silicon compound of the formula (II) at least one group from the group consisting of - (A) - and - [NR7- (A ') j- and - [0- (A ") j- and - [NR ₈ - (A'" )] -

In the two terminal structural units (R50) _c (R6) dSi- and - Si (R6 ') d' (OR5 ') c, the radicals R5, R5', R5 "independently of one another represent a hydrogen atom or a Ci-C6- Alkyl group. The radicals R6, R6 'and R6 ″ stand independently of one another for a Ci-C6-alkyl group.

Here, c stands for an integer from 1 to 3, and d stands for the integer 3 - c. If c is 3, then d is 0. If c is 2, d is 1. If c is 1, d is 2.

Similarly, c ‘stands for an integer from 1 to 3, and d‘ stands for the integer 3 - c ‘. If c ‘stands for the number 3, then d‘ equals 0. If c steht stands for the number 2, then d ‘equals 1. If c ‘stands for the number 1, then d‘ is 2.

Films with the highest stability or dyeings with the best wash fastness could be obtained if the radicals c and c ‘both stand for the number 3. In this case d and d ‘both stand for the number 0.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (II),

(R50) c (R6) dSi- (A) _e - [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A”')] h-Si (R6> ( 0R5 ') c · (II), where

- R5 and R5 ‘independently represent a methyl group or an ethyl group,

- c and c ‘both stand for the number 3 and

- d and d ‘both stand for the number 0.

If c and c 'both stand for the number 3 and d and d' both stand for the number 0, the organic silicon compounds according to the invention correspond to the formula (IIIa) (R50) 3Si- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] h-Si (OR5 ') 3 (lla) .

The radicals e, f, g and h can independently represent the number 0 or 1, at least one radical from e, f, g and h being different from zero. The abbreviations e, f, g and h therefore define which of the groupings - (A) _e - and - [NR7- (A ')] _f - and - [0- (A ”)] _g - and - [ NR8- (A ”')] _h - are located in the central part of the organic silicon compound of the formula (II).

In this context, the presence of certain groups has proven to be particularly advantageous with regard to increasing the wash fastness. Particularly good results could be obtained when at least two of the radicals e, f, g and h stand for the number 1. Very particularly preferably e and f both stand for the number 1. Furthermore, with very particular preference g and h both stand for the number 0.

If e and f both stand for the number 1 and g and h both stand for the number 0, the organic silicon compounds according to the invention correspond to the formula (Mb)

(R50) c (R6) dSi- (A) - [NR7- (A ')] - Si (R6> (0R5') c · (Mb).

The radicals A, A ‘, A“, A “‘ and A ““ stand independently of one another for a linear or branched, divalent Ci-C2o-alkylene group. The radicals A, A ‘, A ″, A ″ and A ″ ″ are preferably, independently of one another, a linear, divalent Ci-C20-alkylene group. The radicals A, A ‘, A ″, A ″ A and A ″ ″ are more preferably, independently of one another, a linear divalent Ci-C6-alkylene group.

The radicals A, A ', A ", A"' and A "" are particularly preferably, independently of one another, a methylene group (-CH2-), an ethylene group (-CH2-CH2-), a propylene group (-CH2-CH2-CH2) -) or a butylene group (-CH2-CH2-CH2-CH2-). The radicals A, A ‘, A ″, A ″ and A ″ ″ are very particularly preferably a propylene group (-CH2-CH2-CH2-).

The divalent Ci-C2o-alkylene group can alternatively be referred to as a divalent or divalent C1-C20-alkylene group, which means that each grouping A, A ‘, A“, A “‘ and A ““ can form two bonds.

The linear propylene group (-CH2-CH2-CH2-) can alternatively also be referred to as propane-1,3-diyl group.

If the radical f stands for the number 1, then contains the organic according to the invention

Silicon compound of formula (II) has a structural grouping - [NR7- (A ’)] -.

If the radical h stands for the number 1, then contains the organic

Silicon compound of the formula (II) has a structural grouping - [NR8- (A ”')] -. Here are the remainders R? and Rs independently of one another for a hydrogen atom, a C1-C6-alkyl group, a hydroxy-Ci-C6-alkyl group, a C2-C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the formula (III)

- (A "") - Si (R ₆ ") d" (OR ₅ "(HO-

The radicals R7 and R8 very particularly preferably stand independently of one another

Hydrogen atom, a methyl group, a 2-hydroxyethyl group, a 2-alkenyl group, a 2-aminoethyl group or for a grouping of the formula (III).

If the radical f stands for the number 1 and the radical h stands for the number 0, the organic silicon compound according to the invention contains the grouping [NR7- (A ')], but not the grouping - [NR8- (A ”')] now the radical R7 represents a grouping of the formula (III), then the agent (a) contains an organic silicon compound with 3 reactive silane groups.

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ")] g- [NR8- (A'")] h-Si (R6 (OR5 ') c (II),

in which

- e and f both stand for the number 1,

- g and h both stand for the number 0,

- A and A ‘independently represent a linear, divalent Ci-C6-alkylene group and

- R7 represents a hydrogen atom, a methyl group, a 2-hydroxyethyl group, a 2-alkenyl group, a 2-aminoethyl group or a grouping of the formula (III).

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one organic silicon compound of the formula (II), where

- e and f both stand for the number 1,

- g and h both stand for the number 0,

- A and A ‘independently represent a methylene group (-CH2-), an ethylene group (-CH2- CH2-) or a propylene group (-CH2-CH2-CH2),

and

Organic silicon compounds of the formula (II) which are well suited for achieving the object of the invention are - 3- (Trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- 2- [bis [3- (trimethoxysilyl) propyl] amino] ethanol

- 3- (Trimethoxysilyl) -N, N-bis [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine - N1, N1 -Bis [3- (trimethoxysilyl) propyl] -1, 2-ethanediamine,

- N1, N1 -Bis [3- (triethoxysilyl) propyl] -1, 2-ethanediamine,

- N, N-bis [3- (trimethoxysilyl) propyl] -2-propen-1-amine

- N, N-bis [3- (triethoxysilyl) propyl] -2-propen-1-amine

The aforementioned organic silicon compounds of the formula (II) are commercially available.

Bis (trimethoxysilylpropyl) amine with the CAS number 82985-35-1 can be purchased from Sigma-Aldrich, for example.

Bis [3- (triethoxysilyl) propyl] amine with the CAS number 13497-18-2 can be purchased from Sigma-Aldrich, for example.

N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine is alternatively referred to as bis (3-trimethoxysilylpropyl) -N-methylamine and can be purchased commercially from Sigma-Aldrich or Fluorochem .

3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine with the CAS number 18784-74-2 can be purchased from Fluorochem or Sigma-Aldrich, for example.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one organic silicon compound (a1) which is selected from the group of

- 3- (Trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine - N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- 2- [bis [3- (trimethoxysilyl) propyl] amino] ethanol

- 2- [bis [3- (triethoxysilyl) propyl] amino] ethanol

- 3- (Trimethoxysilyl) -N, N-bis [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine

- N1, N1 -Bis [3- (trimethoxysilyl) propyl] -1, 2-ethanediamine,

- N1, N1 -Bis [3- (triethoxysilyl) propyl] -1, 2-ethanediamine,

- N, N-bis [3- (trimethoxysilyl) propyl] -2-propene-1-amine and / or

- N, N-bis [3- (triethoxysilyl) propyl] -2-propene-1-amine.

In further tests, in particular dyeing tests, it has also been found to be particularly advantageous if the agent (a) applied to the keratinous material in the process contains at least one organic silicon compound of the formula (IV)

RgSi (ORio) k (Rll) m (IV).

The compounds of the formula (IV) are organic silicon compounds which are selected from silanes having one, two or three silicon atoms, the organic silicon compound comprising one or more hydroxyl groups and / or hydrolyzable groups per molecule.

The organic silicon compound (s) of the formula (IV) can also be referred to as silanes of the alkyl-alkoxy-silane or alkyl-hydroxy-silane type,

R ₉ Si (ORio) k (Rn) m (IV),

in which

- Rg stands for a Ci-Ci8-alkyl group,

- Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k.

In a further preferred embodiment, the process is characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (IV)

RgSi (ORio) k (Rll) m (IV),

in which

Rg stands for a Ci-Ci8-alkyl group,

Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

R11 stands for a Ci-C6-alkyl group k is an integer from 1 to 3, and

m stands for the integer 3 - k.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one further organic silicon compound of the formula (IV) in addition to the organic silicon compound or compounds of the formula (I)

R ₉ Si (ORio) k (Ri i) m (IV),

in which

- Rg stands for a Ci-Ci8-alkyl group,

- Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one further organic silicon compound of the formula (IV) in addition to the organic silicon compound or compounds of the formula (II)

R ₉ Si (ORio) k (Rn) m (IV),

in which

- Rg stands for a Ci-Ci8-alkyl group,

- Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one further organic silicon compound of the formula (IV) in addition to the organic silicon compound or compounds of the formula (I) and / or (II)

RgSi (ORio) k (Rn) m (IV),

in which

- Rg stands for a Ci-Ci8-alkyl group,

- Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k. In the organic silicon compounds of the formula (IV), the radical Rg stands for a C1-C18-alkyl group. This Ci-Ci8-alkyl group is saturated and can be linear or branched. Rg is preferably a linear Ci-Ci8-alkyl group. Rg is preferably a methyl group, a

Ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, an n-hexyl group, an n-octyl group, an n-dodecyl group or an n-octadecyl group. Rg particularly preferably represents a methyl group, an ethyl group, an n-hexyl group or an n-octyl group.

In the organic silicon compounds of the form (IV), the radical R10 represents a hydrogen atom or a Ci-C6-alkyl group. R10 particularly preferably represents a methyl group or an ethyl group.

In the organic silicon compounds of the form (IV), the radical Rn stands for a Ci-C6-alkyl group. Rn particularly preferably represents a methyl group or an ethyl group.

Furthermore, k stands for an integer from 1 to 3, and m stands for the integer 3 - k. If k is the number 3, then m is 0. If k is the number 2, then m is 1. If k is the number 1, then m is 2.

Particularly stable films, i.e. Dyeings with particularly good wash fastness properties could be obtained if an agent (a) was used in the process which contains at least one organic silicon compound (a1) of the formula (IV) in which the radical k stands for the number 3. In this case, the remainder m stands for the number 0.

Organic ones that are particularly well suited to solving the problem according to the invention

Are silicon compounds of formula (IV)

- methyltrimethoxysilane

- methyltriethoxysilane - ethyltriethoxysilane

- n-hexyltriethoxysilane

- n-octyltriethoxysilane

- n-Dodecyltrimethoxysilane and / or

- n-dodecyltriethoxysilane.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (IV) which is selected from the group from

- methyltrimethoxysilane

- methyltriethoxysilane

- ethyltrimethoxysilane

- ethyltriethoxysilane

- hexyltrimethoxysilane

- hexyltriethoxysilane

- Octyltrimethoxysilane

- octyltriethoxysilane

- dodecyltrimethoxysilane

- dodecyltriethoxysilane

- Octadecyltrimethoxysilane and / or

- Octadecyltriethoxysilane.

The organic silicon compounds described above are reactive compounds. In this context, it has been found to be preferred if the agent (a) - based on the total weight of the agent (a) - has one or more organic

Contains silicon compounds (a1) in a total amount of 0.1 to 20% by weight, preferably 1 to 15% by weight and particularly preferably 2 to 8% by weight.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) - based on the total weight of the agent (a) - has one or more organic silicon compounds (a1) in a total amount of 0.1 to 20% by weight , preferably 1 to 15% by weight and particularly preferably 2 to 8% by weight.

To achieve particularly good dyeing results, it is particularly advantageous to use the organic silicon compounds of the formula (I) and / or (II) in certain quantity ranges on average (a) to use. The agent (a) particularly preferably contains - based on the total weight of the agent (a) - one or more organic silicon compounds of the formula (I) and / or (II) in a total amount of 0.1 to 10% by weight, preferably 0.5 to 5% by weight and particularly preferably 0.5 to 3% by weight.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) - based on the total weight of the agent (a) - has one or more organic silicon compounds of the formula (I) and / or (II) in a total amount of 0 , 1 to 10% by weight, preferably 0.5 to 5% by weight and particularly preferably 0.5 to 3% by weight.

Furthermore, it has been found to be very particularly preferred if the organic silicon compound or compounds of the formula (IV) are also contained in the agent (a) in certain quantity ranges. The agent (a) particularly preferably contains - based on the total weight of the agent (a) - one or more organic silicon compounds of the formula (IV) in one

Total amount from 0.1 to 20% by weight, preferably 2 to 15% by weight and particularly preferably 4 to 9% by weight.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) - based on the total weight of the agent (a) - has one or more organic silicon compounds of the formula (IV) in a total amount of 0.1 to 20 wt. -%, preferably 2 to 15% by weight and particularly preferably 3.2 to 10% by weight.

In the course of the work leading to this invention it has been found that on the

keratinic material, particularly stable and uniform films could also be obtained when the agent (a) contains two structurally different organic silicon compounds.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least two structurally different organic silicon compounds.

In a preferred embodiment, a method is characterized in that an agent (a) is applied to the keratinic material, which is at least one organic

Contains silicon compounds of the formula (I) and at least one organic silicon compound of the formula (IV).

In an explicitly very particularly preferred embodiment, a method according to the invention is characterized in that an agent (a) which contains at least one organic silicon compound of the formula (I) selected from the group is used on the keratinic material (3-aminopropyl) triethoxysilane and (3-aminopropyl) trimethoxysilane is selected, and additionally contains at least one organic silicon compound of the formula (IV), which is selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, hexyltrimethoxysilane and hexyltriethoxysilane.

In a further preferred embodiment, a method is characterized in that the agent (a) - based on the total weight of the agent (a) - contains:

- 0.5 to 5 wt .-% of at least one first organic silicon compound (a1) selected from the group consisting of (3-aminopropyl) trimethoxysilane, (3-aminopropyl) triethoxysilane, (2-aminoethyl) trimethoxysilane, (2-aminoethyl) ) triethoxysilane, (3-dimethylaminopropyl) trimethoxysilane, (3-dimethylaminopropyl) triethoxysilane, (2-dimethylaminoethyl) trimethoxysilane and (2-dimethylaminoethyl) triethoxysilane, and

3.2 to 10% by weight of at least one second organic silicon compound (a1) selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, octyltrimethoxysilane,

Octyltriethoxysilane, dodecyltrimethoxysilane, dodecyltriethoxysilane, octadecyltrimethoxysilane and octadecyltriethoxysilane.

In the context of this embodiment, the agent (a) contains one or more organic

Silicon compounds of a first group in a total amount of 0.5 to 3% by weight. The organic silicon compounds of this first group are selected from the group consisting of (3-aminopropyl) trimethoxysilane, (3-aminopropyl) triethoxysilane, (2-aminoethyl) trimethoxysilane, (2- aminoethyl) triethoxysilane, (3-dimethylaminopropyl) trimethoxysilane, (3- Dimethylaminopropyl) triethoxysilane (2-dimethylaminoethyl) trimethoxysilane and / or (2-dimethylaminoethyl) triethoxysilane.

In the context of this embodiment, the agent (a) contains one or more organic

Silicon compounds of a second group in a total amount of 3.2 to 10% by weight. The organic silicon compounds of this second group are selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane,

Hexyltrimethoxysilane, hexyltriethoxysilane, octyltrimethoxysilane, octyltriethoxysilane,

Dodecyltrimethoxysilane, dodecyltriethoxysilane, octadecyltrimethoxysilane and / or

Octadecyltriethoxysilane.

Even the addition of small amounts of water leads to hydrolysis in the case of organic silicon compounds with at least one hydrolyzable group. The hydrolysis products and / or organic silicon compounds with at least one hydroxyl group can be in a

Condensation reaction react with each other. Because of this, both the

organosilicon compounds with at least one hydrolyzable group as well as their Hydrolysis and / or condensation products can be contained in the agent (a). When using organosilicon compounds with at least one hydroxyl group, both the organic silicon compounds with at least one hydroxyl group and their

Condensation products may be contained in the agent (a).

A condensation product is understood to mean a product that is formed by the reaction of at least two organic silicon compounds each having at least one hydroxyl group or hydrolyzable group per molecule with elimination of water and / or with elimination of an alkanol. The condensation products can be, for example, dimers, but also trimers or oligomers, the condensation products being in equilibrium with the monomers. Depending on the amount of water used or consumed in the hydrolysis, the equilibrium shifts from monomeric organic silicon compounds to condensation product.

Particularly good results could be obtained if organic silicon compounds of the formula (I) and / or (II) were used in the process. Since, as already described above, hydrolysis / condensation starts even with traces of moisture, these are also

Condensation products of the organic silicon compounds (I) and / or (II) thereof

Embodiment includes.

Coloring compounds (a2)

When the agent (a) is used on the keratinic material, the organic silicon compound (s) (a1), which comprise one or more hydroxyl groups or hydrolyzable groups per molecule, are first hydrolyzed and oligomerized or polymerized in the presence of water. The hydrolysis products or oligomers formed in this way have a particularly high affinity for the surface of the keratinous material. Due to the simultaneous presence of the coloring compounds (a2) in the means (a), these are integrated into the resulting oligomers or polymers, so that a colored film is produced on the keratinous material. Following the application of the agent (a), the agent (b) is now applied. The successive application of means (a) and (b) creates a color that is particularly resistant to external influences. The coloring compounds included in these resistant films have good wash fastness.

As constituent (a2) essential to the invention, the agent (a) used in the dyeing process therefore contains at least one coloring compound, comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment.

The substrate platelets have an average thickness of at most 50 nm, preferably less than 30 nm, particularly preferably at most 25 nm and particularly preferably at most 20 nm. The average thickness of the substrate platelets is at least 1 nm, preferably at least 2.5 nm, particularly preferably at least 5 nm, for example at least 10 nm.

Preferred ranges for the thickness of the substrate platelets are 2.5 to 50 nm, 5 to 50 nm, 10 to 50 nm; 2.5 to 30 nm, 5 to 30 nm, 10 to 30 nm; 2.5 to 25 nm, 5 to 25 nm, 10 to 25 nm, 2.5 to 20 nm, 5 to 20 nm and 10 to 20 nm. Each substrate plate preferably has a thickness that is as uniform as possible.

Due to the small thickness of the substrate platelets, the pigment is particularly thick

Opacity on.

The substrate platelets are monolithic. In this context, monolithic means consisting of a single closed unit without breaks, layers or inclusions, although changes in structure can occur within the substrate platelets. The substrate platelets are preferably constructed homogeneously, i. E. that no concentration gradient occurs within the platelets. In particular, the substrate platelets are not constructed in layers and have no particles or particles distributed therein.

The size of the substrate platelet can be matched to the particular application, in particular the desired effect on the keratinic material. As a rule, the substrate platelets have a mean largest diameter of about 2 to 200 μm, in particular about 5 to 100 μm.

In a preferred embodiment, the aspect ratio, expressed by the ratio of the mean size to the average thickness, is at least 80, preferably at least 200, more preferably at least 500, particularly preferably more than 750. The average size of the uncoated substrate platelets is the d50 value of the uncoated

Understood substrate platelets. Unless otherwise stated, the d50 value was determined using a Sympatec Helos device with Quixel wet dispersion. It became

Sample preparation the sample to be examined is predispersed in isopropanol for a period of 3 minutes.

The substrate platelets can be constructed from any material that can be brought into platelet form.

They can be of natural origin, but also synthetically produced. Materials from which the substrate platelets can be constructed are, for example, metals and metal alloys, metal oxides, preferably aluminum oxide, inorganic compounds and minerals such as mica and (semi) precious stones, as well as plastics. The substrate platelets are preferably made of

Metal (alloys) built up. Any metal suitable for metallic luster pigments can be considered as the metal. Such metals include iron and steel, as well as all air and water-resistant (semi) metals such as platinum, zinc, chromium, molybdenum and silicon, and their alloys such as

Aluminum bronze and brass. Preferred metals are aluminum, copper, silver and gold.

Preferred substrate flakes are aluminum flakes and brass flakes, where

Substrate platelets made of aluminum are particularly preferred.

Vacuum metallized pigments (VMP) can be obtained, for example, by releasing metals, metal alloys or metal oxides from appropriately coated foils. They are distinguished by a particularly small thickness of the substrate platelets in the range from 5 to 50 nm and by a particularly smooth surface with increased reflectivity. Substrate platelets which comprise a pigment metallized in a vacuum are also referred to in this application as VMP substrate platelets. VMP substrate platelets made of aluminum can be obtained, for example, by releasing aluminum from metallized foils.

The substrate platelets made of metal or metal alloy can be passivated, for example by anodizing (oxide layer) or chromating.

Uncoated VMP substrate platelets, especially those made of metal or metal alloy, reflect the incident light to a high degree and produce a light-dark flop, but no color impression.

A color impression can be generated, for example, due to optical interference effects. Such pigments can be based on at least once coated substrate platelets. These show interference effects due to the superposition of differently refracted and reflected light beams.

Accordingly, preferred pigments are pigments based on a coated VMP substrate platelet. The substrate platelet preferably has at least one coating B made of a high-index metal oxide with a coating thickness of at least 50 nm. A further coating A is preferably located between the coating B and the surface of the substrate platelet. If necessary, another coating C, which is different from the layer B below, is located on the layer B.

Suitable materials for the coatings A, B and C are all substances that can be applied permanently and in film form to the substrate platelets and, in the case of the layers A and B, have the required optical properties. In general, a coating of part of the surface of the substrate flakes is sufficient to obtain a pigment with a glossy effect. For example, only the upper and / or lower side of the substrate platelets can be coated, with the side surface (s) being cut out. Preferably the entire surface is of the optionally passivated substrate platelets, including the side surfaces, covered by coating B. The substrate platelets are therefore completely encased by coating B. This improves the optical properties of the pigment and increases the mechanical and chemical resistance of the pigments. The foregoing also applies to layer A and preferably also to layer C, if any.

Although several coatings A, B and / or C can be present in each case, the coated substrate platelets preferably each have only one coating A, B and, if present, C.

The coating B is made up of at least one high-index metal oxide. High refractive index materials have a refractive index of at least 1.9, preferably at least 2.0 and particularly preferably at least 2.4. The coating B preferably comprises at least 95% by weight, particularly preferably at least 99% by weight, of high-index metal oxide (s).

The coating B has a thickness of at least 50 nm. The thickness of coating B is preferably not more than 400 nm, particularly preferably at most 300 nm.

High refractive index metal oxides suitable for coating B are preferably selective

light-absorbing (i.e. colored) metal oxides, such as iron (III) oxide (a- and y-Fe203, red), cobalt (II) oxide (blue), chromium (III) oxide (green), titanium (III) oxide (blue) , is usually in a mixture with titanium oxynitrides and titanium nitrides) and vanadium (V) oxide (orange) and mixtures thereof. Colorless, high-index oxides such as titanium dioxide and / or zirconium oxide are also suitable.

Coating B can contain a selectively absorbing dye, preferably 0.001 to 5% by weight, particularly preferably 0.01 to 1% by weight, based in each case on the total amount of coating B. Organic and inorganic dyes that are stable in the have a metal oxide coating installed.

The coating A preferably has at least one low refractive index metal oxide and / or metal oxide hydrate. Coating A preferably comprises at least 95% by weight, particularly preferably at least 99% by weight, of low-refractive-index metal oxide (hydrate). Low refractive index

Materials have a refractive index of at most 1.8, preferably at most 1.6.

The low-refractive index metal oxides which are suitable for coating A include, for example, silicon (di) oxide, silicon oxide hydrate, aluminum oxide, aluminum oxide hydrate, boron oxide, germanium oxide, manganese oxide, magnesium oxide and mixtures thereof, silicon dioxide being preferred. The coating A preferably has a thickness of 1 to 100 nm, particularly preferably 5 to 50 nm, particularly preferably 5 to 20 nm. The distance between the surface of the substrate platelets and the inner surface of coating B is preferably at most 100 nm, particularly preferably at most 50 nm, particularly preferably at most 20 nm. Because the thickness of coating A and thus the distance between the surface of the substrate platelets and of a coating B is in the range specified above, it can be ensured that the pigments have a high hiding power.

If the pigment based on a VMP substrate flake has only one layer A, it is preferred for the pigment to have a VMP substrate flake made of aluminum and a layer A made of silicon dioxide. If the pigment based on a VMP substrate flake has a layer A and a layer B, it is preferred for the pigment to have a VMP substrate flake made of aluminum, a layer A made of silicon dioxide and a layer B made of iron oxide.

According to a preferred embodiment, the pigments have a further coating C made of a metal oxide (hydrate), which is different from the coating B below.

Suitable metal oxides are, for example, silicon (di) oxide, silicon oxide hydrate, aluminum oxide, aluminum oxide hydrate, zinc oxide, tin oxide, titanium dioxide, zirconium oxide, iron (III) oxide and chromium (III) oxide. Silica is preferred.

The coating C preferably has a thickness of 10 to 500 nm, particularly preferably 50 to 300 nm. By providing the coating C, for example based on T1O2, better interference can be achieved, with a high hiding power being ensured.

Layers A and C serve in particular as protection against corrosion and also for chemical and physical stabilization. Layers A and C are particularly preferably contained

Silicon dioxide or aluminum oxide, which are applied by the sol-gel process. This method comprises dispersing the uncoated VMP substrate flakes or the VMP substrate flakes already coated with layer A and / or layer B in a solution of a

Metal alkoxide such as tetraethyl orthosilicate or aluminum triisopropoxide (usually in a solution of organic solvent or a mixture of organic solvent and water with at least 50% by weight organic solvent such as a C1 to C4 alcohol), and adding a weak base or acid to hydrolyze the metal alkoxide whereby a film of the metal oxide forms on the surface of the (coated) substrate platelets.

The layer B can, for example, by hydrolytic decomposition of one or more organic metal compounds and / or by precipitation of one or more dissolved metal salts and, if necessary, subsequent aftertreatment (for example conversion of a hydroxide-containing compound formed

Layers in the oxide layers by annealing) are produced. Although each of the coatings A, B and / or C can be built up from a mixture of two or more metal oxides (hydrate), each of the coatings is preferably built up from a metal oxide (hydrate).

The pigments based on coated VMP substrate platelets preferably have a thickness of 70 to 500 nm, particularly preferably 100 to 400 nm, particularly preferably 150 to 320 nm, for example 180 to 290 nm. Due to the small thickness of the substrate platelets, the pigment has a particularly high hiding power. The small thickness of the coated

Substrate platelets are achieved in particular in that the thickness of the uncoated

The substrate platelet is small, but also because the thicknesses of the coatings A and, if present, C are set to the smallest possible value. The thickness of coating B determines the color impression of the pigment.

The adhesion and abrasion resistance of pigments based on coated VMP substrate platelets in the keratinous material can be significantly increased by adding organic compounds such as silanes to the outermost layer, depending on the structure of layer A, B or C,

Phosphoric acid esters, titanates, borates or carboxylic acids is modified. The organic compounds are bound to the surface of the outermost layer A, B or C, preferably containing metal oxide. The outermost layer designates the layer which is spatially furthest away from the VMP substrate plate. The organic compounds are preferably functional silane compounds which can bind to the layer A, B or C containing metal oxide. These can be either mono- or bifunctional compounds. Examples of bifunctional organic compounds are methacryloxypropenyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3- acryloxypropyltrimethoxysilane, 2-acryloxyethyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-acryloxypropyltrimethoxysilane, 2-Methacryloxyethyl- triethoxysilane, 2-acryloxyethyltriethoxysilane, 3-methacryloxypropyltris (methox- yethoxyjsilan, 3- methacryloxypropyltris ( butoxyethoxy) silane, 3-methacryloxypropyltris (propoxy) silane, 3- methacryloxypropyltris (butoxy) silane, 3-acryloxypropyltris (methoxyethoxy) silane, 3- acryloxypropyltris (butoxyethoxy) silane, 3-acryloxypropyltris (butoxy) silane, vinyltrimethoxy Vinylethyl dichlorosilane, vinylmethyldiacetoxysilane, vinylmethyldichlorosilane, vinylmethyldiethoxysilane, vinyltriacetoxysilane, vinyltrichlorosilane, phenylvinyldiethoxysilane, or phenylallyldichlorosilane. Furthermore, a modification with a monofunctional silane or, in particular an arylsilane, can be performed lie. This has only one functional group which can covalently bind pigments based on coated VMP substrate platelets (ie to the outermost metal oxide-containing layer) or, if not completely covered, to the metal surface. The hydrocarbon residue of the silane faces away from the pigment. Depending on the type and nature of the hydrocarbon radical of the silane, a different degree of hydrophobicity of the pigment is achieved. Examples of such silanes are Hexadecyltrimethoxysilane, propyltrimethoxysilane, etc. Pigments based on silicon dioxide-coated aluminum substrate platelets are surface-modified with a monofunctional silane. Octyltrimethoxysilane, octyltriethoxysilane,

Hecadecyltrimethoxysilane and hecadecyltriethoxysilane. By the changed

Surface properties / water repellency can improve adhesion,

Abrasion resistance and alignment in the application can be achieved.

It has been shown that pigments based on VMP substrate platelets with such

Surface modification also show better compatibility with the organosilicon compounds used and / or their condensation or polymerization products.

Particularly good results could be obtained if the agent (a) - based on the total weight of the agent (a) - has one or more pigments based on a VMP substrate platelet in a total amount of 0.01 to 10% by weight, preferably of 0.1 to 8% by weight, more preferably from 0.2 to 6% by weight and very particularly preferably from 0.5 to 4.5% by weight.

Pigments based on a substrate platelet, which comprises a vacuum metallized pigment, are available, for example, under the name Alegrace® Marvelous from Schlenk Metallic Pigments GmbH.

Pigments based on a VMP substrate platelet have a defined particle size in terms of thickness and particle area. With an appropriate amount used, this enables the keratinic material to be completely covered. In addition, dyeings with pigments based on VMP substrate platelets have a very high rub and wash fastness due to their smooth surface structure.

In addition to the pigment based on a VMP substrate platelet, the agent (a) can comprise further coloring compounds selected from the group consisting of pigments and / or substantive dyes.

The use of pigments has proven to be very particularly preferred in this context.

In a further very particularly preferred embodiment, a process is characterized in that the agent (a) contains at least one further coloring compound (a2) from the group of pigments.

Pigments in the context of the present invention are understood to mean coloring compounds which, at 25 ° C., have a solubility in water of less than 0.5 g / l, preferably of less than 0.1 g / L, even more preferably less than 0.05 g / L. The water solubility can be achieved, for example, using the method described below: Weigh out 0.5 g of the pigment in a beaker. A stir fry is added. Then one liter of distilled water is added. This mixture is heated to 25 ° C. for one hour while stirring on a magnetic stirrer. Are still undissolved in the mixture after this period

If components of the pigment are visible, the solubility of the pigment is below 0.5 g / L.

If the pigment-water mixture cannot be assessed visually due to the high intensity of the pigment which may be present in finely dispersed form, the mixture is filtered. If a proportion of undissolved pigments remains on the filter paper, the solubility of the pigment is below 0.5 g / L.

Suitable color pigments can be of inorganic and / or organic origin.

In a preferred embodiment, the agent according to the invention is characterized in that the agent (a) has at least one further coloring compound (a2) from the group of

contains inorganic and / or organic pigments.

Preferred color pigments are selected from synthetic or natural inorganic pigments. Inorganic color pigments of natural origin can be made from chalk, ocher, umber, green earth, burnt Terra di Siena or graphite, for example. Furthermore, as inorganic color pigments, black pigments such. B. iron oxide black, colored pigments such. B. ultramarine or iron oxide red and fluorescent or phosphorescent pigments can be used.

Colored metal oxides, hydroxides and oxide hydrates, mixed-phase pigments, sulfur-containing silicates, silicates, metal sulfides, complex metal cyanides, metal sulfates, metal chromates and / or molybdates are particularly suitable. Particularly preferred color pigments are black iron oxide (CI 77499), yellow iron oxide (CI 77492), red and brown iron oxide (CI 77491), manganese violet (CI 77742), ultramarines (sodium aluminum sulfosilicates, CI 77007, Pigment Blue 29), chromium oxide hydrate

(CI77289), iron blue (Ferric Ferrocyanide, CI77510) and / or carmine (Cochineal).

Color pigments which are likewise particularly preferred according to the invention are colored pearlescent pigments. These are usually based on mica and / or mica and can be coated with one or more metal oxides. Mica is one of the layered silicates. The most important representatives of these silicates are muscovite, phlogopite, paragonite, biotite, lepidolite and margarite. To produce the pearlescent pigments in conjunction with metal oxides, the mica, predominantly muscovite or phlogopite, is coated with a metal oxide. As an alternative to natural mica, synthetic mica coated with one or more metal oxide (s) can also be used as a pearlescent pigment. Particularly preferred pearlescent pigments are based on natural or synthetic mica (mica) and are coated with one or more of the aforementioned metal oxides. The color of the respective pigments can be varied by varying the layer thickness of the metal oxide (s).

Likewise preferred pigments based on mica are synthetically produced mica flakes coated with metal oxide, in particular based on synthetic fluorophlogopite (INCI:

Synthetic fluorophlogopite). The synthetic fluorophlogopite platelets are coated, for example, with tin oxide, iron oxide (s) and / or titanium dioxide. The metal oxide layers can also have pigments such as iron (II l) hexacyanidoferrate (l l / l II) or carmine red. Such mica pigments are available, for example, under the name SYNCRYSTAL from Eckart.

In a further preferred embodiment, the method is characterized in that the agent (a) contains at least one further coloring compound (a2) from the group of inorganic pigments, which is selected from the group of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides , complex metal cyanides, metal sulfates, bronze pigments and / or colored pigments based on mica or mica coated with at least one metal oxide and / or metal oxychloride.

In a further preferred embodiment, the method is characterized in that the agent (a) contains at least one further coloring compound (a2) from the group of pigments, which is selected from pigments based on mica or mica, those with one or more

Metal oxides from the group of titanium dioxide (CI 77891), black iron oxide (CI 77499), yellow iron oxide (CI 77492), red and / or brown iron oxide (CI 77491, CI 77499), manganese violet (CI 77742), ultramarines (sodium aluminum sulfosilicates , CI 77007, Pigment Blue 29), chromium oxide hydrate (CI 77289), chromium oxide (CI 77288) and / or iron blue (Ferric Ferrocyanide, CI 77510) are coated.

Further suitable pigments are based on metal oxide-coated platelet-shaped borosilicates. These are coated, for example, with tin oxide, iron oxide (s), silicon dioxide and / or titanium dioxide. Such borosilicate-based pigments are available, for example, under the name MIRAGE from Eckart or Reflecks from BASF SE.

Examples of particularly suitable color pigments are commercially available, for example under

Trade names Rona®, Colorona®, Xirona®, Dichrona® and Timiron® from Merck, Ariabel® and Unipure® from Sensient, Prestige® from Eckart Cosmetic Colors, Flamenco®, Cellini®, Cloisonne®, Duocrome® , Gemtone®, Timica®, MultiReflections, Chione from BASF SE and Sunshine® from Sunstar. Particularly preferred color pigments with the trade name Colorona® are, for example:

Colorona Copper, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Passion Orange, Merck, Mica, CI 77491 (Iran Oxides), Alumina

Colorona Patina Silver, Merck, MICA, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)

Colorona RY, Merck, CI 77891 (TITANIUM DIOXIDE), MICA, CI 75470 (CARMINE)

Colorona Oriental Beige, Merck, MICA, CI 77891 (TITANIUM DIOXIDE), CI 77491 (IRON OXIDES) Colorona Dark Blue, Merck, MICA, TITANIUM DIOXIDE, FERRIC FERROCYANIDE

Colorona Chameleon, Merck, CI 77491 (IRON OXIDES), MICA

Colorona Aborigine Amber, Merck, MICA, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDES) Colorona Blackstar Blue, Merck, CI 77499 (IRON OXIDES), MICA

Colorona Patagonian Purple, Merck, MICA, CI 77491 (IRON OXIDES), CI 77891 (TITANIUM

DIOXIDE), CI 77510 (FERRIC FERROCYANIDE)

Colorona Red Brown, Merck, MICA, CI 77491 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDES) Colorona Russet, Merck, CI 77491 (TITANIUM DIOXIDES), MICA, CI 77891 (IRON OXIDES)

Colorona Imperial Red, Merck, MICA, TITANIUM DIOXIDE (CI 77891), D&C RED NO. 30 (CI 73360) Colorona Majestic Green, Merck, CI 77891 (TITANIUM DIOXIDE), MICA, CI 77288

(CHROMIUM OXIDE GREENS)

Colorona Light Blue, Merck, MICA, TITANIUM DIOXIDE (CI 77891), FERRIC FERROCYANIDE (CI 77510)

Colorona Red Gold, Merck, MICA, CI 77891 (TITANIUM DIOXIDE), CI 77491 (IRON OXIDES) Colorona Gold Plus MP 25, Merck, MICA, TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491) Colorona Carmine Red, Merck, MICA, TITANIUM DIOXIDE, CARMINE

Colorona Blackstar Green, Merck, MICA, CI 77499 (IRON OXIDES)

Colorona Bordeaux, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Bronze, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Bronze Fine, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Fine Gold MP 20, Merck, MICA, CI 77891 (TITANIUM DIOXIDES), CI 77491 (IRON OXIDES) Colorona Sienna Fine, Merck, CI 77491 (IRON OXIDES), MICA

Colorona Sienna, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Precious Gold, Merck, Mica, CI 77891 (Titanium dioxide), Silica, CI 77491 (Iran oxides), Tin oxide

Colorona Sun Gold Sparkle MP 29, Merck, MICA, TITANIUM DIOXIDE, IRON OXIDES, MICA, CI 77891, CI 77491 (EU)

Colorona Mica Black, Merck, CI 77499 (Iran oxides), Mica, CI 77891 (Titanium dioxide)

Colorona Bright Gold, Merck, Mica, CI 77891 (Titanium dioxide), CI 77491 (Iran oxides)

Colorona Blackstar Gold, Merck, MICA, CI 77499 (IRON OXIDES)

Colorona SynCopper, Merck, Synthetic Fluorphlogopite (and) Iran Oxides Colorona SynBronze, Merck, Synthetic Fluorphiogopite (and) Iron Oxides

Other particularly preferred color pigments with the trade name Xirona® are, for example:

Xirona Golden Sky, Merck, Silica, CI 77891 (Titanium Dioxide), Tin Oxide

Xirona Caribbean Blue, Merck, Mica, CI 77891 (Titanium Dioxide), Silica, Tin Oxide

Xirona Kiwi Rose, Merck, Silica, CI 77891 (Titanium Dioxide), Tin Oxide

Xirona Magic Mauve, Merck, Silica, CI 77891 (Titanium Dioxide), Tin Oxide.

Xirona Le Rouge, Merck, Iron Oxides (and) Silica

In addition, particularly preferred color pigments with the trade name Unipure®

for example:

Unipure Red LC 381 EM, Sensient CI 77491 (Iron Oxides), Silica

Unipure Black LC 989 EM, Sensient, CI 77499 (Iron Oxides), Silica

Unipure Yellow LC 182 EM, Sensient, CI 77492 (Iron Oxides), Silica

Pigments with the trade name Flamenco® are also particularly preferred

for example:

Flamenco® Summit Turquoise T30D, BASF, Titanium Dioxide (and) Mica

Flamenco® Super Violet 530Z, BASF, Mica (and) Titanium Dioxide

In a further embodiment of the process, the agent (a) can also contain one or more coloring compounds from the group of organic pigments as a further coloring compound (a2).

The organic pigments are correspondingly insoluble, organic dyes or color lakes, for example from the group of nitroso, nitro, azo, xanthene, anthraquinone, isoindolinone, isoindoline, quinacridone, perinone, perylene , Diketopyrrolopyorrole, indigo, thioindido, dioxazine, and / or triarylmethane compounds can be selected.

Particularly suitable organic pigments are, for example, carmine, quinacridone, phthalocyanine, sorghum, blue pigments with the color index numbers CI 42090, CI 69800, CI 69825, CI 73000, CI 74100, CI 74160, yellow pigments with the color index numbers CI 1 1680, CI 1 1710, CI 15985, CI 19140, CI 20040, CI 21 100, CI 21 108, CI 47000, CI 47005, green pigments with the Color Index numbers CI 61565, CI 61570, CI 74260, orange pigments with the Color Index numbers CI 1 1725, CI 15510, CI 45370, CI 71 105, red pigments with the color index numbers CI 12085, CI 12120, CI 12370, CI 12420, CI 12490, CI 14700, CI 15525, CI 15580, CI 15620, CI 15630, CI 15800, CI 15850, CI 15865, CI 15880, CI 17200, CI 26100, CI 45380, CI 45410, CI 58000, CI 73360, CI 73915 and / or CI 75470. In a further particularly preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least one further coloring compound (a2) from the group of organic pigments, which is selected from the group of carmine, quinacridone, phthalocyanine, sorgho, blue pigments with the color index numbers CI 42090, CI 69800, CI 69825, CI 73000, CI 74100, CI 74160, yellow pigments with the color index numbers CI 1 1680, CI 1 1710, CI 15985, CI 19140, CI 20040, CI 21 100, CI 21 108, CI 47000, CI 47005, green pigments with the color index numbers CI 61565, CI 61570, CI 74260, orange pigments with the color index numbers CI 1 1725, CI 15510, CI 45370, CI 71 105, red pigments with the color index numbers CI 12085, CI 12120, CI 12370, CI 12420, CI 12490, CI 14700, CI 15525, CI 15580, CI 15620, CI 15630, CI 15800, CI 15850, CI 15865, CI 15880, CI 17200, CI 26100, CI 45380, CI 45410, CI 58000, CI 73360, CI 73915 and / or CI 75470.

The organic pigment can also be a colored lacquer. In the context of the invention, the term “colored varnish” is understood to mean particles which comprise a layer of absorbed dyes, the unit of particles and dyestuff being covered by the above.

Conditions is insoluble. The particles can, for example, be inorganic substrates, which can be aluminum, silica, calcium borosilicate, calcium aluminum borosilicate or also aluminum.

The alizarin color varnish, for example, can be used as the color varnish.

Because of their excellent light and temperature stability, the use of the aforementioned pigments in the agent (a) is particularly preferred. It is also preferred if the pigments used have a certain particle size. This particle size leads, on the one hand, to a uniform distribution of the pigments in the polymer film formed and, on the other hand, avoids a rough hair or skin feel after the cosmetic agent has been applied. It is therefore advantageous according to the invention if the at least one pigment has an average particle size D50 of 1 to 50 μm, preferably 5 to 45 μm, more preferably 10 to 40 μm, in particular 14 to 30 μm. The mean particle size D50 can be determined, for example, using dynamic light scattering (DLS).

In addition to the pigment based on a VMP substrate platelet, the agent (a) can contain other effect pigments, such as pigments based on lamellar substrate platelets and / or pigments based on lenticular substrate platelets, as further coloring compound (s) (a2).

In a further preferred embodiment, the method is characterized in that the agent (a) - based on the total weight of the agent (a) - contains one or more further pigments a total amount of 0.01 to 10% by weight, preferably from 0.1 to 8% by weight, more preferably from 0.2 to 6% by weight and very particularly preferably from 0.5 to 4.5% by weight .-% contains.

The agents (a) used in the process can also contain one or more substantive dyes as further coloring compound (s) (a2). Substantive dyes are dyes that are absorbed directly onto the hair and do not require an oxidative process to develop the color. Substantive dyes are usually nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones, triarylmethane dyes or indophenols.

The substantive dyes for the purposes of the present invention have a solubility in water (760 mmHg) at 25 ° C. of more than 0.5 g / L and are therefore not to be regarded as pigments. The substantive dyes for the purposes of the present invention preferably have a

Solubility in water (760 mmHg) at 25 ° C of more than 1 g / L.

Substantive dyes can be divided into anionic, cationic and nonionic substantive dyes.

In a further preferred embodiment, the process is characterized in that the agent (a) contains at least one anionic, cationic and / or nonionic substantive dye as a further coloring compound (a2).

In a further preferred embodiment, the method is characterized in that the agent (a) contains at least one further coloring compound (a2) from the group of anionic, nonionic and / or cationic substantive dyes.

Suitable cationic substantive dyes are, for example, Basic Blue 7, Basic Blue 26, Basic Violet 2 and Basic Violet 14, Basic Yellow 57, Basic Red 76, Basic Blue 16, Basic Blue 347 (Cationic Blue 347 / Dystar), HC Blue No. 16, Basic Blue 99, Basic Brown 16, Basic Brown 17, Basic Yellow 57, Basic Yellow 87, Basic Orange 31, Basic Red 51 Basic Red 76

As nonionic substantive dyes, for example, nonionic nitro and

Quinone dyes and neutral azo dyes are used. Suitable non-ionic

Direct dyes are those under the international names or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, HC Orange 1, Disperse Orange 3, HC Red 1, HC Red 3, HC Red 10 , HC Red 1 1, HC Red 13, HC Red BN, HC Blue 2, HC Blue 1 1, HC Blue 12, Disperse Blue 3, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9 known compounds, as well 1,4-diamino-2-nitrobenzene, 2-amino-4-nitrophenol, 1,4-bis- (2-hydroxyethyl) -amino-2-nitrobenzene, 3-nitro-4- (2-hydroxyethyl) -aminophenol, 2- (2-hydroxyethyl) amino-4,6-dinitrophenol, 4 - [(2-hydroxyethyl) amino] -3-nitro-1 -methylbenzene, 1-amino-4- (2-hydroxyethyl) - amino-5-chloro-2-nitrobenzene, 4-amino-3-nitrophenol, 1 - (2'-ureidoethyl) amino-4-nitrobenzene, 2 - [(4-amino-2-nitrophenyl) amino] benzoic acid, 6 -Nitro-1, 2,3,4-tetrahydroquinoxaline, 2-hydroxy-1,4-naphthoquinone, picric acid and its salts, 2-amino-6-chloro-4-nitrophenol, 4-ethylamino-3-nitrobenzoic acid and 2- Chloro-6-ethylamino-4-nitrophenol.

In the course of the work leading to this invention it has been found that, in particular with agents (a) which contain at least one anionic substantive dye, dyeings with particularly high color intensity can be produced.

In an explicitly very particularly preferred embodiment, the method is therefore characterized in that the agent (a) also contains at least one anionic substantive dye.

Anionic substantive dyes are also referred to as acid dyes. Under

Acid dyes are substantive dyes understood that at least one

Carboxylic acid grouping (-COOH) and / or a sulfonic acid grouping (-SO3H). Depending on the pH, the protonated forms (-COOH, -SO3H) of the carboxylic acid or sulfonic acid groups are in equilibrium with their deprotonated forms (-COO-, -S03 ^_ ). The proportion of protonated forms increases with decreasing pH. If substantive dyes are used in the form of their salts, the carboxylic acid groups or

Sulphonic acid groups are present in deprotonated form and are neutralized with corresponding stoichiometric equivalents of cations in order to maintain electroneutrality. Acid dyes according to the invention can also be used in the form of their sodium salts and / or their potassium salts.

The acid dyes for the purposes of the present invention have a solubility in water (760 mmHg) at 25 ° C. of more than 0.5 g / L and are therefore not to be regarded as pigments. For the purposes of the present invention, the acid dyes preferably have a solubility in water (760 mmHg) at 25 ° C. of more than 1 g / l.

The alkaline earth salts (such as calcium salts and magnesium salts) or aluminum salts of acid dyes often have a poorer solubility than the corresponding alkali salts. If the solubility of these salts is below 0.5 g / L (25 ° C, 760 mmHg), they do not fall under the definition of a substantive dye.

An essential feature of the acid dyes is their ability to form anionic charges, the carboxylic acid or sulfonic acid groups responsible for this usually being linked to different chromophoric systems. Suitable chromophoric systems can be found, for example, in the structures of nitrophenylenediamines, nitroaminophenols, azo dyes, Anthraquinone dyes, triarylmethane dyes, xanthene dyes, rhodamine dyes, oxazine dyes and / or indophenol dyes.

In the context of one embodiment, a method for coloring keratinic material is therefore preferred, which is characterized in that the agent (a) furthermore contains at least one anionic substantive dye selected from the group of

Nitrophenylenediamines, the nitroaminophenols, the azo dyes, the anthraquinone dyes, the triarylmethane dyes, the xanthene dyes, the rhodamine dyes, the oxazine dyes and / or the indophenol dyes, the dyes from the aforementioned group each having at least one carboxylic acid group (-COOH) (-COONa), a potassium carboxylate group (-COOK), a sulfonic acid group (-SO3H), a sodium sulfonate group (- SOsNa) and / or a potassium sulfonate group (-SO3K).

One or more compounds from the following group can be selected as particularly suitable acid dyes: Acid Yellow 1 (D&C Yellow 7, Citronin A, Ext. D&C Yellow No. 7, Japan Yellow 403, CI 10316, COLIPA n ° B001), Acid Yellow 3 (COLIPA n °: C 54, D&C Yellow N ° 10, Quinoline Yellow, E104, Food Yellow 13), Acid Yellow 9 (CI 13015), Acid Yellow 17 (CI 18965), Acid Yellow 23 (COLIPA n ° C 29, Covacap Jaune W 1 100 (LCW), Sicovit Tartrazine 85 E 102 (BASF), Tartrazine, Food Yellow 4, Japan Yellow 4, FD&C Yellow No. 5), Acid Yellow 36 (CI 13065), Acid Yellow 121 ( CI 18690), Acid Orange 6 (CI 14270), Acid Orange 7 (2-Naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA n ° C015), Acid Orange 10 (Cl 16230; Orange G sodium salt), Acid Orange 1 1 (CI 45370), Acid Orange 15 (CI 50120), Acid Orange 20 (CI 14600), Acid Orange 24 (BROWN 1; CI 20170; KATSU201; nosodiumsalt; Brown No.201; RESORCIN BROWN; ACID ORANGE 24 ; Japan Brown 201; D & C Brown No.1), Acid Red 1 4 (CI14720), acid red 18 (E124, red 18; CI 16255), Acid Red 27 (E 123, CI 16185, C-Red 46, Echtrot D, FD&C Red Nr.2, Food Red 9, Naphtholrot S), Acid Red 33 (Red 33, Fuchsia Red, D&C Red 33, CI 17200), Acid Red 35 (CI Cl18065), Acid Red 51 (CI 45430, Pyrosin B, Tetraiodfluorescein, Eosin J, lodeosin), Acid Red 52 (CI 45100, Food Red 106, Solar Rhodamine B, Acid Rhodamine B, Red n ° 106 Pontacyl Brilliant Pink), Acid Red 73 (CI CI 27290), Acid Red 87 (Eosin, CI 45380), Acid Red 92 (COLIPA n ° C53, CI 45410), Acid Red 95 (CI 45425, Erythtosine.Simacid Erythrosine Y), Acid Red 184 (CI 15685), Acid Red 195, Acid Violet 43 (Jarocol Violet 43, Ext.D&C Violet n ° 2, Cl 60730, COLIPA n ° C063), Acid Violet 49 (CI 42640), Acid Violet 50 (CI 50325), Acid Blue 1 (Patent Blue, CI 42045), Acid Blue 3 (Patent Blau V, CI 42051), Acid Blue 7 (CI 42080), Acid Blue 104 (CI 42735), Acid Blue 9 ( E 133, Patent Blue AE, Amido Blue AE, Erioglaucin A, CI 42090, Cl Food Blue 2), Acid Blue 62 (CI 62045), Acid Blue 74 (E 132, CI 73015), Acid Blue 80 (CI 61 585), Acid Green 3 (CI 42085, Foodgreenl), Acid Green 5 (CI 42095), Acid Green 9 (C.1.42100), Acid Green 22 (C.1.42170), Acid Green 25 (CI 61570, Japan Green 201, D&C Green No. 5), Acid Green 50 (Brillantsäuregrün BS, Cl 44090, Acid Brilliant Green BS, E 142), Acid Black 1 (Black n ° 401, Naphthalene Black 10B, Amido Black 10B, CI 20 470, COLIPA n ° B15), Acid Black 52 (CI 1571 1), Food Yellow 8 (CI 14270), Food Blue 5, D&C Yellow 8, D&C Green 5, D&C Orange 10, D&C Orange 1 1, D&C Red 21, D&C Red 27, D&C Red 33, D&C Violet 2 and / or D&C Brown 1.

The water solubility of the anionic substantive dyes can be determined, for example, in the following way. 0.1 g of the anionic substantive dye are placed in a beaker. A stir bar is added. Then 100 ml of water are added. This mixture is heated to 25 ° C. on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. If there are still undissolved residues, the amount of water is increased - for example in steps of 10 ml. Water is added until the amount of dye used has completely dissolved. If the dye-water mixture cannot be assessed visually due to the high intensity of the dye, the mixture is filtered. If a portion of undissolved dyes remains on the filter paper, the solubility test is repeated with a larger amount of water. If 0.1 g of the anionic substantive dye dissolves in 100 ml of water at 25 ° C., the solubility of the dye is 1 g / L.

Acid Yellow 1 is called 8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid disodium salt and has a solubility in water of at least 40 g / L (25 ° C).

Acid Yellow 3 is a mixture of the sodium salts of mono- and disulfonic acids of 2- (2-quinolyl) -1 H-indene-1, 3 (2H) -dione and has a water solubility of 20 g / L (25 ° C).

Acid Yellow 9 is the disodium salt of 8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid, its water solubility is above 40 g / L (25 ° C).

Acid Yellow 23 is the trisodium salt of 4,5-dihydro-5-oxo-1 - (4-sulfophenyl) -4 - ((4-sulfophenyl) azo) - 1 H-pyrazole-3-carboxylic acid and at 25 ° C well in Water soluble.

Acid Orange 7 is the sodium salt of 4 - [(2-Hydroxy-1-naphthyl) azo] benzene sulfonate. Its water solubility is more than 7 g / L (25 ° C).

Acid Red 18 is the trisodium salt of 7-hydroxy-8 - [(E) - (4-sulfonato-1-naphthyl) -diazenyl)] - 1,3-naphthalenedisulfonate and has a very high solubility in water of more than 20 wt. %.

Acid Red 33 is the disodium salt of 5-amino-4-hydroxy-3- (phenylazo) -naphthalene-2,7-disulphonate, its water solubility is 2.5 g / L (25 ° C).

Acid Red 92 is the disodium salt of 3,4,5,6-tetrachloro-2- (1,4,5,8-tetrabromo-6-hydroxy-3-oxoxanthen-9-yl) benzoic acid, its water solubility is specified with greater than 10 g / L (25 ° C).

Acid Blue 9 is the disodium salt of 2 - ({4- [N-ethyl (3-sulfonatobenzyl] amino] phenyl} {4 - [(N-ethyl (3-sulfonatobenzyl) imino] -2,5-cyclohexadiene-1 - ylidene} methyl) benzene sulfonate and has a water solubility of more than 20% by weight (25 ° C).

A very particularly preferred method is therefore characterized in that the agent (a) has at least one further coloring compound (a2) from the group of anionic contains substantive dyes, which is selected from the group of Acid Yellow 1, Acid Yellow 3, Acid Yellow 9, Acid Yellow 17, Acid Yellow 23, Acid Yellow 36, Acid Yellow 121, Acid Orange 6,

Acid Orange 7, Acid Orange 10, Acid Orange 1 1, Acid Orange 15, Acid Orange 20, Acid Orange 24, Acid Red 14, Acid Red, Acid Red 27, Acid Red 33, Acid Red 35, Acid Red 51, Acid Red 52, Acid Red 73, Acid Red 87, Acid Red 92, Acid Red 95, Acid Red 184, Acid Red 195, Acid Violet 43, Acid Violet 49, Acid Violet 50, Acid Blue 1, Acid Blue 3, Acid Blue 7, Acid Blue 104, Acid Blue 9, Acid Blue 62,

Acid Blue 74, Acid Blue 80, Acid Green 3, Acid Green 5, Acid Green 9, Acid Green 22, Acid Green 25, Acid Green 50, Acid Black 1, Acid Black 52, Food Yellow 8, Food Blue 5, D&C Yellow 8, D&C Green 5, D&C Orange 10, D&C Orange 1 1, D&C Red 21, D&C Red 27, D&C Red 33, D&C Violet 2 and / or D&C Brown 1.

The substantive dye or dyes, in particular the anionic substantive dyes, can be used in various amounts in the means (a) depending on the desired color intensity. Particularly good results could be obtained if the agent (a) - based on its total weight - has one or more substantive dyes (a2) in a total amount of 0.01 to 10 wt.%, Preferably 0.1 to 8 wt. -%, more preferably from 0.2 to 6% by weight and very particularly preferably from 0.5 to 4.5% by weight.

In a further preferred embodiment, the method is characterized in that the agent (a) - based on the total weight of the agent (a) - also has one or more substantive dyes as a further coloring compound (a2) in a total amount of 0.01 to 10 % By weight, preferably from 0.1 to 8% by weight, more preferably from 0.2 to 6% by weight and very particularly preferably from 0.5 to 4.5% by weight.

Silicone pads (a3)

In a further very particularly preferred embodiment, the agent (a) used in the process additionally contains at least one silicone polymer (a3).

Silicone polymers, which can alternatively be called silicones for short, are understood as poly (organo) siloxanes. Silicone polymers are understood to be a group of synthetic polymers in which silicon atoms are linked via oxygen atoms.

Silicone polymers are generally macromolecules with a molecular weight of at least 500 g / mol, preferably at least 1000 g / mol, more preferably at least 2500 g / mol, particularly preferably at least 5000 g / mol, which comprise repeating organic units.

The maximum molecular weight of the silicone polymer depends on the degree of polymerisation (number of polymerised monomers) and the batch size and is also determined by the polymerisation method. For the purposes of the present invention, it is preferred if the maximum Molecular weight of the silicone polymer is not more than 10 ⁷ g / mol, preferably not more than 10 ⁶ g / mol and particularly preferably not more than 10 ⁵ g / mol.

The silicone polymers comprise many Si — O repeat units, it being possible for the Si atoms to carry organic radicals such as, for example, alkyl groups or substituted alkyl groups.

In accordance with the high molecular weight of the silicone polymers, they are based on more than 10 Si-O repeat units, preferably more than 50 Si-O repeat units and particularly preferably more than 100 Si-O repeat units, very particularly preferably more than 500 Si-O repeat units .

The silicone polymers (a3) contained in the agent (a) are therefore different from the silanes (a1) likewise contained in the agent (a).

In the context of one embodiment, therefore, a method for coloring keratinic material is preferred, which is characterized in that the agent (a) contains:

(a3) at least one silicone polymer.

In the work leading to this invention it has been found that the incorporation of the silicone polymer (a3) into the agent (a) led to an improvement in the feel of the hair.

The film produced by the oligomerization or polymerization of the organosilicon compounds (silanes) (a1) can - especially when higher amounts of silanes (a1) are used - have a certain stickiness or softness, which on the one hand has a detrimental effect on the feel of the keratinic materials on the other hand, it can also have a negative effect on the durability of the film. Without being tied to this theory, it is assumed that the joint use of the silane (a1) and the silicone polymer (a3) leads on average (a) to a reaction or interaction of the two components with one another. When the silane and silicone polymer are used together, the silanes appear to form a film, as described above, in which the silicone polymers are either embedded or on which the silicone polymers agglomerate. It has been found that the film formed in this way is much more pliable, flexible, durable and less brittle.

Accordingly, it could be observed that the rheological properties of the film produced with the agent (a) can be greatly improved by adding at least one silicone polymer (a3). In the presence of the silicone polymers (a3), the film became stronger or more rigid, so that the colored keratinic materials left a less sticky, smoother and more pleasant impression. Furthermore, the higher strength of the film also had positive effects on the fastness properties of the keratin materials, in particular on their rub fastness. Since the dyed films were more resistant on contact with combs, brushes and textiles, less severe abrasion was found on contact with these objects.

When using certain silicone polymers (a3), the advantages described above were particularly pronounced. It has therefore been found to be particularly preferred if the agents (a) used in the process contain at least one alkoxy-modified silicone polymer and / or at least one amino-modified silicone polymer (a3).

(a3) at least one alkoxy-modified and / or amino-modified silicone polymer.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (a) contains at least one alkoxy-modified silicone polymer.

Alkoxy-modified silicones are understood as meaning silicones whose structure comprises at least one structural alkoxy unit. This structural alkoxy unit can be, for example, an alkoxy group. Alkoxy groups are understood to mean C2-Cio-alkoxy groups. The alkoxy group can be at the end of the silicone (i.e. it can be present as a group -O-CH3 or as a group -O-CH2-CH3). However, it is also according to the invention if the alkoxy group itself also carries a substituent; in this case, under an alkoxy modification, at least one group on the silicone such as (-CH2-CH2-0-), (-CH2-CH2-CH2-0-), (-CH (CH3) -CH2-0- ), (-CH2-CH (CH3) -CH2-0-) or (-CH2-CH2-CH2-CH2-0-). The alkoxy-modified silicones (A) preferably have at least one grouping (-CH2-CH2-0-) and / or (-CH2-CH2-CH2-0-)

The alkoxy groups can be linked to the silicone either via a carbon atom or via an oxygen atom, for example the silicones can carry the structural units of the formula (Sa), (S-b), (Sc) and / or (Sd):

It is particularly preferred if the alkoxy-modified silicone polymer or polymers (a3) carry more than one alkoxy group, ie if the silicone polymers (a3) are polyalkoxylated. Polyalkoxylated silicones carry polyoxyalkylene groups as structural units, in particular polyoxyethylene groups (ie groups of the [-CH2-CH2-0-] _{m type} ) and / or polyoxypropylene groups (ie groups of the [-CH (CH3) -CH2-0-] _m and / or type [-CH2-CH2-CH2-0-] _m ). The number is preferably

Polyoxyalkyl units in the silicone polymer is at least 2. m is therefore an integer greater than or equal to 2.

The alkoxy-modified silicone (a3) is particularly preferably a nonionic silicone. Nonionic silicones carry neither positive nor negative charges.

Very particularly suitable polyalkoxylated silicones (a3) comprise at least one

Structural unit of the formula (SI)

wherein

n for an integer from 2 to 20, preferably for an integer from 4 to 18, more preferably for an integer from 6 to 16, even more preferably for an integer from 8 to 14 and very particularly preferably for the number 12 stands.

The positions marked with an asterisk * in the above Here formulas stand for the free valences of the corresponding bonds, it being possible for the bond to be made to a further Si atom, a further O atom and / or a further C atom.

(a3) at least one silicone polymer which comprises at least one structural unit of the formula (S-l)

wherein n for an integer from 2 to 20, preferably for an integer from 4 to 18, more preferably for an integer from 6 to 16, even more preferably for an integer from 8 to 14 and very particularly preferably for the number 12 stands.

A preferred alkoxy-modified silicone polymer (a3) can in addition to one or more

Structural units of the general formula (S-l) also contain further structural units which differ structurally from the units of the formula (S-l). The alkoxy-modified silicone polymer particularly preferably additionally comprises one or more dimethylsiloxane units. Depending on whether the silicone according to the invention is linear or branched, it has two (in the case of one

chain-shaped, linear silicone) or several (in the case of a branched silicone) end groups. It has been found to be particularly advantageous if a silicone polymer (a3) according to the invention has a trimethylsilyloxy group (i.e. a -0-Si (CH3) 3 group) as end groups.

In a further very particularly preferred embodiment, the method is therefore characterized in that the agent (a) contains at least one silicone polymer (a3) which is composed of structural units of the formula (S1), the formula (S-II), the formula (S -Ill) and the formula (S-IV),

where n - independently in each structural unit (S1) - in each case for an integer from 2 to 20, preferably for an integer from 4 to 18, more preferably for an integer from 6 to 16, even more preferably for an integer from 8 to 14 and very particularly preferably the number 12 stands.

A silicone polymer (a3) which is composed of structural units of the formula (SI), the formula (S-II), the formula (S-II I) and the formula (S-IV) is understood in this context to be a silicone , which exclusively (in each case one or more) structural units of the formulas (S1), (S-II), (S-II I) and (S-IV) has. Here, the silicone can also contain various structural units of the formula (S-1), which each differ in their number n.

The positions marked with an asterisk in the abovementioned structural units each represent the points of attachment to the other structural units. For example, a very particularly preferred silicone polymer (a3), which is composed of structural units of the formula (S1), the formula (S-II), the Formula (Sl II) and the formula (S-IV) composed, which have the following structure:

x and y are selected depending on the desired molecular weight of the silicone, and n represents one of the preferred or particularly preferred integers according to the invention described above.

Both low molecular weight and higher molecular weight alkoxy-modified silicones can be used as silicone polymers (a3). Particularly advantageous effects were found with silicone polymers (a3) with a molar mass of 800 to 10,000 g / mol, preferably from 1,000 to 9,000 g / mol, more preferably from 2,000 to 8,000 g / mol and particularly preferably from 2,500 to 5,000 g / mol observed. Particularly suitable silicone polymers are, for example:

Abil B 8843 from Evonik, PEG-14 DIMETHICONE

Xiameter OFX 0193 Fluid from Dow Corning, PEG-12 Dimethicone

In addition, it was also possible to obtain particularly good results if an agent (a) was used in the process which contains an amino-modified silicone polymer (a3). The amino-modified silicone polymer can alternatively also be referred to as an amino-functionalized silicone polymer or also as an amino silicone.

In a further preferred embodiment, a method is characterized in that the agent (a) contains at least one amino-modified silicone polymer.

The agent (a) can contain one or more different amino-modified silicone polymers (a3). Such silicones can e.g. by the formula (S-V)

M (RaQbSiO (4-a-b) / 2) x (RcSiO (4-c) / 2) yM (S-V), where in the above formula R is a hydrocarbon or a

Is a hydrocarbon radical having 1 to about 6 carbon atoms, Q is a polar radical of the general formula -R ¹ HZ, where R ^{1 is} a divalent linking group bonded to hydrogen and the radical Z, composed of carbon and hydrogen atoms, carbon -, hydrogen and oxygen atoms or carbon, hydrogen and nitrogen atoms, and Z is an organic, amino-functional radical which contains at least one amino-functional group; "a" takes values in the range of about 0 to about 2, "b" takes values in the range of about 1 to about 3, "a" + "b" is less than or equal to 3, and "c" is a number in the range from about 1 to about 3, and x is a number in the range from 1 to about 2,000, preferably from about 3 to about 50, and most preferably from about 3 to about 25, and y is a number in the range from about 20 to about 10,000 , preferably from about 125 to about 10,000, and most preferably from about 150 to about 1,000, and M is a suitable silicone end group as known in the art, preferably trimethylsiloxy. Non-limiting examples of the radicals represented by R include

Alkyl groups such as methyl, ethyl, propyl, isopropyl, isopropyl, butyl, isobutyl, amyl, isoamyl, hexyl, isohexyl and the like; Alkenyl radicals such as vinyl, halovinyl, alkylvinyl, allyl, haloallyl, alkylallyl; Cycloalkyl groups such as cyclobutyl, cyclopentyl, cyclohexyl and the like; Phenyl residues, benzyl residues, halogenated hydrocarbon residues such as 3-chloropropyl, 4-bromobutyl, 3,3,3-trifluoropropyl, chlorocyclohexyl, bromophenyl, chlorophenyl and similar as well as sulfur-containing residues such as mercaptoethyl,

Mercaptopropyl, mercaptohexyl, mercaptophenyl, and the like; preferably R is an alkyl radical containing 1 to about 6 carbon atoms, and most preferably R is methyl. Examples of R ¹ include methylene, ethylene, propylene, hexamethylene, decamethylene, -CH ₂ CH (CH3) CH ₂ -, phenylene, naphthylene, -CH2CH2SCH2CH 2-, -CH2CH2OCH2-, -OCH2CH2-, -OCH ₂ CH2CH2- , -CH ₂ CH (CH3) C (0) 0CH ₂ -, - (CH ₂ ) 3 CC (0) 0CH ₂ CH ₂ -, -C6H 4C6H4-, -C6H ₄ CH ₂ C ₆ H4-; and - (CH

2) ₃ C (0) SCH ₂ CH ₂ - a.

Z is an organic, amino-functional radical containing at least one functional amino group. One possible formula for Z is NH (CH ₂ ) _Z NH ₂ , where z is 1 or more. Another possible formula for Z is -NH (CH ₂ ) _z (CH ₂ ) _ZZ NH, where both z and zz are independently 1 or more, this structure including diamino ring structures such as piperazinyl. Most preferably Z is an -NHCH ₂ CH ₂ NH ₂ radical. Another possible formula for Z is - N (CH ₂ ) _Z (CH ₂ ) _ZZ NX ₂ or -NX ₂ , wherein each X of X _{2 is} independently selected from the group consisting of hydrogen and alkyl groups having 1 to 12 carbon atoms, and zz is 0.

Q is most preferably a polar, amine-functional radical of the formula -CH ₂ CH ₂ CH ₂ NHCH ₂ CH ₂ NH ₂ . In the formulas, "a" takes values in the range from about 0 to about 2, "b" takes values in the range from about 2 to about 3, "a" + "b" is less than or equal to 3, and "c "is a number in the range from about 1 to about 3. The molar ratio of the R _a Qb SiO ( _4-a -b) / ₂ units to the R _c SiO ( _{4-C) / 2} units is in the range of about 1: 2 to 1:65, preferably from about 1: 5 to about 1:65, and most preferably from about 1:15 to about 1:20. If one or more silicones of the above formula are used, the various variable substituents In the above formula, the different silicone components that are present in the silicone mixture may be different.

In a particularly preferred embodiment, a method according to the invention is characterized by the use of an agent (a) on the keratinous material, the agent (a) being an amino-modified silicone polymer (a3) of the formula (S-VI)

R ' _a G _{3 a} -Si (OSiG ₂ ) _n - (OSiG _b R' ₂ - b) m-0-SiG _3-a -R ' _a (S-VI), in which means:

G is -H, a phenyl group, -OH, -O-CH3, -CH ₃ , -0-CH ₂ CH ₃ , -CH ₂ CH ₃ , -0-CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₃ , -0-CH (CH ₃ ) ₂ , -CH (CH ₃ ) ₂ , -O-CH ₂ CH ₂ CH ₂ CH ₃ , -CH ₂ CH ₂ CH ₂ CH ₃ , -O- CH ₂ CH (CH ₃ ) ₂ , -CH ₂ CH (CH ₃ ) ₂ , -0-CH (CH ₃ ) CH ₂ CH3, -CH (CH ₃ ) CH ₂ CH3, -0-C (CH ₃ ) 3, -C (CH ₃ ) 3 a stands for a number between 0 and 3, in particular 0;

b stands for a number between 0 and 1, in particular 1,

m and n are numbers whose sum (m + n) is between 1 and 2000, preferably between 50 and 150, where n is preferably values from 0 to 1999 and in particular from 49 to 149 and m preferably values from 1 to 2000, in particular from 1 to 10 assumes

R ^' is a monovalent radical selected from

o -QN (R ") - CH ₂ -CH ₂ -N (R") ₂

o -QN (R ") ₂ o -QN ⁺ (R ") ₃ A- o -QN ⁺ H (R") ₂ A- o -QN ⁺ H ₂ (R ") A- o -QN (R") - CH ₂ -CH ₂ -N ⁺ R "H ₂ A-,

where each Q represents a chemical bond, -CH ₂ -, -CH ₂ -CH ₂ -, -CH ₂ CH ₂ CH ₂ -, -C (CH3) ₂ -, - CH ₂ CH ₂ CH ₂ CH ₂ -, - CH ₂ C (CH ₃ ) ₂ -, -CH (CH ₃ ) CH ₂ CH ₂ -,

R "stands for identical or different radicals from the group -H, -phenyl, -benzyl, -CH ₂ - CH (CH ₃ ) Ph, the Ci- ₂ o-alkyl radicals, preferably -CH ₃ , -CH ₂ CH ₃ , - CH ₂ CH ₂ CH ₃ , -CH (CH ₃ ) ₂ , -CH ₂ CH ₂ CH ₂ H ₃ , -CH ₂ CH (CH ₃ ) ₂ , -CH (CH ₃ ) CH ₂ CH ₃ , -C (CH ₃ ) ₃ , and A represents an anion, which is preferably selected from chloride, bromide, iodide or methosulfate.

In the context of a further preferred embodiment, a method is characterized by the use of an agent (a) on the keratinous material, the agent (a) containing at least one amino-modified silicone polymer (a3) of the formula (S-VII),

where m and n are numbers whose sum (m + n) is between 1 and 2000, preferably between 50 and 150, where n is preferably values from 0 to 1999 and in particular from 49 to 149 and m preferably values from 1 to 2000, in particular from 1 to 10 assumes.

These silicones are referred to as trimethylsilylamodimethicones according to the INCI declaration.

In a further preferred embodiment, a method is characterized by the use of an agent (a) on the keratinous material, the agent (a) containing at least one amino-modified silicone polymer (a3) of the formula (S-VII I) (S- Vlll), where R is -OH, -0-CH ₃ or a -CH ₃ group and m, n1 and n2 are numbers whose sum (m + n1 + n2) is between 1 and 2000, preferably between 50 and 150 , the sum (n1 + n2) preferably assuming values from 0 to 1999 and in particular from 49 to 149 and m preferably from 1 to 2000, in particular from 1 to 10. These amino-modified or amino-functionalized silicone polymers are referred to as amodimethicones according to the INCI declaration.

Regardless of which amino-modified silicones are used, agents (a) are preferred which contain an amino-modified silicone polymer whose amine number is above 0.25 meq / g, preferably above 0.3 meq / g and in particular above 0.4 meq / g. The amine number stands for the milli-equivalents of amine per gram of the amino-functional silicone. It can be determined by titration and also given in the unit mg KOH / g.

In a further preferred embodiment, a method is characterized by the use of an agent (a) on the keratinous material, the agent (a) containing at least one amino-modified silicone polymer (a3) of the formula of the formula (S-IX),

in which

m and n mean numbers that are chosen so that the sum (n + m) is in the range from 1 to 1000,

n is a number in the range from 0 to 999 and m is a number in the range from 1 to 1000,

R1, R2 and R3, which are identical or different, represent a hydroxyl group or a C1-4 alkoxy group,

where at least one of the groups R1 to R3 is a hydroxyl group;

Further preferred methods are characterized by the use of an agent (a) on the keratinic material, the agent (a) at least amino-functional silicone polymer of the formula of the formula (SX)

contains, in the

- p and q mean numbers that are chosen so that the sum (p + q) is in the range from 1 to 1000,

- p is a number in the range from 0 to 999 and q is a number in the range from 1 to 1000,

R1 and R2, which are different, denote a hydroxyl group or a C1-4 alkoxy group, where at least one of the groups R1 to R2 denotes a hydroxyl group.

The silicones of the formulas (S-IX) and (SX) differ in the grouping on the Si atom that carries the nitrogen-containing group: In formula (S-IX), R2 denotes a hydroxyl group or a C1-4 alkoxy group, while the Radical in formula (SX) is a methyl group. The individual Si groupings, which are marked with the indices m and n or p and q, do not have to be present as blocks, rather the individual units can also be present in a statistically distributed manner, ie in the formulas (S-IX) and (SX) not necessarily every R1 -Si (CH3) ₂ group is bound to a - [0-Si (CH3) ₂ ] group.

Processes in which an agent (a) is applied to the keratin fibers which contains at least one amino-modified silicone polymer (a3) of the formula of the formula (S-Xl) have also proven to be particularly effective with regard to the desired effects

in the

A represents a group -OH, -0-Si (CH3) 3, -0-Si (CH ₃ ) ₂ 0H, -0-Si (CH ₃ ) ₂ 0CH3,

D is a group -H, -Si (CH3) 3, -Si (CH ₃ ) ₂ 0H, -Si (CH ₃ ) ₂ 0CH ₃ ,

b, n and c stand for whole numbers between 0 and 1000,

with the stipulations - n> 0 and b + c> 0

- At least one of the conditions A = -OH or D = -H is met.

In the above formula (S-Xl), the individual siloxane units with the indices b, c and n are randomly distributed, i.e. they do not necessarily have to be block copolymers.

Very good effects with regard to improving the rub fastness could be observed when an agent (a) was applied to the keratinous material in the process, which agent contained a special 4-morpholinomethyl-substituted silicone polymer (a3). This very particularly preferred amino-functionalized silicone polymer comprises at least one structural unit of the formula (S-XIII)

(a3) at least one silicone polymer which comprises at least one structural unit of the formula (S-XIII)

Particularly good effects with regard to the improvement of the rubbing fastness could also be observed when an agent (a) which contained a special 4-morpholinomethyl-substituted silicone polymer (a3) was applied to the keratinic material in the process. This very particularly preferred amino-functionalized silicone polymer comprises structural units of the formulas (S-Xll) and the formula (S-Xlll)

Xlll).

In the context of an explicitly very particularly preferred embodiment, a method according to the invention is characterized in that the agent (a) is at least one amino-modified

Contains silicone polymer (a3) which comprises structural units of the formula (S-Xll) and of the formula (S-Xlll)

Xlll).

Corresponding 4-morpholinomethyl-substituted silicone polymers are described below.

A very particularly preferred, amino-functionalized silicone polymer is known under the name Amodimethicone / Morpholinomethyl Silsesquioxane Copolymer and is commercially available from Wacker in the form of the raw material Belsil ADM 8301 E.

The 4-morpholinomethyl-substituted silicone that can be used, for example, is a silicone which has structural units of the formulas (S-XII), (S-XII l ') and (S-XIV')

in which

R1 is -CH ₃ , -OH, -OCH3, -O-CH2CH3, -O-CH2CH2CH3, or -O-0H (OH ₃ ) ₂ ;

R2 stands for -CH3, -OH, or -OCH3.

Particularly preferred agents (a) according to the invention contain at least one 4-morpholinomethyl-substituted silicone of the formula (S-XV)

(S-V)

in the

R1 is -CH ₃ , -OH, -OCH3, -O-CH2CH3, -O-CH2CH2CH3, or -0-CH (CH ₃ ) 2;

R2 stands for -CH3, -OH, or -OCH3.

B is a group -OH, -0-Si (CH3) 3, -0-Si (CH ₃ ) ₂ 0H, -0-Si (CH ₃ ) ₂ 0CH3,

D is a group -H, -Si (CH3) 3, -Si (CH ₃ ) ₂ 0H, -Si (CH ₃ ) ₂ 0CH ₃ ,

a, b and c independently represent integers between 0 and 1000, with the

Condition a + b + c> 0

m and n stand independently of each other for integers, numbers between 1 and 1000 with the proviso that

at least one of the conditions B = -OH or D = -H is met,

the units a, b, c, m and n are distributed randomly or in blocks in the molecule. Structural formula (Si-VI) is intended to make it clear that the siloxane groups n and m do not necessarily have to be bound directly to an end grouping B or D. Rather, in preferred formulas (Si-VI) a> 0 or b> 0 and in particularly preferred formulas (Si-VI) a> 0 and c> 0, ie the terminal grouping B or D is preferably on a dimethylsiloxy grouping bound. In formula (Si-VI) too, the siloxane units a, b, c, m and n are preferably distributed randomly.

The silicones according to the invention represented by formula (Si-VI) can be trimethylsilyl-terminated (D or B = -Si (CH3) 3), but they can also be dimethylsilylhydroxy on two sides or dimethylsilylhydroxy and dimethylsilylmethoxy on one side. Silicones used with particular preference in the context of the present invention are selected from silicones in which

B = -0-Si (CH ₃ ) 20H and D = -Si (CH ₃ ) 3

B = -0-Si (CH ₃₎ ₂ 0H and D = -Si (CH ₃₎ ₂ OH

B = -0-Si (CH ₃ ) 20H and D = -Si (CH ₃ ) 20CH ₃

B = -0-Si (CH ₃ ) 3 and D = -Si (CH ₃ ) ₂ OH

B = -0-Si (CH ₃ ) 20 CH ₃ and D = -Si (CH ₃ ) ₂ OH

means.

To produce particularly resistant films, the means (a) contains the one or more

Silicone polymers, especially the alkoxy-modified and / or the amino-modified

Silicone polymers, preferably in certain quantity ranges.

Particularly flexible films of low tack were obtained when an agent (a) was used in the process which - based on the total weight of the agent (a) - contains one or more silicone polymers (a3) in a total amount of 0.1 to 8 wt. -%, preferably 0.1 to 5% by weight, more preferably from 0.1 to 3% by weight and very particularly preferably from 0.1 to 0.5% by weight.

In the context of a further preferred embodiment, a method is characterized in that the agent (a) - based on the total weight of the agent (a) - one or more

Contains silicone polymers in a total amount of 0.1 to 15% by weight, preferably 0.5 to 12% by weight, more preferably 1 to 10% by weight and very particularly preferably 2 to 8% by weight.

In the context of an explicitly very particularly preferred embodiment, a method is characterized in that the agent (a) - based on the total weight of the agent (a) - one or more alkoxy-modified silicone polymers in a total amount of 0.1 to 15 wt. %, preferably 0.5 to 12% by weight, more preferably from 1 to 10% by weight and very particularly preferably from 2 to 8% by weight.

In the context of an explicitly very particularly preferred embodiment, a method is characterized in that the agent (a) - based on the total weight of the agent (a) - one or several amino-modified silicone polymers in a total amount of 0.1 to 15% by weight, preferably 0.5 to 12% by weight, more preferably from 1 to 10% by weight and very particularly preferably from 2 to 8% by weight. -% contains. pH of the agent (a)

It has been found to be preferred if the agent (a) is packaged in the form of a water-containing agent which is adjusted to an alkaline pH.

To adjust the pH, the agent (a) can contain at least one alkalizing agent.

To set the desired pH, the agents (a) can therefore also contain at least one alkalizing agent. The pH values in the context of the present invention are pH values that were measured at a temperature of 22 ° C.

The agent (a) can contain, for example, ammonia, alkanolamines and / or basic amino acids as the alkalizing agent.

The alkanolamines which can be used in the agent are preferably selected from primary amines with a C2-C6-alkyl parent structure which carries at least one hydroxyl group. Preferred alkanolamines are selected from the group which is formed from 2-aminoethan-1 -ol (monoethanolamine), 3-aminopropan-1 -ol, 4-aminobutan-1 -ol, 5-aminopentan-1 -ol, 1-aminopropane -2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1 - Amino-2-methylpropan-2-ol, 3-aminopropan-1, 2-diol, 2-amino-2-methylpropan-1, 3-diol.

Particularly preferred alkanolamines are selected from 2-aminoethan-1-ol and / or 2-amino-2-methylpropan-1 -ol. A particularly preferred embodiment is therefore characterized in that the agent according to the invention contains an alkanolamine selected from 2-aminoethan-1-ol and / or 2-amino-2-methylpropan-1 -ol as alkalizing agent.

For the purposes of the invention, an amino acid is an organic compound which, in its structure, contains at least one protonatable amino group and at least one —COOH or one —SOβH group. Preferred amino acids are aminocarboxylic acids, in particular a- (alpha) - aminocarboxylic acids and w-aminocarboxylic acids, with a-aminocarboxylic acids being particularly preferred.

Basic amino acids are to be understood as meaning those amino acids which have an isoelectric point p1 greater than 7. Basic α-aminocarboxylic acids contain at least one asymmetric carbon atom. In the context of the present invention, both possible enantiomers can be used equally as specific compounds or mixtures thereof, in particular as racemates. However, it is particularly advantageous to use the naturally preferred isomer form, usually in the L configuration.

The basic amino acids are preferably selected from the group that is formed from arginine, lysine, ornithine and histidine, particularly preferably from arginine and lysine. In a further particularly preferred embodiment, a method is therefore characterized in that the alkalizing agent is a basic amino acid from the group arginine, lysine,

Ornithine and / or histidine.

In addition, the agent can contain other alkalizing agents, in particular inorganic ones

Contain alkalizing agents. Inorganic alkalizing agents which can be used according to the invention are preferably selected from the group formed from sodium hydroxide, potassium hydroxide, calcium hydroxide, barium hydroxide, sodium phosphate, potassium phosphate, sodium silicate,

Sodium metasilicate, potassium silicate, sodium carbonate and potassium carbonate.

Particularly preferred alkalizing agents are ammonia and 2-aminoethan-1-ol

(Monoethanolamine), 3-aminopropan-1-ol, 4-aminobutan-1 -ol, 5-aminopentan-1 -ol, 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2- ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1-amino-2-methylpropan-2-ol, 3-aminopropan-1, 2- diol, 2-amino-2-methylpropane-1, 3-diol, arginine, lysine, ornithine, histidine, sodium hydroxide, potassium hydroxide, calcium hydroxide, barium hydroxide, sodium phosphate, potassium phosphate, sodium silicate, sodium metasilicate, potassium silicate, sodium carbonate and potassium carbonate.

Although the agents (a) are preferably adjusted to pH values in the alkaline range, it may in principle still be necessary to use small amounts of acidifying agents for fine adjustment of the desired pH value. Acidifying agents suitable according to the invention are, for example, citric acid, lactic acid, acetic acid or else dilute mineral acids (such as, for example, hydrochloric acid, sulfuric acid, phosphoric acid).

In the context of the work leading to this invention, it has been found, however, that the presence of the alkalizing agent or the setting of the alkaline pH for the

Formation of resistant films on the keratin material is essential. The presence of too large amounts of acids can have a negative effect on the strength of the films. For this reason, it has been found to be preferred to keep the amounts of acids used on average (a) as low as possible. For this reason it is advantageous if the total amount of the mean (a) contained organic and / or inorganic acids does not exceed a certain value.

In a further preferred embodiment, a method is characterized in that the total amount of the organic acids contained in the agent (a) from the group of citric acid, tartaric acid, malic acid and lactic acid at a content below 1% by weight, preferably below 0, 7% by weight, more preferably below 0.5% by weight, even more preferably below 0.1% by weight and very particularly preferably below 0.01% by weight.

In a further preferred embodiment, a method is characterized in that the total amount of the inorganic acids contained in the agent (a) from the group of hydrochloric acid, sulfuric acid and phosphoric acid at a content below 1 wt .-%, preferably below 0.7 wt .-%, more preferably below 0.5% by weight, even more preferably below 0.1% by weight and very particularly preferably below 0.01% by weight.

The maximum total amounts of acids contained in the agent (a) indicated above are always based on the total weight of the agent (a).

Medium (bl

The method for the treatment of keratinic material comprises not only the application of the agent (a) but also the application of the agent (b). The agent (b) used in the method is characterized in that it contains at least one sealing reagent (b1).

The agent (b) is an aftertreatment agent and the application of the agent (b) to the keratinic material treated with agent (a) has the effect that the colorations achieved in the process are made more durable. In particular, the wash fastness and the rub fastness of the dyeings obtained in the process can be improved by using the agent (b).

It is preferred that the sealing reagent (b1) comprises a compound selected from the group consisting of film-forming polymers, alkalizing agents, acidifying agents and mixtures thereof.

It can be preferred that the sealing reagent (b1) comprises a film-forming polymer.

Polymers are understood to mean macromolecules with a molecular weight of at least 1000 g / mol, preferably of at least 2500 g / mol, particularly preferably of at least 5000 g / mol, which consist of identical, repeating organic units. The polymers of the present invention can be synthetically produced polymers that are structurally formed by polymerizing one type of monomer or by polymerizing different ones different types of monomers are produced. If the polymer is produced by polymerizing one type of monomer, it is called a homo-polymer. If structurally different types of monomers are used in the polymerization, the resulting polymer is referred to as a copolymer.

The maximum molecular weight of the polymer depends on the degree of polymerisation (number of polymerised monomers) and the batch size and is also determined by the polymerisation method. For the purposes of the present invention, it is preferred if the maximum

Molecular weight of the film-forming, hydrophobic polymer is not more than 10 ⁷ g / mol, preferably not more than 10 ⁶ g / mol and particularly preferably not more than 10 ⁵ g / mol.

In the context of the invention, a film-forming polymer is understood to mean a polymer which is capable of forming a film on a substrate, for example on a keratin material or a keratin fiber. The formation of a film can be detected, for example, by viewing the keratinic material treated with the polymer under a microscope.

The film-forming polymers in means (b) can be hydrophilic or hydrophobic.

In the context of a first embodiment, it can be preferred to use at least one hydrophobic, film-forming polymer as sealing reagent (b1) in the means (b).

A hydrophobic polymer is understood to mean a polymer that has a solubility in water at 25 ° C. (760 mmHg) of less than 1% by weight.

The water solubility of the film-forming, hydrophobic polymer can be determined, for example, in the following way. 1 g of the polymer is placed in a beaker. Make up to 100 g with water. A stir bar is added and the mixture is warmed to 25 ° C on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. If the polymer-water mixture cannot be assessed visually due to the high turbidity of the mixture, the mixture is filtered. If a proportion of undissolved polymer remains on the filter paper, the solubility of the polymer is less than 1% by weight.

The polymers of the acrylic acid type, the polyurethanes, the polyesters, the polyamides, the polyureas, the cellulose polymers, the nitro-cellulose polymers, the silicone polymers, the polymers of the acrylamide type and the polyisoprenes can be mentioned here in particular . Particularly suitable film-forming, hydrophobic polymers are, for example, polymers from the group of copolymers of acrylic acid, copolymers of methacrylic acid, homopolymers or copolymers of acrylic acid esters, homopolymers or copolymers of methacrylic acid esters, homopolymers or copolymers of acrylic acid amides, homopolymers or copolymers of methacrylic acid amides, copolymers of vinyl pyrrolidone, copolymers of vinyl alcohol, copolymers of vinyl acetate, homopolymers or copolymers of ethylene, homopolymers or copolymers of propylene, homopolymers or copolymers of styrene, polyurethanes, polyesters and / or the polyamides.

In a further preferred embodiment, a method is characterized in that the agent (b) contains at least one film-forming, hydrophobic polymer as sealing reagent (b1), which is selected from the group of copolymers of acrylic acid, the copolymers of

Methacrylic acid, the homopolymers or copolymers of acrylic acid esters, the homopolymers or copolymers of methacrylic acid esters, the homopolymers or copolymers of acrylic acid amides, the homopolymers or copolymers of methacrylic acid amides, the copolymers of

Vinyl pyrrolidone, copolymers of vinyl alcohol, copolymers of vinyl acetate,

Homopolymers or copolymers of ethylene, homopolymers or copolymers of propylene, homopolymers or copolymers of styrene, polyurethanes, polyesters and / or polyamides.

The film-forming hydrophobic polymers which are selected from the group of synthetic polymers, the polymers obtainable by free radical polymerization or the natural polymers have proven particularly suitable for achieving the object of the invention.

Further particularly suitable film-forming hydrophobic polymers can be selected from the homopolymers or copolymers of olefins, such as cycloolefins, butadiene, isoprene or styrene, vinyl ethers, vinyl amides, the esters or amides of (meth) acrylic acid with at least one Ci-C2o-alkyl group, an aryl group or a C2-Cio-hydroxyalkyl group.

Further film-forming hydrophobic polymers can be selected from the homo- or

Copolymers of isooctyl (meth) acrylate, isononyl (meth) acrylate, 2-ethylhexyl (meth) acrylate,

Lauryl (meth) acrylate), isopentyl (meth) acrylate, n-butyl (meth) acrylate), isobutyl (meth) acrylate,

Ethyl (meth) acrylate, methyl (meth) acrylate, tert-butyl (meth) acrylate, stearyl (meth) acrylate, hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate and / or mixtures thereof.

Further film-forming hydrophobic polymers can be selected from the homo- or

Copolymers of (meth) acrylamide, N-alkyl (meth) acrylamides, especially those with C2-C18 Alkyl groups, such as, for example, N-ethyl acrylamide, N-tert-butyl acrylamide, N-octyl acrylamide, N-di (C1 -C4) alkyl (meth) acrylamide.

Further preferred anionic copolymers are, for example, copolymers of acrylic acid, methacrylic acid or their Ci-C6-alkyl esters, as described under the INCI declaration Acrylates

Copolymers are sold. A suitable commercial product is, for example Aculyn ^® 33 from Rohm & Haas. However, copolymers of acrylic acid, methacrylic acid or their Ci-C6-alkyl esters and the esters of an ethylenically unsaturated acid and an alkoxylated fatty alcohol are also preferred. Suitable ethylenically unsaturated acids are, in particular, acrylic acid, methacrylic acid and itaconic acid; suitable alkoxylated fatty alcohols are, in particular, steareth-20 or ceteth-20.

Particularly preferred polymers on the market are, for example, Aculyn® 22 (Acrylates / Steareth-20 Methacrylate Copolymer), Aculyn® 28 (Acrylates / Beheneth-25 Methacrylate Copolymer), Structure 2001® (Acryla-tes / Steareth-20 Itaconate Copolymer) , Structure 3001®

(Acrylates / Ceteth-20 Itaconate Copolymer), Structure Plus® (Acrylates / Aminoacrylates C10-30 Alkyl PEG-20 Itaconate Copolymer), Carbopol® 1342, 1382, Ultrez 20, Ultrez 21 (Acrylates / C10-30 Alkyl Acrylate Crosspolymer), Synthalen W 2000® (Acrylates / Palmeth-25 Acrylate Copolymer) or the Soltex OPT (Acrylates / C 12-22 Alkyl methacrylate Copolymer) sold by Rohme and Haas.

Suitable polymers based on vinyl monomers include, for example, the homo- and copolymers of N-vinylpyrrolidone, vinylcaprolactam, vinyl (C1 -C6) alkyl pyrrole, vinyl oxazole, vinyl thiazole, vinyl pyrimidine or des Vinylimidazole.

The copolymers octylacrylamide / acrylates /

butylaminoethyl methacrylate copolymer, as it is, for example, under the trade name

AMPHOMER® or LOVOCRYL® 47 is sold commercially by NATIONAL STARCH, or the copolymers of acrylates / octylacrylamides which are sold under the trade names DERMACRYL® LT and DERMACRYL® 79 by NATIONAL STARCH.

Examples of suitable polymers based on olefins are the homo- and copolymers of ethylene, propylene, butene, isoprene and butadiene.

In a further embodiment, the block copolymers which comprise at least one block made of styrene or the derivatives of styrene can be used as film-forming hydrophobic polymers. These block copolymers can be copolymers which, in addition to a styrene block, contain one or more other blocks, such as, for example, styrene / ethylene, styrene / ethylene / butylene, styrene / butylene, styrene / isoprene, styrene / butadiene. Corresponding polymers are sold commercially by BASF under the trade name “Luvitol HSB”. Surprisingly, it has been found that particularly intense and washfast colors could be obtained if the agent (b) contained at least one film-forming polymer as sealing reagent (b1), which was selected from the group of homopolymers and copolymers of acrylic acid, the homopolymers and copolymers of methacrylic acid, the homopolymers and copolymers of acrylic acid esters, the homopolymers and copolymers of methacrylic acid esters, the homopolymers and copolymers of acrylic acid amides, the

Homopolymers and copolymers of methacrylic acid amides, homopolymers and copolymers of vinyl pyrrolidone, homopolymers and copolymers of vinyl alcohol, homopolymers and copolymers of vinyl acetate, homopolymers and copolymers of ethylene, homopolymers and copolymers of propylene, homopolymers and copolymers of styrene, of polyurethanes, polyesters and polyamides.

In a further preferred embodiment, a method is characterized in that the agent (b) contains at least one film-forming polymer as sealing reagent (b1), which is selected from the group of homopolymers and copolymers of acrylic acid, the

Homopolymers and copolymers of methacrylic acid, the homopolymers and copolymers of acrylic acid esters, the homopolymers and copolymers of methacrylic acid esters, the

Homopolymers and copolymers of acrylic acid amides, the homopolymers and copolymers of methacrylic acid amides, the homopolymers and copolymers of vinylpyrrolidone, the

Homopolymers and copolymers of vinyl alcohol, homopolymers and copolymers of vinyl acetate, homopolymers and copolymers of ethylene, homopolymers and copolymers of propylene, homopolymers and copolymers of styrene, polyurethanes, polyesters and polyamides.

In a further embodiment, it can be preferred to use at least one hydrophilic, film-forming polymer as sealing reagent (b1) in the means (b).

A hydrophilic polymer is understood to mean a polymer that has a solubility in water at 25 ° C. (760 mmHg) of more than 1% by weight, preferably more than 2% by weight.

The water solubility of the film-forming hydrophilic polymer can be determined, for example, in the following way. 1 g of the polymer is placed in a beaker. Make up to 100 g with water. A stir bar is added and the mixture is warmed to 25 ° C on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. A completely dissolved polymer appears macroscopically homogeneous. If the polymer-water mixture cannot be assessed visually due to the high turbidity of the mixture, the mixture is filtered. If no undissolved polymer remains on the filter paper, then the solubility of the polymer is more than 1% by weight. Nonionic, anionic and cationic polymers can be used as film-forming, hydrophilic polymers.

Suitable film-forming, hydrophilic polymers can, for example, from the group of

Polyvinylpyrrolidone (co) polymers, polyvinyl alcohol (co) polymers, vinyl acetate (co) polymers, carboxyvinyl (co) polymers, acrylic acid (co) polymers, methacrylic acid (co) polymers, natural rubbers , the polysaccharides and / or the acrylamide (co) polymers can be selected.

Furthermore, it is very particularly preferred to use polyvinylpyrrolidone (PVP) and / or a vinylpyrrolidone-containing copolymer as the film-forming hydrophilic polymer.

In a further very particularly preferred embodiment, a method is characterized in that the agent (b) at least one film-forming, hydrophilic polymer as

Sealing reagent (b1) which is selected from the group consisting of polyvinylpyrrolidone (PVP) and the copolymers of polyvinylpyrrolidone.

It is also preferred if the agent contains polyvinylpyrrolidone (PVP) as the film-forming, hydrophilic polymer. Surprisingly, the washfastness of the dyeings which could be obtained with PVP-containing agents (b) was also very good.

Particularly suitable polyvinylpyrrolidones are available, for example, under the name Luviskol® K from BASF SE, in particular Luviskol® K 90 or Luviskol® K 85 from BASF SE.

The polymer PVP K30, which is sold by Ashland (ISP, POI Chemical), can also be used as another polyvinylpyrrolidone (PVP) that is explicitly very particularly suitable. PVP K 30 is a polyvinylpyrrolidone which is very soluble in cold water and has the CAS number 9003-39-8. The molecular weight of PVP K 30 is approx. 40,000 g / mol.

Other particularly suitable polyvinylpyrrolidones are the substances known under the trade names LUVITEC K 17, LUVITEC K 30, LUVITEC K 60, LUVITEC K 80, LUVITEC K 85, LUVITEC K 90 and LUVITEC K 115 and available from BASF.

The use of film-forming hydrophilic polymers as sealing reagent (b1) from the group of copolymers of polyvinylpyrrolidone has also led to particularly good and washable color results.

Particularly suitable film-forming, hydrophilic polymers that can be mentioned in this context are vinylpyrrolidone-vinyl ester copolymers, such as those listed under the Trademark Luviskol ^® (BASF). Luviskol ^® VA 64 and Luviskol ^® VA 73, each vinyl pyrrolidone / vinyl acetate copolymers, are particularly preferred nonionic polymers.

Of the vinylpyrrolidone-containing copolymers, a styrene / VP copolymer and / or a vinylpyrrolidone-vinyl acetate copolymer and / or a VP / DMAPA acrylates copolymer and / or a VP / vinyl caprolactam / DMAPA acrylates copolymer are very particularly preferably used in the cosmetic compositions .

Vinylpyrrolidone-vinyl acetate copolymers are sold under the name Luviskol® VA by BASF SE. A VP / vinyl caprolactam / DMAPA Acrylates copolymer is sold by Ashland Inc. under the trade name Aquaflex® SF-40. A VP / DMAPA Acrylates copolymer is sold, for example, under the name Styleze CC-10 by Ashland and is a highly preferred vinylpyrrolidone-containing copolymer.

Other suitable copolymers of polyvinylpyrrolidone that can be mentioned are the copolymers which are obtained by reacting N-vinylpyrrolidone with at least one further monomer from the group of V-vinylformamide, vinyl acetate, ethylene, propylene, acrylamide, vinyl caprolactam,

Vinyl caprolactone and / or vinyl alcohol can be obtained.

Sealing reagent (b1) which is selected from the group consisting of polyvinylpyrrolidone (PVP), vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / styrene copolymers,

Vinyl pyrrolidone / ethylene copolymers, vinyl pyrrolidone / propylene copolymers,

Vinyl pyrrolidone / vinyl caprolactam copolymers, vinyl pyrrolidone / vinyl formamide copolymers and / or vinyl pyrrolidone / vinyl alcohol copolymers.

Another suitable copolymer of vinyl pyrrolidone is that under the INCI name

Maltodextrin / VP copolymer known polymer.

Furthermore, intensely colored keratinic material, in particular hair, with very good wash fastness properties could be obtained if a nonionic, film-forming, hydrophilic polymer was used as the film-forming, hydrophilic polymer.

In a further embodiment, the agent (b) can contain at least one nonionic, film-forming, hydrophilic polymer as sealing reagent (b1).

According to the invention, a nonionic polymer is understood to mean a polymer that does not contain any in a protic solvent - such as water, for example - under standard conditions Structural units with permanent cationic or anionic groups which carry through

Counterions must be compensated while maintaining the electrical neutrality. Cationic groups include, for example, quaternized ammonium groups, but not protonated amines. Anionic groups include, for example, carboxyl and sulfonic acid groups.

The agents are very particularly preferred which contain, as the nonionic, film-forming, hydrophilic polymer, at least one polymer selected from the group consisting of

Polyvinylpyrrolidone,

Copolymers of N-vinylpyrrolidone and vinyl esters of carboxylic acids with 2 to 18

Carbon atoms, in particular from N-vinylpyrrolidone and vinyl acetate,

Copolymers of N-vinylpyrrolidone and N-vinylimidazole and methacrylamide,

Copolymers of N-vinylpyrrolidone and N-vinylimidazole and acrylamide,

Copolymers of N-vinylpyrrolidone with N, N-di (C1 to C4) -alkylamino- (C2 to C4) -alkylacrylamide.

If copolymers of N-vinylpyrrolidone and vinyl acetate are used, it is again preferred if the molar ratio of the structural units contained in the monomer N-vinylpyrrolidone to the structural units of the polymer contained in the monomer vinyl acetate is in the range from 20:80 to 80:20, in particular from 30 to 70 to 60 to 40. Suitable copolymers from

Vinylpyrrolidone and vinyl acetate are available, for example, under the trademarks Luviskol® VA 37, Luviskol® VA 55, Luviskol® VA 64 and Luviskol® VA 73 from BASF SE.

Another particularly preferred polymer is selected from the polymers of the INCI name VP / Methacrylamide / Vinyl Imidazole Copolymer, for example under the

Trade names Luviset Clear are available from BASF SE.

Another very particularly preferred nonionic, film-forming, hydrophilic polymer is a copolymer of N-vinylpyrrolidone and N, N-dimethylaminiopropyl methacrylamide, which

for example with the INCI name VP / DMAPA Acrylates Copolymer z. B. under the

The trade name Styleze® CC 10 is sold by ISP.

A cationic polymer is the copolymer of N-vinylpyrrolidone, N-vinylcaprolactam, N- (3-dimethylaminopropyl) methacrylamide and 3- (methacryloylamino) propyl-lauryl-dimethylammonium chloride (INCI name: Polyquaternium-69), which is available for example under the trade name AquaStyle ^® 300 (28-32% by weight active substance in an ethanol-water mixture,

Molecular weight 350,000) is sold by ISP.

Further suitable film-forming, hydrophilic polymers are, for example Vinylpyrrolidone-vinylimidazolium methochloride copolymers, as offered under the names Luviquat ^® FC 370, FC 550 and the INCI name Polyquaternium-16 as well as FC 905 and HM 552,

Vinylpyrrolidone-vinylcaprolactam-acrylate terpolymers, such as those with acrylic acid esters and

Acrylic acid amides are commercially available as a third monomer component, for example under the name Aquaflex ^® SF 40.

Polyquaternium-1 1 is the reaction product of diethyl sulfate with a copolymer of

Vinyl pyrrolidone and dimethylaminoethyl methacrylate. Suitable commercial products are available, for example, under the names Dehyquart® CC 11 and Luviquat® PQ 11 PN from BASF SE or Gafquat 440, Gafquat 734, Gafquat 755 or Gafquat 755N from Ashland Inc.

Polyquaternium-46 is the reaction product of vinyl caprolactam and vinyl pyrrolidone with

Methyl vinylimidazolium methosulfate and is available, for example, under the name Luviquat® Hold from BASF SE. Polyquaternium-46 is preferably used in an amount of 1 to 5% by weight, based on the total weight of the cosmetic composition. It is very particularly preferred that Polyquaternium-46 is used in combination with a cationic guar compound. It is even highly preferred that Polyquaternium-46 is used in combination with a cationic guar compound and Polyquaternium-11.

Acrylic acid polymers, for example, which can be present in uncrosslinked or crosslinked form, can be used as suitable anionic film-forming, hydrophilic polymers.

Corresponding products are sold commercially, for example, under the trade names Carbopol 980, 981, 954, 2984 and 5984 by Lubrizol or also under the names Synthalen M and Synthalen K by 3V Sigma (The Sun Chemicals, Inter Harz).

Examples of suitable film-forming, hydrophilic polymers from the group of natural gums are xanthan gum, gellan gum, carob gum.

Examples of suitable film-forming, hydrophilic polymers from the group of the polysaccharides are hydroxyethyl cellulose, hydroxypropyl cellulose, ethyl cellulose and carboxymethyl cellulose.

Suitable film-forming, hydrophilic polymers from the group of acrylamides are, for example, polymers which are produced from monomers of (meth) acrylamido-C1-C4-alkyl-sulfonic acid or the salts thereof. Corresponding polymers can be selected from the polymers of polyacrylamidomethanesulfonic acid, polyacrylamidoethanesulfonic acid,

Polyacrylamidopropanesulfonic acid, poly2-acrylamido-2-methylpropanesulfonic acid, poly-2-methylacrylamido-2-methylpropanesulfonic acid and / or poly-2-methylacrylamido-n-butanesulfonic acid. Preferred polymers of the poly (meth) arylamido-C1-C4-alkyl-sulfonic acids are crosslinked and at least 90% neutralized. These polymers can be crosslinked or also uncrosslinked.

Crosslinked and completely or partially neutralized polymers of the poly-2-acrylamido-2-methylpropanesulfonic acid type are known under the INCI names "Ammonium Polyacrylamido-2-methylpropanesulphonate" or "Ammonium Polyacryldimethyltauramide".

Another preferred polymer of this type is the crosslinked poly-2-acrylamido-2methyl-propanesulphonic acid polymer sold by Clariant under the trade name Hostacerin AMPS, which is partially neutralized with ammonia.

In a further explicitly very particularly preferred embodiment, a method is characterized in that the agent (b) has at least one anionic, film-forming polymer as

Contains sealing reagent (b1).

In this context, the best results could be obtained when the agent (b) contains at least one film-forming polymer as sealing reagent (b1) which comprises at least one structural unit of the formula (P-I) and at least one structural unit of the formula (P-II)

in which

M stands for a hydrogen atom or for ammonium (NH4), sodium, potassium, magnesium or calcium.

In a further preferred embodiment, a method according to the invention is characterized in that the agent (b) contains at least one film-forming polymer as sealing reagent (b1) which comprises at least one structural unit of the formula (P-I) and at least one structural unit of the formula (P-II)

ii), in which

M for a hydrogen atom or for ammonium (NFU), sodium, potassium, or magnesium Calcium stands.

When M represents a hydrogen atom, the structural unit of the formula (P-1) is based on one

Acrylic acid unit.

When M stands for an ammonium counterion, the structural unit of the formula (P-1) is based on the ammonium salt of acrylic acid.

When M is a sodium counterion, the structural unit of the formula (P-1) is based on the

Sodium salt of acrylic acid.

When M is a potassium counterion, the structural unit of formula (P-1) is based on the

Potassium salt of acrylic acid.

When M stands for half an equivalent of a magnesium counterion, the structural unit of the formula (P-1) is based on the magnesium salt of acrylic acid.

When M stands for half an equivalent of a calcium counterion, the structural unit of the formula (P-1) is based on the calcium salt of acrylic acid.

The film-forming polymer (s) are preferably used in certain quantity ranges in the agent (b). In this context, the solution according to the invention has been found

Task proved to be particularly preferred if the means (b) - based on the

Total weight of the agent (b) - one or more film-forming polymers as sealing reagent (b1) in a total amount of 0.1 to 18% by weight, preferably from 1 to 16% by weight, more preferably from 5 to 14.5% by weight .-% and very particularly preferably from 8 to 12% by weight.

In a further preferred embodiment, a method is characterized in that the agent (b) - based on the total weight of the agent (b) - has one or more film-forming polymers as sealing reagent (b1) in a total amount of 0.1 to 18 wt. %, preferably from 1 to 16% by weight, more preferably from 5 to 14.5% by weight and very particularly preferably from 8 to 12% by weight.

With the use of the agent (b), comprising a film-forming polymer as sealing reagent (b1), the colored film initially produced by the application of the agent (a) is intended to be sealed and / or fixed. With application of the second agent (b) with a film-forming polymer as sealing reagent (b1), the film-forming polymer is deposited in the form of a further film on the colored film produced in the first layer. The multi-layer film system produced in this way has improved resistance to external influences. The film produced by means (b) comprising a film-forming polymer as sealing reagent (b1) is preferably not itself colored. In this way it can also be ensured that abrasion of the second film formed by means (b) to a certain extent does not lead to any color changes in the entire film system. It is therefore very particularly preferred if the agent (b) contains no or only very small amounts of coloring compounds.

In an alternative embodiment, the sealing reagent (b1) contains an alkalizing agent.

The alkalizing agent is particularly preferably selected from the group consisting of ammonia, C2-C6 alkanolamines, basic amino acids, alkali metal hydroxides and alkaline earth metal hydroxides.

In the context of a further particularly preferred embodiment, a method is characterized in that the agent (b) contains at least one alkalizing agent as sealing reagent (b1) which is selected from the group of ammonia, C2-C6-alkanolamines, basic amino acids, alkali metal hydroxides, alkaline earth metal hydroxides , Alkali metal silicates,

Alkali metal metasilicates, alkaline earth metal silicates, alkaline earth metal metasilicates, alkali metal carbonates and alkaline earth metal carbonates.

It has been found that the aftertreatment with an agent (b) which contains ammonia has a particularly good influence on improving the wash fastness and the rub fastness of the dyeings obtained in the process.

In the context of a further very particularly preferred embodiment, a method is characterized in that the composition (b) contains ammonia as sealing reagent (b1).

Also good results could be obtained when the composition (b) as

Sealing reagent (b1) contained at least one C2-C6-alkanolamine.

The alkanolamines which can be used in composition (b) can be selected, for example, from the group of primary amines with a C2-C6-alkyl parent structure which carries at least one hydroxyl group. Preferred alkanolamines are selected from the group that is formed from 2-aminoethan-1-ol (monoethanolamine), 3-aminopropan-1-ol, 4-aminobutan-1-ol, 5-aminopentan-1-ol, 1-aminopropane -2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1 -Amino-2-methylpropan-2-ol, 3-aminopropan-1,2-diol, 2-amino-2-methylpropan-1,3-diol.

In a further preferred embodiment, a method according to the invention is characterized in that the composition (b) is used as sealing reagent (b1) at least one Contains alkalizing agent from the group of alkanolamines, which is preferably selected from the group of 2-aminoethan-1-ol (monoethanolamine), 3-aminopropan-1-ol, 4-aminobutan-1-ol, 5-aminopentan-1-ol , 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1 -ol, 1-amino-2-methylpropan-2-ol, 3-aminopropane-1, 2-diol and 2-amino-2-methylpropan-1, 3-diol.

Also good results could be obtained when the composition (b) as

Sealing reagent (b1) contained at least one basic amino acid.

An amino acid in the context of the invention is an organic compound which in its structure contains at least one protonatable amino group and at least one —COOH or one —SOsH group. Preferred amino acids are aminocarboxylic acids, in particular α- (alpha) -aminocarboxylic acids and w-aminocarboxylic acids, α-aminocarboxylic acids being particularly preferred.

According to the invention, basic amino acids are to be understood as meaning those amino acids which have an isoelectric point p1 of greater than 7.0.

Basic α-aminocarboxylic acids contain at least one asymmetric carbon atom. In the context of the present invention, both possible enantiomers can be used equally as specific compounds or mixtures thereof, in particular as racemates. However, it is particularly advantageous to use the naturally preferred isomer form, usually in the L configuration.

The basic amino acids are preferably selected from the group that is formed from arginine, lysine, ornithine and histidine, particularly preferably from arginine and lysine. In a further particularly preferred embodiment, the method is therefore characterized in that the sealing reagent (b1) is an alkalizing agent comprising a basic one

Amino acid from the group arginine, lysine, ornithine and / or histidine.

In a further preferred embodiment, the method is characterized in that the agent (b) contains as sealing reagent (b1) at least one alkalizing agent from the group of basic amino acids, which is preferably selected from the group of arginine, lysine, ornithine and histidine.

Good results could also be obtained when the agent (b) contains at least one alkali metal hydroxide as the sealing reagent (b1). Sodium hydroxide and potassium hydroxide, for example, can be mentioned as very suitable alkali metal hydroxides. Good results could also be obtained when the composition (b) is an alkalizing agent comprising at least one as sealing reagent (b1)

Alkaline earth metal hydroxide. Magnesium hydroxide, calcium hydroxide and barium hydroxide can be mentioned as well-suited alkaline earth metal hydroxides.

Good results could also be obtained if the agent (b) contained at least one alkali metal silicate and / or alkali metal metasilicate as sealing reagent (b1). Suitable

Alkali metal silicates are, for example, sodium silicate and potassium silicate. Suitable

Examples of alkali metal metasilicates are sodium metasilicate and potassium metasilicate.

Good results could also be obtained if the agent (b) contained at least one alkali metal carbonate and / or alkaline earth metal carbonate as sealing reagent (b1). Suitable alkali metal carbonates are, for example, sodium carbonate and potassium carbonate. Suitable

Alkaline earth metal carbonates are, for example, magnesium carbonate and calcium carbonate.

Within the group of the aforementioned sealing reagent (b1) in the form of a

Alkalizing agents, ammonia, C2-C6-alkanolamines, basic amino acids and alkali metal hydroxides have proven to be particularly suitable.

In the context of a further particularly preferred embodiment, the method is characterized in that the agent (b) acts as a sealing reagent (b1) at least one

Alkalizing agents selected from the group consisting of ammonia, C2-C6-alkanolamines, basic amino acids and alkali metal hydroxides.

Contains alkalizing agent selected from the group consisting of ammonia, 2-aminoethan-1 -ol, 3-aminopropan-1 -ol, 4-aminobutan-1 -ol, 5-aminopentan-1 -ol, 1-aminopropane-2- ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1-amino 2-methylpropan-2-ol, 3-aminopropan-1, 2-diol, 2-amino-2-methylpropan-1, 3-diol, arginine, lysine, ornithine, histidine, sodium hydroxide and potassium hydroxide.

The agent (b) contains the alkalizing agent as a sealing reagent (b1) in a cosmetic carrier, preferably in an aqueous cosmetic carrier.

In this context, it has been found to be preferred if the agent (b) - based on the total weight of the agent (b) - 5.0 to 99.0 wt .-%, preferably 15.0 to 97.0 wt .-% %, more preferably 25.0 to 97.0% by weight, even more preferably 35.0 to 97.0% by weight and very particularly preferably 45.0 to 97.0% by weight of water. In a further embodiment, the method is characterized in that the agent (b) - based on the total weight of the agent (b) - 5.0 to 99.0 wt .-%, preferably 15.0 to 97.0 wt .-% %, more preferably 25.0 to 97.0% by weight, even more preferably 35.0 to 97.0% by weight and very particularly preferably 45.0 to 97.0% by weight of water.

The alkalizing agents contained in the agent (b) exert an influence on the pH of the agent (b). It was found here that certain alkaline pH values in particular have an advantageous effect on the dyeing performance that can be achieved in the process and the fastness properties of the dyeings.

For this reason it is preferred that the agent (b), comprising an alkalizing agent as sealing reagent (b1), has a pH of from 7.0 to 12.0, preferably from 7.5 to 11.5, more preferably from 8.0 to 11.0 and very particularly preferably from 8.5 to 9.5.

The pH value can be measured using the usual methods known from the prior art, such as, for example, pH value measurement using glass electrodes using single-rod electrodes or using pH indicator paper.

In a further very particularly preferred embodiment, the method is characterized in that the agent (b) contains an alkalizing agent as sealing reagent (b1) and has a pH of 7.0 to 12.0, preferably from 7.5 to 11 .5, more preferably from 8.0 to 11.0 and very particularly preferably from 8.5 to 9.5.

The pH values in the context of the present invention are pH values that were measured at a temperature of 22 ° C.

In yet another alternative embodiment, the sealing reagent (b1) contains an acidifying agent.

The acidifying agent is particularly preferably selected from the group consisting of inorganic acids, organic acids and mixtures thereof.

Good results could be obtained if the agent (b) contains at least one inorganic acid as the sealing reagent (b1). Suitable inorganic acids are, for example, phosphoric acid, sulfuric acid and / or hydrochloric acid, sulfuric acid being particularly preferred.

In a further preferred embodiment, the method is characterized in that the agent (b) is used as a sealing reagent (b1) at least one acidifying agent from the group of Contains inorganic acids, which is preferably selected from the group consisting of

Phosphoric acid, sulfuric acid, hydrochloric acid and mixtures thereof.

In a further, even more preferred embodiment, the method is thereby

characterized in that the agent (b) contains sulfuric acid as the sealing reagent (b1).

Good results could also be obtained if the agent (b) contains at least one organic acid as the sealing reagent (b1). The organic acid is preferably selected from the group consisting of formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, glyceric acid, glyoxylic acid, adipic acid, pimelic acid, propic acid, azelaic acid, Crotonic acid, isocrotonic acid, elaidic acid, maleic acid, fumaric acid, muconic acid, citraconic acid, mesaconic acid, camphoric acid, benzoic acid, o, m, p-phthalic acid, naphthoic acid, toluic acid, hydratropic acid, atropic acid, cinnamic acid, isonicotinic acid, nicotinic acid,

Bicarbamic acid, 4,4'-dicyano-6,6'-binicotinic acid, 8-carbamoyloctanoic acid, 1,2,4-pentane tricarboxylic acid, 2-pyrrolecarboxylic acid, 1,2,4,6,7-naphthalene pentaacetic acid, malonaldehyde, 4-hydroxy phthalamic acid, 1-pyrazolecarboxylic acid, gallic acid or propane tricarboxylic acid, glycolic acid, gluconic acid, lactic acid, maleic acid, ascorbic acid, malic acid, tartaric acid,

Citric acid and mixtures thereof.

In a further preferred embodiment, the method is characterized in that the agent (b) contains at least one acidifying agent from the group of organic acids as sealing reagent (b1), the organic acid preferably being selected from the group consisting of formic acid, acetic acid, propionic acid , Butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, glyceric acid, glyoxylic acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, propiolic acid, crotonic acid, isocrotonic acid, maleinic acid, mesaconic acid, muconic acid, maleinic acid , Camphoric acid, benzoic acid, o, m, p-phthalic acid, naphthoic acid, toluic acid, hydratropic acid, atropic acid, cinnamic acid, isonicotinic acid, nicotinic acid, bicarbamic acid, 4,4'-dicyano-6,6'-binicotinic acid, 8-carbamoyloctanoic acid, 1, 2 , 4-pentane tricarboxylic acid, 2-pyrrole carboxylic acid, 1, 2,4,6, 7-naphthalene pentaacetic acid e, malonaldehydic acid, 4-hydroxyphthalamic acid, 1-pyrazole carboxylic acid, gallic acid or propane tricarboxylic acid, glycolic acid, gluconic acid, lactic acid, maleic acid, ascorbic acid, malic acid, tartaric acid, citric acid and mixtures thereof.

In a further, even more preferred embodiment, the method is thereby

characterized in that the agent (b) contains acetic acid as a sealing reagent (b1). Likewise suitable acidifying agents include methanesulfonic acid and / or 1-hydroxyethane-1,1-diphosphonic acid.

Within the group of the aforementioned sealing reagents (b1) in the form of a

Acidifying agents, sulfuric acid and / or acetic acid have proven to be particularly well suited.

Acidifying agents selected from the group consisting of sulfuric acid, acetic acid and mixtures thereof.

The agent (b) contains the acidifying agent as sealing reagent (b1) in a cosmetic carrier, preferably in an aqueous cosmetic carrier.

The acidifying agents contained in the agent (b) exert an influence on the pH of the agent (b). It was found here that acidic pH values also have an advantageous effect on the dyeing performance that can be achieved in the process and the fastness properties of the dyeings.

For this reason, it is preferred that the agent (b), comprising an acidifying agent as sealing reagent (b1), has a pH of 2.0 to 6.5, preferably from 3.0 to 6.0, more preferably from 4 , 0 to 6.0 and very particularly preferably from 4.5 to 5.5.

In a further very particularly preferred embodiment, the method is characterized in that the agent (b) contains an acidifying agent as sealing reagent (b1) and has a pH of 2.0 to 6.5, preferably from 3.0 to 6, 0, more preferably from 4.0 to 6.0 and very particularly preferably from 4.5 to 5.5.

Further ingredients in means (a) and Cb)

The means (a) and (b) described above can also contain one or more optional ingredients. The agents can additionally contain one or more surfactants. The term surfactants is understood to mean surface-active substances. A distinction is made between anionic surfactants consisting of a hydrophobic residue and a negatively charged hydrophilic head group, amphoteric surfactants, which carry both a negative and a compensating positive charge, cationic surfactants, which have a positively charged hydrophilic group in addition to a hydrophobic residue, and nonionic surfactants, which have no charges but rather strong dipole moments and are strongly hydrated in aqueous solution.

Zwitterionic surfactants are surface-active compounds which have at least one quaternary ammonium group and at least one -COO ⁽⁾ - or -S03 ^(_) - group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinates, for example coconut alkyl dimethylammonium glycinate, N-acyl aminopropyl-N, N-dimethylammonium glycinate, for example cocoacylaminopropyl dimethylammonium glycinate, and 2-alkyl -3-carboxymethyl-3-hydroxyethyl-imidazolines each with 8 to 18 carbon atoms in the alkyl or acyl group and that

Cocoacylaminoethyl hydroxyethyl carboxymethyl glycinate. A preferred zwitterionic surfactant is the fatty acid amide derivative known under the INCI name Cocamidopropyl Betaine.

Ampholytic surfactants are surface-active compounds which, in addition to a Cs-C ₂₄ -alkyl or -acyl group, contain at least one free amino group and at least one —COOH or —SOsH group and are capable of forming internal salts. Examples of suitable ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids, each with about 8 to 24 C. Atoms in the alkyl group. Typical examples of amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates,

Imidazolinium betaines and sulfobetaines.

Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, the

Cocoacylaminoethylaminopropionate and the C ₁₂ - Cis acyl sarcosine.

The agents can also contain at least one nonionic surfactant. Suitable nonionic surfactants are alkyl polyglycosides and alkylene oxide addition products with fatty alcohols and fatty acids with 2 to 30 moles of ethylene oxide per mole of fatty alcohol or fatty acid. Preparations with good properties are also obtained if, as nonionic surfactants, they contain fatty acid esters of ethoxylated glycerol which have been reacted with at least 2 mol of ethylene oxide. Furthermore, the agents can also contain at least one cationic surfactant. Cationic surfactants are understood to mean surfactants, that is to say surface-active compounds, each with one or more positive charges. Cationic surfactants only contain positive charges. These surfactants are usually composed of a hydrophobic part and a hydrophilic head group, the hydrophobic part usually consisting of a hydrocarbon structure (e.g. consisting of one or two linear or branched alkyl chains), and the positive charge (s) are located in the hydrophilic head group. Examples of cationic surfactants are

- Quaternary ammonium compounds, which can carry one or two alkyl chains with a chain length of 8 to 28 carbon atoms as hydrophobic radicals,

- Quaternary phosphonium salts, substituted with one or more alkyl chains with a chain length of 8 to 28 carbon atoms or

- tertiary sulfonium salts.

Furthermore, the cationic charge can also be part of a heterocyclic ring (e.g. an imidazolium ring or a pyridinium ring) in the form of an onium structure. In addition to the functional unit that carries the cationic charge, the cationic surfactant can also contain other uncharged functional groups, as is the case, for example, with esterquats. The cationic surfactants are used in a total amount of 0.1 to 45% by weight, preferably 1 to 30% by weight and very particularly preferably 1 to 15% by weight, based on the total weight of the respective agent.

Furthermore, the agents can also contain at least one anionic surfactant. Anionic surfactants are surface-active agents with exclusively anionic charges (neutralized by a corresponding counter cation). Examples of anionic surfactants are fatty acids, alkyl sulfates, alkyl ether sulfates and ether carboxylic acids with 12 to 20 carbon atoms in the alkyl group and up to 16 glycol ether groups in the molecule.

The anionic surfactants are used in a total amount of 0.1 to 45% by weight, preferably 1 to 30% by weight and very particularly preferably 1 to 15% by weight, based on the total weight of the respective agent.

The agent (a) and / or the agent (b) can also contain a matting agent. Suitable matting agents include, for example, (modified) starches, waxes, talc and / or (modified) silicas. The amount of matting agent is preferably between 0.1 and 10% by weight based on the total amount of agent (a) or agent (b). Agent (a) preferably contains a matting agent. The agents can also contain other active ingredients, auxiliaries and additives, such as solvents, fat components such as, for example, the C8-C30 fatty acid triglycerides, the C8-C30 fatty acid monoglycerides, the C8-C3o fatty acid diglycerides and / or the hydrocarbons;

Structurants such as glucose, maleic acid and lactic acid, hair conditioning compounds such as phospholipids, for example lecithin and cephalins; Perfume oils, dimethyl isosorbide and

Cyclodextrins; fiber structure-improving active ingredients, in particular mono-, di- and oligosaccharides such as, for example, glucose, galactose, fructose, fruit sugar and lactose; Dyes for coloring the agent; Anti-dandruff ingredients such as Piroctone Olamine, Zinc Omadine and Climbazole;

Amino acids and oligopeptides; Protein hydrolyzates based on animals and / or plants, and in the form of their fatty acid condensation products or optionally anionically or cationically modified derivatives; vegetable oils; Sunscreens and UV blockers; Active ingredients such as panthenol, pantothenic acid, pantolactone, allantoin, pyrrolidinone carboxylic acids and their salts, and bisabolol; Polyphenols, in particular hydroxycinnamic acids, 6,7-dihydroxycoumarins, hydroxybenzoic acids, catechins, tannins, leucoanthocyanidins, anthocyanidins, flavanones, flavones and flavonols; Ceramides or pseudoceramides; Vitamins, provitamins and vitamin precursors; Plant extracts; Fats and waxes such as fatty alcohols, beeswax, montan wax and paraffins; Source and

Penetrants such as glycerine, propylene glycol monoethyl ether, carbonates, hydrogen carbonates, guanidines, ureas and primary, secondary and tertiary phosphates; Opacifiers such as latex, styrene / PVP and styrene / acrylamide copolymers; Pearlescent agents such as ethylene glycol mono- and distearate and PEG-3 distearate; and propellants such as propane-butane mixtures, N2O, dimethyl ether, CO2 and air.

The person skilled in the art will select these additional substances according to the desired properties of the agents. With regard to further optional components and the amounts of these components used, express reference is made to the relevant manuals known to the person skilled in the art. The additional active ingredients and auxiliaries are preferably used in the preparations according to the invention in amounts of 0.0001 to 25% by weight, in particular 0.0005 to 15% by weight, based on the total weight of the respective agent.

Process for coloring keratinic materials

In the context of the method according to the invention, agents (a) and (b) are applied to the keratinic materials, in particular to human hair. Thus means (a) and (b) are the means ready to use. The means (a) and (b) are different from each other.

The means (a) and (b) can in principle be used simultaneously or successively, the successive application being preferred. The best results could be obtained if the agent (a) was first applied to the keratinic materials in a first step and the agent (b) was applied in a second step.

A method for treating keratin material, in particular for dyeing keratin material, in particular human hair, is therefore very particularly preferred, comprising the following steps in the order given:

o In a first step, application of an agent (a) on the keratinic material, the agent (a) containing:

o in a second step, application of an agent (b) to the keratinic material, the agent (b) containing:

(b1) at least one sealing reagent.

In order to give the colored keratinic material a high washout resistance over a longer period of time, means (a) and (b) are also particularly preferably used within one and the same dyeing process, which means that between the use of means (a) and (b ) is a maximum of a few hours.

In a further preferred embodiment, the method is characterized in that the agent (a) is applied first and then the agent (b) is applied, the period between the application of the agents (a) and (b) being a maximum of 24 hours , preferably a maximum of 12 hours and particularly preferably a maximum of 6 hours.

A characteristic feature of the agent (a) is its content of at least one reactive organic silicon compound (a1). The reactive organic silicon compound or compounds (a1) enter into an oligomerization or polymerization reaction and in this way functionalize the hair surface as soon as they come into contact with it. In this way a first film is formed. The coloring compounds (a2) are incorporated into the film so that it is colored. In the second step of the process, a second agent (b) is then applied to the hair. During the application of the agent (b), comprising at least one film-forming polymer as sealing reagent (b1), this interacts with the silane film and is thus bound to the keratinic materials. During the application of the agent (b), comprising at least one alkalizing agent or acidifying agent as

Sealing reagent (b1), the formation of the silane film is positively influenced. In the context of a further embodiment, a method comprising the following steps in the specified order is very particularly preferred

(1) Application of the agent (a) on the keratin material,

(2) Allowing agent (a) to act for a period of 10 seconds to 10 minutes, preferably 10 seconds to 5 minutes,

(3) if necessary, rinsing the keratinous material with water,

(4) application of the agent (b) on the keratinic material,

(5) allowing the agent (b) to act for a period of 30 seconds to 30 minutes, preferably 30 seconds to 10 minutes,

(6) Rinse the keratinous material with water.

Rinsing out the keratinic material with water in steps (3) and (6) of the method is understood according to the invention to mean that only water is used for the rinsing process, without any further means other than means (a) and (b) would be used.

In a step (1), the agent (a) is first applied to the keratinic materials, in particular the human hair.

After application, the agent (a) is allowed to act on the keratinic materials. In this context, exposure times of 10 seconds to 10 minutes, preferably from 20 seconds to 5 minutes and very particularly preferably from 30 seconds to 2 minutes on the hair have proven to be particularly advantageous.

In a preferred embodiment of the method according to the invention, the agent (a) can now be rinsed out of the keratinic materials before the agent (b) is applied to the hair in the subsequent step.

Dyeings with likewise good wash fastness properties were obtained when the agent (b) was applied to the keratinic materials to which the agent (a) was still applied.

In step (4), the agent (b) is now applied to the keratinic materials. After application, the agent (b) is now allowed to act on the hair.

Even if the agent (b) is left to act for a short time, the process allows dyeings to be produced with particularly good intensity and washfastness. Contact times of 10 seconds to 10 minutes, preferably of 20 seconds to 5 minutes and very particularly preferably of 30 seconds to 3 minutes on the hair have proven to be particularly advantageous. In step (6), agent (b) (and any agent (a) that is still present) is then rinsed out of the keratinic material with water.

In this embodiment, the sequence of steps (1) to (6) takes place preferably within 24 hours.

The agent (a) contains the organic silicon compound (s) a class of

highly reactive compounds which can undergo hydrolysis or oligomerization and / or polymerization when used. Due to their high reactivity, these form organic

Silicon compounds form a film on the keratinous material.

To avoid premature oligomerization or polymerization, it is of considerable advantage for the user to prepare the ready-to-use agent (a) just before use.

In the context of a further embodiment, a method is preferred which comprises the following steps in the specified order

(1) Production of an agent (a) by mixing a first agent (a ‘) and a second agent (a“), where

o the first agent (a ‘) contains at least one organic silicon compound (a1) from the group of the silanes with one, two or three silicon atoms, and

o the second agent (a ") contains at least one coloring compound (a2), comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment,

(2) application of the agent (a) on the keratin material,

(3) allowing the agent (a) to act for a period of 10 seconds to 10 minutes, preferably 10 seconds to 5 minutes,

(4) if necessary, rinsing the keratinous material with water,

(5) application of the agent (b) on the keratin material,

(6) Allowing agent (b) to act for a period of 30 seconds to 30 minutes, preferably 30 seconds to 10 minutes,

(7) Rinsing the keratinous material with water.

In order to be able to provide a formulation that is as stable as possible in storage, the agent (a ‘) itself is preferably formulated with a low water content or anhydrous.

In a preferred embodiment, a multi-component packaging unit (kit-of-parts) is characterized in that the agent (a ') - based on the total weight of the agent (a') - preferably has a water content of 0.001 to 10% by weight from 0.5 to 9% by weight, more preferably from 1 to 8% by weight and very particularly preferably from 1.5 to 7% by weight. The agent (a “) contains water. In a preferred embodiment, a multi-component packaging unit (kit-of-parts) is characterized in that the agent (a ”) - based on the total weight of the agent (a2) - has a water content of 15 to 100% by weight, preferably from 35 to 100% by weight, more preferably from 55 to 100% by weight, even more preferably from 65 to 100% by weight and very particularly preferably from 75 to 100% by weight.

Within this embodiment, the ready-to-use agent (a) is now produced by mixing the agents (a ‘) and (a“).

For example, the user can first stir or spill the agent (a ‘), which contains the organic silicon compound (s) (a1), with the aqueous, coloring agent-containing agent (a“). This mixture of (a ‘) and (a“) can now be applied to the keratinic materials by the user - either immediately after its manufacture or after a short reaction time of 10 seconds to 20 minutes. The user can then use means (b) as described above.

The optionally contained silicone polymer (a3) can be contained in the agent (a ‘) or in the agent (a“). The silicone polymer (a3) is preferably contained in the agent (a ”).

o the first agent (a ‘) contains at least one organic silicon compound (a1) from the group of the silanes with one, two or three silicon atoms and furthermore at least one silicone polymer (a3), and

(2) application of the agent (a) on the keratin material,

(4) if necessary, rinsing the keratinous material with water,

(5) application of the agent (b) on the keratin material,

(7) Rinsing the keratinous material with water. In a further embodiment, particularly preferred is a method comprising the following steps in the order given

o the second agent (a ") contains at least one coloring compound (a2), comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, and furthermore contains at least one silicone polymer (a3),

(2) application of the agent (a) on the keratin material,

(4) if necessary, rinsing the keratinous material with water,

(5) application of the agent (b) on the keratin material,

(7) Rinsing the keratinous material with water.

In the context of a further preferred embodiment, a method can also be characterized in that the silicone polymer or polymers (a3) are separated in a third

made-up means (a “‘) are made available.

In the context of this further embodiment, preference is given to a method comprising the following steps in the order given

(1) Production of an agent (a) by mixing a first agent (a ‘) and a second agent (a“) and a third agent (a “‘), where

the first agent (a ‘) contains at least one organic silicon compound (a1) from the group of the silanes having one, two or three silicon atoms, and

the second agent (a ”) contains at least one coloring compound (a2) comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, and

the third agent (a “‘) contains at least one silicone polymer (a3),

(2) application of the agent (a) on the keratin material,

(4) if necessary, rinsing the keratinous material with water,

(5) application of the agent (b) on the keratin material,

(6) Allowing agent (b) to act for a period of 30 seconds to 30 minutes, preferably 30 seconds to 10 minutes, (7) Rinsing the keratinous material with water.

Multi-component packaging unit (kit-of-parts)

To increase the user comfort, the user is preferably provided with all the necessary means in the form of a multi-component packaging unit (kit-of-parts).

A second subject of the present invention is therefore a multi-component packaging unit (kit-of-parts) for coloring keratinic material, comprehensively packaged separately from one another

a first container with a means (a ‘), the means (a‘) containing:

a second container with a means (a "), the means (a") containing:

a third container with a means (b), the means (b) containing:

(b1) at least one sealing reagent,

components (a1), (a2) and (b1) being disclosed in detail above.

The organic silicon compounds (a1) contained in the mean (a ‘) of the kit from the group of the silanes with one, two or three silicon atoms correspond to the organic silicon compounds which were also used in the mean (a) of the method described above.

The coloring compound (a2) contained in the mean (a ″) of the kit, comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, correspond to the pigments based on VMP substrate platelets, which are also based on the mean (a) of the procedure described above were used.

The sealing reagent (b1) contained in the middle (b) of the kit corresponds to the

Sealing reagent which was also used in means (b) of the method described above.

In this context, too, it is again possible to use the optionally contained silicone polymer (a3)

To be assembled in the middle (a ‘), in the middle (a“) or in a further medium (a “).

Within the scope of a further embodiment, a multi-component packaging unit (kit-of-parts) for coloring keratinous material is packaged comprehensively separately from one another

- a first container with a means (a '), the means (a') containing: at least one organic silicon compound (a1) from the group of the silanes with one, two or three silicon atoms and furthermore at least one silicone polymer (a3), and

- a second container with a means (a "), the means (a") containing:

- a third container with a means (b), the means (b) containing:

(b1) at least one sealing reagent,

the components (a1), (a2), (a3) and (b1) being disclosed in detail above.

a first container with a means (a ‘), the means (a‘) containing:

at least one organic silicon compound (a1) from the group of the silanes with one, two or three silicon atoms and furthermore at least one silicone polymer (a3), and

a second container with a means (a "), the means (a") containing:

a third container with an agent (a “‘), the agent (a “‘) being a water-based cosmetic carrier

a fourth container with a means (b), the means (b) containing:

(b1) at least one sealing reagent,

the components (a1), (a2), (a3) and (b1) being disclosed in detail above.

In the context of this embodiment, the means (a ‘) and (a ″) have a low water content. To produce the ready-to-use agent (a), the agents (a ‘), (a“) and (a “‘) are mixed. The means (a “‘) represents a water-based cosmetic carrier.

a first container with a means (a ‘), the means (a‘) containing:

at least one organic silicon compound (a1) from the group of the silanes with one, two or three silicon atoms,

a second container with a means (a "), the means (a") containing:

(a2) at least one coloring compound, comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, and furthermore at least one silicone polymer (a3), and

a third container with a means (b), the means (b) containing: (b1) at least one sealing reagent,

the components (a1), (a2), (a3) and (b1) being disclosed in detail above.

a first container with a means (a ‘), the means (a‘) containing:

a second container with a means (a "), the means (a") containing:

(a2) at least one coloring compound comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment,

a third container with a means (a “‘), where the means (a “‘) contains:

at least one silicone polymer (a3), and

a fourth container with a means (b), the means (b) containing:

(b1) at least one sealing reagent,

the components (a1), (a2), (a3) and (b1) being disclosed in detail above.

With regard to the further preferred embodiments of the multi-component packaging unit, what has been said about the method applies mutatis mutantis.

Examples

example 1

The following formulations were produced (unless otherwise stated, all data are in% by weight)

Medium (a ‘)

Medium (a ")

The ready-to-use agent (a) was prepared by mixing 5 g of the agent (a ‘) and 20 g of the agent (a“). The pH of the agent (a) was determined by adding ammonia or

Lactic acid adjusted to a value of 10.5. Then the agent (a) was left to stand for about 5 minutes.

Medium (b)

The agent (a) was massaged into a strand of hair (Kerling, Euronaturhaar, white) and allowed to act for 1 minute. The agent (a) was then rinsed out with water.

Subsequently, the agent (b) was applied to the strand of hair, left to act for 1 minute and then also rinsed out with water. The tresses were then assessed visually. A whitish-metallic coloring of the hair with high intensity and fastness was obtained.

Claims

1. Process for coloring keratinic material, in particular human hair,

comprising the following steps:

Application of an agent (a) to the keratinous material, the agent (a) containing: (a1) at least one organic silicon compound from the group of the silanes with one, two or three silicon atoms, and

(a2) at least one coloring compound comprising at least one pigment based on a substrate platelet, which comprises a vacuum metallized pigment, and application of an agent (b) to the keratinic material, the agent (b) containing: (b1) at least one sealing reagent .

2. The method according to claim 1, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (I) and / or (II)

RiR2N-L-Si (OR ₃ ) a (R4) b (I), where

Ri, R ₂ independently represent a hydrogen atom or a Ci-C6-alkyl group,

L stands for a linear or branched, divalent Ci-C ₂ o-alkylene group,

R3, R ₄ independently represent a Ci-C6-alkyl group,

a, stands for an integer from 1 to 3, and

b stands for the integer 3 - a, and

wherein in the organic silicon compound of the formula (II)

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] _h -Si (R6 ^, ) d (OR5 ^, ) c (II),

R5, R5 ‘, R5“, R6, R6 ‘and R6“ independently of one another represent a Ci-C6-alkyl group,

A, A ', A “, A“' and A ““ independently of one another represent a linear or branched, divalent Ci-C ₂ o-alkylene group,

R7 and Re independently represent a hydrogen atom, a Ci-C6-alkyl group, a hydroxy-Ci-C6-alkyl group, a C ₂ -C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the formula (III ) stand

- (A ““) - Si (R6 “) d“ (OR ₅ “) c“ (III), c, stands for an integer from 1 to 3, d stands for the integer 3 - c,

c ‘stands for an integer from 1 to 3,

d ‘stands for the integer 3 - c‘,

c "stands for an integer from 1 to 3,

d "stands for the whole number 3 - c",

e stands for 0 or 1,

f stands for 0 or 1,

g stands for 0 or 1,

h stands for 0 or 1,

with the proviso that at least one of the radicals from e, f, g and h is different from 0.

3. The method according to any one of claims 1 to 2, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (I),

RiR ₂ NL-Si (OR ₃ ) a (R4) b (I),

in which

Ri, R ₂ both represent a hydrogen atom, and

L stands for a linear, divalent Ci-C6-alkylene group, preferably for a propylene group (- CH ₂ --CH ₂ --CH ₂ -) or for an ethylene group (--CH ₂ --CH ₂ -),

R ₃ , R ₄ independently of one another represent a methyl group or an ethyl group, a represents the number 3 and

b stands for the number 0.

4. The method according to any one of claims 1 to 3, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (I) which is selected from the group

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

- -1 - (3-aminopropyl) silanetriol

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

- -1 - (2-aminoethyl) silanetriol

- (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane

- -1 - (3-dimethylaminopropyl) silanetriol

- (2-Dimethylaminoethyl) triethoxysilane.

- (2-Dimethylaminoethyl) trimethoxysilane and / or

- 1 - (2-dimethylaminoethyl) silanetriol. 5. The method according to any one of claims 1 to 4, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (II),

in which

- e and f both stand for the number 1,

- g and h both stand for the number 0,

6. The method according to any one of claims 1 to 5, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (II) which is selected from the group

- 3- (Trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- 2- [bis [3- (trimethoxysilyl) propyl] amino] ethanol

- 2- [bis [3- (triethoxysilyl) propyl] amino] ethanol

- 3- (Trimethoxysilyl) -N, N-bis [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine

- N1, N1-bis [3- (trimethoxysilyl) propyl] -1, 2-ethanediamine,

- N1, N1-bis [3- (triethoxysilyl) propyl] -1, 2-ethanediamine,

- N, N-bis [3- (trimethoxysilyl) propyl] -2-propene-1-amine and / or

- N, N-bis [3- (triethoxysilyl) propyl] -2-propen-1-amine.

7. The method according to any one of claims 1 to 6, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (IV).

R ₉ Si (ORio) k (Rn) m (IV),

in which

- Rg stands for a Ci-Ci8-alkyl group,

- Rio stands for a hydrogen atom or a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k. 8. The method according to any one of claims 1 to 7, characterized in that the agent (a) contains at least one organic silicon compound (a1) of the formula (IV) which is selected from the group

- methyltrimethoxysilane

- methyltriethoxysilane

- ethyltrimethoxysilane

- ethyltriethoxysilane

- hexyltrimethoxysilane

- hexyltriethoxysilane

- Octyltrimethoxysilane

- octyltriethoxysilane

- dodecyltrimethoxysilane,

- dodecyltriethoxysilane,

- octadecyltrimethoxysilane,

- Octadecyltriethoxysilane and

- Mixtures of it.

9. The method according to any one of claims 1 to 8, characterized in that the agent (a) contains at least two structurally different organic silicon compounds (a1).

10. The method according to any one of claims 1 to 9, characterized in that the

Substrate platelets a material selected from the group consisting of metals,

Contains metal alloys and metal oxides.

11. The method according to any one of claims 1 to 10, characterized in that the

Substrate plate comprises aluminum.

12. The method according to any one of claims 1 to 1 1, characterized in that the

The substrate platelet has a coating A made of at least one low-refractive-index metal oxide and / or metal oxide hydrate which has a refractive index of at most 1.8.

13. The method according to any one of claims 1 to 12, characterized in that the

Substrate plate has a coating B made of at least one high-index metal oxide which has a refractive index of at least 1.9.

14. The method according to 13, characterized in that the substrate plate is a further

Coating C of at least one metal oxide and / or metal oxide hydrate, which is different from the underlying coating B, has. 15. Multi-component packaging unit (kit-of-parts) for coloring keratinic material, comprehensively packaged separately from one another

a first container with a means (a ‘), the means (a‘) containing:

a second container with a means (a "), the means (a") containing:

a third container with a means (b), the means (b) containing:

(b1) at least one sealing reagent.