WO1997046211A1 - Compositions cosmetiques detergentes et utilisation - Google Patents
Compositions cosmetiques detergentes et utilisation Download PDFInfo
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- WO1997046211A1 WO1997046211A1 PCT/FR1997/001008 FR9701008W WO9746211A1 WO 1997046211 A1 WO1997046211 A1 WO 1997046211A1 FR 9701008 W FR9701008 W FR 9701008W WO 9746211 A1 WO9746211 A1 WO 9746211A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/737—Galactomannans, e.g. guar; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
Definitions
- the present invention relates to new cosmetic compositions with improved properties intended simultaneously for cleaning and conditioning the hair, and comprising, in a cosmetically acceptable support, a washing base consisting of surfactants with detergent power in which are also present as conditioning agents , cationic polymers in combination with a particular silicone.
- a washing base consisting of surfactants with detergent power in which are also present as conditioning agents , cationic polymers in combination with a particular silicone.
- the invention also relates to the use of said compositions in the above-mentioned cosmetic application.
- detergent compositions for cleaning and / or washing the hair, the use of detergent compositions (or shampoos) based essentially on conventional surfactants of the type in particular anionic, nonionic and / or amphoteric, but more particularly of anionic type, is These compositions are applied to wet hair and the foam generated by massage or friction with the hands allows, after rinsing with water, the elimination of the various soils initially present on the hair.
- conditioning agents intended mainly to repair or limit the harmful or undesirable effects induced by the various treatments or aggressions which undergo , more or less repeatedly, the hair fibers.
- conditioning agents can of course also improve the cosmetic behavior of natural hair.
- the conditioning agents most commonly used to date in shampoos are cationic polymers, silicones and / or silicone derivatives, which in effect give washed, dry or wet hair, ease of disentangling, increased smoothness and smoothness. compared to what can be obtained with the corresponding cleaning compositions which are free thereof.
- cationic polymers silicones and / or silicone derivatives
- silicones and / or silicone derivatives which in effect give washed, dry or wet hair, ease of disentangling, increased smoothness and smoothness. compared to what can be obtained with the corresponding cleaning compositions which are free thereof.
- silicone and cationic polymer it is known to preferably use a mixture of silicone and cationic polymer.
- the latter are not really entirely satisfactory, so that there is still a great need for new products having, at the level of one or more of the cosmetic properties mentioned above, better performance.
- the present invention aims to satisfy such a need.
- compositions according to the invention give the hair, after rinsing, a remarkable treating effect which is manifested in particular by an ease of disentangling, as well as an addition of volume, lightness, straightening, softness and suppleness.
- R 1 R 2 , R 3 and R 4 , identical or different, denote a C r C 4 alkyl radical or a phenyl group
- R 5 denotes a C r C 4 alkyl radical or a hydroxyl group
- - n is an integer varying from 1 to 5
- - m is an integer varying from 1 to 5
- x is chosen such that the amine index is between 0.01 and 1 meq / g.
- Another subject of the invention is the use in cosmetics of the above compositions for cleaning and conditioning the hair.
- the essential elements included in the composition of the products according to the invention are (A) a washing base, (B) a conditioning system comprising (i) the cationic polymer (s), (ii) the particular amino silicone (s) .
- compositions in accordance with the invention necessarily comprise a washing base, generally aqueous.
- the surfactant (s) forming the washing base can be chosen either, alone or as a mixture, from anionic, amphoteric, nonionic, zwitterionic and cationic surfactants.
- the washing base preferably comprises anionic surfactants or mixtures of anionic surfactants and amphoteric surfactants, and even more preferably contains only this type of surfactant or mixture of surfactants.
- washing base is that just sufficient to give the final composition a satisfactory foaming and / or detergent power, and too large quantities of washing base do not really bring any additional advantages.
- the washing base can represent from 4% to 50% by weight, preferably from 10% to 35% by weight, and even more preferably from 12% to 25% by weight, of the total weight of the final composition.
- surfactants which are suitable for carrying out the present invention are in particular the following:
- anionic surfactants which can be used, alone or as mixtures, in the context of the present invention, there may be mentioned in particular (non-limiting list) the salts (in particular alkali salts, in particular sodium salts, ammonium, amine salts, amino alcohol salts or magnesium salts) of the following compounds: alkyl sulfates, alkyl ether sulfates, alkylamidoethersulfates, alkylaryl polyethersulfates, monoglycerides sulfates; alkylsulfonates, alkylphosphates, alkylamidesulfonates, alkylarylsulfonates, ⁇ -olefin-sulfonates, paraffin-sulfonates; alkylsulfosuccinates, alkylethersulfosuccinates, alkylamidesulfosuccinates;
- the salts in particular alkali salts, in particular sodium salts, ammonium, amine salt
- anionic surfactants which can still be used, mention may also be made of the salts of fatty acids such as the salts of oleic, ricinoleic, palmitic, stearic acids, coconut oil or hydrogenated coconut oil acids; acyl-lactylates whose acyl radical contains 8 to 20 carbon atoms.
- Weakly anionic surfactants can also be used, such as uronic alkyl D galactoside acids and their salts as well as polyoxyalkylenated ether carboxylic acids and their salts, in particular those comprising from 2 to 50 ethylene oxide groups, and their mixtures.
- the anionic surfactants of the acid or salt type of polyoxyalkylenated carboxylic ethers are in particular those which correspond to the following formula (1):
- Rl denotes an alkyl or alkaryl group
- n is an integer or decimal number (average value) which can vary from 2 to 24 and preferably from 3 to 10, the alkyl radical having between 6 and 20 carbon atoms approximately, and aryl denoting preferably phenyl,
- A denotes H, ammonium, Na, K, Li, Mg or a monoethanolamine or triethanolamine residue. It is also possible to use mixtures of compounds of formula (1), in particular mixtures in which the groups R-j are different.
- anionic surfactants it is preferred to use, according to the invention, the salts of alkyl sulfates and of alkyl ether sulfates and their mixtures.
- Non-ionic surfactants are also well known compounds per se (see in particular in this regard "Handbook of Surfactants” by MR PORTER, Blackie & Son editions (Glasgow and London), 1991, pp 116-178) and their nature is not, in the context of the present invention, of a character critical.
- alcohols alpha-diols, aikylphenols or polyethoxylated, polypropoxylated or polyglycerol fatty acids, having a fatty chain comprising for example 8 to 18 carbon atoms, the number of ethylene oxide or propylene oxide groups which may range in particular from 2 to 50 and the number of glycerol groups which may range in particular from 2 to 30.
- copolymers of ethylene oxide and of propylene, condensates of ethylene and propylene oxide on fatty alcohols ; polyethoxylated fatty amides preferably having from 2 to 30 moles of ethylene oxide, polyglycerol fatty amides comprising on average 1 to 5 glycerol groups and in particular 1, 5 to 4; polyethoxylated fatty amines preferably having 2 to 30 moles of ethylene oxide; esters of oxyethylenated sorbitan fatty acids having from 2 to 30 moles of ethylene oxide; sucrose fatty acid esters, polyethylene glycol fatty acid esters, alkylpolyglycosides, N-alkyl glucamine derivatives, amine oxides such as amino (C ⁇
- the alkylpolyglycosides constitute nonionic surfactants which fall particularly well within
- Amphoteric or zwitterionic surfactants may in particular be (non-limiting list) derivatives of aliphatic secondary or tertiary amines, in which the aliphatic radical is a chain linear or branched having 8 to 18 carbon atoms and containing at least one water-soluble anionic group (for example carboxylate, sulfonate, sulfate, phosphate or phosphonate); mention may also be made of (C8-C20) alkyl betaines, sulfobetaines, (C8-C20) alkyl amidoalkyl (C ⁇ -Cs) betaines or (C8-C20) amidoalkyl (C-j-C ⁇ ) sulfobetaines alkyl.
- aliphatic secondary or tertiary amines in which the aliphatic radical is a chain linear or branched having 8 to 18 carbon atoms and containing at least one water-soluble anionic group (for example carb
- R 2 denotes an alkyl radical of an acid R 2 -COOH present in the hydrolyzed coconut oil, a heptyl, nonyl or undecyl radical, R3 denotes a beta-hydroxyethyl group and R4 denotes a carboxymethyl group;
- X' denotes the group -CH 2 CH 2 -COOH or a hydrogen atom
- Y 'de notes - COOH or the radical -CH 2 - CHOH - SO3H
- R 2 'de notes an alkyl radical of an acid Rg -COOH present in coconut oil or in hydrolysed linseed oil, an alkyl radical, in particular C7, Cg , C-
- cocoamphocarboxyglycinate sold under the trade name MIRANOL C2M concentrated by the company MIRANOL.
- cationic surfactants that may be mentioned in particular (non-limiting list): the salts of primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated; quaternary ammonium salts such as chlorides or bromides of tetraalkylammonium, alkylamidoalkyltrialkylammonium, trialkylbenzylammonium, trialkylhydroxyalkylammonium or alkylpyridinium; imidazoline derivatives; or cationic amine oxides.
- cationic surfactants the use of which is not excluded, do not constitute preferred surfactants for the implementation of the present invention.
- compositions in accordance with the invention also necessarily comprise a cationic polymer.
- conditioning agents of cationic polymer type which can be used in accordance with the present invention can be chosen from all those already known per se as improving the cosmetic properties of hair treated with detergent compositions, namely in particular those described in patent application EP-A- 0 337 354 and in French patent applications FR-A- 2 270 846, 2 383 660, 2 598 611, 2 470 596 and 2 519 863.
- cationic polymer designates any polymer containing cationic groups and / or groups which can be ionized into cationic groups.
- the preferred cationic polymers are chosen from those which contain units comprising primary, secondary, tertiary and / or quaternary amine groups which can either be part of the main polymer chain, or be carried by a lateral substituent directly connected thereto.
- the cationic polymers used generally have a number-average molecular mass of between 500 and 5.10 6 approximately, and preferably between 10 3 and 3.10 6 approximately.
- cationic polymers there may be mentioned more particularly quaternized proteins (or protein hydrolysates) and polymers of the polyamine, polyaminoamide and quaternary polyammonium type. These are known products.
- the proteins or hydrolysates of quaternized proteins are in particular chemically modified polypeptides carrying at the end of the chain, or grafted onto it, quaternary ammonium groups.
- Their molecular mass can vary for example from 1,500 to 10,000, and in particular from 2,000 to 5,000 approximately.
- these compounds there may be mentioned in particular:
- protein hydrolysates carrying quaternary ammonium groups on the polypeptide chain comprising at least one alkyl radical having from 1 to 18 carbon atoms.
- CROQUAT M the quaternary ammonium groups of which comprise C 10 -C 18 alkyl groups
- CROQUAT S the quaternary ammonium groups of which comprise a C 18 alkyl group
- CROTEIN Q the quaternary ammonium groups of which comprise at least one alkyl group having from 1 to 18 carbon atoms.
- X " is an anion of an organic or mineral acid
- A denotes a protein residue derived from collagen protein hydrolysates
- R 5 denotes a lipophilic group containing up to 30 carbon atoms
- R 6 represents a group Alkylene having 1 to 6 carbon atoms, for example the products sold by the company Inolex, under the name "LEXEIN QX 3000", called in the CTFA dictionary "Cocotrimonium Collagen Hydrolysate".
- quaternized vegetable proteins such as wheat, corn or soy proteins: as quaternized wheat proteins
- polymers of the polyamine, polyamidoamide, quaternary polyammonium type which can be used in accordance with the present invention, which may be mentioned in particular, are those described in French patents No. 2,505,348 or 2,542,997. Among these polymers, there may be mentioned:
- Vinylpyrrolidone-acrylate or -dialkylamino-alkyl methacrylate copolymers such as the products sold under the name "GAFQUAT” by the company ISP, such as for example GAFQUAT 734, 755 or HS100 or the product called " Copolymer 937 ".
- Cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer, and described in particular in US Pat. No. 4,131,576, such as hydroxyalkyl celluloses, such as hydroxymethyl- , hydroxyethyl- or hydroxypropyl celluloses grafted in particular with a salt of methacryloylethyl trimethylammonium, of methacrylmidopropyl trimethylammonium, of diallyl dimethyl ammonium.
- cationic polysaccharides described more particularly in US patents 3,589,578 and 4,031,307 such as guar gums containing cationic trialkylammonium groups.
- Guar gums modified with a salt (eg chloride) of 2,3-epoxypropyl trimethylammonium are used, for example.
- Such products are marketed in particular under the trade names of JAGUAR C13 S, JAGUAR C 15, JAGUAR C 17 or JAGUAR C162 by the company MEYHALL.
- polymers consisting of piperazinyl units and of radicals alkylene or hydroxyalkylene with straight or branched chains, optionally interrupted by oxygen, sulfur, nitrogen atoms or by aromatic or heterocyclic rings, as well as the products of oxidation and / or quaternization of these polymers.
- Such polymers are described in particular in French patents 2,162,025 and 2,280,361;
- polyaminoamide derivatives resulting from the condensation of polyalkylene polyamines with polycarboxylic acids followed by alkylation by bifunctional agents Mention may be made, for example, of the adipic acid-diacoylaminohydroxyalkoyldialoylene triamine polymers in which the alkyl radical contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl, propyl.
- the alkyl radical contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl, propyl.
- Such polymers are described in particular in French patent 1,583,363.
- these derivatives there may be mentioned more particularly the adipic acid / dimethylaminohydroxypropyl / diethylene triamine polymers sold under the name "CARTARETINE F, F4 or F8" by the company SANDOZ.
- the molar ratio between the polyalkylene polylamine and the dicarboxylic acid being between 0.8: 1 and 1.4: 1; the resulting polyaminoamide being reacted with epichlorohydrin in a molar ratio of epichlorohydrin relative to the secondary amine group of the polyaminoamide of between 0.5: 1 and 1.8: 1.
- Such polymers are described in particular in the patents American 3,227,615 and 2,961,347.
- Polymers of this type are in particular sold under the name "Hercosett 57” by the company Hercules Inc. or else under the name of "PD 170” or “Delsette 101” by the company Hercules in the case of the adipic acid copolymer / epoxypropyl / diethylene-triamine.
- R12 denotes a hydrogen atom or a methyl radical
- R10 and R11 independently of one another, denote an alkyl group having from 1 to 22 carbon atoms, a hydroxyalkyl group in which the alkyl group preferably has 1 to 5 carbon atoms, a lower amidoalkyl group or R10 and R11 can denote, jointly with the nitrogen atom to which they are attached, heterocyclic groups, such as piperidinyl or morpholinyl
- Y " is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate.
- R13, R14, R15 and R16 identical or different, represent aliphatic, alicyclic or arylaliphatic radicals containing from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals, or else R13, R14, R15 and R16, together or separately, constitute with the nitrogen atoms to which they are attached heterocycles optionally containing a second heteroatom other than nitrogen or else R13, R14, R15 and R16 represent a linear or branched C1-C6 alkyl radical substituted by a nitrile, ester group, acyl, amide or -CO-O-R17-D or -CO-NH-R17-D where R17 is an alkylene and D is a quaternary ammonium group;
- A1 and B1 represent polymethylenic groups containing from 2 to 20 carbon atoms which may be linear or branched, saturated or unsaturated, and which may contain, linked to or intercalated in the main chain, one or more aromatic rings, or one or more atoms of oxygen, sulfur or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and
- X denotes an anion derived from a mineral or organic acid
- A1, R13 and R15 can form with the two nitrogen atoms to which they are attached a piperazine ring; in addition if A1 denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene radical, B1 can also denote a group (CH2) n-CO-D-OC- (CH2) n-
- a bis-secondary diamine residue such as a piperazine derivative
- X " is an anion such as chloride or bromide.
- These polymers have a number-average molecular mass generally between 1000 and 100,000.
- R18, R19, R20 and R21 identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, ⁇ -hydroxyethyl, ⁇ -hydroxypropyl or -CH2CH2 (OCH2CH2) pOH radical, where p is equal to 0 or to an integer between 1 and 6, provided that R18, R19, R20 and R21 do not simultaneously represent a hydrogen atom, r and s, identical or different, are whole numbers between 1 and 6 , q is equal to 0 or an integer between 1 and 34, X denotes a halogen atom, A denotes a radical of a dihalide or preferably represents -CH2-
- MIRAPOL A 15 Mention may, for example, be made, among these, of the products "MIRAPOL A 15", “MIRAPOL AD1", “MIRAPOL AZ1” and “MIRAPOL 175" sold by the company MIRANOL.
- X 2 denotes an anion, for example methosulfate or halide, such as chloride or bromide.
- the comonomer (s) that can be used in the preparation of the corresponding copolymers belong to the family of acrylamides, methacrylamides, diacetone acrylamides, acrylamides and methacrylamides substituted with nitrogen by lower alkyls, alkyl esters, acrylic or methacrylic acids, vinylpyrrolidone or vinyl esters.
- Quaternary polymers of vinylpyrrolidone and of vinylimidazole such as for example the products sold under the names LUVIQUAT FC 905, FC 550 and FC 370 by the company B.A.S.F ..
- Crosslinked polymers of methacryloyloxyethyltrimethylammonium chloride such as the polymers obtained by homopolymerization of dimethylaminoethylmethacrylate quaternized with methyl chloride, or by copolymerization of acrylamide with dimethylaminoethylmethacrylate quaternized with methyl chloride, homo or copolymerization being followed by crosslinking with an olefinically unsaturated compound, in particular methylene bis acrylamide.
- This dispersion is marketed under the name of "SALCARE SC 92" by the company ALLIED COLLOIDS. You can also use a homopolymer crosslinked methacryloyloxyethyl trimethylammonium chloride containing about 50% by weight of the homopolymer in mineral oil. This dispersion is marketed under the name of "SALCARE SC 95" by the company ALLIED COLLOIDS.
- cationic polymers which can be used in the context of the invention are polyalkyleneimines, in particular polyethyleneimines, polymers containing vinylpyridine or vinylpyridinium units, polyamine and epichlorohydrin condensates, quaternary polyureylenes and chitin derivatives.
- the polymers chosen from MIRAPOL the compound of formula (VII) in which R13, R14, R15 and R16 represent the methyl radical
- A1 represents the radical of formula - (CH2) 3- and B1 represents the radical of formula - (CH2) 6- and X " represents the chloride anion (subsequently named Mexomer PO)
- A1 and B1 represent the radical of formula - (CH2) 3- and X " represents the bromide anion (subsequently named Mexomer PAK).
- quaternary cellulose ether derivatives such as the products sold under the name “JR 400” by the company UNION CARBIDE CORPORATION, cyclopolymers, in particular copolymers of dimethyldiallylammonium chloride and of acrylamide, sold under the names “MERQUAT 550” and “MERQUAT S” by the company MERCK, cationic polysaccharides and more particularly guar gum modified with 2 chloride , 3-epoxypropyl trimethylammonium sold under the name "JAGUAR C13S" by the company MEYHALL
- the cationic polymer (s) can represent from 0.001% to 10% by weight, preferably from 0.005% to 5% by weight, and even more preferably from 0.01% to 3% by weight, of the total weight of the final composition.
- the latter also contain at least one amino silicone of formula (I) defined above.
- the amino silicones of general formula (I) are used which correspond to at least one of, and preferably to all, the following conditions: - R ⁇ R 2 , R 3 and R 4 denote the methyl radical,
- the groups (C n H 2n ) and (C m H 2m ) can be linear or branched.
- Such silicones are for example sold under the names SF1921 or SF1925 by the company GENERAL ELECTRIC.
- the cosmetic compositions in accordance with the invention contain the amino silicones defined above at weight contents which can be between 0.05% and 10%, preferably between 0.1% and 5% and even more preferably between 0, 2% and 3%, relative to the total weight of the composition.
- the vehicle, or support, of the detergent compositions according to the invention is preferably water or an aqueous-alcoholic solution of a lower alcohol such as ethanol, isopropanol or butanol.
- the detergent compositions according to the invention have a final pH generally between 3 and 10. Preferably, this pH is between 5 and 8.
- the adjustment of the pH to the desired value can be carried out conventionally by adding a base ( organic or mineral) in the composition, for example ammonia or a primary, secondary or tertiary (poly) amine such as monoethanolamine, diethanolamine, triethanolamine, isopropanolamine or propanediamine-1, 3, or by addition of an acid, preferably a carboxylic acid such as for example citric acid.
- a base organic or mineral
- a primary, secondary or tertiary (poly) amine such as monoethanolamine, diethanolamine, triethanolamine, isopropanolamine or propanediamine-1, 3, or by addition of an acid, preferably a carboxylic acid such as for example citric acid.
- the detergent compositions according to the invention can of course also contain all the usual adjuvants encountered in the field of shampoos, such as, for example, perfumes, preservatives, sequestering agents, thickeners, softeners, foam modifiers, colorants , pearlescent agents, moisturizing agents, anti-dandruff or anti-seborrheic agents, vitamins, sunscreens, suspending agents and others.
- adjuvants encountered in the field of shampoos such as, for example, perfumes, preservatives, sequestering agents, thickeners, softeners, foam modifiers, colorants , pearlescent agents, moisturizing agents, anti-dandruff or anti-seborrheic agents, vitamins, sunscreens, suspending agents and others.
- compositions can be in the form of more or less thickened liquids, creams or gel and they are mainly suitable for washing, caring for and / or styling the hair. They can also be in the form of rinse-off lotions.
- compositions in accordance with the invention are used like conventional shampoos, they are simply applied to wet hair and the foam generated by massage or friction with the hands is then eliminated, after a possible pause time, by rinsing with water, the operation being able to be repeated one or more times.
- the invention also relates to a process for washing and conditioning keratin fibers such as the hair, consisting in applying to said wet fibers an effective amount of a composition as defined above, then in rinsing with water after a possible pause time.
- compositions in accordance with the invention give the hair, after rinsing, a remarkable styling effect which is manifested in particular by ease of styling and maintenance, as well as a contribution of volume and lightness, markedly improved.
- composition A Two shampoo compositions were produced, one in accordance with the invention (composition A) and the other comparative (composition B):
- x is chosen such that the amine index is approximately 0.5 meq / g.
- Shampooing is carried out by applying approximately 12 g of composition A to sensitized hair previously wet. The shampoo is lathered and then rinsed thoroughly with water.
- composition A according to the invention All the experts indicate a clear improvement in these properties for the hair treated with composition A according to the invention.
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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EP97927252A EP0906082B1 (fr) | 1996-06-07 | 1997-06-06 | Compositions cosmetiques detergentes et utilisation |
US09/194,971 US6153570A (en) | 1996-06-07 | 1997-06-06 | Detergent cosmetic compositions and use |
AU31806/97A AU3180697A (en) | 1996-06-07 | 1997-06-06 | Detergent cosmetic compositions and use |
DE69704662T DE69704662T2 (de) | 1996-06-07 | 1997-06-06 | Kosmetische waschmittelzusammensetzungen und deren verwendung |
JP50029098A JP3332931B2 (ja) | 1996-06-07 | 1997-06-06 | 洗浄化粧品組成物及びその使用 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR96/07193 | 1996-06-07 | ||
FR9607193A FR2749507B1 (fr) | 1996-06-07 | 1996-06-07 | Compositions cosmetiques detergentes et utilisation |
Publications (1)
Publication Number | Publication Date |
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WO1997046211A1 true WO1997046211A1 (fr) | 1997-12-11 |
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ID=9492908
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/FR1997/001008 WO1997046211A1 (fr) | 1996-06-07 | 1997-06-06 | Compositions cosmetiques detergentes et utilisation |
Country Status (7)
Country | Link |
---|---|
US (1) | US6153570A (fr) |
EP (1) | EP0906082B1 (fr) |
JP (1) | JP3332931B2 (fr) |
AU (1) | AU3180697A (fr) |
DE (1) | DE69704662T2 (fr) |
FR (1) | FR2749507B1 (fr) |
WO (1) | WO1997046211A1 (fr) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2001028505A1 (fr) * | 1999-10-19 | 2001-04-26 | Wella Aktiengesellschaft | Produit transparent de traitement capillaire |
US6290944B1 (en) * | 1999-02-16 | 2001-09-18 | L'oreal S.A. | Detergent compositions containing an hydroxylalkyl ether surfactant and a cationic guar gum |
US6808701B2 (en) | 2000-03-21 | 2004-10-26 | Johnson & Johnson Consumer Companies, Inc. | Conditioning compositions |
EP1726295A1 (fr) | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée pipéridine et trois tensioactifs et utilisation de ces dernières |
EP1726293A1 (fr) * | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée et utilisation |
EP1726294A1 (fr) * | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée pipéridine et un polymère cationique et utilisation de ces dernières |
US7514091B2 (en) | 1998-07-23 | 2009-04-07 | L'oreal S.A. | Aminated silicone detergent cosmetic composition and use |
US8246941B2 (en) | 2005-05-24 | 2012-08-21 | L'oreal S.A. | Detergent cosmetic compositions comprising at least one amino silicone, and use thereof |
WO2013082096A1 (fr) | 2011-11-29 | 2013-06-06 | Dow Corning Corporation | Émulsions de silicone aminofonctionnelle pour des traitements de fibre |
WO2010111576A3 (fr) * | 2009-03-27 | 2014-01-23 | Hercules Incorporated | Polymères aminés et leur utilisation dans des compositions aqueuses |
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US6528046B1 (en) | 1999-10-22 | 2003-03-04 | Wella Ag | Clear hair treatment composition |
JP2005519658A (ja) * | 2001-11-14 | 2005-07-07 | ザ プロクター アンド ギャンブル カンパニー | 毛髪の美容処置のための方法及びこの方法を実行するための用具 |
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US9051406B2 (en) | 2011-11-04 | 2015-06-09 | Akzo Nobel Chemicals International B.V. | Graft dendrite copolymers, and methods for producing the same |
BR112014008874A2 (pt) | 2011-11-04 | 2017-04-25 | Akzo Nobel Chemicals Int Bv | composição de copolímero híbrido de dendrito |
US8945314B2 (en) | 2012-07-30 | 2015-02-03 | Ecolab Usa Inc. | Biodegradable stability binding agent for a solid detergent |
US9365805B2 (en) | 2014-05-15 | 2016-06-14 | Ecolab Usa Inc. | Bio-based pot and pan pre-soak |
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- 1997-06-06 DE DE69704662T patent/DE69704662T2/de not_active Expired - Fee Related
- 1997-06-06 US US09/194,971 patent/US6153570A/en not_active Expired - Fee Related
- 1997-06-06 JP JP50029098A patent/JP3332931B2/ja not_active Expired - Fee Related
- 1997-06-06 EP EP97927252A patent/EP0906082B1/fr not_active Expired - Lifetime
- 1997-06-06 AU AU31806/97A patent/AU3180697A/en not_active Abandoned
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7514091B2 (en) | 1998-07-23 | 2009-04-07 | L'oreal S.A. | Aminated silicone detergent cosmetic composition and use |
US6290944B1 (en) * | 1999-02-16 | 2001-09-18 | L'oreal S.A. | Detergent compositions containing an hydroxylalkyl ether surfactant and a cationic guar gum |
WO2001028505A1 (fr) * | 1999-10-19 | 2001-04-26 | Wella Aktiengesellschaft | Produit transparent de traitement capillaire |
US6808701B2 (en) | 2000-03-21 | 2004-10-26 | Johnson & Johnson Consumer Companies, Inc. | Conditioning compositions |
EP1726295A1 (fr) | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée pipéridine et trois tensioactifs et utilisation de ces dernières |
EP1726294A1 (fr) * | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée pipéridine et un polymère cationique et utilisation de ces dernières |
FR2886149A1 (fr) * | 2005-05-24 | 2006-12-01 | Oreal | Compositions cosmetiques detergentes comprenant une silicone aminee piperidine et trois tensioactifs et utilisation de ces derniers |
FR2886145A1 (fr) * | 2005-05-24 | 2006-12-01 | Oreal | Compositions cosmetiques detergentes comprenant une silicone aminee piperidine et polymere cationique et utilisation de ces derniers |
FR2886148A1 (fr) * | 2005-05-24 | 2006-12-01 | Oreal | Compositions cosmetiques detergentes comprenant une silicone aminee et utilisation |
EP1726293A1 (fr) * | 2005-05-24 | 2006-11-29 | L'oreal | Compositions cosmétiques détergentes comprenant une silicone aminée et utilisation |
US8246941B2 (en) | 2005-05-24 | 2012-08-21 | L'oreal S.A. | Detergent cosmetic compositions comprising at least one amino silicone, and use thereof |
WO2010111576A3 (fr) * | 2009-03-27 | 2014-01-23 | Hercules Incorporated | Polymères aminés et leur utilisation dans des compositions aqueuses |
WO2013082096A1 (fr) | 2011-11-29 | 2013-06-06 | Dow Corning Corporation | Émulsions de silicone aminofonctionnelle pour des traitements de fibre |
Also Published As
Publication number | Publication date |
---|---|
EP0906082B1 (fr) | 2001-04-25 |
JP3332931B2 (ja) | 2002-10-07 |
DE69704662T2 (de) | 2001-08-09 |
US6153570A (en) | 2000-11-28 |
DE69704662D1 (de) | 2001-05-31 |
FR2749507B1 (fr) | 1998-08-07 |
FR2749507A1 (fr) | 1997-12-12 |
JPH11513998A (ja) | 1999-11-30 |
EP0906082A1 (fr) | 1999-04-07 |
AU3180697A (en) | 1998-01-05 |
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