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EP0503221A1 - Concentrated fabric softening compositions - Google Patents

Concentrated fabric softening compositions Download PDF

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Publication number
EP0503221A1
EP0503221A1 EP91870187A EP91870187A EP0503221A1 EP 0503221 A1 EP0503221 A1 EP 0503221A1 EP 91870187 A EP91870187 A EP 91870187A EP 91870187 A EP91870187 A EP 91870187A EP 0503221 A1 EP0503221 A1 EP 0503221A1
Authority
EP
European Patent Office
Prior art keywords
weight
fabric softening
composition
composition according
concentrated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP91870187A
Other languages
German (de)
French (fr)
Other versions
EP0503221B1 (en
Inventor
Bruno Albert Jean Hubesch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26129188&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0503221(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from EP91870105.3A external-priority patent/EP0503218A1/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US08/178,243 priority Critical patent/US5484540A/en
Priority to HU9302549A priority patent/HUT66690A/en
Priority to CS931846A priority patent/CZ184693A3/en
Priority to AU14445/92A priority patent/AU1444592A/en
Priority to PCT/US1992/000661 priority patent/WO1992015745A1/en
Priority to NZ24186292A priority patent/NZ241862A/en
Priority to IE920735A priority patent/IE920735A1/en
Priority to MX9200990A priority patent/MX9200990A/en
Priority to PT10021092A priority patent/PT100210A/en
Priority to CN 92102202 priority patent/CN1046774C/en
Publication of EP0503221A1 publication Critical patent/EP0503221A1/en
Publication of EP0503221B1 publication Critical patent/EP0503221B1/en
Application granted granted Critical
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3734—Cyclic silicones
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/835—Mixtures of non-ionic with cationic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/001—Softening compositions
    • C11D3/0015—Softening compositions liquid
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2003—Alcohols; Phenols
    • C11D3/2006—Monohydric alcohols
    • C11D3/2017—Monohydric alcohols branched
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2003—Alcohols; Phenols
    • C11D3/2006—Monohydric alcohols
    • C11D3/2017—Monohydric alcohols branched
    • C11D3/202—Monohydric alcohols branched fatty or with at least 8 carbon atoms in the alkyl chain
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3707—Polyethers, e.g. polyalkyleneoxides
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/144—Alcohols; Metal alcoholates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165—Ethers
    • D06M13/17—Polyoxyalkyleneglycol ethers
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35—Heterocyclic compounds
    • D06M13/352—Heterocyclic compounds having five-membered heterocyclic rings
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35—Heterocyclic compounds
    • D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46—Compounds containing quaternary nitrogen atoms
    • D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46—Compounds containing quaternary nitrogen atoms
    • D06M13/47—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
    • D06M13/473—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/227—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
    • D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53—Polyethers
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38—Cationic compounds
    • C11D1/58—Heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38—Cationic compounds
    • C11D1/62—Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50—Modified hand or grip properties; Softening compositions

Definitions

  • the present invention relates to fabric softeners.
  • the compositions according to the invention are concentrated aqueous fabric softening compositions which retain viscosity upon dilution.
  • Concentrated aqueous fabric softening compositions have been extensively described in the art, and one aspect which has often been discussed is the viscosity of these concentrated compositions; indeed these concentrated compositions are typically extremely viscous and the prior art has often described means by which the viscosity of these concentrated compositions could be controlled or decreased.
  • One aspect which has been much less dealt with is the viscosity of these concentrated compositions upon dilution; indeed it has been observed that the viscosity of such concentrated compositions dramatically drops upon dilution, and this viscosity loss is clearly undesirable, essentially in terms of consumer acceptance.
  • Concentrated aqueous fabric softeners have been described for instance in EP 56 695, EP 13 780, DE 26 31 114 and EP 60 003, and a process for the preparation of concentrated fabric softening compositions is disclosed in EP-A-316 996.
  • a concentrated aqueous fabric softening composition comprising from 10% to 35% by weight of a cationic fabric softening active or mixtures thereof, said composition further comprising:
  • the present invention also encompasses a method for the softening of fabrics, wherein the above concentrated compositions are diluted in water before they are contacted with said fabrics in the rinse water.
  • compositions according to the invention are concentrated fabric softeners; by concentrated, it is meant that the compositions comprise from 10% to 35% by weight of the total composition of a cationic fabric softening active or mixtures thereof, preferably 15% to 25%.
  • cationic it is meant any softening compound which is in cationic form in the concentrated softening composition.
  • Suitable cationic fabric softening actives include
  • Component (i) are the well-known dialkyldimethylammonium salts such as ditallowdimethylammonium chloride (DTDMAC), ditallowdimethylammonium methylsulfate, di(hydrogenated tallow) dimethylammonium chloride, dibehenyldimethylammonium chloride.
  • DTDMAC ditallowdimethylammonium chloride
  • ditallowdimethylammonium methylsulfate di(hydrogenated tallow) dimethylammonium chloride
  • dibehenyldimethylammonium chloride ditallowdimethylammonium chloride
  • Component (ii) and (iii) are methylbis(tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate and methylbis(hydrogenated tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate, wherein R1 is an acyclic aliphatic C15-C17 hydrocarbon group, R2 is an ethylene group, R5 is a methyl group, R8 is a hydroxyalkyl group and A is a methylsulfate anion; these materials are available from Sherex Chemical Company under the trade names Varisoft 222 R and Varisoft 110 R, respectively.
  • Component (iv) are 1-methyl-1-tallowamino-ethyl-2-tallowimidazolinium methylsulfate and 1-methyl-1-(hydrogenated tallowamidoethyl)-methylsulfate.
  • Suitable fabric softening actives include the following amines, provided they are present in the concentrated softening composition in a protonated form; such amines are of the formula : wherein n is 2 or 3, preferably 2; R1 and R2 are, independently, a C8-C30 alkyl or alkenyl, preferably C12-C20 alkyl, more preferably C15-C18 alkyl, or mixtures of such alkyl radicals. Examples of such mixtures are the alkyl radicals obtained from coconut oil, "soft" (non-hardened) tallow, and hardened tallow.
  • Q is CH2 or N, preferably N
  • X is wherein T is O or NR5, R5 being H or C1-C4 alkyl, preferably H, and R4 is a divalent C1-C3 alkylene group or (C2H4O)m, wherein m is an integer of from 1 to 8; or X is R4.
  • Most preferred softening agents according to the above formula are imidazolines of the following formula : wherein R1 is a tallow group.
  • the softening amines described herein above are suitable for the purpose of the present invention provided they are present in the concentrated softening composition in a protonated form; a suitable means to protonate these amines is described for instance in EP 199 383.
  • a preferred softening active mixture for use herein is a mixture of 20% to 70% by weight of the softening active of ditallow dimethyl ammonium chloride (DTDMAC) and 30% to 80% ditallow imidazoline.
  • DTDMAC ditallow dimethyl ammonium chloride
  • the concentrated compositions according to the invention comprise from 15% to 25% by weight of the finished product of such a mixture.
  • the softening active comprises a ditallow imidazoline ester such as described herein above (i.e. when T is O and R1 and R2 are both tallow in the formula above). This embodiment is particularly preferred for environmental reasons.
  • compositions according to the invention further comprise from 0.3% to 3% by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox) n , wherein R is a linear C8-18 alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof.
  • a linear fatty alcohol ethoxylate of the formula RO(Etox) n wherein R is a linear C8-18 alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof.
  • R is a linear C8-18 alkyl chain
  • n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof.
  • Preferred are linear fatty alcohol ethoxylates wherein R is a linear chain having from 10 to 13 carbon atoms, and wherein n is from 5 to 10, preferably 8.
  • these compounds, or mixtures thereof are present at levels
  • compositions according to the present invention further comprise from 0.5% to 6% , preferably from 1.5% to 2.5% by weight of the composition of a nonionic hydrophylic polymer, or mixtures thereof.
  • suitable polymers include polyethylene glycol, polypropylene glycol, polyvinylalcolhol and the like. Particularly preferred is a polyethylene glycol having a molecular weight of from 300 to 50000, preferably 2000 to 10000.
  • the softening active is a mixture of DTDMAC and ditallow imidasoline
  • the softening active comprises ditallow imidazoline ester
  • compositions according to the present invention further comprise from 0% to 2%, preferably from 0% to 0.1% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, preferably 12 to 14, or mixtures thereof, most preferably 13.
  • Branched compounds similar to said highly branched fatty alcohols are often present in perfumes; thus, the level of said highly branched fatty alcohol to be added to the composition must be adjusted depending on the perfume which is used, if any.
  • Such highly branched fatty alcohols suitable for use in the compositions according to the present invention are commercially available from EXXON under the trade name EXXAL®.
  • compositions according to the invention may further comprise from 0% to 0.5% by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula: where R is a C1-C5 alkyl group and m is an integer of 1 to 500, or mixtures thereof.
  • Said polydialkylsiloxanes components are not essential ingredients in the compositions according to the invention, as the compositions will retain viscosity upon dilution even in the abscence of such polydialkylsiloxanes.
  • several benefits can be obtained from these polydialkylsiloxane, including improved stability of the finished product, improved water absorbancy of the treated fabrics.
  • compositions according to the present invention comprise from 0.05% to 0.5%, most preferably from 0.1% to 0.3% by weight of the total composition of the above polydialkylsiloxanes, or mixtures thereof.
  • the softening active comprises the ditallow imidazoline ester described herein above
  • Suitable polydialkylsiloxanes are commercially available from DOW CORNING under the trade name 200 fluid, and the preferred polydialkylsiloxanes for use herein are DOW CORNING's 200 fluid 350 CS (R is methyl and m is 203) and 5 CS (R is methyl and m is 7).
  • compositions according to the invention may additionally comprise such conventional ingredients as perfumes, preservatives, germicides, colorants, fungicides, stabilizers, brighteners, opacifiers and the like, at conventional levels, i.e. up to about 5% by weight of the composition.
  • compositions in their concentrated form have a viscosity of from 40 to 400 cps at 60 RPM shear rate.
  • the compositions according to the invention can be used directly in the concentrated form, or they can preferably be diluted before they are used.
  • the compositions according to the present invention are meant to be diluted in water, preferably in 2 to 3 times their weight of water.
  • the compositions In diluted form, the compositions have a viscosity of from 20 to 60 cps at 60 RPM shear rate, preferably 30 to 50 cps at 6o RPM shear rate.
  • the present invention also encompasses a method for the softening of fabrics wherein the concentrated fabric softening compositions described herein above are diluted in water before they are contacted with said fabrics.
  • a concentrated softening composition as described hereinabove which has a viscosity of from 40 to 400 cps at 60 RPM shear rate, is diluted in two times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of from 20 to 60, preferably 30 to 50 cps at 60 RPM shear rate, and said diluted fabric softening composition is contacted with said fabrics in the rinse water.
  • compositions according to the present invention are illustrated by the following examples.
  • a composition according to the present invention is made, which comprises : - Ditallow dimethyl ammonium chloride 7.60% - Ditallow dimethyl imidazoline 14.20% - HCl 0.82% - Polyethylene glycol 4000 MW 2.00%% - Silicone oil 5CS 0.19% - Lutensol® TO8 1.30% - Exxal® 13 0.08% - CaCl2 0.20% - Perfume 0.70% - water and minors to 100% silicone oil 5 CS is a polydialkylsiloxane as defined in the description.
  • Lutensol® TO 8 is a linear fatty alcohol ethoxylate
  • EXXAL® 13 is a highly branched fatty alcohol, both according to the description hereinbefore.
  • the above composition was made by adding the HCl to a water seat at 60°C-65°C. To this solution, a molten permix of ditallow dimethyl ammonium chloride, ditallowimidazoline and Lutensol TO 8 is added at about 80°C-85°C, under agitation during about 10 minutes. An aqueous solution of CaCl2 is then injected for about 5 minutes. A mixture of perfume and the silicone oil is then added. The composition is then cooled to room temperature. Finally a 50% solution of the polyethylene glycol 4000 MW is added. The composition thus obtained has a viscosity of about 65cps before dilution, and 50cps after dilution in 2 times its weight of water.
  • a composition which contains:
  • a composition which contains:

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Abstract

Concentrated fabric softening compositions are described which retain viscosity upon dilution in water. The compositions comprise cationic fabric softening actives, as well as a specific combination of emulsifiers and polymers. The present invention also encompasses a method for the softening of fabrics.

Description

    Technical field
  • The present invention relates to fabric softeners. The compositions according to the invention are concentrated aqueous fabric softening compositions which retain viscosity upon dilution.
    • Background
  • Concentrated aqueous fabric softening compositions have been extensively described in the art, and one aspect which has often been discussed is the viscosity of these concentrated compositions; indeed these concentrated compositions are typically extremely viscous and the prior art has often described means by which the viscosity of these concentrated compositions could be controlled or decreased. One aspect which has been much less dealt with is the viscosity of these concentrated compositions upon dilution; indeed it has been observed that the viscosity of such concentrated compositions dramatically drops upon dilution, and this viscosity loss is clearly undesirable, essentially in terms of consumer acceptance.
  • It is therefore an object of the present invention to provide a concentrated aqueous fabric softening composition which has an acceptable viscosity in the concentrated form, and which retains acceptable viscosity after it has been diluted.
  • This technical problem was discussed in GB 2 007 734 which proposes to use a combination of a fatty quaternary ammonium salt having two long chain alkyl groups together with an oily substance.
  • Concentrated aqueous fabric softeners have been described for instance in EP 56 695, EP 13 780, DE 26 31 114 and EP 60 003, and a process for the preparation of concentrated fabric softening compositions is disclosed in EP-A-316 996.
    • Summary of the invention
  • It has now been found that the above object can be achieved by formulating a concentrated aqueous fabric softening composition comprising from 10% to 35% by weight of a cationic fabric softening active or mixtures thereof, said composition further comprising:
    • from 0.3% to 3 % by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear C₈-C₁₈ alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof;
    • From 0.5% to 6% by weight of the total composition of a nonionic hydrophilic polymer, or mixtures thereof;
    • from 0% to 2% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, or mixtures thereof;
    • from 0% to 0.5 % by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula
      Figure imgb0001
       wherein R is a C₁-C₅ alkyl chain, and m is an integer of from 1 to 500, or mixtures thereof.
  • The present invention also encompasses a method for the softening of fabrics, wherein the above concentrated compositions are diluted in water before they are contacted with said fabrics in the rinse water.
    • Detailed description of the invention
  • The compositions according to the invention are concentrated fabric softeners; by concentrated, it is meant that the compositions comprise from 10% to 35% by weight of the total composition of a cationic fabric softening active or mixtures thereof, preferably 15% to 25%. By cationic, it is meant any softening compound which is in cationic form in the concentrated softening composition. Suitable cationic fabric softening actives include
    • (i) acylic quaternary ammonium salts having the formula :
      Figure imgb0002
       wherein R₂ is an acylic aliphatic C₁₅-C₂₂ hydrocarbon group which may be interrupted by ester groups, R₃ is a C₁-C₄ saturated alkyl or hydroalkyl group, R₄ is selected from R₂ and R₃, and A is an anion; rapidly biodegradable compounds of formula (i) where R₂, and possibly R₄, are interrupted by ester groups, are disclosed in EPA 239 910;
    • (ii) diamido quaternary ammonium salts having the formula :
      Figure imgb0003
       wherein R is an acyclic aliphatic C₁₅-C₂₂ hydrocarbon group, R₂ is a divalent alkylene group having 1 to 3 carbon atoms, R₅ and R₈ are C₁-C₄ saturated alkyl or hydroxyalkyl groups, and A⁻ is an anion.
    • (iii) diamido alkoxylated quaternary ammonium salts having the formula :
      Figure imgb0004
       wherein n is an integer of from about 1 to about 5, and R₁, R₂, R₅ and A⁻ are as defined above.
    • (iv) quaternary imidazolinium compounds having the formula:
      Figure imgb0005
       wherein R₁ = C₁₅-C₁₇ saturated alkyl, R₂ = C₁-C₄ saturated alkyl, Z = NH or O, and A⁻ is an anion.
  • Examples of Component (i) are the well-known dialkyldimethylammonium salts such as ditallowdimethylammonium chloride (DTDMAC), ditallowdimethylammonium methylsulfate, di(hydrogenated tallow) dimethylammonium chloride, dibehenyldimethylammonium chloride.
  • Examples of Component (ii) and (iii) are methylbis(tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate and methylbis(hydrogenated tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate, wherein R₁ is an acyclic aliphatic C₁₅-C₁₇ hydrocarbon group, R₂ is an ethylene group, R₅ is a methyl group, R₈ is a hydroxyalkyl group and A is a methylsulfate anion; these materials are available from Sherex Chemical Company under the trade names Varisoft 222 R and Varisoft 110 R, respectively.
    Examples of Component (iv) are 1-methyl-1-tallowamino-ethyl-2-tallowimidazolinium methylsulfate and 1-methyl-1-(hydrogenated tallowamidoethyl)-methylsulfate.
  • Other suitable fabric softening actives include the following amines, provided they are present in the concentrated softening composition in a protonated form; such amines are of the formula :
    Figure imgb0006
    wherein n is 2 or 3, preferably 2; R₁ and R₂ are, independently, a C₈-C₃₀ alkyl or alkenyl, preferably C₁₂-C₂₀ alkyl, more preferably C₁₅-C₁₈ alkyl, or mixtures of such alkyl radicals. Examples of such mixtures are the alkyl radicals obtained from coconut oil, "soft" (non-hardened) tallow, and hardened tallow. Q is CH₂ or N, preferably N, X is
    Figure imgb0007
    wherein T is O or NR₅, R₅ being H or C₁-C₄ alkyl, preferably H, and R₄ is a divalent C₁-C₃ alkylene group or (C₂H₄O)m, wherein m is an integer of from 1 to 8; or X is R₄.
  • Most preferred softening agents according to the above formula are imidazolines of the following formula :
    Figure imgb0008
    wherein R1 is a tallow group.
  • The softening amines described herein above are suitable for the purpose of the present invention provided they are present in the concentrated softening composition in a protonated form; a suitable means to protonate these amines is described for instance in EP 199 383.
  • A preferred softening active mixture for use herein is a mixture of 20% to 70% by weight of the softening active of ditallow dimethyl ammonium chloride (DTDMAC) and 30% to 80% ditallow imidazoline. Preferably, the concentrated compositions according to the invention comprise from 15% to 25% by weight of the finished product of such a mixture.
  • In an alternative preferred embodiment of the present invention, the softening active comprises a ditallow imidazoline ester such as described herein above (i.e. when T is O and R₁ and R₂ are both tallow in the formula above). This embodiment is particularly preferred for environmental reasons.
  • The compositions according to the invention further comprise from 0.3% to 3% by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear C₈-₁₈ alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof. Preferred are linear fatty alcohol ethoxylates wherein R is a linear chain having from 10 to 13 carbon atoms, and wherein n is from 5 to 10, preferably 8. Preferably, these compounds, or mixtures thereof are present at levels of from about 1 to about 1.5% by weight of the total composition. These compounds are commercially available from BASF under the trade name LUTENSOL TO®.
  • The compositions according to the present invention further comprise from 0.5% to 6% , preferably from 1.5% to 2.5% by weight of the composition of a nonionic hydrophylic polymer, or mixtures thereof. Such suitable polymers include polyethylene glycol, polypropylene glycol, polyvinylalcolhol and the like. Particularly preferred is a polyethylene glycol having a molecular weight of from 300 to 50000, preferably 2000 to 10000. In the preferred embodiment herein where the softening active is a mixture of DTDMAC and ditallow imidasoline, it is preferred to use a polyethylene glycol with a molecular weight of about 4000. In the alternative preferred embodiment where the softening active comprises ditallow imidazoline ester, it is preferred to use a polyethylene glycol with a molecular weight of about 8000.
  • The compositions according to the present invention further comprise from 0% to 2%, preferably from 0% to 0.1% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, preferably 12 to 14, or mixtures thereof, most preferably 13. Branched compounds similar to said highly branched fatty alcohols are often present in perfumes; thus, the level of said highly branched fatty alcohol to be added to the composition must be adjusted depending on the perfume which is used, if any. Such highly branched fatty alcohols suitable for use in the compositions according to the present invention are commercially available from EXXON under the trade name EXXAL®.
  • The compositions according to the invention may further comprise from 0% to 0.5% by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula:
    Figure imgb0009
    where R is a C₁-C₅ alkyl group and m is an integer of 1 to 500, or mixtures thereof. Said polydialkylsiloxanes components are not essential ingredients in the compositions according to the invention, as the compositions will retain viscosity upon dilution even in the abscence of such polydialkylsiloxanes. However, several benefits can be obtained from these polydialkylsiloxane, including improved stability of the finished product, improved water absorbancy of the treated fabrics. Said polydialkylsiloxanes can also be helpful in avoiding the formation of fabric softener residues which may occur in the dispenser of the washing machine. Thus, preferred compositions according to the present invention comprise from 0.05% to 0.5%, most preferably from 0.1% to 0.3% by weight of the total composition of the above polydialkylsiloxanes, or mixtures thereof. In the compositions according to the present invention where the softening active comprises the ditallow imidazoline ester described herein above, it is preferred to use a polydialkylsiloxane where R is methyl and m is about 200. In other compositions, it is preferred to use a polydialkylsiloxane where R is methyl and m is 7. Suitable polydialkylsiloxanes are commercially available from DOW CORNING under the trade name 200 fluid, and the preferred polydialkylsiloxanes for use herein are DOW CORNING's 200 fluid 350 CS (R is methyl and m is 203) and 5 CS (R is methyl and m is 7).
  • The compositions according to the invention may additionally comprise such conventional ingredients as perfumes, preservatives, germicides, colorants, fungicides, stabilizers, brighteners, opacifiers and the like, at conventional levels, i.e. up to about 5% by weight of the composition.
  • The compositions in their concentrated form have a viscosity of from 40 to 400 cps at 60 RPM shear rate. The compositions according to the invention can be used directly in the concentrated form, or they can preferably be diluted before they are used. The compositions according to the present invention are meant to be diluted in water, preferably in 2 to 3 times their weight of water. In diluted form, the compositions have a viscosity of from 20 to 60 cps at 60 RPM shear rate, preferably 30 to 50 cps at 6o RPM shear rate.
  • Thus, the present invention also encompasses a method for the softening of fabrics wherein the concentrated fabric softening compositions described herein above are diluted in water before they are contacted with said fabrics. In a preferred embodiment of said method, a concentrated softening composition as described hereinabove, which has a viscosity of from 40 to 400 cps at 60 RPM shear rate, is diluted in two times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of from 20 to 60, preferably 30 to 50 cps at 60 RPM shear rate, and said diluted fabric softening composition is contacted with said fabrics in the rinse water.
  • The compositions according to the present invention are illustrated by the following examples.
    • Example 1
  • A composition according to the present invention is made, which comprises :
    - Ditallow dimethyl ammonium chloride 7.60%
    - Ditallow dimethyl imidazoline 14.20%
    - HCl 0.82%
    - Polyethylene glycol 4000 MW 2.00%%
    - Silicone oil 5CS 0.19%
    - Lutensol® TO8 1.30%
    - Exxal® 13 0.08%
    - CaCl₂ 0.20%
    - Perfume 0.70%
    - water and minors to 100%

    silicone oil 5 CS is a polydialkylsiloxane as defined in the description. Lutensol® TO 8 is a linear fatty alcohol ethoxylate, and EXXAL® 13 is a highly branched fatty alcohol, both according to the description hereinbefore.
  • The above composition was made by adding the HCl to a water seat at 60°C-65°C. To this solution, a molten permix of ditallow dimethyl ammonium chloride, ditallowimidazoline and Lutensol TO 8 is added at about 80°C-85°C, under agitation during about 10 minutes. An aqueous solution of CaCl₂ is then injected for about 5 minutes. A mixture of perfume and the silicone oil is then added. The composition is then cooled to room temperature. Finally a 50% solution of the polyethylene glycol 4000 MW is added.
    The composition thus obtained has a viscosity of about 65cps before dilution, and 50cps after dilution in 2 times its weight of water.
    • Example 2
  • A composition is made which contains:
    Figure imgb0010
    • Example 3
  • A composition is made which contains:
    Figure imgb0011

Claims (15)

  1. A concentrated aqueous fabric softening composition comprising from 10 to 35 % by weight of a cationic fabric softening active or mixtures thereof, said composition further comprising
    - from 0.3% to 3% by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear C₈-C₁₈ alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof;
    - from 0.5% to 6% by weight of the total composition of a nonionic hydrophilic polymer, or mixtures thereof;
    - from 0 to 2% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, or mixtures thereof;
    - from 0 to 0.5 %by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula:
    Figure imgb0012
     wherein R is a C₁-C₅ alkyl chain, and m is an integer of from 1 to 500, or mixtures thereof.
  2. A composition according to claim 1 which comprises from 15 % to 25% by weight of the total composition of said cationic fabric softening active, or mixtures thereof.
  3. A concentrated fabric softening composition according to the preceding claims wherein said cationic softening active is a mixture of ditallow dimethyl ammonium chloride and ditallow imidazoline.
  4. A concentrated fabric softening composition according to claim 3 which consists of from 20% to 70% by weight of said softening active of ditallowdimethyl ammonium chloride and from 30% to 80% by weight of said softening active of ditallow imidazoline.
  5. A concentrated fabric softening composition according to claims 3 and 4 which comprises from 1.5% to 2.5% by weight of the total composition of a polyethylene glycol having a molecular weight of 4000.
  6. A concentrated fabric softening composition according to claims 3-5 which comprises from 0.05% to 0.5 %, preferably 0.1% to 0.3% by weight of the total composition of said linear or cyclic polydialkylsiloxane of the formula
    Figure imgb0013
     wherein R is methyl, and m is 7.
  7. A concentrated fabric softening composition according to claims 1 and 2 wherein said softening active comprises ditallow imidazoline ester.
  8. A concentrated fabric softening composition according to claim 7 which comprises a polyethylene glycol having a molecular weight of 8000.
  9. A concentrated fabric softening composition according to claims 7-8 which comprises from 0.05% to 0.5 %, preferably from 0.1% to 0.3% by weight of the total composition of said linear or cyclic polydialkylsiloxane of the formula:
    Figure imgb0014
     wherein R is a methyl, and m is 203.
  10. A concentrated fabric softening composition according to the preceding claims which comprises from 1% to 1.5% by weight of the total composition of said fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear C₁₀-C₁₃ alkyl chain, and n representing the weighted average ethoxylation degree is from 5 to 10, preferably 8.
  11. A concentrated fabric softening composition according to the preceding claims which comprises from 0% to 0.1% by weight of the total composition of said highly branched fatty alcohol, said highly branched fatty alcohol having from 12 to 14 carbon atoms, preferably 13.
  12. A concentrated fabric softening composition according to any of the preceeding claims, said composition having a viscosity of from 40 to 400 cps at 60 RPM shear rate before dilution, and said composition having a viscosity of from 20 to 60cps at 60 RPM shear rate after it has been diluted in 2 times its weight of water.
  13. A concentrated fabric softening composition according to claim 12 which has a viscosity of from 30 to 50 cps at 60 RPM shear rate after it has been diluted in 2 times its weight of water.
  14. A method for the softening of fabrics wherein a concentrated fabric softening composition according to claims 1 to 10 and having a viscosity of from 40 to 400 cps at 60 RPM Shear rate is diluted in 2 times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of 20 to 60 cps at 60 RPM shear rate, and wherein said diluted fabric softening composition is contacted with said fabrics in the rinse water.
  15. A method according to claim 14 wherein the concentrated fabric softening composition having a viscosity of from 40 to 400 cps at 60 RPM shear rate is diluted in 2 times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of from 30 to 50 cps at 60 RPM shear rate.
EP19910870187 1991-03-08 1991-11-22 Concentrated fabric softening compositions Revoked EP0503221B1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
US08/178,243 US5484540A (en) 1991-03-08 1992-01-30 Concentrated fabric softening compositions
HU9302549A HUT66690A (en) 1991-03-08 1992-01-30 Concentrated fabric softening compositions
CS931846A CZ184693A3 (en) 1991-03-08 1992-01-30 Concentrated textile plasticizing mixtures
AU14445/92A AU1444592A (en) 1991-03-08 1992-01-30 Concentrated fabric softening compositions
PCT/US1992/000661 WO1992015745A1 (en) 1991-03-08 1992-01-30 Concentrated fabric softening compositions
PT10021092A PT100210A (en) 1991-03-08 1992-03-06 AQUEOUS CONCENTRATE COMPOSITIONS FOR CARRYING UP TISSUES THAT UNDERSTAND CATIONIC ACTIVE INGREDIENTS OF TISSUE LOTION AS WELL AS A SPACING COMBINATION OF EMULSIFYING AND POLYMERING AGENTS
NZ24186292A NZ241862A (en) 1991-03-08 1992-03-06 Concentrated aqueous fabric softener containing cationic active; linear fatty alcohol ethoxylate; nonionic hydrophilic polymer and optionally fatty alcohol or/and polydialkyl siloxane
IE920735A IE920735A1 (en) 1991-03-08 1992-03-06 Concentrated fabric softening compositions
MX9200990A MX9200990A (en) 1991-03-08 1992-03-06 CONCENTRATED FABRIC SOFTENING COMPOSITIONS.
CN 92102202 CN1046774C (en) 1991-03-08 1992-03-07 Concentrated fabric softening compositions

Applications Claiming Priority (4)

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EP91200507 1991-03-08
EP91200507 1991-03-08
EP91870105.3A EP0503218A1 (en) 1991-03-08 1991-07-03 Concentrated fabric softening compositions
EP91870105 1991-07-03

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EP0839947A2 (en) * 1996-11-04 1998-05-06 Schill & Seilacher GmbH & Co. Composition for the permanent hydrophilic treatment of polyolefines, use of the composition and the fibres treated therewith
EP0869168A2 (en) * 1997-04-05 1998-10-07 Henkel Kommanditgesellschaft auf Aktien Composition for imparting hydrophilic properties to textiles
US5856287A (en) * 1995-03-01 1999-01-05 Colgate-Palmolive Co. Laundry concentrates
US7056881B2 (en) 2000-09-05 2006-06-06 Unilever Home & Personal Care Usa A Division Of Conopco, Inc. Fabric conditioning compositions
US7078374B2 (en) 2000-09-05 2006-07-18 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Method of preparing fabric conditioning compositions
EP1290124B2 (en) † 2000-06-16 2007-01-03 Unilever Plc Fabric softening compositions
US7282116B2 (en) * 1998-10-15 2007-10-16 The Procter & Gamble Company Paper softening compositions containing bilayer disrupter
EP2270123A1 (en) 2009-06-30 2011-01-05 The Procter and Gamble Company Packaged particulate bleaching compositions
US8916512B2 (en) 2010-06-21 2014-12-23 Basf Se Surfactant component and a composition including the same

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EP0330261A2 (en) * 1988-02-25 1989-08-30 The Procter & Gamble Company Stable biodegradable fabric softening compositions containing 2-hydroxypropyl monoester quaternized ammonium salts
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FR2298600A1 (en) * 1975-01-25 1976-08-20 Hoechst Ag SOFTENERS FOR TEXTILE MATERIALS
FR2457336A1 (en) * 1979-05-21 1980-12-19 Unilever Nv LIQUID FABRIC SOFTENING COMPOSITION, AND PROCESS FOR PREPARING THE SAME
EP0167382A2 (en) * 1984-07-03 1986-01-08 The Procter & Gamble Company Liquid cleansing composition
GB2177108A (en) * 1985-07-10 1987-01-14 Procter & Gamble Shampoo compositions
EP0234717A1 (en) * 1986-01-23 1987-09-02 The Procter & Gamble Company Detergent composition providing rinse cycle suds and turbidity control
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5856287A (en) * 1995-03-01 1999-01-05 Colgate-Palmolive Co. Laundry concentrates
EP0730023A3 (en) * 1995-03-01 1999-08-11 Colgate-Palmolive Company Laundry concentrates
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EP0839947A2 (en) * 1996-11-04 1998-05-06 Schill & Seilacher GmbH & Co. Composition for the permanent hydrophilic treatment of polyolefines, use of the composition and the fibres treated therewith
DE19645380B4 (en) * 1996-11-04 2008-04-17 Schill + Seilacher Ag Composition for the permanent hydrophilization of polyolefin fibers, and use of the composition
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EP0869168A3 (en) * 1997-04-05 1999-01-20 Henkel Kommanditgesellschaft auf Aktien Composition for imparting hydrophilic properties to textiles
US7282116B2 (en) * 1998-10-15 2007-10-16 The Procter & Gamble Company Paper softening compositions containing bilayer disrupter
EP1290124B2 (en) † 2000-06-16 2007-01-03 Unilever Plc Fabric softening compositions
US7056881B2 (en) 2000-09-05 2006-06-06 Unilever Home & Personal Care Usa A Division Of Conopco, Inc. Fabric conditioning compositions
US7078374B2 (en) 2000-09-05 2006-07-18 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Method of preparing fabric conditioning compositions
EP2270123A1 (en) 2009-06-30 2011-01-05 The Procter and Gamble Company Packaged particulate bleaching compositions
WO2011002640A1 (en) 2009-06-30 2011-01-06 The Procter & Gamble Company Packaged particulate bleaching compositions
US8916512B2 (en) 2010-06-21 2014-12-23 Basf Se Surfactant component and a composition including the same

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EP0503221B1 (en) 1998-02-11

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