WO1996003967A1 - Hair cosmetic compositions - Google Patents
Hair cosmetic compositions Download PDFInfo
- Publication number
- WO1996003967A1 WO1996003967A1 PCT/US1995/008336 US9508336W WO9603967A1 WO 1996003967 A1 WO1996003967 A1 WO 1996003967A1 US 9508336 W US9508336 W US 9508336W WO 9603967 A1 WO9603967 A1 WO 9603967A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hair
- hair cosmetic
- cosmetic composition
- composition according
- gelling agent
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 66
- 239000002537 cosmetic Substances 0.000 title claims abstract description 33
- 239000003349 gelling agent Substances 0.000 claims abstract description 36
- 229920000642 polymer Polymers 0.000 claims abstract description 30
- 239000000834 fixative Substances 0.000 claims abstract description 22
- 229920001577 copolymer Polymers 0.000 claims abstract description 17
- 150000001993 dienes Chemical class 0.000 claims abstract description 12
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims abstract description 8
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 7
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 claims abstract description 6
- 229920003118 cationic copolymer Polymers 0.000 claims abstract description 6
- 230000007062 hydrolysis Effects 0.000 claims abstract description 4
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 4
- 239000001913 cellulose Substances 0.000 claims abstract description 3
- 229920002678 cellulose Polymers 0.000 claims abstract description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002585 base Substances 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 4
- 150000001414 amino alcohols Chemical class 0.000 claims description 3
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical group 0.000 claims 1
- 235000011114 ammonium hydroxide Nutrition 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 claims 1
- 229920005862 polyol Polymers 0.000 claims 1
- 150000003077 polyols Chemical class 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract 1
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- 125000002091 cationic group Chemical group 0.000 description 13
- 239000000178 monomer Substances 0.000 description 12
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- 239000003795 chemical substances by application Substances 0.000 description 9
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- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
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- 235000002639 sodium chloride Nutrition 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
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- UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 description 2
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 206010019049 Hair texture abnormal Diseases 0.000 description 2
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229920013750 conditioning polymer Polymers 0.000 description 2
- 239000003581 cosmetic carrier Substances 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
- 229940043276 diisopropanolamine Drugs 0.000 description 2
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
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- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
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- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
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- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
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- 229920006037 cross link polymer Polymers 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- WSDISUOETYTPRL-UHFFFAOYSA-N dmdm hydantoin Chemical compound CC1(C)N(CO)C(=O)N(CO)C1=O WSDISUOETYTPRL-UHFFFAOYSA-N 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- VEUUMBGHMNQHGO-UHFFFAOYSA-N ethyl chloroacetate Chemical compound CCOC(=O)CCl VEUUMBGHMNQHGO-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 230000003741 hair volume Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- MJVGBKJNTFCUJM-UHFFFAOYSA-N mexenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=C(C)C=C1 MJVGBKJNTFCUJM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229940073555 nonoxynol-10 Drugs 0.000 description 1
- 229940060184 oil ingredients Drugs 0.000 description 1
- 229940095127 oleth-20 Drugs 0.000 description 1
- 229940101267 panthenol Drugs 0.000 description 1
- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical class [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920002851 polycationic polymer Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940068977 polysorbate 20 Drugs 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical class [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- 229960000368 sulisobenzone Drugs 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- 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
-
- 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
-
- 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
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8194—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; Compositions of derivatives of such polymers
-
- 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
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
-
- 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 present invention relates to hair cosmetic compositions. More particularly, this invention relates to hair cosmetic compositions containing a gelling agent and a hair fixative/conditioning polymer and having improved "in-use” and "on-hair” feel properties in addition to manageability and style retention benefits.
- compositions for centuries, typically to damp or dry hair. These compositions provide temporary setting benefits, and should be removable by water and/or by shampooing.
- the materials used in the compositions to provide the setting benefits are generally applied in the form of mousses, gels, lotions or sprays.
- Style retention in gel products is typically achieved by use of one or more hair fixative polymers, such as polyvinylpyrollidone (PVP) and the copolymer of PVP with vinyl acetate (PVP/VA) in combination with a gelling agent.
- PVP polyvinylpyrollidone
- PVP/VA vinyl acetate
- a commonly used gelling agent is crosslinked polyacrylic acid, known by the CTFA name of Carbomer.
- a hair cosmetic composition comprising:-
- gelling agent comprising a copolymer of methyl vinyl ether/maleic anhydride, crosslinked with C4-C 16 alkadiene or hydrolysis products thereof;
- hair fixative polymer comprising a cationic copolymer of nonionic cellulose and diallyl dimethyl ammonium chloride
- compositions of the present invention contain from about 0.01% to about 3% preferably from about 0.05% to about 2%, more preferably from about 0.5% to about 1.5%, most preferably from about 0.6% to about 1% by weight of gelling agent. It is this gelling agent which in combination with a cationic hair fixative polymer imparts hair setting and conditioning benefits without the tacky dry-hair feel and on-hand stickiness normally associated with hair styling cosmetics.
- the gelling agents suitable for use in the present invention comprise a copolymer of methyl vinyl ether/maleic anhydride, and hydrolysis products thereof, crosslinked with C4-C16, preferably C6-C12, more preferably Cg-Cjo alkadiene.
- the gelling agents typically have a viscosity in the region of from about 50,000 cps to about 150,000 cps, preferably from about 70,000 cps to about 100,000 cps (measured as 0.5% gelling agent in non-alcoholic solution at pH7; Brookfield RVT, Spindle TE, 10 ⁇ m).
- the copolymer utilised in the present application comprise a copolymer of methyl vinyl ether/maleic anhydride (hereafter identified as A) crosslinked with C4-C16, preferably C6-C12, more preferably Cg-Cio alkadiene (hereafter identified as B).
- A methyl vinyl ether/maleic anhydride
- B Cg-Cio alkadiene
- suitable polymers and their preparations are described in detail in "Polymers and Thickeners” Vol. 108, May 1993, p61-67, S.L. Kopolow, Y.T. Kwak and M.Helioff. These polymers comprise part A and B as defined above.
- B comprises C6-C14 alkadiene, more preferably a C -C ⁇ 2 alkadiene, most preferably a Cg-C ⁇ o alkadiene.
- the preferred gelling agent for use herein is methyl vinyl ether/maleic anhydride, crosslinked with 1 ,9-decadiene (PVM/MA decadiene crosspolymer), available from ISP as Stabileze 06 (RTM).
- the hair gelling agents, herein are preferably utilised in at least partially neutralised form in order to obtain the required gel structure and overall pH of the hair cosmetic compositions.
- the gelling agent can be neutralised to a level of from about 30% to about 100%, preferably from about 40% to about 98%, more preferably from about 50% to about 95% with base. Any conventionally used base, organic or inorganic, may be used for neutralisation of the acidic gelling agents. Hydroxides of alkali and alkaline earth metals and amino alcohols are suitable neutralisers for use in the present hair cosmetic compositions.
- suitable organic neutralising agents which may be included in the hair cosmetic compositions of the present invention include amines, especially amino alcohols such as 2-amino-2-methyl- 1 ,3-propanediol (AMPD), 2-amine-2-ethyl-l,3-propanediol (AEPD), 2-amino-2-methyl-l- propanol (AMP), 2-amino-l-butanol (AB), monethanolamine (ME A), diethanolamine (DEA), triethanolamine (TEA), monoisopropanolamine (MIPA), diisopropanolamine (DIPA), triisopropanolamine (TIPA), dimethyl steramine (DMS) and amino methyl propanol (AMP) and mixtures thereof.
- amines especially amino alcohols such as 2-amino-2-methyl- 1 ,3-propanediol (AMPD), 2-amine-2-ethyl-l,3-propanediol (AEPD), 2-amino-2
- Preferred neutralising agents for use in compositions of the present invention are potassium and sodium hydroxides, aminomethyl propanol (AMP) and triethanolamine (TEA) and mixtures thereof.
- compositions may optionally include an auxiliary gelling agent at from about 0.01% to about 1%, preferqably from about 0.1% to about 0.5% by weight.
- Suitable auxiliary gelling agents can be selected from any conventional gelling agent such as a crosslinked polyacrylic acid copolymer, ethylene maleic anhydride copolymers or hydroxyethylcellulose and its derivatives.
- the preferred auxiliary gelling for use herein is hydroxyethylcellulose.
- Carrier The hair cosmetic compositions of the present invention also include a carrier which can be aqueouse or non-aqueous and mixtures thereof. This can comprise any of those conventionally used in polymer containing hair cosmetic formulations.
- the carrier is generally present in the hair cosmetic compositions at from about 70% to about 99.89%, preferably from about 78% to about 99.5% by weight. More preferably, the carrier is present at from about 80% to about 99% by weight of the total composition.
- Organic solvents suitable for use in the carrier in compositions according to the present invention include C ⁇ C ⁇ alkanols, carbitol, acetone and mixtures thereof.
- C ⁇ -C alkanols preferred for use in the present compositions are C2-C4 monohydric alcohols such as ethanol, isopropanol and mixtures thereof.
- the preferred hair compositions according to the present invention contain from 70% to about 99.89% by weight of water, preferably from 78% to about 99.5%, more preferably from about 80% to about 99% by weight of water as the carrier.
- compositions according to the present invention comprise, as a second essential component, a hair fixative polymer.
- This hair fixative polymer is preferably solubilized or colloidally dispersed in the hair cosmetic carrier along with the gelling agent copolymer.
- the preferred hair fixative polymer component of the hair cosmetic compositions of the present invention comprises a cationic copolymer of hydroxyethyl cellulose and diallyl dimethyl ammonium chloride which is known by the CTFA name Polyquaternium 4 and marketed under the trade names Celquat L200 (RTM) and Celquat HI 00 (RTM) by National Starch and Chemical Ltd.
- the hair fixative polymer is present in an amount of from about 0.1% to about 10%, preferably from about 0.3% to about 8%, more preferably from about 0.5% to about 6%, most preferably from about 0.8% to about 3% by weight of composition.
- the weight ratio of gelling agent:hair fixative polymer is in the range of from about 10: 1 to about 1 : 10.
- hair fixative polymers suitable for use herein in conjunction with the above material include any polymer which is soluble or colloidally dispersible in the hair cosmetic carrier. Solubility and dispersibility are determined at ambient conditions of temperature and pressure (25°C and at 101.3 kPa (1 Atm)). Such copolymers may be cationic or nonionic in character. Copolymers suitable for use herein have a molecular weight in the range of from about 1,000 to about 5,000,000, preferably from about 50,000 to about 4,000,000, more preferably from about 100,000 to about 3,000,000, most preferably from about 500,000 to about 2,000,000.
- cationic and nonionic resins may be utilised as detailed below.
- Polycationic hair conditioning polymer resins suitable for use herein are described below.
- monomeric units present in the polymers may be referred to as the monomers from which they can be derived.
- the cationic monomers can be derived from polymerizable cationic starting monomers, or from polymerizable nonionic monomers which are modified subsequent to polymerization to be of cationic character.
- cationic unsaturated monomers can be polymerized in cationic form, or as an alternative they can be polymerized in the form of their precursors, which are then modified to be cationic, for example, by a quaternizing agent (eg. ethyl monochloroacetate, diemethyl sulfate, etc.).
- Preferred cationic monomers include dimethylaminoethyl methacrylate, quaternized dimethylaminoethyl methacrylate, diallyldimethyl ammonium chloride, vinylimidazolium quaternary ammonium monomers and mixtures thereof.
- Nonionic monomers are acrylic or methacrylic acid esters of C 1-C24 alcohols, such as methanol, ethanol, 1- propanol, 2-pro ⁇ anol, 1-butanol, 2-methyl-l -propanol, 1-pentanol, 2- pentanol, 3-pentanol, 2-methyl- l-butanol, 1 -methyl- 1-butanol, 3-methyl-l- butanol, 1 -methyl- 1 -pentanol, 2-methyl-l -pentanol, 3-methyl-l -pentanol, t-butaonl, cyclohexanol, 2-ethyl-l -butanol, 3-heptanol, benzyl alcohol, 2- octanol, 6-methyl-l-heptanol, 2-ethyl-l -hexanol, 3,5-dimethyl-l-hexanol, 3,5,5-
- nonionic monomers include acrylate and methacrylate derivatives such as allyl acrylate and methacrylate, cyclohexyl acrylate and methacrylate, oleyl acrylate and methacrylate, benzyl acrylate and methacylate, tetrahydrofurfuryl acrylate and methacrylate, ethylene glycol di-acrylate and -methacrylate, 1,3- butyleneglycol di-acrylate and -methacrylate, diacetonacylamide, isobornyl (meth)acrylate, and the like.
- acrylate and methacrylate derivatives such as allyl acrylate and methacrylate, cyclohexyl acrylate and methacrylate, oleyl acrylate and methacrylate, benzyl acrylate and methacylate, tetrahydrofurfuryl acrylate and methacrylate, ethylene glycol di-acrylate and -methacrylate
- Preferred nonionic monomers include n-butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, methyl methacrylate, t- butylacrylate, t-butylmethacrylate, and mixtures thereof.
- Representative polar nonionic monomers include acrylamide, N,N- dimethylacrylamide, methacrylamide, N-t-butyl acylamide, methacrylonitrile, acrylamide, acrylate alcohols (eg. C2-C6 acrylate alcohols such as hydroxyethyl acrylate, hydroxyproxyl acrylate), hydroxyethyl methacrylate, hydroxpropyl methacrylate, vinyl pyrrolidone, vinyl ethers, such as methyl vinyl ether, acyl lactones and vinyl pyridine, allyl alcohols, vinyl alcohols and vinyl caprolactam.
- acrylate alcohols eg. C2-C6 acrylate alcohols such as hydroxyethyl acrylate, hydroxyproxyl acrylate
- hydroxyethyl methacrylate hydroxyethyl methacrylate
- hydroxpropyl methacrylate vinyl pyrrolidone
- vinyl ethers such as methyl vinyl ether,
- Preferred polycationic polymer resins for use herein include cationic guar gum, cationic polysaccharides, homopolymers of dimethyldiallyl ammonium chloride, copolymers of dimethyldiallyl ammonium chloride and acrylamide, cationic amino-functional homopolymers and copolymers derived from acrylic acid and/or methacrylic acid, especially from alkylaminoalkyl acrylate and methacrylate monomers such as dimethylacmonoethyl acrylate and methacrylate, polyalkylene imines and ethoxy polyalkylene imines, vinylimidazolium vinylpyrrolidone quaternary ammonium copolymers, and mixtures thereof.
- the auxilliary hair fixative polymer is incorporated with the Polyquaternium 4 at levels of from about 0.01% to about 10%, preferably from about 0.15 to about 5% by weight.
- the combination of Polyquat 4 and auxilliary hair fixative polymer is valuable for providing overall hair feel benefits, particularity with respect to flakiness.
- the present compositions can be formulated as leave-in hair cosmetic compositions such as gels or creams. Methods of making the hair cosmetic compositions of the present invention are described more specifically in the examples.
- the hair cosmetic compositions of the present invention may contain a chelating agent at a level of from about 0.01% to about 5%, preferably from about 0.5% to about 3%, more preferably from about 0.08% to about 1% by weight.
- Chelating agents suitable for the compositions according to the present invention include salts of ethylenediamine tetraacetic acid including ethylenediamine tetraacetic acid, disodium ethylenediamine tetraacetic acid and pentasodium pentatate.
- the preferred chelating agent for use in compositions according to the present invention is tetrasodium ethylenediamine tetraacetic acid.
- the hair cosmetic compositions of the present invention can also contain a variety of non-essential, optional components such as preservatives, surfactants, block polymers, thickeners and viscosity modifiers, electrolytes, fatty alcohols, pH adjusting agents, perfume oils; UV screening agents; hair conditioning agents, Pearlescants, emollients; lubricants and penetrants such as various lanolin components; protein hydrolysates and other protein derivatives; ethylene adducts and polv oxyethylene cholesterol; volatile and non-volatile silicone fluids.
- non-essential, optional components such as preservatives, surfactants, block polymers, thickeners and viscosity modifiers, electrolytes, fatty alcohols, pH adjusting agents, perfume oils; UV screening agents; hair conditioning agents, Pearlescants, emollients; lubricants and penetrants such as various lanolin components; protein hydrolysates and other protein derivatives; ethylene adducts and polv oxyethylene cholesterol
- surfactants used as perfume solubilizing agents such as anionics (e.g., sodium alkyl sulphates, nonionics (a ine oxides); amphoterics (aliphatic secondary or tertiary amine derivatives) zwitterionics (aliphatic quaternary ammonium; phosphonium or sulphonium derivatives) and fluorinated surfactants (e.g.
- anionics e.g., sodium alkyl sulphates, nonionics (a ine oxides)
- amphoterics aliphatic secondary or tertiary amine derivatives
- zwitterionics aliphatic quaternary ammonium; phosphonium or sulphonium derivatives
- fluorinated surfactants e.g.
- Zonyl FSK) RTM
- preferred surfactants for use herein being nonionics such as polyethylene glycol fatty acid esters, isosteareth-20, polysorbate-20, PPG- 12-PEG-65 lanolin oil, PEG-40 hydrogenated caster oil, polysorbate 80, Oleth-20 and Nonoxynol- 10, thickeners and viscosity modifiers such as diethanolamides of long chain fatty acids, sodium chloride, sodium sulphate, and ethyl alcohol; block polymers of ethylene oxide and propylene oxide such as Pluronic (RTM) F88 offered by BASF Wyandotte; preservatives such as DMDM hydantoin, methyl paraben, propyl paraben and diaxolidinyl urea; fatty alcohols such as cetearyl alcohol; electrolyte such as earth and alkaline-earth metal salts; quaternary ammonium ions and cationic amines and halogen ions; pH
- the hair cosmetic compositions of the present invention are used in conventional ways to provide the hair styling/holding benefits of the present invention in combination with reduced on-hair and on-hand tack. Such methods can involve applying an effective amount of the product to dry or damp hair before or after the hair is styled, or both.
- effective amount is meant an amount sufficient to provide the hair volume and style benefits desired considering the length and texture of the hair.
- the hair cosmetic compositions according to the present invention may be effectively applied to the hair using the hands, using a comb or brush or by applying with a sponge or 'wipe'.
- the invention is illustrated by the following non-limiting examples.
- the hair cosmetic formulations are prepared by (a) dispersing the gelling agent(s) into water, allowing sufficient time for hydration of the gelling agent (30 minutes to 1 hour), then partially neutralising the gelling agent with a suitable base and (b) in a separate step, solubilising the fixative polymer(s) in water along with any non-essential optional ingredients and the chelating agent.
- the premixes (a) and (b) are combined and the resulting mixture is modified to the desired viscosity and pH characteristics using the remainder of the neutralising base.
- compositions provide effective style retention, deliver a hair conditioning effect with low on-hand and on-hair tack.
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- Public Health (AREA)
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- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX9700667A MX9700667A (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic compositions. |
EP95925443A EP0768864A4 (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic compositions |
US08/776,453 US5922312A (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic compositions |
JP8506495A JPH10503514A (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic composition |
CA002192799A CA2192799A1 (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic compositions |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9415324.4 | 1994-07-29 | ||
GB9415324A GB9415324D0 (en) | 1994-07-29 | 1994-07-29 | Hair cosmetic compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996003967A1 true WO1996003967A1 (en) | 1996-02-15 |
Family
ID=10759083
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/008336 WO1996003967A1 (en) | 1994-07-29 | 1995-06-30 | Hair cosmetic compositions |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0768864A4 (en) |
JP (1) | JPH10503514A (en) |
CN (1) | CN1086936C (en) |
CA (1) | CA2192799A1 (en) |
GB (1) | GB9415324D0 (en) |
MX (1) | MX9700667A (en) |
WO (1) | WO1996003967A1 (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5714135A (en) * | 1996-03-18 | 1998-02-03 | Chesebrough-Pond' S Usa Co., Division Of Conopco, Inc. | Hair treatment compostion |
FR2755607A1 (en) * | 1996-11-08 | 1998-05-15 | Oreal | COSMETIC COMPOSITION BASED ON FIXING POLYMER AND GELIFYING AGENT, METHOD AND USE |
WO1999053890A1 (en) * | 1998-04-22 | 1999-10-28 | Amway Corporation | Conditioning shampoo |
WO2000048555A3 (en) * | 1999-02-19 | 2001-01-11 | Procter & Gamble | Leave-on cosmetic compositions containing a cationic polymer |
FR2833487A1 (en) * | 2001-12-18 | 2003-06-20 | Oreal | Cosmetic composition for treating keratinic materials comprises two polymers that have complementary non-photoactivatable functional groups |
WO2003053379A1 (en) * | 2001-12-18 | 2003-07-03 | L'oreal | Cosmetic composition forming an adhesive film comprising a polymer with silicone-free skeleton including reactive functions |
EP2319487A1 (en) * | 2009-06-29 | 2011-05-11 | L'oreal S.A. | Refreshing cream foundation in gel form |
EP2319491A1 (en) * | 2009-06-29 | 2011-05-11 | L'oreal S.A. | Refreshing cream foundation in gel form |
US8475816B2 (en) | 2008-12-16 | 2013-07-02 | L'oreal S.A. | Emulsion lipstick composition |
US8551461B2 (en) | 2008-12-09 | 2013-10-08 | L'oreal | Moisturizing and shine-imparting emulsion lip compositions |
US8597626B2 (en) | 2009-06-29 | 2013-12-03 | L'oreal | Long wear, waterproof mascara composition with water washability |
US8597621B2 (en) | 2008-12-16 | 2013-12-03 | L'oreal | Shine-imparting hydrating and moisturizing emulsion lipstick composition |
US8647611B2 (en) | 2009-06-29 | 2014-02-11 | L'oréal | Composition containing a polyol and a reaction product |
US8652451B2 (en) | 2009-06-29 | 2014-02-18 | L'oreal | Composition comprising a sugar silicone surfactant and a oil-soluble polar modified polymer |
US8663609B2 (en) | 2009-06-29 | 2014-03-04 | L'oreal | Composition comprising a polyol, a sugar silicone surfactant and a oil-soluble polar modified polymer |
US8663667B2 (en) | 2009-06-29 | 2014-03-04 | L'oreal | Refreshing cream foundation in gel form |
US8747868B2 (en) | 2010-12-30 | 2014-06-10 | L'oreal | Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product |
US8778316B2 (en) | 2008-12-11 | 2014-07-15 | L'oreal | Non-sticky, hydrating and moisturizing aqueous lip gloss composition |
US8828366B2 (en) | 2009-06-29 | 2014-09-09 | L'oreal | Hydrating cream foundation in emulsion form |
US8932566B2 (en) | 2009-06-29 | 2015-01-13 | L'oreal | Composition comprising a polyol and a oil-soluble polar modified polymer |
US9023387B2 (en) | 2008-12-09 | 2015-05-05 | L'oreal | Transfer-resistant emulsion containing a surfactant |
US9040593B2 (en) | 2008-12-16 | 2015-05-26 | L'oreal | Water-insoluble reaction product of a polyamine and an oil-soluble high carbon polar modified polymer |
US9308396B2 (en) | 2008-12-16 | 2016-04-12 | L'oreal | Transfer-resistant and long wear foundation in emulsion form containing oil absorbing powders |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012532109A (en) * | 2009-06-29 | 2012-12-13 | ロレアル | Compositions containing polar modified polymers |
BR112017003439B1 (en) * | 2014-09-03 | 2020-12-01 | Unilever Nv | transparent composition and method for hair treatment |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5066481A (en) * | 1990-11-05 | 1991-11-19 | Isp Investments Inc. | Mousse hair composition |
US5118498A (en) * | 1990-11-19 | 1992-06-02 | Isp Investments Inc. | Hair setting shampoo composition |
US5194260A (en) * | 1990-08-23 | 1993-03-16 | L'oreal | Cosmetic composition for the hair contains a film forming polymer and a silicone incorporated in a wax microdispersion and a cosmetic treatment using the same |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU83349A1 (en) * | 1981-05-08 | 1983-03-24 | Oreal | AEROSOL FOAM COMPOSITION BASED ON CATIONIC POLYMER AND ANIONIC POLYMER |
US5085856A (en) * | 1990-07-25 | 1992-02-04 | Elizabeth Arden Co., Division Of Conopco, Inc. | Cosmetic water-in-oil emulsion lipstick comprising a phospholipid and glycerol fatty acid esters emulsifying system |
US5254636A (en) * | 1992-05-28 | 1993-10-19 | Isp Investments Inc. | Rapid hydrolysis of crosslinked maleic anhydride/lower alkyl vinyl ether copolymers |
DE4232944A1 (en) * | 1992-10-01 | 1994-04-07 | Wella Ag | Hair treatment products and methods for use |
FR2702958B1 (en) * | 1993-03-24 | 1995-05-24 | Oreal | Cosmetic composition containing at least one nonionic surfactant of the alkylpolyglycoside and / or polyglycerolated type and at least one crosslinked copolymer of maleic anhydride / alkyl (C1-C5) vinyl ether. |
-
1994
- 1994-07-29 GB GB9415324A patent/GB9415324D0/en active Pending
-
1995
- 1995-06-30 CA CA002192799A patent/CA2192799A1/en not_active Abandoned
- 1995-06-30 MX MX9700667A patent/MX9700667A/en unknown
- 1995-06-30 WO PCT/US1995/008336 patent/WO1996003967A1/en not_active Application Discontinuation
- 1995-06-30 CN CN95194394A patent/CN1086936C/en not_active Expired - Fee Related
- 1995-06-30 JP JP8506495A patent/JPH10503514A/en active Pending
- 1995-06-30 EP EP95925443A patent/EP0768864A4/en not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5194260A (en) * | 1990-08-23 | 1993-03-16 | L'oreal | Cosmetic composition for the hair contains a film forming polymer and a silicone incorporated in a wax microdispersion and a cosmetic treatment using the same |
US5066481A (en) * | 1990-11-05 | 1991-11-19 | Isp Investments Inc. | Mousse hair composition |
US5118498A (en) * | 1990-11-19 | 1992-06-02 | Isp Investments Inc. | Hair setting shampoo composition |
Non-Patent Citations (1)
Title |
---|
See also references of EP0768864A4 * |
Cited By (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5714135A (en) * | 1996-03-18 | 1998-02-03 | Chesebrough-Pond' S Usa Co., Division Of Conopco, Inc. | Hair treatment compostion |
FR2755607A1 (en) * | 1996-11-08 | 1998-05-15 | Oreal | COSMETIC COMPOSITION BASED ON FIXING POLYMER AND GELIFYING AGENT, METHOD AND USE |
WO1998020846A1 (en) * | 1996-11-08 | 1998-05-22 | L'oreal | Cosmetic composition with fixing polymer and gelling agent base, method and use |
WO1999053890A1 (en) * | 1998-04-22 | 1999-10-28 | Amway Corporation | Conditioning shampoo |
AU771906B2 (en) * | 1999-02-19 | 2004-04-08 | Procter & Gamble Company, The | Cosmetic compositions |
WO2000048555A3 (en) * | 1999-02-19 | 2001-01-11 | Procter & Gamble | Leave-on cosmetic compositions containing a cationic polymer |
FR2833487A1 (en) * | 2001-12-18 | 2003-06-20 | Oreal | Cosmetic composition for treating keratinic materials comprises two polymers that have complementary non-photoactivatable functional groups |
EP1321126A1 (en) * | 2001-12-18 | 2003-06-25 | L'Oreal | Cosmetic compositions comprising polymers having complementary chemical functions |
WO2003053379A1 (en) * | 2001-12-18 | 2003-07-03 | L'oreal | Cosmetic composition forming an adhesive film comprising a polymer with silicone-free skeleton including reactive functions |
US9023387B2 (en) | 2008-12-09 | 2015-05-05 | L'oreal | Transfer-resistant emulsion containing a surfactant |
US8551461B2 (en) | 2008-12-09 | 2013-10-08 | L'oreal | Moisturizing and shine-imparting emulsion lip compositions |
US8778316B2 (en) | 2008-12-11 | 2014-07-15 | L'oreal | Non-sticky, hydrating and moisturizing aqueous lip gloss composition |
US8597621B2 (en) | 2008-12-16 | 2013-12-03 | L'oreal | Shine-imparting hydrating and moisturizing emulsion lipstick composition |
US9308396B2 (en) | 2008-12-16 | 2016-04-12 | L'oreal | Transfer-resistant and long wear foundation in emulsion form containing oil absorbing powders |
US9040593B2 (en) | 2008-12-16 | 2015-05-26 | L'oreal | Water-insoluble reaction product of a polyamine and an oil-soluble high carbon polar modified polymer |
US8475816B2 (en) | 2008-12-16 | 2013-07-02 | L'oreal S.A. | Emulsion lipstick composition |
US8562961B2 (en) | 2009-06-29 | 2013-10-22 | L'oreal | Refreshing cream foundation in gel form |
US8647611B2 (en) | 2009-06-29 | 2014-02-11 | L'oréal | Composition containing a polyol and a reaction product |
US8652451B2 (en) | 2009-06-29 | 2014-02-18 | L'oreal | Composition comprising a sugar silicone surfactant and a oil-soluble polar modified polymer |
US8663609B2 (en) | 2009-06-29 | 2014-03-04 | L'oreal | Composition comprising a polyol, a sugar silicone surfactant and a oil-soluble polar modified polymer |
US8663667B2 (en) | 2009-06-29 | 2014-03-04 | L'oreal | Refreshing cream foundation in gel form |
US8597626B2 (en) | 2009-06-29 | 2013-12-03 | L'oreal | Long wear, waterproof mascara composition with water washability |
US8828366B2 (en) | 2009-06-29 | 2014-09-09 | L'oreal | Hydrating cream foundation in emulsion form |
US8932566B2 (en) | 2009-06-29 | 2015-01-13 | L'oreal | Composition comprising a polyol and a oil-soluble polar modified polymer |
US8540973B2 (en) | 2009-06-29 | 2013-09-24 | L'oréal | Refreshing cream foundation in gel form |
EP2319491A1 (en) * | 2009-06-29 | 2011-05-11 | L'oreal S.A. | Refreshing cream foundation in gel form |
EP2319487A1 (en) * | 2009-06-29 | 2011-05-11 | L'oreal S.A. | Refreshing cream foundation in gel form |
US8747868B2 (en) | 2010-12-30 | 2014-06-10 | L'oreal | Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product |
US8846062B2 (en) | 2010-12-30 | 2014-09-30 | L'oreal | Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product |
Also Published As
Publication number | Publication date |
---|---|
GB9415324D0 (en) | 1994-09-21 |
MX9700667A (en) | 1997-04-30 |
EP0768864A1 (en) | 1997-04-23 |
CN1086936C (en) | 2002-07-03 |
JPH10503514A (en) | 1998-03-31 |
CA2192799A1 (en) | 1996-02-15 |
CN1154651A (en) | 1997-07-16 |
EP0768864A4 (en) | 1997-08-20 |
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