RU97110777A - COMPOSITION FOR PROCESSING KERATIN MATERIALS CONTAINING, AT LEAST, ONE SILICON ORGANIC GRAVITY COPOLYMER WITH POLYSILOXANE SKELETON TO WHICH GRAVES ARE NOT CONCERNED - Google Patents
COMPOSITION FOR PROCESSING KERATIN MATERIALS CONTAINING, AT LEAST, ONE SILICON ORGANIC GRAVITY COPOLYMER WITH POLYSILOXANE SKELETON TO WHICH GRAVES ARE NOT CONCERNEDInfo
- Publication number
- RU97110777A RU97110777A RU97110777/14A RU97110777A RU97110777A RU 97110777 A RU97110777 A RU 97110777A RU 97110777/14 A RU97110777/14 A RU 97110777/14A RU 97110777 A RU97110777 A RU 97110777A RU 97110777 A RU97110777 A RU 97110777A
- Authority
- RU
- Russia
- Prior art keywords
- composition according
- vinyl
- acid
- copolymers
- acrylate
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 38
- 229920001577 copolymer Polymers 0.000 title claims 28
- -1 POLYSILOXANE SKELETON Polymers 0.000 title claims 20
- 239000000463 material Substances 0.000 title claims 5
- 102000011782 Keratins Human genes 0.000 title claims 4
- 108010076876 Keratins Proteins 0.000 title claims 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 title claims 2
- 229910052710 silicon Inorganic materials 0.000 title claims 2
- 239000010703 silicon Substances 0.000 title claims 2
- 230000005484 gravity Effects 0.000 title 1
- 229920000642 polymer Polymers 0.000 claims 19
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 13
- 125000000129 anionic group Chemical group 0.000 claims 13
- 239000000178 monomer Substances 0.000 claims 13
- 150000003254 radicals Chemical class 0.000 claims 13
- 125000004432 carbon atoms Chemical group C* 0.000 claims 8
- 150000002148 esters Chemical class 0.000 claims 8
- 238000006116 polymerization reaction Methods 0.000 claims 7
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 5
- 229920001567 Vinyl ester Polymers 0.000 claims 4
- 230000002209 hydrophobic Effects 0.000 claims 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 4
- XTXRWKRVRITETP-UHFFFAOYSA-N vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N Itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 150000008064 anhydrides Chemical class 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims 3
- 239000000194 fatty acid Substances 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 3
- 125000005395 methacrylic acid group Chemical class 0.000 claims 3
- 150000003839 salts Chemical group 0.000 claims 3
- 239000011780 sodium chloride Substances 0.000 claims 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- 125000003903 2-propenyl group Chemical class [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-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
- 239000002202 Polyethylene glycol Substances 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive Effects 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 239000002537 cosmetic Substances 0.000 claims 2
- 239000006260 foam Substances 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
- 229910052751 metal Chemical class 0.000 claims 2
- 239000002184 metal Chemical class 0.000 claims 2
- 229920003145 methacrylic acid copolymer Polymers 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- 125000000962 organic group Chemical group 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 229920001223 polyethylene glycol Polymers 0.000 claims 2
- 229920001296 polysiloxane Polymers 0.000 claims 2
- 239000002453 shampoo Substances 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 239000007921 spray Substances 0.000 claims 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N 2-methyl-2-propenoic acid methyl ester Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical class C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- XVQUOJBERHHONY-UHFFFAOYSA-N Isometheptene Chemical group CNC(C)CCC=C(C)C XVQUOJBERHHONY-UHFFFAOYSA-N 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N Methacrylamide Chemical group CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N Methyl radical Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N Methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims 1
- 210000004080 Milk Anatomy 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-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
- 229940029983 VITAMINS Drugs 0.000 claims 1
- 229940021016 Vitamin IV solution additives Drugs 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
- 239000000443 aerosol Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000007942 carboxylates Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 239000006071 cream Substances 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
- 238000004043 dyeing Methods 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical group CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N fumaric acid Chemical compound OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
- 239000001530 fumaric acid Substances 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 239000000499 gel Substances 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 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
- 239000006210 lotion Substances 0.000 claims 1
- 239000011976 maleic acid Substances 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
- 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
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 229920002401 polyacrylamide Polymers 0.000 claims 1
- 229920001515 polyalkylene glycol Polymers 0.000 claims 1
- 230000002335 preservative Effects 0.000 claims 1
- 239000003755 preservative agent Substances 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 229920005573 silicon-containing polymer Polymers 0.000 claims 1
- 159000000000 sodium salts Chemical class 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
- LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 230000001225 therapeutic Effects 0.000 claims 1
- 239000002562 thickening agent Substances 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
- 239000011782 vitamin Substances 0.000 claims 1
- 235000013343 vitamin Nutrition 0.000 claims 1
- 229930003231 vitamins Natural products 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
Claims (28)
где радикалы G1, одинаковые или разные, означают водород или алкильный радикал с 1-10 атомами углерода или фенильный радикал;
радикалы G2, одинаковые или разные, означают алкиленовую группу с 1-10 атомами углерода;
G3 означает полимерный остаток, получающийся в результате (гомо)полимеризации по крайней мере одного анионного мономера с двойной связью;
G4 означает полимерный остаток, получающийся в результате (гомо)полимеризации по крайней мере одного гидрофобного мономера с двойной связью;
"m" и "n" равны 0 или 1;
"а" означает целое число 0 - 50;
"b" означает целое число, которое может составлять 10-350;
"с" означает целое число 0 - 50;
при условии, что один из параметров "а" и "с" отличен от нуля.9. A composition according to any one of claims 1 to 8, characterized in that the organosilicon grafted copolymer is selected from silicon-containing polymers including a unit of the following formula (1) in its structure:
where the radicals G 1 , identical or different, are hydrogen or an alkyl radical with 1-10 carbon atoms or a phenyl radical;
G 2 radicals, identical or different, mean an alkylene group with 1-10 carbon atoms;
G 3 means a polymer residue resulting from the (homo) polymerization of at least one double bond anionic monomer;
G 4 means a polymer residue resulting from the (homo) polymerization of at least one hydrophobic double bond monomer;
"m" and "n" are 0 or 1;
"a" means the integer 0 to 50;
"b" means an integer that may be 10-350;
"c" means the integer 0 to 50;
provided that one of the parameters "a" and "c" is nonzero.
где "n" означает целое число от 0 до 10;
А означает метиленовую группу, возможно соединенную с атомом углерода ненасыщенной группы или с соседней метиленовой группой, когда "n" больше 1, через гетероатом, такой, как кислород или сера;
R1 означает атом водорода, фенильную или бензильную группу;
R2 означает атом водорода, низшую алкильную или карбоксильную группу;
R3 означает атом водорода, низшую алкильную группу, группу -СН2-СООН, фенильную или бензильную группу;
полимеры, включающие звенья, происходящие от сульфокислоты, такие, как винилсульфоновые, стиропсульфоновые, акриламидоалкилсульфоновые звенья.14. The composition according to any one of claims 1 to 13, characterized in that the anionic polymer is selected among the following: polymers comprising carboxyl units derived from monomeric mono- or dicarboxylic unsaturated acids of the formula (V):
where "n" means an integer from 0 to 10;
A means a methylene group, possibly connected to a carbon atom of an unsaturated group or to an adjacent methylene group when “n” is greater than 1, through a heteroatom such as oxygen or sulfur;
R 1 means a hydrogen atom, a phenyl or benzyl group;
R 2 means a hydrogen atom, a lower alkyl or carboxyl group;
R 3 means a hydrogen atom, a lower alkyl group, a —CH 2 —COOH group, a phenyl or benzyl group;
polymers comprising sulfonic acid-derived units, such as vinyl sulfonic, styrene sulfonic, acrylamidoalkyl sulfonic units.
В) сополимеры, происходящие от кротоновой кислоты, такие, как сополимеры, содержащие в своей цепи винилацетатное или винилпропионатное звено и возможно звенья других мономеров, таких, как сложные аллиловые или металлиловые эфиры, простой виниловый эфир или сложный виниловый эфир линейной или разветвленной насыщенной карбоновой кислоты с длинной углеводородной цепью, таких, которые содержат, по крайней мере 5 атомов углерода, причем эти полимеры могут быть привитыми сополимерами или сшитыми; Г) полимеры, происходящие от малеиновой, фумаровой, итаконовой кислот или их ангидридов со сложными виниловыми эфирами, простыми виниловыми эфирами, винилгалогенидами, фенилвиниловыми производными, акриловой кислотой и ее эфирами; сополимеры малеинового, цитраконового, итаконового ангидридов со сложным аллиловым или металлиловым эфиром, включающие в свою цепь акриламидную, метакриламидную группу, α-олефин, сложные акриловые или метакриловые эфиры, акриловую или метакриловую кислоты или винилпирролидон, причем ангидридные функции моноэтерифицированы или моноамидированы; Д) полиакриламиды, содержащие карбоксилатные группы.15. The composition according to p. 14, wherein the anionic polymer is selected from the following: A) homo- and copolymers of acrylic or methacrylic acid or their salts, copolymers of acrylic acid with acrylamide and their salts, sodium salts of polyhydroxycarboxylic acids; B) copolymers of acrylic or methacrylic acids with a monomer containing a double bond, such as ethylene, styrene, vinyl esters, esters of acrylic or methacrylic acid, possibly grafted to polyalkylene glycol, such as polyethylene glycol, and possibly crosslinked; copolymers of this type, including in their chain an acrylamide unit, optionally N-alkylated and / or hydroxyalkylated; copolymers of acrylic acid with (C 1 -C 4 ) -alkyl methacrylate;
C) copolymers derived from crotonic acid, such as copolymers containing in their chain a vinyl acetate or vinyl propionate unit and optionally other monomers such as allyl or metal esters, vinyl ether or a linear or branched saturated carboxylic acid vinyl ester with a long hydrocarbon chain, such that contain at least 5 carbon atoms, and these polymers can be grafted copolymers or crosslinked; D) polymers derived from maleic, fumaric, itaconic acids or their anhydrides with complex vinyl esters, simple vinyl ethers, vinyl halides, phenyl vinyl derivatives, acrylic acid and its esters; copolymers of maleic, citraconic, itaconic anhydrides with an allyl or metal ester complex, including an acrylamide, methacrylamide group, α-olefin, acrylic or methacrylic esters, acrylic or methacrylic acids or vinyl pyrrolidone in their chain, moreover, the mono ethers are anhydride or monoester; E) polyacrylamides containing carboxylate groups.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9511478A FR2739279B1 (en) | 1995-09-29 | 1995-09-29 | COMPOSITION FOR THE TREATMENT OF KERATINIC MATERIALS COMPRISING AT LEAST ONE SILICONE POLYMER GRAFT WITH A POLYSILOXANE SKELETON GRAFT WITH NON-SILICON ORGANIC MONOMERS AND AT LEAST ONE ANIONIC POLYMER |
FR9511478 | 1995-09-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU97110777A true RU97110777A (en) | 1999-07-10 |
RU2166926C2 RU2166926C2 (en) | 2001-05-20 |
Family
ID=9483068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU97110777/14A RU2166926C2 (en) | 1995-09-29 | 1996-09-16 | Composition for treating keratinous materials containing at least one organosilicon grafted copolymer with polysyloxane skeleton having grafted organic monomers containing no silicon and at least one anion polymer |
Country Status (12)
Country | Link |
---|---|
US (1) | US6086862A (en) |
EP (1) | EP0793482B1 (en) |
JP (2) | JPH10500432A (en) |
AT (1) | ATE222089T1 (en) |
BR (1) | BR9606672A (en) |
CA (1) | CA2207478C (en) |
DE (1) | DE69622987T2 (en) |
ES (1) | ES2181910T3 (en) |
FR (1) | FR2739279B1 (en) |
PL (1) | PL185547B1 (en) |
RU (1) | RU2166926C2 (en) |
WO (1) | WO1997012592A1 (en) |
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JP3679569B2 (en) * | 1997-09-24 | 2005-08-03 | 花王株式会社 | Aqueous hair tonic composition for hair and scalp treatment |
FR2795316B1 (en) * | 1999-06-28 | 2004-12-24 | Oreal | PERMANENT PROCESS COMPRISING THE PRELIMINARY APPLICATION OF A COMPOSITION COMPRISING AT LEAST ONE ANIONIC POLYMER |
US6605577B1 (en) | 2001-11-07 | 2003-08-12 | Chemsil Silicones, Inc. | Clear conditioning detersive compositions containing polysiloxanes with at least one cyclic side chain |
US6642194B2 (en) | 2001-11-07 | 2003-11-04 | Chemsil Silicones, Inc. | Clear conditioning detersive compositions and methods for making the same |
US7959198B2 (en) * | 2002-05-16 | 2011-06-14 | Labor Saving Systems, Ltd. | Magnetic line retrieval system and method |
US20050074260A1 (en) * | 2003-10-03 | 2005-04-07 | Xerox Corporation | Printing apparatus and processes employing intermediate transfer with molten intermediate transfer materials |
US7128412B2 (en) | 2003-10-03 | 2006-10-31 | Xerox Corporation | Printing processes employing intermediate transfer with molten intermediate transfer materials |
US20050196368A1 (en) * | 2004-02-12 | 2005-09-08 | Ludivine Laurent | Cosmetic composition comprising at least one anionic fixing polymer and at least one nonionic compound, and a process for shaping keratin fibers therewith by applying heat |
WO2006086444A1 (en) * | 2005-02-09 | 2006-08-17 | Farouk Systems, Inc. | Composition and system for hair coloring and color retention |
US7687574B2 (en) * | 2006-05-01 | 2010-03-30 | Momentive Performance Materials Inc. | Acrylate cross linked silicone copolymer networks |
US7833541B2 (en) * | 2006-05-01 | 2010-11-16 | Momentive Performance Materials Inc. | Cosmetic compositions utilizing acrylate cross linked silicone copolymer networks |
JP6641227B2 (en) * | 2016-04-28 | 2020-02-05 | 信越化学工業株式会社 | Emulsified cosmetic |
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DK0412704T3 (en) * | 1989-08-07 | 1999-11-01 | Procter & Gamble | Hair conditioning and styling compositions |
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DE69005283D1 (en) * | 1990-01-09 | 1994-01-27 | Dow Corning | Siloxane composition for hair care. |
GB2245279B (en) * | 1990-06-20 | 1993-04-07 | Unilever Plc | Shampoo composition |
US5034218A (en) * | 1990-07-13 | 1991-07-23 | Helene Curtis, Inc. | Stable conditioning shampoo containing compatible anionic surfactant/cationic conditioning agent-non-volatile silicone emulsion |
US5468477A (en) * | 1992-05-12 | 1995-11-21 | Minnesota Mining And Manufacturing Company | Vinyl-silicone polymers in cosmetics and personal care products |
ES2089822T3 (en) * | 1992-05-12 | 1996-10-01 | Minnesota Mining & Mfg | POLYMERS FOR COSMETIC AND PERSONAL CARE PRODUCTS. |
SK136194A3 (en) * | 1992-05-15 | 1995-08-09 | Procter & Gamble | Adhesive agent containing polysiloxane-grafted polymer, and cosmetic compositions thereof |
EP0582152B1 (en) * | 1992-07-28 | 2003-04-16 | Mitsubishi Chemical Corporation | A hair cosmetic composition |
EP0640643B1 (en) * | 1993-08-10 | 2000-04-26 | Kao Corporation | Organopolysiloxanes and a method of setting hair using the same |
EP0748204B1 (en) * | 1994-03-01 | 1998-11-25 | The Procter & Gamble Company | Hair care compositions providing hair conditioning and style retention |
WO1997001321A1 (en) * | 1995-06-26 | 1997-01-16 | Revlon Consumer Products Corporation | Glossy transfer resistant cosmetic compositions |
ATE155341T1 (en) * | 1995-08-01 | 1997-08-15 | Goldwell Gmbh | HAIR TREATMENT PRODUCTS |
-
1995
- 1995-09-29 FR FR9511478A patent/FR2739279B1/en not_active Expired - Fee Related
-
1996
- 1996-09-06 US US08/849,185 patent/US6086862A/en not_active Expired - Lifetime
- 1996-09-16 RU RU97110777/14A patent/RU2166926C2/en not_active IP Right Cessation
- 1996-09-16 ES ES96931850T patent/ES2181910T3/en not_active Expired - Lifetime
- 1996-09-16 WO PCT/FR1996/001432 patent/WO1997012592A1/en active IP Right Grant
- 1996-09-16 DE DE69622987T patent/DE69622987T2/en not_active Expired - Lifetime
- 1996-09-16 BR BR9606672A patent/BR9606672A/en not_active IP Right Cessation
- 1996-09-16 PL PL96320481A patent/PL185547B1/en not_active IP Right Cessation
- 1996-09-16 AT AT96931850T patent/ATE222089T1/en active
- 1996-09-16 JP JP9514004A patent/JPH10500432A/en active Pending
- 1996-09-16 EP EP96931850A patent/EP0793482B1/en not_active Expired - Lifetime
- 1996-09-16 CA CA002207478A patent/CA2207478C/en not_active Expired - Fee Related
-
1999
- 1999-07-28 JP JP11214326A patent/JP2000038325A/en active Pending
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