RU2000123753A - COSMETIC COMPOSITION, INCLUDING, AT LEAST, ONE SILICONE AND ACRYLATE COPOLYMER AND AT LEAST, ONE PRIVATED SILICONE COPOLYMER - Google Patents
COSMETIC COMPOSITION, INCLUDING, AT LEAST, ONE SILICONE AND ACRYLATE COPOLYMER AND AT LEAST, ONE PRIVATED SILICONE COPOLYMERInfo
- Publication number
- RU2000123753A RU2000123753A RU2000123753/04A RU2000123753A RU2000123753A RU 2000123753 A RU2000123753 A RU 2000123753A RU 2000123753/04 A RU2000123753/04 A RU 2000123753/04A RU 2000123753 A RU2000123753 A RU 2000123753A RU 2000123753 A RU2000123753 A RU 2000123753A
- Authority
- RU
- Russia
- Prior art keywords
- acrylate
- composition according
- meth
- monomer
- silicone
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 30
- 229920001296 polysiloxane Polymers 0.000 title claims 20
- 229920001577 copolymer Polymers 0.000 title claims 5
- 239000002537 cosmetic Substances 0.000 title claims 3
- -1 polysiloxane skeleton Polymers 0.000 claims 30
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 18
- 239000000178 monomer Substances 0.000 claims 16
- 125000004432 carbon atoms Chemical group C* 0.000 claims 8
- 229920000642 polymer Polymers 0.000 claims 7
- 238000006116 polymerization reaction Methods 0.000 claims 7
- 125000000129 anionic group Chemical group 0.000 claims 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 230000002209 hydrophobic Effects 0.000 claims 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 4
- 229910052710 silicon Inorganic materials 0.000 claims 4
- 239000010703 silicon Substances 0.000 claims 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 4
- 210000004209 Hair Anatomy 0.000 claims 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 3
- 125000000962 organic group Chemical group 0.000 claims 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 2
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical class C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims 2
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims 2
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 claims 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-Vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N Itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 2
- 125000003277 amino 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
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- 239000001530 fumaric acid Substances 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- 239000011976 maleic acid Substances 0.000 claims 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000006832 (C1-C10) alkylene group Chemical group 0.000 claims 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-Dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 claims 1
- MLMGJTAJUDSUKA-UHFFFAOYSA-N 2-ethenyl-1H-imidazole Chemical compound C=CC1=NC=CN1 MLMGJTAJUDSUKA-UHFFFAOYSA-N 0.000 claims 1
- BQBSIHIZDSHADD-UHFFFAOYSA-N 2-ethenyl-4,5-dihydro-1,3-oxazole Chemical compound C=CC1=NCCO1 BQBSIHIZDSHADD-UHFFFAOYSA-N 0.000 claims 1
- QQBUHYQVKJQAOB-UHFFFAOYSA-N 2-ethenylfuran Chemical compound C=CC1=CC=CO1 QQBUHYQVKJQAOB-UHFFFAOYSA-N 0.000 claims 1
- SFPNZPQIIAJXGL-UHFFFAOYSA-N 2-ethoxyethyl 2-methylprop-2-enoate Chemical compound CCOCCOC(=O)C(C)=C SFPNZPQIIAJXGL-UHFFFAOYSA-N 0.000 claims 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical group CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N 2-hydroxyethyl 2-methylacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 claims 1
- AGBXYHCHUYARJY-UHFFFAOYSA-M 2-phenylethenesulfonate Chemical compound [O-]S(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-M 0.000 claims 1
- MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical group C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 claims 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims 1
- XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims 1
- 210000004709 Eyebrows Anatomy 0.000 claims 1
- 210000000720 Eyelashes Anatomy 0.000 claims 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N Hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 claims 1
- 210000000088 Lip Anatomy 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N Methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- 229940088644 N,N-dimethylacrylamide Drugs 0.000 claims 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N N,N-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N N-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims 1
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N N-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 claims 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N N-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 claims 1
- 210000000282 Nails Anatomy 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 210000003491 Skin Anatomy 0.000 claims 1
- 229940029983 VITAMINS Drugs 0.000 claims 1
- 229940021016 Vitamin IV solution additives Drugs 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
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive Effects 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 1
- 150000001447 alkali salts 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
- 125000005210 alkyl ammonium group Chemical group 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 150000001722 carbon compounds Chemical class 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 230000000875 corresponding Effects 0.000 claims 1
- GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 claims 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 claims 1
- 125000005131 dialkylammonium group Chemical group 0.000 claims 1
- 229940008099 dimethicone Drugs 0.000 claims 1
- 239000004205 dimethyl polysiloxane Substances 0.000 claims 1
- 235000013870 dimethyl polysiloxane Nutrition 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
- BRLQWZUYTZBJKN-UHFFFAOYSA-N epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims 1
- 125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000003205 fragrance Substances 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 150000002391 heterocyclic compounds Chemical group 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 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
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 239000003921 oil 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
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 1
- 229920001515 polyalkylene glycol Polymers 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride 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
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- 239000004094 surface-active agent Substances 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
- 125000005207 tetraalkylammonium group Chemical group 0.000 claims 1
- 125000005208 trialkylammonium group Chemical group 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
- 235000013311 vegetables Nutrition 0.000 claims 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 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
- 0 C=C(*=C(N)N)P Chemical compound C=C(*=C(N)N)P 0.000 description 1
Claims (23)
в которой Х выбирают из группы, состоящей из ОН, ОМ, OR8, NH2, NHR8, N(R8)2;
M означает катион, выбираемый из группы, состоящей из Ni+, К-, Mg++, NH4+, алкиламмония, диалкиламмония, триалкиламмония и тетраалкиламмония;
радикалы R8 могут быть одинаковыми или разными и их выбирают из группы, состоящей из водорода; линейных или разветвленных (С1-С40)-алкильных групп; моно- или полигидроксилированных (C1-C40)-алкильных групп, возможно замещенных одной или несколькими алкоксильными группами, аминогруппами или карбоксильными группами; гидроксилированных простых полиэфирных групп; N, N-диметиламиноэтильной, 2-гидроксиэтильной, 2-метоксиэтильной, 2-этоксиэтильной, гидроксипропильной, метоксипропильной и этоксипропильной групп;
R7 и R6, независимо друг от друга, выбирают из группы, состоящей из водорода, линейных или разветвленных (C1-C8)-алкильных групп, метокси-, этокси-, 2-гидроксиэтокси-, 2-метоксиэтоксигруппы и 2-этоксиэтильной группы, групп CN, СООН и СООМ.2. The composition according to p. 1, characterized in that the monomer (a) corresponds to the formula (Ia)
wherein X is selected from the group consisting of OH, OHM, OR 8 , NH 2 , NHR 8 , N (R 8 ) 2 ;
M means a cation selected from the group consisting of Ni + , K - , Mg ++ , NH 4+ , alkylammonium, dialkyl ammonium, trialkylammonium and tetraalkylammonium;
R 8 radicals may be the same or different and are selected from the group consisting of hydrogen; linear or branched (C 1 -C 40 ) -alkyl groups; mono- or polyhydroxylated (C 1 -C 40 ) -alkyl groups optionally substituted by one or more alkoxy groups, amino groups or carboxyl groups; hydroxylated polyether groups; N, N-dimethylaminoethyl, 2-hydroxyethyl, 2-methoxyethyl, 2-ethoxyethyl, hydroxypropyl, methoxypropyl and ethoxypropyl groups;
R 7 and R 6 , independently of each other, are selected from the group consisting of hydrogen, linear or branched (C 1 -C 8 ) -alkyl groups, methoxy, ethoxy, 2-hydroxyethoxy, 2-methoxyethoxy and 2- ethoxyethyl group, groups CN, COOH and COOM.
в которой R2 выбирают из СН3 или группы
R3 выбирают из СН3 или группы R2;
R4 выбирают из водорода, СН3 или групп:
R6 означает органическую группу с 1-40 атомами углерода, которая может содержать аминогруппы, карбоксильные группы или сульфонатные группы, и, если с= 0, R6 означает анион неорганической кислоты;
радикалы R1 могут быть одинаковыми или разными и их выбирают из алифатических углеводородов с 1-20 атомами углерода, алифатических или циклоалифатических углеводородов с 3-20 атомами углерода и групп R5, отвечающих следующей формуле
n означает целое число от 1 до 6;
х и у означают целые числа, выбираемые таким образом, чтобы молекулярная масса полисилоксана составляла 300-30000;
а и b означают целые числа от 0 до 50; и
с означает 0 или 1.3. The composition according to p. 1 for hair care, characterized in that the silicone derivative (b) corresponds to the formula (I)
in which R 2 choose from CH 3 or group
R 3 is selected from CH 3 or the group R 2 ;
R 4 is selected from hydrogen, CH 3 or groups:
R 6 means an organic group with 1-40 carbon atoms, which may contain amino groups, carboxyl groups or sulphonate groups, and, if c = 0, R 6 means an anion of an inorganic acid;
R 1 radicals may be the same or different and are selected from aliphatic hydrocarbons with 1-20 carbon atoms, aliphatic or cycloaliphatic hydrocarbons with 3-20 carbon atoms and R 5 groups corresponding to the following formula
n means an integer from 1 to 6;
x and y are integers selected so that the molecular weight of the polysiloxane is 300 to 30,000;
a and b are integers from 0 to 50; and
c means 0 or 1.
в которой радикалы G1, одинаковые или разные, означают водород или (C1-С10)-алкил или еще фенил;
радикалы G2, одинаковые или разные, означают (С1-С10)-алкиленовую группу;
G3 означает полимерный остаток, образующийся в результате (гомо)полимеризации по крайней мере одного анионного мономера с двойной связью;
G4 означает полимерный остаток, образующийся в результате (гомо)полимеризации по крайней мере одного гидрофобного мономера с двойной связью;
m и n равны 0 или 1;
а означает целое число от 0 до 50;
b означает целое число, которое может составлять от 10 до 350;
с означает целое число от 0 до 50;
при условии, что один из параметров а и с отличается от 0.15. Composition according to any one of paragraphs. 1-5, characterized in that the grafted silicone copolymer is selected from silicone polymers, containing in its structure the link of the following formula (I)
in which the radicals G 1 , the same or different, mean hydrogen or (C 1 -C 10 ) -alkyl or else phenyl;
the radicals G 2 , which are the same or different, mean a (C 1 -C 10 ) alkylene group;
G 3 means a polymer residue resulting from the (homo) polymerization of at least one anionic monomer with a double bond;
G 4 means a polymer residue resulting from the (homo) polymerization of at least one hydrophobic monomer with a double bond;
m and n are 0 or 1;
and means an integer from 0 to 50;
b means an integer that can be from 10 to 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 |
|---|---|---|---|
| FR9911596A FR2798844B1 (en) | 1999-09-16 | 1999-09-16 | COSMETIC COMPOSITION COMPRISING AT LEAST ONE SILICONE / ACRYLATE COPOLYMER AND AT LEAST ONE GRAFTED SILICONE POLYMER |
| FR9911596 | 1999-09-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2000123753A true RU2000123753A (en) | 2002-08-10 |
| RU2197221C2 RU2197221C2 (en) | 2003-01-27 |
Family
ID=9549922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2000123753/04A RU2197221C2 (en) | 1999-09-16 | 2000-09-15 | Cosmetic composition including, at least, one copolymer of silicone and acrylate and, at least, one grafted silicone copolymer |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1084698B1 (en) |
| JP (2) | JP2001114655A (en) |
| KR (1) | KR100364307B1 (en) |
| CN (1) | CN1293028A (en) |
| AT (1) | ATE244550T1 (en) |
| AU (1) | AU750093B2 (en) |
| BR (1) | BR0004351A (en) |
| CA (1) | CA2319959A1 (en) |
| DE (1) | DE60003763T2 (en) |
| ES (1) | ES2202018T3 (en) |
| FR (1) | FR2798844B1 (en) |
| PL (1) | PL342564A1 (en) |
| RU (1) | RU2197221C2 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2825630B1 (en) * | 2001-06-11 | 2003-09-19 | Oreal | COSMETIC AND / OR DERMATOLOGICAL COMPOSITION IN THE FORM OF A WATER IN OIL EMULSION STABILIZED BY A (CO) POLYMER OF SULFONIC 2-ACRYLAMIDO-2-METHYLPROPANE WITH HYDROPHOBIC GRAFTS |
| JP6224557B2 (en) * | 2014-09-04 | 2017-11-01 | 信越化学工業株式会社 | Film-forming composition and cosmetic |
| US9988590B1 (en) * | 2017-11-10 | 2018-06-05 | Afton Chemical Corporation | Polydialkylsiloxane poly (meth)acrylate brush polymers for lubricant additive application |
| JP6850268B2 (en) * | 2018-02-09 | 2021-03-31 | 信越化学工業株式会社 | (Meta) Acrylic Silicone Graft Copolymer and Its Manufacturing Method |
| TW202023523A (en) * | 2018-10-11 | 2020-07-01 | 美商陶氏全球科技責任有限公司 | Color cosmetic formulation |
| CN110437944A (en) * | 2019-08-15 | 2019-11-12 | 广州立白企业集团有限公司 | A kind of dedicated purificant of automatic dish-washing machine with resistive connection film and spotting performance |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5166276A (en) * | 1989-07-12 | 1992-11-24 | Mitsubishi Petrochemical Company Ltd. | Polymer for hair-care products |
| FR2735689B1 (en) * | 1995-06-21 | 1997-08-01 | Oreal | COMPOSITION COMPRISING A DISPERSION OF POLYMER PARTICLES IN A NON-AQUEOUS MEDIUM |
| FR2740037B1 (en) * | 1995-10-18 | 1997-12-05 | Rhone Poulenc Chimie | COSMETIC COMPOSITIONS FOR HAIR AND SKIN BASED ON FUNCTIONALIZED POLYORGANOSILOXANES |
| ES2318872T3 (en) * | 1997-07-23 | 2009-05-01 | Basf Se | EMPLOYMENT OF POLYMERS THAT CONTAIN POLYSYLOXANE FOR COSMETIC FORMULATIONS. |
-
1999
- 1999-09-16 FR FR9911596A patent/FR2798844B1/en not_active Expired - Fee Related
-
2000
- 2000-08-28 EP EP00402377A patent/EP1084698B1/en not_active Revoked
- 2000-08-28 ES ES00402377T patent/ES2202018T3/en not_active Expired - Lifetime
- 2000-08-28 DE DE60003763T patent/DE60003763T2/en not_active Expired - Fee Related
- 2000-08-28 AT AT00402377T patent/ATE244550T1/en not_active IP Right Cessation
- 2000-09-05 AU AU56487/00A patent/AU750093B2/en not_active Ceased
- 2000-09-12 JP JP2000277134A patent/JP2001114655A/en active Pending
- 2000-09-15 RU RU2000123753/04A patent/RU2197221C2/en not_active IP Right Cessation
- 2000-09-15 CN CN00128741A patent/CN1293028A/en active Pending
- 2000-09-15 CA CA002319959A patent/CA2319959A1/en not_active Abandoned
- 2000-09-15 PL PL00342564A patent/PL342564A1/en not_active Application Discontinuation
- 2000-09-15 BR BR0004351-6A patent/BR0004351A/en not_active IP Right Cessation
- 2000-09-16 KR KR1020000054438A patent/KR100364307B1/en not_active IP Right Cessation
-
2004
- 2004-08-02 JP JP2004226152A patent/JP2004307517A/en not_active Withdrawn
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