RU2000133183A - Composition for the oxidation dyeing of keratin fibers, contain a thickening polymer comprising at least one fatty chain, and fatty alcohols having more than twenty CARBON ATOMS - Google Patents
Composition for the oxidation dyeing of keratin fibers, contain a thickening polymer comprising at least one fatty chain, and fatty alcohols having more than twenty CARBON ATOMSInfo
- Publication number
- RU2000133183A RU2000133183A RU2000133183/14A RU2000133183A RU2000133183A RU 2000133183 A RU2000133183 A RU 2000133183A RU 2000133183/14 A RU2000133183/14 A RU 2000133183/14A RU 2000133183 A RU2000133183 A RU 2000133183A RU 2000133183 A RU2000133183 A RU 2000133183A
- Authority
- RU
- Russia
- Prior art keywords
- composition according
- alkyl
- composition
- fatty chain
- fatty
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims 83
- 229920000642 polymer Polymers 0.000 title claims 22
- 239000000835 fiber Substances 0.000 title claims 15
- 150000002191 fatty alcohols Chemical class 0.000 title claims 14
- 102000011782 Keratins Human genes 0.000 title claims 13
- 108010076876 Keratins Proteins 0.000 title claims 13
- 238000004043 dyeing Methods 0.000 title claims 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title 1
- 230000003647 oxidation Effects 0.000 title 1
- 238000007254 oxidation reaction Methods 0.000 title 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 12
- 230000001590 oxidative Effects 0.000 claims 11
- -1 ethyleneoxy radical Chemical group 0.000 claims 9
- 239000002585 base Substances 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000000975 dye Substances 0.000 claims 8
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000000129 anionic group Chemical group 0.000 claims 7
- 229920001577 copolymer Polymers 0.000 claims 7
- 239000007800 oxidant agent Substances 0.000 claims 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 6
- 125000002091 cationic group Chemical group 0.000 claims 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 6
- 230000002209 hydrophobic Effects 0.000 claims 6
- 239000000178 monomer Substances 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 5
- 239000011780 sodium chloride Substances 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 3
- 239000001913 cellulose Substances 0.000 claims 3
- 229920002678 cellulose Polymers 0.000 claims 3
- 238000004040 coloring Methods 0.000 claims 3
- 230000000875 corresponding Effects 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 229920002635 polyurethane Polymers 0.000 claims 3
- 239000004814 polyurethane Substances 0.000 claims 3
- 239000004094 surface-active agent Substances 0.000 claims 3
- 239000002562 thickening agent Substances 0.000 claims 3
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical group C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 claims 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-Aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 2
- 240000005497 Cyamopsis tetragonoloba Species 0.000 claims 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N P-Phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 2
- 230000002378 acidificating Effects 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 230000001264 neutralization Effects 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000002736 nonionic surfactant Substances 0.000 claims 2
- 229920000570 polyether Polymers 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- KEUDMLLLHGLIGH-UHFFFAOYSA-N 1H-pyrazole;pyrimidine Chemical class C=1C=NNC=1.C1=CN=CN=C1 KEUDMLLLHGLIGH-UHFFFAOYSA-N 0.000 claims 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-Aminophenol Chemical class NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-O 4,5-dihydro-1H-imidazol-1-ium Chemical compound C1CN=C[NH2+]1 MTNDZQHUAFNZQY-UHFFFAOYSA-O 0.000 claims 1
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- NOPFSRXAKWQILS-UHFFFAOYSA-N Docosanol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N Erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N Hydrogen peroxide - urea Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims 1
- 108010029541 Laccase Proteins 0.000 claims 1
- 229940018564 M-PHENYLENEDIAMINE Drugs 0.000 claims 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N M-Phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinylpyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N O-Phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 1
- 108090000854 Oxidoreductases Proteins 0.000 claims 1
- 102000004316 Oxidoreductases Human genes 0.000 claims 1
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 108090000437 Peroxidases Proteins 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 102000014961 Protein Precursors Human genes 0.000 claims 1
- 108010078762 Protein Precursors Proteins 0.000 claims 1
- 229940083082 Pyrimidine derivatives acting on arteriolar smooth muscle Drugs 0.000 claims 1
- 150000001242 acetic acid derivatives Chemical class 0.000 claims 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 239000003945 anionic surfactant Substances 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims 1
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- 229960000735 docosanol Drugs 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 150000003840 hydrochlorides Chemical class 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- 150000003903 lactic acid esters Chemical class 0.000 claims 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 1
- 230000000813 microbial Effects 0.000 claims 1
- 150000002829 nitrogen Chemical group 0.000 claims 1
- 230000033116 oxidation-reduction process Effects 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims 1
- 150000003217 pyrazoles Chemical class 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 150000003230 pyrimidines Chemical class 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 239000003638 reducing agent Substances 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 150000003899 tartaric acid esters Chemical class 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
Claims (1)
CH2= CR'CH2OBnR
в которой R' обозначает Н или СН3, В обозначает радикал этиленокси, n равно 0 или целому числу от 1 до 100, R обозначает углеводородный радикал, выбранный из алкила, арилалкила, арила, алкиларила, циклоалкила, содержащих от 8 до 30, преимущественно от 10 до 24 и, более предпочтительно, от 12 до 18 атомов углерода.9. The composition according to p. 1, characterized in that the link is simple allyl ether with a fatty chain is a monomer of the following formula I:
CH 2 = CR'CH 2 OB n R
in which R ′ is H or CH 3 , B is an ethyleneoxy radical, n is 0 or an integer from 1 to 100, R is a hydrocarbon radical selected from alkyl, arylalkyl, aryl, alkylaryl, cycloalkyl containing from 8 to 30, preferably from 10 to 24 and, more preferably, from 12 to 18 carbon atoms.
в которой R1 обозначает Н, СН3 или C2H5, а гидрофобное звено типа С10-С30-алкилового эфира ненасыщенной карбоновой кислоты представляет собой мономер приведенной ниже формулы III:
в которой R2 обозначает Н, СНз или C2H5, а R3 обозначает С10-С30-алкил, преимущественно С12-С22-алкил.11. The composition according to p. 10, characterized in that the hydrophilic unit type olefinically unsaturated carboxylic acid is a monomer of the following formula II:
in which R 1 denotes H, CH 3 or C 2 H 5 , and the hydrophobic unit of the type C 10 -C 30 -alkyl ester of unsaturated carboxylic acid is a monomer of the following formula III:
in which R 2 denotes H, CH3 or C 2 H 5 , and R 3 denotes C 10 -C 30 alkyl, preferably C 12 -C 22 alkyl.
(a) карбоновую кислоту с α,β-моноэтиленовой ненасыщенностью,
(b) отличный от (а) мономер с α,β-моноэтиленовой ненасыщенностью, не обладающий поверхностно-активными свойствами,
(c) неионный моноуретан, полученный реакцией одноосновного ПАВ с моноизоцианатом с моноэтиленовой ненасыщенностью.13. The composition according to p. 6, characterized in that the anionic thickening polymer with a fatty chain is an acrylic ternary copolymer containing:
(a) carboxylic acid with α, β-monoethylene unsaturation,
(b) a monomer other than (a) with α, β-monoethylene unsaturation, which does not have surface-active properties,
(c) non-ionic monourethane obtained by the reaction of a monobasic surfactant with monoethylenically unsaturated monoisocyanate.
(1) целлюлозы, модифицированные группами, содержащими по крайней мере одну жирную цепь;
(2) гидроксипропилгуары, модифицированные группами, содержащими по крайней мере одну жирную цепь 10-30 атомами углерода;
(3) полиуретаны - простые полиэфиры, содержащие в своей цепи полиоксиэтиленированные гидрофильные последовательности и одновременно гидрофобные последовательности, которые могут составлять только алифатические цепи и/или циклоалифатические цепи и/или ароматические цепи.15. The composition according to p. 6, characterized in that the non-ionic thickening polymer with a fatty chain is chosen from the group which includes:
(1) cellulose modified with groups containing at least one fatty chain;
(2) hydroxypropyl guars, modified by groups containing at least one fatty chain of 10-30 carbon atoms;
(3) polyurethanes are polyethers containing polyoxyethylenated hydrophilic sequences in their chains and at the same time hydrophobic sequences that can constitute only aliphatic chains and / or cycloaliphatic chains and / or aromatic chains.
(5) сополимеры C2-C6-алкилметакрилатов или C1-C6-алкилакрилатов с амфифильными мономерами, содержащими по крайней мере одну жирную цепь;
(6) сополимеры гидрофильных метакрилатов или акрилатов с гидрофобными мономерами, содержащими по крайней мере одну жирную цепь;
(7) полимеры со скелетом аминопласт-простой эфир, содержащие по крайней мере одну жирную цепь.(4) copolymers of vinylpyrrolidone and fatty chain hydrophobic monomers;
(5) copolymers of C 2 -C 6 alkyl methacrylates or C 1 -C 6 alkyl acrylates with amphiphilic monomers containing at least one fatty chain;
(6) copolymers of hydrophilic methacrylates or acrylates with hydrophobic monomers containing at least one fatty chain;
(7) polymers with an aminoplast-ether skeleton containing at least one fatty chain.
в которой R1 обозначает атом водорода, С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, С1-С4-алкокси-С1-С4-алкил или С1-С4-алкил, замещенный азотсодержащей группой, фенил или 4-аминофенил;
R2 обозначает атом водорода, С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, С1-С4-алкокси-С1-С4-алкил или С1-С4-алкил, замещенный азотсодержащей группой;
R1 и R2 могут образовывать вместе с атомом азота, с которым они связаны, 5- или 6-членный гетероцикл, который может быть замещен одной или несколькими группами алкила, гидрокси или уреидо;
R3 обозначает атом водорода, атом галогена, такого как хлор, С1-С4-алкил, сульфо, карбокси, моногидрокси-С1-С4-алкил или гидрокси-С1-С4-алкокси, ацетиламино-С1-С4-алкокси, мезил-амино-С1-С4-алкокси или карбамоиламино-С1-С4-алкокси; и
R4 обозначает атом водорода, галогена или С1-С4-алкильный радикал.23. The composition according to p. 22, characterized in that the p-phenylenediamine selected from compounds with the following structure I:
in which R 1 denotes a hydrogen atom, C 1 -C 4 -alkyl, monohydroxy-C 1 -C 4 -alkyl, polyhydroxy-C 2 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 - alkyl or C 1 -C 4 -alkyl substituted with a nitrogen-containing group, phenyl or 4-aminophenyl;
R 2 denotes a hydrogen atom, C 1 -C 4 -alkyl, monohydroxy-C 1 -C 4 -alkyl, polyhydroxy-C 2 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl or C 1 -C 4 -alkyl substituted with a nitrogen-containing group;
R 1 and R 2 may form, together with the nitrogen atom to which they are bound, a 5 or 6 membered heterocycle, which may be substituted with one or more alkyl, hydroxy or ureido groups;
R 3 represents a hydrogen atom, a halogen atom such as chlorine, C 1 -C 4 alkyl radical, sulfo, carboxy, monohydroxy C 1 -C 4 -alkyl or hydroxy-C 1 -C 4 alkoxy, acetylamino-C 1 - C 4 -alkoxy, mesyl-amino-C 1 -C 4 -alkoxy or carbamoylamino-C 1 -C 4 -alkoxy; and
R 4 denotes a hydrogen atom, halogen or a C 1 -C 4 -alkyl radical.
в которой: Z1 и Z2, одинаковые или разные, обозначают радикал гидроксил или -NH2, которые могут быть замещены С1-С4-алкилом или связкой Y;
связка Y обозначает линейную или разветвленную алкиленовую цепь с 1-14 атомами углерода, которая может быть прервана или завершена одной или несколькими азотсодержащими группами и/или одним или несколькими гетероатомами, такими как кислород, сера или азот, и, возможно, замещена одним или несколькими гидроксильными или С1-С6-алкокси-группами;
R5 и R6 обозначают атом водорода или галогена, С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, амино-С1-С4-алкил или связку Y;
R7, R8, R9, R10, R11 и R12, одинаковые или разные, обозначают атом водорода, связку Y или С1-С4-алкил; при условии, что соединения формулы II содержат только одну связку Y на молекулу.24. The composition according to p. 22, characterized in that the double bases are selected from compounds with the following structure II:
in which: Z 1 and Z 2 , which are the same or different, denote a hydroxyl or -NH 2 radical, which may be substituted with C 1 -C 4 alkyl or a bond Y;
the Y bond refers to a linear or branched alkylene chain with 1-14 carbon atoms, which may be interrupted or terminated by one or more nitrogen-containing groups and / or one or several heteroatoms, such as oxygen, sulfur or nitrogen, and may be substituted by one or several hydroxyl or C 1 -C 6 alkoxy groups;
R 5 and R 6 represent a hydrogen atom or a halogen, C 1 -C 4 -alkyl, mono-hydroxy-C 1 -C 4 -alkyl, polyhydroxy-C 2 -C 4 -alkyl, amino-C 1 -C 4 -alkyl or a bond Y;
R 7 , R 8 , R 9 , R 10 , R 11 and R 12 , which are the same or different, represent a hydrogen atom, a bond of Y or C 1 -C 4 -alkyl; provided that the compounds of formula II contain only one bundle of Y per molecule.
в которой R13 обозначает атом водорода или галогена, такого как фтор, С1-С4-алкил, моногидрокси-С1-С4-алкил, С1-С4-алкокси-С1-С4-алкил, амино-С1-С4-алкил или гидрокси-С1-С4-алкиламино-С1-С4-алкил,
R14 обозначает атом водорода или галогена, такого как фтор, С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, амино-С1-С4-алкил, циано-С1-С4-алкил или С1-С4-алкокси-С1-С4-алкил.26. The composition according to p. 22, characterized in that the p-aminophenols are selected from compounds of the structure III below:
in which R 13 denotes a hydrogen atom or a halogen, such as fluorine, C 1 -C 4 -alkyl, mono-hydroxy-C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy-C 1 -C 4 -alkyl, amino C 1 -C 4 -alkyl or hydroxy-C 1 -C 4 -alkylamino-C 1 -C 4 -alkyl,
R 14 denotes a hydrogen atom or a halogen, such as fluorine, C 1 -C 4 -alkyl, mono-hydroxy-C 1 -C 4 -alkyl, polyhydroxy-C 2 -C 4 -alkyl, amino-C 1 -C 4 -alkyl, cyano C 1 -C 4 alkyl or C 1 -C 4 alkoxy C 1 -C 4 alkyl.
44. Композиция по п. 42, отличающаяся тем, что катионный полимер представляет собой поли(четвертично-аммониевое) соединение, построенное из структурных звеньев, соответствующих приведенной ниже формуле U:
45. Композиция по п. 42, отличающаяся тем, что амфотерный полимер представляет собой сополимер, содержащий по меньшей мере один мономер акриловой кислоты и соль диметилдиаллиламмония.43. The composition according to p. 42, characterized in that the cationic polymer is a poly (quaternary ammonium) compound constructed from structural units corresponding to the following formula W:
44. The composition according to p. 42, characterized in that the cationic polymer is a poly (quaternary ammonium) compound, built of structural units corresponding to the following formula U:
45. The composition according to p. 42, characterized in that the amphoteric polymer is a copolymer containing at least one acrylic acid monomer and a dimethyldiallylammonium salt.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9916762 | 1999-12-30 | ||
FR9916762A FR2803197B1 (en) | 1999-12-30 | 1999-12-30 | COMPOSITION FOR OXIDATION DYEING OF KERATINIC FIBERS COMPRISING A THICKENING POLYMER COMPRISING AT LEAST ONE FATTY CHAIN AND A FATTY ALCOHOL HAVING MORE THAN TWENTY CARBON ATOMS |
Publications (2)
Publication Number | Publication Date |
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RU2000133183A true RU2000133183A (en) | 2002-11-10 |
RU2204989C2 RU2204989C2 (en) | 2003-05-27 |
Family
ID=9554073
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000133183/14A RU2204989C2 (en) | 1999-12-30 | 2000-12-28 | Composition for oxidizing dying of keratin fibers, comprising thickening polymer comprising at least one aliphatic chain, and fatty alcohol with at least twenty carbon atoms |
Country Status (17)
Country | Link |
---|---|
US (1) | US6436151B2 (en) |
EP (1) | EP1142555B1 (en) |
JP (1) | JP2001220330A (en) |
KR (1) | KR100416826B1 (en) |
CN (1) | CN100379401C (en) |
AR (1) | AR027109A1 (en) |
AT (1) | ATE353240T1 (en) |
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JP2001240520A (en) * | 1999-12-20 | 2001-09-04 | Lion Corp | Hair dye composition |
-
1999
- 1999-12-30 FR FR9916762A patent/FR2803197B1/en not_active Expired - Fee Related
-
2000
- 2000-12-11 ES ES00403470T patent/ES2281334T3/en not_active Expired - Lifetime
- 2000-12-11 PT PT00403470T patent/PT1142555E/en unknown
- 2000-12-11 AT AT00403470T patent/ATE353240T1/en not_active IP Right Cessation
- 2000-12-11 DK DK00403470T patent/DK1142555T3/en active
- 2000-12-11 EP EP00403470A patent/EP1142555B1/en not_active Expired - Lifetime
- 2000-12-11 DE DE60033277T patent/DE60033277T2/en not_active Expired - Lifetime
- 2000-12-14 AU AU72284/00A patent/AU749655B2/en not_active Ceased
- 2000-12-27 AR ARP000106936A patent/AR027109A1/en not_active Application Discontinuation
- 2000-12-27 BR BRPI0006551-0B1A patent/BR0006551B1/en active IP Right Grant
- 2000-12-27 CA CA002330342A patent/CA2330342A1/en not_active Abandoned
- 2000-12-27 BR BRPI0006551A patent/BRPI0006551B8/en unknown
- 2000-12-28 RU RU2000133183/14A patent/RU2204989C2/en not_active IP Right Cessation
- 2000-12-28 PL PL00344852A patent/PL344852A1/en not_active Application Discontinuation
- 2000-12-29 CN CNB001372564A patent/CN100379401C/en not_active Expired - Fee Related
- 2000-12-30 KR KR10-2000-0087154A patent/KR100416826B1/en not_active IP Right Cessation
-
2001
- 2001-01-02 US US09/750,718 patent/US6436151B2/en not_active Expired - Lifetime
- 2001-01-04 JP JP2001000251A patent/JP2001220330A/en active Pending
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