RU97121885A - A COMPOSITION FOR HANDLING KERATIN SUBSTANCES, INCLUDING, AT LEAST, ONE INIQUE SILICONE POLYMER AND, AT LEAST, ONE AMID OF FATTY ACID, AND ITS APPLICATION - Google Patents
A COMPOSITION FOR HANDLING KERATIN SUBSTANCES, INCLUDING, AT LEAST, ONE INIQUE SILICONE POLYMER AND, AT LEAST, ONE AMID OF FATTY ACID, AND ITS APPLICATIONInfo
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- RU97121885A RU97121885A RU97121885/14A RU97121885A RU97121885A RU 97121885 A RU97121885 A RU 97121885A RU 97121885/14 A RU97121885/14 A RU 97121885/14A RU 97121885 A RU97121885 A RU 97121885A RU 97121885 A RU97121885 A RU 97121885A
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- Prior art keywords
- composition according
- paragraphs
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- radical
- monomers
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- 239000000203 mixture Substances 0.000 title claims 62
- 229920001296 polysiloxane Polymers 0.000 title claims 31
- 229920000642 polymer Polymers 0.000 title claims 28
- 235000014113 dietary fatty acids Nutrition 0.000 title claims 6
- 239000000194 fatty acid Substances 0.000 title claims 6
- 150000004665 fatty acids Chemical class 0.000 title claims 6
- 239000000126 substance Substances 0.000 title claims 6
- 102000011782 Keratins Human genes 0.000 title claims 4
- 108010076876 Keratins Proteins 0.000 title claims 4
- -1 polysiloxane part Polymers 0.000 claims 46
- 239000000178 monomer Substances 0.000 claims 21
- 150000003254 radicals Chemical class 0.000 claims 19
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 15
- 239000005977 Ethylene Substances 0.000 claims 14
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 9
- 150000002148 esters Chemical class 0.000 claims 9
- 229910052710 silicon Inorganic materials 0.000 claims 9
- 239000010703 silicon Substances 0.000 claims 9
- 239000004215 Carbon black (E152) Substances 0.000 claims 7
- 238000006116 polymerization reaction Methods 0.000 claims 7
- 125000000129 anionic group Chemical group 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 6
- 125000000524 functional group Chemical group 0.000 claims 5
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims 4
- 210000002356 Skeleton Anatomy 0.000 claims 4
- 150000001298 alcohols Chemical class 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 4
- 230000002209 hydrophobic Effects 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 229920000098 polyolefin Polymers 0.000 claims 4
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-Vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 3
- 150000001408 amides Chemical class 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- 241000195940 Bryophyta Species 0.000 claims 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 2
- 229940088644 N,N-dimethylacrylamide Drugs 0.000 claims 2
- YLGYACDQVQQZSW-UHFFFAOYSA-N N,N-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000005396 acrylic acid ester group Chemical group 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive Effects 0.000 claims 2
- 239000000443 aerosol Substances 0.000 claims 2
- 125000000033 alkoxyamino group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 230000000875 corresponding Effects 0.000 claims 2
- 239000002537 cosmetic Substances 0.000 claims 2
- 125000003700 epoxy group Chemical group 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 239000011976 maleic acid Substances 0.000 claims 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 claims 2
- 125000005395 methacrylic acid group Chemical class 0.000 claims 2
- 235000011929 mousse Nutrition 0.000 claims 2
- 125000000962 organic group Chemical group 0.000 claims 2
- 238000010526 radical polymerization reaction Methods 0.000 claims 2
- 238000007142 ring opening reaction Methods 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 1
- MGNZXYYWBUKAII-UHFFFAOYSA-N 1,3-Cyclohexadiene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 claims 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 claims 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N 2-methyl-2-propenoic acid methyl ester Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 claims 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 claims 1
- MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical compound C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 claims 1
- XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N Itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N Methyl radical Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 210000004080 Milk Anatomy 0.000 claims 1
- MJQIARGPQMNBGT-WWUCIAQXSA-N N-[(9Z)-octadecenoyl]sphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(=O)CCCCCCC\C=C/CCCCCCCC MJQIARGPQMNBGT-WWUCIAQXSA-N 0.000 claims 1
- XFHJDMUEHUHAJW-UHFFFAOYSA-N N-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 claims 1
- 241001602876 Nata Species 0.000 claims 1
- 229920001774 Perfluoroether Polymers 0.000 claims 1
- 239000004698 Polyethylene (PE) Substances 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 claims 1
- 229940029983 VITAMINS Drugs 0.000 claims 1
- 229940021016 Vitamin IV solution additives Drugs 0.000 claims 1
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- ATMLPEJAVWINOF-UHFFFAOYSA-N acrylic acid acrylic acid Chemical compound OC(=O)C=C.OC(=O)C=C ATMLPEJAVWINOF-UHFFFAOYSA-N 0.000 claims 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 150000001280 alpha hydroxy acids Chemical class 0.000 claims 1
- 150000003863 ammonium salts Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 1
- SOGAXMICEFXMKE-UHFFFAOYSA-N butyl 2-methylprop-2-enoate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical group [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 239000006071 cream Substances 0.000 claims 1
- 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 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims 1
- 238000001125 extrusion Methods 0.000 claims 1
- 239000000796 flavoring agent Substances 0.000 claims 1
- 235000013355 food flavoring agent Nutrition 0.000 claims 1
- 239000001530 fumaric acid Substances 0.000 claims 1
- 125000002519 galactosyl group Chemical group C1([C@H](O)[C@@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 claims 1
- 239000000499 gel Substances 0.000 claims 1
- 239000011521 glass Substances 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- 125000003147 glycosyl group Chemical group 0.000 claims 1
- 229920000578 graft polymer Polymers 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 239000006210 lotion Substances 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 235000013336 milk Nutrition 0.000 claims 1
- 239000008267 milk Substances 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 238000006068 polycondensation reaction Methods 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 150000003141 primary amines Chemical class 0.000 claims 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims 1
- WRIRWRKPLXCTFD-UHFFFAOYSA-N propanediamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 150000003839 salts Chemical group 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 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 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
- 235000013311 vegetables Nutrition 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 239000011782 vitamin Substances 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229930003231 vitamins Natural products 0.000 claims 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N α-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims 1
Claims (44)
где R1 обозначает либо линейный или разветвленный, насыщенный или ненасыщенный, С9-С30 углеводородный радикал, причем этот радикал может быть замещен одной или более гидроксильными группами, необязательно этерифицированными насыщенной или ненасыщенной С16-С30 жирной кислотой; либо радикал R"-(NR-CO)n-R', где n равно 0 или 1, R обозначает водород или гидроксиэтил, R' и R" представляют углеводородные радикалы, сумма углеродных атомов которых находится между 9 и 30, причем R' представляет двухвалентный радикал;
R2 обозначает атом водорода или (гликозил)n, (галактозил)m или сульфогалактозильный радикал, в котором n представляет целое число в пределах 1 - 4, и m представляет целое число в пределах 1 - 8;
R3 обозначает атом водорода или насыщенный или ненасыщенный, С16-С27 углеводородный радикал, причем этот радикал может быть замещен одним или более С1-С14 алкильными углеводородными радикалами; R3 может также обозначать С15-С26 α-гидроксиалкильный радикал, причем гидроксильная группа необязательно этерифицирована C16-C30 α-гидpoкcи кислотой;
R4 обозначает атом водорода, C1-C4 алкильный радикал, насыщенный или ненасыщенный С16-С27 углеводородный радикал или группу -CH2-CHOH-CH2-O-R6, где R6 обозначает С10-С26 углеводородный радикал;
R5 обозначает атом водорода или моно- или полигидроксилированный С1-С4 углеводородный радикал.1. Cosmetic or dermatological composition intended for the treatment of keratin substances, characterized in that it contains, in a cosmetically or dermatologically acceptable medium, at least one grafted silicone polymer, including a polysiloxane part, and a part consisting of a silicon-free organic chain, one of two parts is the main chain of the polymer, and the other is grafted to the specified main chain and at least one fatty acid amide corresponding to the general formula (I):
where R 1 denotes either a linear or branched, saturated or unsaturated, C 9 -C 30 hydrocarbon radical, and this radical may be substituted by one or more hydroxyl groups, optionally esterified with a saturated or unsaturated C 16 -C 30 fatty acid; or the radical R "- (NR-CO) n -R ', where n is 0 or 1, R denotes hydrogen or hydroxyethyl, R' and R" represent hydrocarbon radicals, the sum of carbon atoms of which is between 9 and 30, and R ' represents a bivalent radical;
R 2 denotes a hydrogen atom or (glycosyl) n , (galactosyl) m or a sulfo-galactosyl radical, in which n represents an integer in the range of 1 to 4, and m represents an integer in the range of 1 to 8;
R 3 denotes a hydrogen atom or a saturated or unsaturated, C 16 -C 27 hydrocarbon radical, and this radical may be substituted with one or more C 1 -C 14 alkyl hydrocarbon radicals; R 3 may also be a C 15 -C 26 α-hydroxyalkyl radical, the hydroxyl group optionally being esterified with a C 16 -C 30 α-hydroxy acid;
R 4 denotes a hydrogen atom, a C 1 -C 4 alkyl radical, a saturated or unsaturated C 16 -C 27 hydrocarbon radical, or a group —CH 2 —CHOH — CH 2 -OR 6 , where R 6 is a C 10 -C 26 hydrocarbon radical;
R 5 denotes a hydrogen atom or a mono - or polyhydroxylated C 1 -C 4 hydrocarbon radical.
а) 0 - 98% по весу по крайней мере одного липофильного мономера (А) низкой полярности, содержащего этиленовую ненасыщенность низкой полярности, который полимеризуется по радикальному пути;
б) 0 - 98% по весу по крайней мере одного полярного гидрофильного мономера (В), содержащего этиленовую ненасыщенность, который сополимеризуют с (А)-типа мономером(ами);
в) 0,01 - 50% по весу по крайней мере одного полисиликсанового макромера (С) общей формулы (II):
X(Y)nSi(R)3-mZm
где X обозначает винильную группу, по которой макромер сополимеризуется с мономерами (А) и (В);
Y обозначает двухвалентную связывающую группу;
R обозначает водород, С1-С6 алкил или алкокси или С6-С12 арил;
Z обозначает моновалентную полисилоксановую единицу, имеющую средне-числовую молекулярную массу, по крайней мере, 500;
n равно 0 или 1 и m представляет целое число в пределах от 1 до 3,
причем процентное содержание рассчитывают относительно суммарного веса мономеров (А), (В) и (С).5. Composition according to any one of paragraphs. 1-4, characterized in that it contains at least one silicone graft copolymer, including:
a) 0 to 98% by weight of at least one lipophilic monomer (A) of low polarity, containing ethylene unsaturation of low polarity, which polymerizes in a radical way;
b) 0 to 98% by weight of at least one polar hydrophilic monomer (B) containing ethylene unsaturation, which is copolymerized with (A) -type monomer (s);
c) 0.01 to 50% by weight of at least one polysilixane macromer (C) of the general formula (II):
X (Y) n Si (R) 3-m Z m
where X denotes a vinyl group, in which the macromer is copolymerized with monomers (A) and (B);
Y denotes a divalent linking group;
R is hydrogen, C 1 -C 6 alkyl or alkoxy, or C 6 -C 12 aryl;
Z represents a monovalent polysiloxane unit having a number average molecular weight of at least 500;
n is 0 or 1 and m represents an integer ranging from 1 to 3,
moreover, the percentage is calculated relative to the total weight of the monomers (A), (B) and (C).
где R1 представляет водород или -СООН;
R2 представляет водород, метил или -СН2СООН;
R3 представляет С1-С6 алкил, алкокси или алкиламино, С6-С12, арил или гидроксил;
R4 представляет С1-С6 алкил, алкокси или алкиламино, С6-С12 арил или гидроксил;
q равно целому числу 2 - 6;
р равно 0 или 1;
r равно целому числу 5 - 700;
m равно целому числу 1 - 3.10. Composition according to any one of paragraphs. 5-9, characterized in that the polysiloxane macromer (C) has the general formula (III):
where R 1 represents hydrogen or-COOH;
R 2 represents hydrogen, methyl or -CH 2 COOH;
R 3 is C 1 -C 6 alkyl, alkoxy or alkylamino, C 6 -C 12 , aryl or hydroxyl;
R 4 is C 1 -C 6 alkyl, alkoxy or alkylamino, C 6 -C 12 aryl or hydroxyl;
q is an integer from 2 to 6;
p is 0 or 1;
r is an integer of 5-700;
m is an integer of 1 - 3.
где n равно целому числу в пределах 5 - 700.11. Composition according to any one of paragraphs. 5-10, characterized in that the polysiloxane macromer (C) has the general formula:
where n is an integer in the range of 5-700.
а) 60% по весу трет-бутилакрилата;
b) 20% по весу акриловой кислоты;
с) 20% по весу силиконового макромера формулы:
где n равно целому числу в пределах от 5 до 700; причем весовые процентные содержания рассчитывают относительно суммарного веса мономеров.12. Composition according to any one of paragraphs. 1-11, characterized in that it contains at least one copolymer, which can be obtained by radical polymerization, based on the monomer mixture consisting of:
a) 60% by weight of t-butyl acrylate;
b) 20% by weight acrylic acid;
c) 20% by weight of a silicone macromer of the formula:
where n is an integer ranging from 5 to 700; moreover, the weight percentages are calculated relative to the total weight of the monomers.
а) 80% по весу трет-бутилакрилата;
б) 20% по весу силиконового макромера формулы:
где n равно целому числу в пределах 5 - 700; причем весовые процентные содержания рассчитывают относительно суммарного веса мономеров.13. Composition according to any one of paragraphs. 1-11, characterized in that it contains at least one copolymer, which can be obtained by radical polymerization, based on the monomer mixture consisting of:
a) 80% by weight of tert-butyl acrylate;
b) 20% by weight of a silicone macromer of the formula:
where n is an integer in the range of 5-700; moreover, the weight percentages are calculated relative to the total weight of the monomers.
T-(CH2)s-Si-[(OSiR5R6)t-R7]y (IV)
где Т выбирают из группы, состоящей из NH2, NHR', эпокси, ОН, или SH группы; R5, R6, R7 и R', независимо, обозначают С1-С6 алкил, фенил, бензил, С6-С12 алкилфенил или водород; s представляет число 2 - 100; t представляет число 0 - 1000 и y представляет число 1 - 3.19. Composition according to any one of paragraphs. 15-18, characterized in that the polysiloxane macromer is polysiloxane corresponding to the General formula (IV):
T- (CH 2 ) s —Si - [(OSiR 5 R 6 ) t —R 7 ] y (IV)
where T is selected from the group consisting of NH 2 , NHR ', epoxy, OH, or SH groups; R 5 , R 6 , R 7 and R ', independently, represent C 1 -C 6 alkyl, phenyl, benzyl, C 6 -C 12 alkylphenyl or hydrogen; s represents the number 2 - 100; t represents the number 0 - 1000 and y represents the number 1 - 3.
где радикалы G1, которые могут быть одинаковыми или различными, представляют водород или С1-С10 алкильный радикал или, альтернативно, фенильный радикал; радикалы G2, которые могут быть одинаковыми или различными, представляют С1-С10 алкиленовую группу, G3 представляет полимерный остаток, образующийся при гомо- или полимеризации по крайней мере одного анионного мономера, содержащего этиленовую ненасыщенность; G4 представляет полимерный остаток, образующийся при гомо- или полимеризации по крайней мере одного гидрофобного мономера, содержащего этиленовую ненасыщенность; m и n равны 0 или 1; а представляет целое число в пределах 0 - 50; b представляет целое число, которое может быть между 10 и 350; с представляет целое число в пределах 0 - 50; при условии, что один из параметров а и с отличен от 0.27. Composition according to any one of paragraphs. 20-26, characterized in that the grafted silicone polymer is chosen from silicone polymers containing in its structure a unit of the following formula (V):
where the radicals G 1 , which may be the same or different, are hydrogen or a C 1 -C 10 alkyl radical or, alternatively, a phenyl radical; the G 2 radicals, which may be the same or different, represent a C 1 -C 10 alkylene group, G 3 represents a polymer residue resulting from the homo- or polymerization of at least one anionic monomer containing ethylene unsaturation; G 4 is a polymer residue formed by the homo- or polymerization of at least one hydrophobic monomer containing ethylene unsaturation; m and n are 0 or 1; a represents an integer in the range of 0-50; b is an integer that can be between 10 and 350; c is an integer from 0 to 50; provided that one of the parameters a and c is different from 0.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9511484A FR2739284B1 (en) | 1995-09-29 | 1995-09-29 | COMPOSITION FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING AT LEAST ONE GRAFTED SILICONE POLYMER AND AT LEAST ONE FATTY CHAIN AMIDE AND USES THEREOF |
| FR95/11484 | 1995-09-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU97121885A true RU97121885A (en) | 1999-09-10 |
| RU2168324C2 RU2168324C2 (en) | 2001-06-10 |
Family
ID=9483075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU97121885/14A RU2168324C2 (en) | 1995-09-29 | 1996-09-16 | Composition for treatment of keratin substances involving at least one silicone graft-polymer and at least one fatty acid amide and its using |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6165444A (en) |
| EP (1) | EP0862405B1 (en) |
| JP (1) | JP3053649B2 (en) |
| KR (1) | KR100263217B1 (en) |
| AT (1) | ATE209025T1 (en) |
| BR (1) | BR9610760A (en) |
| CA (1) | CA2223000C (en) |
| DE (1) | DE69617262T2 (en) |
| ES (1) | ES2168507T3 (en) |
| FR (1) | FR2739284B1 (en) |
| PL (1) | PL186015B1 (en) |
| RU (1) | RU2168324C2 (en) |
| WO (1) | WO1997012587A1 (en) |
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| AU9449198A (en) * | 1997-10-07 | 1999-04-27 | Reckitt & Colman France | Detergent composition |
| DE19828643A1 (en) * | 1998-06-26 | 1999-12-30 | Wella Ag | Single-phase, foam-like hair treatment agent to achieve a pomade effect |
| FR2799972B1 (en) * | 1999-10-20 | 2001-12-07 | Oreal | COSMETIC COMPOSITIONS CONTAINING A VINYL DIMETHICONE / DIMETHICONE COPOLYMER IN AQUEOUS EMULSION AND A THICKENER AND USES THEREOF |
| FR2799970B1 (en) * | 1999-10-20 | 2001-12-07 | Oreal | COSMETIC COMPOSITIONS CONTAINING A VINYLDIMETHICONE / DIMETHICONE COPOLYMER AND A CONDITIONING AGENT AND USES THEREOF |
| FR2799955B1 (en) * | 1999-10-20 | 2001-12-07 | Oreal | COSMETIC COMPOSITIONS CONTAINING AN EMULSION OF A VINYLDIMETHICONE / DIMETHICONE COPOLYMER AND A CATIONIC SURFACTANT AND USES THEREOF |
| US6520186B2 (en) | 2001-01-26 | 2003-02-18 | L'oreal | Reshapable hair styling composition comprising silicon-containing polycondensates |
| US6576329B2 (en) | 2001-06-12 | 2003-06-10 | Exxonmobil Oil Corporation | Multilayer thermoplastic film |
| US7959198B2 (en) * | 2002-05-16 | 2011-06-14 | Labor Saving Systems, Ltd. | Magnetic line retrieval system and method |
| US20040219177A1 (en) * | 2003-04-29 | 2004-11-04 | Jacobs Randy J. | Depleted skin barrier replenishing skin creams composition and method of application |
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| US20050074260A1 (en) * | 2003-10-03 | 2005-04-07 | Xerox Corporation | Printing apparatus and processes employing intermediate transfer with molten intermediate transfer materials |
| WO2005035631A1 (en) * | 2003-10-07 | 2005-04-21 | Clariant International Ltd | Amino-functional silicone waxes |
| US7511165B2 (en) * | 2004-10-04 | 2009-03-31 | Clariant Finance (Bvi) Limited | Amino-functional silicone waxes |
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| FR2925311B1 (en) * | 2007-12-21 | 2009-12-18 | Oreal | PROCESS FOR LIGHTENING HUMAN KERATINOUS FIBERS USING ANHYDROUS COMPOSITION AND A PARTICULAR ORGANIC AMINE AND APPROPRIATE DEVICE |
| FR2925307B1 (en) | 2007-12-21 | 2009-12-18 | Oreal | METHOD FOR DIRECT LIGHTENING OR OXIDATION COLORING IN THE PRESENCE OF A PARTICULAR ORGANIC AMINE AND DEVICE |
| FR2940101B1 (en) * | 2008-12-19 | 2011-02-18 | Oreal | KERATIN FIBER OXIDATION DYEING COMPOSITION COMPRISING A FATTY BODY AND A 4,5-DIAMINOPYRAZOLE DERIVATIVE |
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| FR2940061B1 (en) * | 2008-12-19 | 2011-03-04 | Oreal | KERATIN FIBER OXIDATION DYE COMPOSITION COMPRISING A FATTY BODY AND A DIAMINOPYRAZOLONE DERIVATIVE. |
| JP5808077B2 (en) * | 2008-12-19 | 2015-11-10 | ロレアル | Method and kit for coloring or brightening in the presence of an inorganic base |
| FR2940105B1 (en) * | 2008-12-19 | 2011-04-08 | Oreal | COMPOSITION COMPRISING A PARTICULAR OXYETHYLENE FIBER AND SURFACTANT, METHOD FOR COLORING THE SAME AND DEVICES THEREFOR |
| FR2940108B1 (en) * | 2008-12-19 | 2011-04-29 | Oreal | METHOD FOR LIGHTENING KERATINIC MATERIALS USING ANHYDROUS COMPOSITION COMPRISING AN ALKALI AGENT AND AN OXIDIZING COMPOSITION |
| EP2198831B1 (en) * | 2008-12-19 | 2017-05-10 | L'Oréal | Method for lightening, lightening direct dyeing or oxidation dyeing carried out in the presence of an organic amine and a mineral base; suitable kit |
| US7918902B2 (en) * | 2008-12-19 | 2011-04-05 | L'oreal S.A. | Process for lightening or process for direct dyeing or oxidation dyeing of keratin fibers in the presence of at least one ammonium salt and device therefor |
| FR2940092B1 (en) * | 2008-12-19 | 2011-02-18 | Oreal | KERATIN FIBER OXIDATION DYE COMPOSITION COMPRISING AN AMIDE OR ESTER FATTY BODY |
| FR2940067B1 (en) * | 2008-12-19 | 2011-02-25 | Oreal | OXIDIZING COMPOSITION FOR THE TREATMENT OF KERATIN FIBERS COMPRISING A CATIONIC POLYMER, A FATTY AMIDE AND AN OXYGEN AGENT |
| JP5826454B2 (en) * | 2008-12-19 | 2015-12-02 | ロレアル | Lightening or dyeing human keratin fibers using an anhydrous composition containing a monoethanolamine / basic amino acid mixture and device therefor |
| FR2940077B1 (en) * | 2008-12-19 | 2012-07-20 | Oreal | METHOD FOR LIGHTENING COLORING KERATINIC MATERIALS USING A COLORING ANHYDROUS COMPOSITION COMPRISING AN ALKALI AGENT AND AN OXIDIZING COMPOSITION |
| FR2940100B1 (en) * | 2008-12-19 | 2011-02-18 | Oreal | KERATIN FIBER OXIDATION DYE COMPOSITION COMPRISING A FATTY BODY AND N, N BIS (BETA-HYDROXYETHYL) -PARAPHENYLENE DIAMINE |
| FR2940055B1 (en) * | 2008-12-19 | 2015-03-27 | Oreal | KERATIN FIBER OXIDATION DYEING COMPOSITION COMPRISING PARA-AMINOPHENOL, DIPROPYLENE GLYCOL, AND ADDITIONAL COLOURANT PRECURSOR |
| FR2940079B1 (en) | 2008-12-19 | 2011-02-18 | Oreal | COMPOSITION COMPRISING AT LEAST ONE SOLID FATTY ALCOHOL, METHOD FOR COLORING THE SAME AND DEVICES THEREOF |
| FR2940107B1 (en) * | 2008-12-19 | 2011-03-18 | Oreal | PROCESS FOR LIGHTENING KERATINIC MATERIALS USING AN EMULSION COMPRISING AN ALKALI AGENT AND AN OXIDIZING COMPOSITION |
| FR2940078B1 (en) * | 2008-12-19 | 2011-05-13 | Oreal | COMPOSITION COMPRISING A FATTY BODY AND A CATIONIC POLYMER, A METHOD FOR COLORING THE SAME AND DEVICES |
| US7927381B2 (en) * | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of an aqueous composition comprising at least one fatty substance, and device |
| FR2940104B1 (en) * | 2008-12-19 | 2011-08-19 | Oreal | HAIR PROCESSING METHOD USING DIRECT EMULSION COMPRISING OXIDIZING AGENT AND COMPOSITION CONTAINING ALKALINE AGENT |
| FR2940102B1 (en) * | 2008-12-19 | 2016-03-11 | Oreal | KERATIN FIBER OXIDATION DYEING COMPOSITION COMPRISING A FATTY BODY, A THICKENER AND AN OXIDATION COLORING PRECURSOR |
| FR2940090B1 (en) * | 2008-12-19 | 2011-02-25 | Oreal | OXIDIZING COMPOSITION FOR THE TREATMENT OF KERATIN FIBERS COMPRISING OIL, FATTY ALCOHOL AND OXYALKYLENE FATTY ALCOHOL |
| FR2940106B1 (en) * | 2008-12-19 | 2013-04-12 | Oreal | COMPOSITION COMPRISING A FATTY BODY AND A SILICATE, COLORING PROCESS USING THE SAME AND DEVICES |
| CN101780015A (en) * | 2008-12-19 | 2010-07-21 | 莱雅公司 | Coloring or lightening human keratin fiber, using anhydrous composition comprising fatty substance and surfactants, a composition comprising mono ethanolamine and basic amino acids, and composition comprising oxidizing agents |
| FR2954121B1 (en) | 2009-12-22 | 2016-03-25 | Oreal | COLORING AND / OR DECOLOURING AGENT OF TWO - PART KERATIN FIBERS, COMPRISING A PARTICULAR FOLDER AND A REDUCTONE. |
| FR2954159B1 (en) * | 2009-12-22 | 2012-02-10 | Oreal | A KERATIN FIBER COLORING AND / OR DECOLOURING AGENT COMPRISING A COMPOSITION COMPRISING AN ALKALINIZING AGENT AND AN ANHYDROUS COMPOSITION COMPRISING AN OXIDANT, EITHER OF THE COMPOSITIONS CONTAINING A FATTY BODY |
| FR2954127B1 (en) * | 2009-12-22 | 2015-10-30 | Oreal | COLORING AND / OR DECOLOURING AGENT OF TWO-PART KERATINOUS FIBERS, COMPRISING A BODY AND A SEQUESTRING AGENT. |
| FR2954160B1 (en) * | 2009-12-22 | 2012-03-30 | Oreal | COLORING OR LIGHTENING COMPOSITION COMPRISING A FATTY BODY AND AN AMPHOTERIC POLYMER |
| CN115947666A (en) * | 2023-02-02 | 2023-04-11 | 深圳市迪克曼生物科技有限公司 | Rice bran oil ceramide and synthesis method and application thereof |
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| DE69006556T2 (en) * | 1989-08-07 | 1994-06-09 | Procter & Gamble | Hair conditioning and styling agents. |
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| US5118507A (en) * | 1991-06-25 | 1992-06-02 | Elizabeth Arden Co., Division Of Conopco, Inc. | Silicone based cosmetic composition |
| FR2679770A1 (en) * | 1991-08-01 | 1993-02-05 | Oreal | Cationic dispersions for treatment of the hair or skin based on ceramides and/or glycoceramides, cosmetic compositions containing them and their cosmetic applications |
| CZ35294A3 (en) * | 1991-08-19 | 1994-07-13 | Procter & Gamble | Hair aerosol preparations containing ionic polymers forming the hair style |
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| EP0582152B1 (en) * | 1992-07-28 | 2003-04-16 | Mitsubishi Chemical Corporation | A hair cosmetic composition |
| DE4225138A1 (en) * | 1992-07-30 | 1994-02-03 | Daimler Benz Ag | Multichip module and method for its production |
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| BR9510141A (en) * | 1995-01-09 | 1997-12-30 | Procter & Gamble | Aqueous composition to fix hair |
| DE69619759T2 (en) * | 1995-10-05 | 2002-11-21 | Wako Pure Chem Ind Ltd | Base material for hair cosmetics |
-
1995
- 1995-09-29 FR FR9511484A patent/FR2739284B1/en not_active Expired - Fee Related
-
1996
- 1996-09-16 ES ES96931855T patent/ES2168507T3/en not_active Expired - Lifetime
- 1996-09-16 JP JP9514009A patent/JP3053649B2/en not_active Expired - Fee Related
- 1996-09-16 BR BR9610760A patent/BR9610760A/en not_active IP Right Cessation
- 1996-09-16 US US08/983,335 patent/US6165444A/en not_active Expired - Lifetime
- 1996-09-16 EP EP96931855A patent/EP0862405B1/en not_active Expired - Lifetime
- 1996-09-16 KR KR1019970709983A patent/KR100263217B1/en not_active IP Right Cessation
- 1996-09-16 WO PCT/FR1996/001437 patent/WO1997012587A1/en active IP Right Grant
- 1996-09-16 RU RU97121885/14A patent/RU2168324C2/en not_active IP Right Cessation
- 1996-09-16 PL PL96324203A patent/PL186015B1/en not_active IP Right Cessation
- 1996-09-16 AT AT96931855T patent/ATE209025T1/en active
- 1996-09-16 DE DE69617262T patent/DE69617262T2/en not_active Expired - Lifetime
- 1996-09-16 CA CA002223000A patent/CA2223000C/en not_active Expired - Fee Related
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