WO2004041224A1 - Agent de traitement capillaire presentant des caracteristiques de film et une odeur ameliorees - Google Patents

Agent de traitement capillaire presentant des caracteristiques de film et une odeur ameliorees Download PDF

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Publication number
WO2004041224A1
WO2004041224A1 PCT/EP2003/012135 EP0312135W WO2004041224A1 WO 2004041224 A1 WO2004041224 A1 WO 2004041224A1 EP 0312135 W EP0312135 W EP 0312135W WO 2004041224 A1 WO2004041224 A1 WO 2004041224A1
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Prior art keywords
weight
hair
agent
polymer
composition according
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PCT/EP2003/012135
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German (de)
English (en)
Inventor
Marion Detert
Thomas Döring
Kerstin Franck
Bettina Primmel
Original Assignee
Beiersdorf Ag
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Application filed by Beiersdorf Ag filed Critical Beiersdorf Ag
Priority to AU2003282063A priority Critical patent/AU2003282063A1/en
Publication of WO2004041224A1 publication Critical patent/WO2004041224A1/fr

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Classifications

    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • 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
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
    • 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
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
    • 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
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8164—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
    • 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
    • A61K8/85—Polyesters
    • 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
    • A61K8/87—Polyurethanes
    • 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
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • 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
    • A61K2800/5424—Polymers characterized by specific structures/properties characterized by the charge anionic
    • 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
    • A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic
    • 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
    • A61K2800/59—Mixtures
    • A61K2800/594—Mixtures of polymers

Definitions

  • the invention comprises hair treatment compositions containing at least one polymer with acidic or amphoteric groups and. at least one polyhydroxyalkylamine.
  • the hair treatment composition according to the invention shows good sensors and improved odor properties.
  • the hair treated with the preparation according to the invention has a natural, permanent bounce.
  • hair treatment products such as shampoos, cures, conditioners, and top fluids for cleaning and maintaining the hair, which are used in a wide variety of applications, for example as leave on or rinse off products.
  • hair care products such as shampoos, cures, conditioners, and top fluids for cleaning and maintaining the hair, which are used in a wide variety of applications, for example as leave on or rinse off products.
  • three other product categories are used in hair care and treatment; namely permanent or temporary hair colorants, permanent hair shaping agents as well as agents that only allow temporary shaping and stabilization of the hairstyle and are generally known as styling agents.
  • These include products such as hair sprays, hair lacquers, setting lotions, setting foams, hair gels, glossy products, hairstyle creams, etc. All these agents have in common that they usually consist of a large number of individual substances or components that perform a wide variety of tasks within the formulation.
  • the formulations are varied, and the components of the hair treatment agent must be compatible in an ethanolic, aqueous-ethanolic or aqueous medium.
  • Styling agents with anionic or amphoteric polymers mostly equipped with carboxy functionalities, require a neutralizing agent to achieve their optimal performance.
  • the neutralization improves the solubility of the film, the viscous elasticity, the film formation property and the KW propellant compatibility.
  • Common neutralizing agents have the disadvantage that they are either volatile and have an undesirable odor such as ammonia, etha . nolamine or aminomethylpropanol or adversely affect the quality of the film (sodium hydroxide or ammonia).
  • the films show a lack of flexibility, the hair has an unnatural feel, residues in the form of fine or coarse scales can be formed.
  • DE 19808824 describes a hair treatment composition containing at least one polymer with acidic groups and at least one N-unsubstituted or N-substituted polyhydroxyamine in a suitable cosmetic base.
  • the polyhydroxyamine has at least 4, particularly preferably 4 to 6, hydroxyl groups.
  • the object of the present invention is to provide a hair treatment composition which overcomes the disadvantages of the prior art, in particular to provide an composition with good film-forming properties and improved odor properties. Furthermore, it is an object of the present invention to provide an alternative hair treatment agent to the prior art.
  • the tasks are solved by a hair treatment agent according to claim 1.
  • the subclaims relate to advantageous embodiments of the agents according to the invention.
  • the invention further comprises the use of such agents.
  • a hair treatment composition comprising at least one polymer with acidic and / or amphoteric groups in alcoholic, aqueous-alcoholic or aqueous medium and at least one polyhydroxyalkylamine of the formula
  • R mono-, di- or trihydroxyalkyl radical with a carbon chain C 2 - C 6 ,
  • R 2 , R 3 H, alkyl radical with a carbon chain Ci - C 18 or mono-, di- or
  • the agent according to the invention contains 0.01 to 5% by weight of polyhydroxyalkylamine, preferably 0.01 to 2% by weight, in each case based on the total weight of the preparation.
  • the preferred polyhydroxyalkylamine is 1-amino-2,3-propanediol and / or 2-amino-1,3-propanediol (serinol).
  • the salts of the polyhydroxyalkylamines, in particular the lactates, can likewise be regarded as particularly preferred.
  • Other hydroxyalkylamines, which belong to the class of compounds according to the invention, have also made possible good film-forming properties and improved odor properties in the cosmetic composition.
  • the film formed by the agent becomes highly elastic, the hair has a natural, permanent bounce without impairing the good firmness of the hair in high humidity and without stickiness of the film.
  • the film shows a good one
  • the polymers with acidic or amphoteric groups can be partially or completely neutralized with the polyhydroxyalkylamine in the hair treatment composition according to the invention. Preference is given to agents in which 20 to 100%, particularly preferably 50 to 100%, of the acid groups in the polymer are neutralized with the amine of the neutralizing agent.
  • the polymer with acid groups can be a natural or a synthetic homo- or copolymer with monomer units containing acid groups, which is optionally copolymerized with comonomers which do not contain acid groups.
  • Suitable acid groups are sulfonic acid, phosphoric acid and carboxylic acid groups, of which the carboxylic acid groups are preferred.
  • Suitable monomers containing acid groups are, for example, acrylic acid, methacrylic acid, crotonic acid, maleic acid or maleic anhydride, aldehydocarboxylic acids or ketocarboxylic acids.
  • comonomers are for example acrylamide, methacrylamide, alkyl- and dialkylacrylamide, alkyl- and dialkylmethacrylamide, alkyl acrylate, alkyl methacrylate, vinyl caprolactone, vinyl pyrrolidone, Vinylester, vinyl alcohol, propylene glycol or ethylene glycol, amine substituted vinyl monomers such as dialkylaminoalkyl acrylate, dialkylaminoalkyl methacrylate, monoalkylaminoalkyl acrylate and
  • Monoalkylaminoalkyl methacrylate with the alkyl groups of these monomers preferably C1 to C7 alkyl groups, particularly preferably C1 to C3 alkyl groups.
  • Suitable polymers with acid groups are in particular uncrosslinked or crosslinked with polyfunctional agents, homopolymers of acrylic acid or methacrylic acid, copolymers of acrylic acid or methacrylic acid with monomers selected from acrylic acid or methacrylic acid esters, acrylamides, methacrylamides and vinylpyrrolidone, homopolymers of crotonic acid and copolymers of crotonic acid with monomers selected from Vinyl esters, acrylic or methacrylic acid esters, acrylamides and methacrylamides.
  • a suitable natural polymer is shellac, for example.
  • polymers are: cross-linked or uncross-linked vinyl acetate / crotonic acid copolymers (INCI VA / crotonates copolymer) e.g. Resyn 28-1310 from National Starch or Luviset CA66 from BASF; Terpolymers of vinyl acetate, crotonate and vinyl alkanoate, in particular vinyl acetate crotonate vinyl noedecanoate copolymers (INCI: VA / Crotonates /
  • Vinyl neodecanoate copolymer e.g. National Starch Resyn 28-2930; partially esterified copolymers between vinyl methyl ether and maleic anhydride (INCI: ethyl, isopropyl, butyl ester of PVM / MA copolymer) e.g.
  • Gantrez ES 225 or Gantrez ES 425 from ISP Copolymers of acrylic acid or methacrylic acid with alkyl acrylates and / or N-alkyl acrylamides, in particular copolymers of methacrylic acid and alkyl acrylates, and terpolymers of acrylic acid, alkyl acrylates and N-alkyl acrylamides such as acrylic acid / ethyl acrylate / N-tert.-butylacrylamide terpolymer (INCI: acrylates / acrylates Copolymer) e.g.
  • Ultrahold 8 from BASF or tert-butyl acrylate / ethyl acrylate / methacrylic acid terpolymer (INCI: Acrylates Copolymer), e.g. Luvimer from BASF; Polystyrene sulfonates (INCI: Sodium Polystyrene Sulfonate) e.g. Flexan 130 from National Starch.
  • Suitable anionic polymers are also water-soluble or dispersible anionic polyurethanes, e.g. Luviset PUR from BASF or polyester.
  • Suitable amphoteric polymers are octylacrylamides / acrylates / butylaminoethyl methacrylate copolymers (Amphomer 28-4910; National Starch) or methacryloyl ethyl betaines / methacrylates copolymers (Diaformer; Mitsubishi).
  • copolymers of monomers containing carboxyl groups or sulfone groups for example (meth) acrylic acid and itaconic acid with basic monomers containing in particular amino groups, such as, for example, mono- or dialkylaminoalkyl (meth) acrylates and / or mono- or dialkylaminoalkyl (meth) acrylamides, Copolymers of N- Octylacrylamide, methyl methacrylate, hydroxypropyl methacrylate, N-tert.-
  • the polymers according to the invention therefore include, in particular, polymers with carboxy, sulfonic acid, phosphoric acid, acid amide, anhydride and / or anionic polyurethane functionality.
  • the aforementioned polymers are among the polymers with acidic and / or amphoteric groups, the amphoteric polymers being composed of an anioic and a cationic functionality in the same molecule.
  • the polymers are preferably film-forming and hair-fixing polymers.
  • Film-forming, hair-fixing polymers are understood to mean those polymers which are used alone in 0.01 to 20%, preferably in 0.1 to 10%, particularly preferably in 1.0 to 5.0% aqueous, alcoholic or aqueous alcoholic solution used, are able to deposit a polymer film on the hair and in this way to strengthen the hair.
  • the agent according to the invention can, as a further component, 0.01 to 20% by weight, preferably 0.1 to 10% by weight, particularly preferably 1.0 to 5.0% by weight, of at least one synthetic or natural, film-forming, nonionic or contain cationic hair-fixing polymer.
  • the hair-fixing polymers can be used individually or in a mixture. Furthermore, polymers with a thickening effect can be used.
  • Suitable synthetic, nonionic, film-forming, hair-fixing polymers are, for example, homopolymers of vinylpyrrolidone, which are sold, for example, under the trade names LUVISKOL TM K by BASF, Germany or PVP-K by ISP, USA, and homopolymers of N-vinylformamide, which are sold, for example, under the trade name PVF by the company National Starch / USA.
  • Other suitable synthetic film-forming, nonionic hair-fixing polymers are, for example, copolymers of vinylpyrrolidone and vinyl acetate, which are sold, for example, under the trade names LUVISKOL TM VA by the company BASF / Germany; Terpolymers
  • Vinyl pyrrolidone, vinyl acetate and vinyl propionate for example, under the Trade name LUVISKOL TM VAP from BASF / Germany; Polyvinylcaprolactam, polyvinylamides and their salts and copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate, terpolymers of vinylcaprolactam, vinylpyrrolidone and dimethylaminomethacrylate; Polyacrylamides, for example under
  • Suitable cationic polymers are e.g. Copolymers of amine-substituted vinyl monomers and non-amine-substituted, non-cationic monomers.
  • Amine-substituted vinyl monomers include dialkylaminoalkyl acrylate,
  • alkyl groups such as C1-C7 alkyl groups, particularly preferably C1-C3 alkyl groups.
  • Suitable ammonium substituted vinyl monomers are e.g. Trialkylmethacryloxy- alkylammonium, trialkylacryloxyalkylammonium, dialkyldiallylammonium and quaternary vinylammonium monomers with cyclic, cationic nitrogen-containing groups
  • alkyl groups of these monomers are preferably lower alkyl groups such as e.g. C1-C7 alkyl groups, particularly preferably C1-C3 alkyl groups.
  • Suitable polymers are polymers described under the names polyquaternium, such as quaternized copolymers of vinylimidazole, vinylpyrrolidone and / or vinylcaprolactam
  • Non-amine-substituted, non-cationic comonomers are e.g. acrylamide,
  • cationic polymers are: quaternized vinyl pyrrolidone / dialkylaminoalkyl methacrylate copolymers, in particular quaternized vinyl pyrrolidone / dimethylaminoethyl methyl acrylate copolymer (INCI: Polyquatemium-11), for example Gafquat 755 from ISP or Luviquat PQ11 from BASF; Methyl vinylimidazolium chlori ⁇ vinyl pyrrolidone.
  • Copolymer for example the Luviquat types FC 370, FC 550, FC 905 or HM552 from BASF; Methyl vinyl imidazolium methyl sulfate / vinyl pyrrolidone copolymer (I ⁇ CI: Polyquaternium-44), for example Luviquat Care or Luviquat MS 370 from BASF; or the copolymer of vinyl caprolactam, vinyl pyrrolidone and quaternized vinyl imidazole (I ⁇ CI Polyquatemium-46), for example Luviquat Hold from BASF.
  • Luviquat types FC 370, FC 550, FC 905 or HM552 from BASF
  • Methyl vinyl imidazolium methyl sulfate / vinyl pyrrolidone copolymer (I ⁇ CI: Polyquaternium-44), for example Luviquat Care or Luviquat MS 370 from BASF
  • Suitable natural film-forming polymers with hair-setting action are, for example, various types of saccharides such as, for example, polysaccharides or mixtures of oligo-, mono- and disaccharides, which are sold, for example, under the trade name C-PUR TM by the company Cerestar, Belgium.
  • Other suitable, natural polymers are Chinese balsam resin and cellulose derivatives, for example hydroxypropyl cellulose with a molecular weight of 30,000 to 50,000 g / mol, which is sold, for example, under the trade name ⁇ ISSO SL TM by Lehmann & Voss / Germany.
  • the agent according to the invention is in an aqueous, alcoholic or in a. ready-made aqueous-alcoholic milieu.
  • solvents or a mixture of solvents with a boiling point below 400 ° C. can be used in an amount of 0.1 to 90% by weight, preferably 1 to 50% by weight.
  • the lower alcohols with 1 to 4 carbon atoms usually used for cosmetic purposes, such as ethanol and isopropanol can be included as alcohols.
  • particularly preferred water-soluble solvents are glycerol and propylene glycol in an amount of up to 30% by weight.
  • the agent according to the invention can also contain the usual additional ingredients for hair treatment agents, for example, wetting agents or emulsifiers from the classes of anionic, amphoteric or nonionic surface-active surfactants, such as fatty alcohol sulfates, alkylbenzenesulfonates, alkyltrimethylammonium salts, alkylbetaines,
  • wetting agents or emulsifiers from the classes of anionic, amphoteric or nonionic surface-active surfactants, such as fatty alcohol sulfates, alkylbenzenesulfonates, alkyltrimethylammonium salts, alkylbetaines,
  • BEST ⁇ TIGU ⁇ GSKOPIE ethoxylated fatty alcohols, ethoxylated nonylphenols, fatty acid alkanolamides, ethoxylated fatty acid esters, in an amount of 0.1 to 30% by weight; Humectants; Perfume oils in an amount of 0.1 to 0.5% by weight; Opacifiers such as ethylene glycol distearate in an amount of about 0.2 to 5.0% by weight; Pearlescent agents, such as a mixture of fatty acid monoalkylolamide and ethylene glycol distearate, in an amount of about 1.0 to 10% by weight; bactericidal and fungicidal active ingredients such as, for example, 2,4,4-trichloro-2-hydroxydiphenyl ether or methyl chloroisothiazole ion, in an amount of 0.01 to 1.0% by weight; Thickeners, such as, for example, coconut fatty acid diethanolamide, in an amount of about 0.2 to 3.0% by weight, buffer substances, such
  • the care substances advantageous according to the invention are cationic surfactants such as monomeric quaternary ammonium compounds or silicone polymers.
  • the cationic substances cetyltrimethylammonium chloride and cetyltrimethylammonium phosphate are very particularly advantageous.
  • Suitable silicone polymers are e.g. Polydimethylsiloxane, ⁇ -hydrp- ⁇ -hydroxypolyoxydimethylsilylene, cyclic dimethylpolysiioxane, dimethylsiloxane-glycol copolymer or
  • the agent according to the invention can be used in various forms of application, for example in aerosol preparations as a foam or as a spray, furthermore as a non-aerosol which is applied by means of a pump or as a "pump and spray" Commitment comes.
  • Use in conventional O / W and W / O emulsions is just as possible as in application forms as a gel, wax or microemulsion.
  • the agent according to the invention is in the form of an aerosol hairspray or aerosol hair lacquer, it additionally contains 3 to 85% by weight of a propellant and is filled into a pressure vessel.
  • a propellant for example, lower alkanes, such as n-butane, i-butane and propane or their mixtures, or also dimethyl ether and fluorocarbons such as F 152 (1,1-difluoroethane) or F 134 (tetrafluoroethane) and, furthermore, in the in Pressurizing gaseous propellants, such as N2, N2O and. CO2 or compressed air and mixtures of the above-mentioned propellants are suitable.
  • the agent according to the invention can also be in the form of a non-aerosol hairspray sprayable with the aid of a suitable mechanically operated spraying device or a non-aerosol hair lacquer.
  • Mechanical spray devices are to be understood as devices which enable the spraying of a liquid without using a propellant.
  • a suitable mechanical spraying device can be, for example, a spray pump or an elastic container provided with a spray valve, in which the cosmetic agent according to the invention is filled under pressure, the elastic container expanding and from which the agent due to the contraction of the elastic container when the spray valve is opened continuously released, can be used.
  • the preparation can further advantageously contain cosmetic substances, although not necessarily, fillers which, for. B. further improve the sensory and cosmetic properties of the formulations.
  • thickeners are used in the preparations according to the invention.
  • these can advantageously be selected from the group of gums.
  • Gums include plant or tree sap that harden in the air and form resins or extracts from aquatic plants. Gum arabic, locust bean gum, tragacanth, karaya, guar gum, pectin, gellan gum, carrageenan, agar, algins, alginates, chondrus and xanthan gum can advantageously be selected from this group for the purposes of the present invention.
  • derivatized gums such as hydroxypropyl guar (Jaguar® HP 8) is also advantageous.
  • polysaccharides and derivatives are e.g. Hyaluronic acid, chitin and chitosan, chondroitin sulfates, starch and starch derivatives as advantageous thickeners according to the invention.
  • cellulose derivatives are e.g. Methyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose as advantageous thickeners according to the invention.
  • Layered silicates contain naturally occurring and synthetic clays such as Montmorillonite, bentonite, hectorite, laponite, aluminum silicates, magnesium aluminum silicates such as Veegum®. These can be used as such or in a modified form as thickeners, e.g. Stearylalkonium hektorite.
  • silica gels can also advantageously be used.
  • homopolymers of acrylic acid are e.g. Carbopol types from Goodrich (Carbopol 940, 980, 981,, 5984, 2984, ETD 2001, ETD 2050 or Ultrez 10). ,
  • Copolymers of acrylic acid or methacrylic acid such as e.g. Carbopol types from Goodrich (Carbopol 1342, 1382, ETD 2020, Ultrez 21, Permulen TR-1 or Pemulen TR-2.
  • the polymers include, for example, polyacrylamides (Seppigel 305), polyvinyl alcohols, PVP, PVP / VA copolymers, polyglycols and ammonium acryloyldimethyltaurates / VP copolymers.
  • polyacrylamides Silicone 305
  • PVP polyvinyl alcohols
  • PVP / VA copolymers polyglycols
  • ammonium acryloyldimethyltaurates / VP copolymers The following examples demonstrate the synergy effect of the preparations according to the invention in comparison to the individual components.

Abstract

La présente invention concerne un agent de traitement capillaire qui comprend au moins un polymère présentant des groupes acides ou amphotères et au moins une polyhydroxyalkylamine dans un milieu alcoolique, aqueux-alcoolique ou aqueux. Cet agent de traitement capillaire présente une texture agréable et une odeur améliorée. Les cheveux traités avec la préparation selon cette invention présentent un ressort naturel durable.
PCT/EP2003/012135 2002-11-02 2003-10-31 Agent de traitement capillaire presentant des caracteristiques de film et une odeur ameliorees WO2004041224A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2003282063A AU2003282063A1 (en) 2002-11-02 2003-10-31 Hair conditioning agents having improved coating and olfactory properties

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2002151122 DE10251122A1 (de) 2002-11-02 2002-11-02 Haarbehandlungsmittel mit verbesserten Film- und Geruchseigenschaften
DE10251122.5 2002-11-02

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Publication Number Publication Date
WO2004041224A1 true WO2004041224A1 (fr) 2004-05-21

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DE (1) DE10251122A1 (fr)
WO (1) WO2004041224A1 (fr)

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DE2404070A1 (de) * 1974-01-29 1975-08-14 Henkel & Cie Gmbh Hautpflege- und hautschutzmittel mit einem gehalt an haut-feuchthaltemitteln
GB1595649A (en) * 1978-05-25 1981-08-12 Nat Starch Chem Corp Aerosol hair spray compositions
FR2697160A1 (fr) * 1992-10-28 1994-04-29 Oreal Composition cosmétique aqueuse pour la fixation de la chevelure à base d'un pseudo-latex.
DE4316242A1 (de) * 1993-05-14 1994-11-17 Henkel Kgaa Haarbehandlungsmittel
US5853706A (en) * 1997-03-19 1998-12-29 Townley Jewelry, Inc. Scented hair gel having particulate matter in the form of glitter
DE19808824C1 (de) * 1998-03-03 1999-10-28 Wella Ag Haarbehandlungsmittel mit einem Gehalt an mit Polyhydroxyaminen neutralisierten sauren Polymeren
EP1075835A1 (fr) * 1999-08-09 2001-02-14 Shiseido Company Limited Utilisation de dérivés d'aminodiols dans des cosmétiques pour la peau
WO2003053381A1 (fr) * 2001-12-11 2003-07-03 Basf Aktiengesellschaft Agent cosmetique contenant au moins un copolymere comportant des unites n-vinyllactame

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