RU2000133186A - COMPOSITION FOR OXIDATIVE DYEING OF KERATIN FIBERS CONTAINING A CONSTANTING POLYMER CONTAINING A LESS MEASURING ONE FAT CHAIN AND ONE FAT MONO-GOLIES GODS. - Google Patents
COMPOSITION FOR OXIDATIVE DYEING OF KERATIN FIBERS CONTAINING A CONSTANTING POLYMER CONTAINING A LESS MEASURING ONE FAT CHAIN AND ONE FAT MONO-GOLIES GODS.Info
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- RU2000133186A RU2000133186A RU2000133186/14A RU2000133186A RU2000133186A RU 2000133186 A RU2000133186 A RU 2000133186A RU 2000133186/14 A RU2000133186/14 A RU 2000133186/14A RU 2000133186 A RU2000133186 A RU 2000133186A RU 2000133186 A RU2000133186 A RU 2000133186A
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- 239000000203 mixture Substances 0.000 title claims 77
- 229920000642 polymer Polymers 0.000 title claims 24
- 239000000835 fiber Substances 0.000 title claims 15
- 102000011782 Keratins Human genes 0.000 title claims 13
- 108010076876 Keratins Proteins 0.000 title claims 13
- 230000001590 oxidative Effects 0.000 title claims 13
- 238000004043 dyeing Methods 0.000 title claims 10
- 239000002585 base Substances 0.000 claims 9
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 8
- 239000007800 oxidant agent Substances 0.000 claims 8
- 125000000129 anionic group Chemical group 0.000 claims 7
- 125000004432 carbon atoms Chemical group C* 0.000 claims 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 7
- 125000002091 cationic group Chemical group 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 239000000975 dye Substances 0.000 claims 6
- -1 ethyleneoxy Chemical group 0.000 claims 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 6
- 229920001577 copolymer Polymers 0.000 claims 5
- 230000002209 hydrophobic Effects 0.000 claims 5
- 125000005647 linker group Chemical group 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 5
- 229920000223 polyglycerol Polymers 0.000 claims 5
- 150000002191 fatty alcohols Chemical class 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 239000004094 surface-active agent Substances 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 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
- 239000001913 cellulose Substances 0.000 claims 3
- 229920002678 cellulose Polymers 0.000 claims 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 229920002635 polyurethane Polymers 0.000 claims 3
- 239000004814 polyurethane 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
- 239000004215 Carbon black (E152) Substances 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
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive Effects 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 238000004040 coloring Methods 0.000 claims 2
- 230000000875 corresponding Effects 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
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 230000001264 neutralization Effects 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 229920001897 terpolymer Polymers 0.000 claims 2
- APXRHPDHORGIEB-UHFFFAOYSA-N 1H-pyrazolo[4,3-d]pyrimidine Chemical class N1=CN=C2C=NNC2=C1 APXRHPDHORGIEB-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
- 108090000790 Enzymes Proteins 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 229920002907 Guar gum Polymers 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical class COC(=O)C=C BAPJBEWLBFYGME-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
- 102000003992 Peroxidases Human genes 0.000 claims 1
- 108090000437 Peroxidases Proteins 0.000 claims 1
- 229940083082 Pyrimidine derivatives acting on arteriolar smooth muscle Drugs 0.000 claims 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 1
- 150000001242 acetic acid derivatives Chemical class 0.000 claims 1
- 150000001298 alcohols 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
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000003277 amino 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
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000004429 atoms 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000007822 coupling agent Substances 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- 125000001033 ether group Chemical group 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical group 0.000 claims 1
- 239000000665 guar gum Substances 0.000 claims 1
- 229960002154 guar gum Drugs 0.000 claims 1
- 235000010417 guar gum Nutrition 0.000 claims 1
- 125000005842 heteroatoms Chemical group 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 150000003903 lactic acid esters Chemical class 0.000 claims 1
- 230000000813 microbial Effects 0.000 claims 1
- 239000002736 nonionic surfactant 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
- 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
- 125000002924 primary amino group Chemical group [H]N([H])* 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
- 239000003638 reducing agent Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 239000011347 resin 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)
RO-(-CH2-CH(CH2OH)-O-)n-H
в которой R означает насыщенный или ненасыщенный, линейный или разветвленный, содержащий от 8 до 40 атомов углерода радикал;
n означает число, равное от 1 до 30.2. The composition according to p. 1, characterized in that the fatty mono - or polyglycerol alcohol has the following formula:
RO - (- CH 2 -CH (CH 2 OH) -O-) n -H
in which R is saturated or unsaturated, linear or branched, containing from 8 to 40 carbon atoms;
n means a number equal to from 1 to 30.
СН2 = CR' CH2 О BnR,
в которой R' означает Н или СН3, В означает этиленокси, n равно нулю или означает целое число от 1 до 100, R означает углеводородный радикал, выбранный из радикалов алкил, арилалкил, арил, алкиларил, циклоалкил, содержащий от 8 до 30 атомов углерода, предпочтительно от 10 до 24, и предпочтительнее, от 12 до 18 атомов углерода.9. The composition according to p. 7, characterized in that the link allyl ether with a fatty chain corresponds to the following formula (I):
CH 2 = CR 'CH 2 About Bn R,
in which R ′ is H or CH 3 , B is ethyleneoxy, n is zero or an integer from 1 to 100, R is a hydrocarbon radical selected from alkyl radicals, arylalkyl, aryl, alkylaryl, cycloalkyl containing from 8 to 30 atoms carbon, preferably from 10 to 24, and preferably, from 12 to 18 carbon atoms.
в которой R1 означает Н или СН3 или C2H5, а гидрофобное звено типа сложного (С10-С30)-алкилового эфира ненасыщенной карбоновой кислоты представляет собой мономер следующей формулы (III):
в которой R2 означает Н или СН3 или C2H5, R3 означает радикал алкил с 10-30 атомами углерода, а предпочтительнее с 12-22 атомами углерода.11. The composition according to p. 10, characterized in that the hydrophilic link of the type of olefinic unsaturated carboxylic acid is a monomer of the following formula (II):
in which R 1 means H or CH 3 or C 2 H 5 , and the hydrophobic unit of the complex (C 10 -C 30 ) -alkyl ester of the unsaturated carboxylic acid is a monomer of the following formula (III):
in which R 2 means H or CH 3 or C 2 H 5 , R 3 means an alkyl radical with 10-30 carbon atoms, and more preferably with 12-22 carbon atoms.
(а) α, β-моноэтиленненасыщенную карбоновую кислоту,
(б) α, β-моноэтиленненасыщенный мономер, отличающийся от (а) и не являющийся поверхностно-активным веществом,
(с) неионный моноуретан, полученный в результате реакции одноосновного поверхностно-активного вещества с моно-этиленненасыщенным моноизоцианатом.13. The composition according to p. 6, characterized in that the anionic thickening polymer with a fat chain is an acrylic terpolymer, including:
(a) α, β-monoethylenically unsaturated carboxylic acid,
(b) α, β-monoethylenically unsaturated monomer, different from (a) and not a surface-active substance,
(c) a non-ionic monourethane obtained by the reaction of a monobasic surfactant with a mono-ethylenically unsaturated monoisocyanate.
(1) целлюлозы, модифицированные группами, содержащими, по меньшей мере, одну жирную цепь;
(2) гидроксипропилгуаровые смолы, модифицированные группами, содержащими, по меньшей мере, одну жирную цепь,
(3) полиэфир-полиуретаны, содержащие в своей цепи одновременно гидрофильные звенья полиоксиэтилированного типа и гидрофобные звенья, которые представляют собой одни алифатические последовательности и/или циклоалифатические и/или ароматические последовательности;
(4) сополимеры винилпирролидона и гидрофобных мономеров с жирной цепью;
(5) сополимеры (C1-C6)-алкилметакрилатов или -акрилатов и амфифильных мономеров, содержащих, по меньшей мере, одну жирную цепь;
(6) сополимеры гидрофильных метилакрилатов или акрилатов и гидрофобных мономеров, содержащих, по меньшей мере, одну жирную цепь;
(7) полимеры со структурой эфира аминопласта, содержащего, по меньшей мере, одну жирную цепь.15. The composition according to p. 6, characterized in that the non-ionic thickening polymer with a fat chain is selected in the group containing:
(1) cellulose modified with groups containing at least one fatty chain;
(2) hydroxypropylguar gums modified with groups containing at least one fatty chain,
(3) polyether-polyurethanes, containing simultaneously hydrophilic units of polyoxyethylated type and hydrophobic units, which are aliphatic sequences and / or cycloaliphatic and / or aromatic sequences;
(4) copolymers of vinylpyrrolidone and fatty chain hydrophobic monomers;
(5) copolymers of (C 1 -C 6 ) alkyl methacrylates or acrylates and amphiphilic monomers containing at least one fatty chain;
(6) copolymers of hydrophilic methyl acrylates or acrylates and hydrophobic monomers containing at least one fatty chain;
(7) polymers with an aminoplast ether structure, containing at least one fatty chain.
в которой R1 означает атом водорода, радикал С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, (C1-C4)-алкокси-(C1-C4)-алкил,
С1-С4-алкил, замещенный азотсодержащей группой, фенильной или 4'-аминофенильной;
R2 означает атом водорода, радикал С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, (C1-C4)-алкокси-(C1-C4)-алкил или С1-С4-алкил, замещенный азотсодержащей группой;
R1 и R2 могут также вместе с азотом, который их содержит, образовывать азотсодержащий гетероцикл с 5 или 6 звеньями, возможно, замещенный одной или несколькими группами алкил, гидрокси или уреидо;
R3 означает атом водорода, атом галогена, такой как атом хлора, радикал С1-С4-алкил, сульфо, карбокси, моногид-рокси-С1-С4-алкил или гидрокси-С1-С4-алкокси, ацетиламино-С1-С4-алкокси, мезиламино-С1-С4-алкокси или карбамоиламино-С1-С4-алкокси,
R4 означает атом водорода, галогена или радикал C1-C4-алкил.23. The composition according to p. 22, characterized in that the paraphenylenediamine selected from compounds of formula (I):
in which R 1 means a hydrogen atom, a radical 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,
C 1 -C 4 -alkyl substituted with a nitrogen-containing group, phenyl or 4'-aminophenyl;
R 2 means a hydrogen atom, a C 1 -C 4 -alkyl radical, mono-hydroxy-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 can also, together with the nitrogen that contains them, form a nitrogen-containing heterocycle with 5 or 6 units, possibly substituted by one or more alkyl, hydroxy or ureido groups;
R 3 means a hydrogen atom, a halogen atom such as a chlorine atom, a 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, mesylamino-C 1 -C 4 -alkoxy or carbamoylamino-C 1 -C 4 -alkoxy,
R 4 means a hydrogen atom, a halogen or a C 1 -C 4 -alkyl radical.
в которой Z1 и Z2, идентичные или разные, представляют радикал гидроксил или -NH2, который может быть замещен радикалом С1-С4-алкил или связующую группу Y;
связующая группа Y означает линейную или разветвленную алкиленовую цепь, содержащую от 1 до 14 атомов углерода, которая может прерываться или заканчиваться одной или несколькими азотсодержащими группами и/или одним или несколькими гетероатомами, такими как атомы кислорода, серы или азота, и, при необходимости, замещенную одним или несколькими радикалами гидроксил или С1-С6-алкокси;
R5 и R6 означают атом водорода или галогена, радикал С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, амино-С1-С4-алкил или связующую группу Y;
R7, R8, R9, R10, R11 и R12, одинаковые или разные, означают атом водорода, связующую группу Y или радикал C1-C4-алкил;
при этом соединения формулы (II) содержат только одну связующую группу Y на молекулу.24. The composition according to p. 22, characterized in that the double bases are selected from compounds of the following formula (II):
in which Z 1 and Z 2 , identical or different, represent a hydroxyl or -NH 2 radical, which may be substituted with a C 1 -C 4 -alkyl radical or a linking group Y;
linking group Y means a linear or branched alkylene chain containing from 1 to 14 carbon atoms, which may be interrupted or terminated by one or more nitrogen-containing groups and / or one or more heteroatoms, such as oxygen, sulfur or nitrogen, and, if necessary, hydroxyl or C 1 -C 6 alkoxy substituted with one or more radicals;
R 5 and R 6 mean a hydrogen atom or halogen, a C 1 -C 4 -alkyl radical, a mono-hydroxy-C 1 -C 4 -alkyl, polyhydroxy-C 2 -C 4 -alkyl, amino-C 1 -C 4 -alkyl or linking group 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 linking group Y or a C 1 -C 4 -alkyl radical;
however, the compounds of formula (II) contain only one linking group Y per molecule.
в которой R13 означает атом водорода, атом галогена, такой как фтор, радикал С1-С4-алкил, моногидрокси-С1-С4-алкил, (С1-С4)-алкокси-(С1-С4) -алкил или амино-С1-С4-алкил, или гидрокси-С1-С4-алкиламино-С1-С4-алкил; R14 означает атом водорода или атом галогена, такой как фтор, радикал С1-С4-алкил, моногидрокси-С1-С4-алкил, полигидрокси-С2-С4-алкил, амино-С1-С4-алкиал, циано-С1-С4-алкил или (С1-С4)-алкокси-(С1-С4)-алкил. 27. Композиция по п. 22, отличающаяся тем, что гетероциклические основания выбраны из пиридиновых производных, пиримидиновых производных, а именно, пиразолопиримидины, и пиразоловых производных.26. The composition according to p. 22, characterized in that the para-aminophenols selected from compounds of the following formula (III):
in which R 13 means a hydrogen atom, a halogen atom such as fluorine, a C 1 -C 4 -alkyl radical, a mono-hydroxy-C 1 -C 4 -alkyl, (C 1 -C 4 ) -alkoxy- (C 1 -C 4 -alkyl or amino-C 1 -C 4 -alkyl, or hydroxy-C 1 -C 4 -alkylamino-C 1 -C 4 -alkyl; R 14 means a hydrogen atom or a halogen atom, such as fluorine, a C 1 -C 4 -alkyl radical, 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. 27. The composition according to p. 22, characterized in that the heterocyclic bases are selected from pyridine derivatives, pyrimidine derivatives, namely, pyrazolopyrimidines, and pyrazole derivatives.
43. Композиция по п. 41, отличающаяся тем, что катионным полимером является четвертичный полиаммоний, состоящий из повторяющихся звеньев, отвечающих формуле (U):
44. Композиция по п. 41, отличающаяся тем, что амфотерным полимером является сополимер, содержащий, по меньшей мере, один мономер акриловой кислоты и одну соль диметилдиаллиламмония.42. The composition according to p. 41, characterized in that the cationic polymer is a Quaternary polyammonium, consisting of repeating units corresponding to the formula (W):
43. The composition according to p. 41, characterized in that the cationic polymer is a Quaternary polyammonium, consisting of repeating units corresponding to the formula (U):
44. The composition according to p. 41, wherein the amphoteric polymer is a copolymer containing at least one acrylic acid monomer and one dimethyldiallylammonium salt.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9916757A FR2803195B1 (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 SINGLE- OR POLY-GLYCEROLE FATTY ALCOHOL |
FR9916757 | 1999-12-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000133186A true RU2000133186A (en) | 2002-11-10 |
RU2207840C2 RU2207840C2 (en) | 2003-07-10 |
Family
ID=9554067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000133186/14A RU2207840C2 (en) | 1999-12-30 | 2000-12-28 | Composition comprising thickening polymer with at least one saturated chain and one saturated mono- or polyglycerol alcohol for oxidative staining keratin fiber |
Country Status (16)
Country | Link |
---|---|
US (3) | US20010023514A1 (en) |
EP (1) | EP1142556B1 (en) |
JP (2) | JP4025020B2 (en) |
KR (1) | KR100416825B1 (en) |
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-
1999
- 1999-12-30 FR FR9916757A patent/FR2803195B1/en not_active Expired - Lifetime
-
2000
- 2000-12-11 DE DE60037720T patent/DE60037720T2/en not_active Expired - Lifetime
- 2000-12-11 PT PT00403471T patent/PT1142556E/en unknown
- 2000-12-11 ES ES00403471T patent/ES2299419T3/en not_active Expired - Lifetime
- 2000-12-11 EP EP00403471A patent/EP1142556B1/en not_active Expired - Lifetime
- 2000-12-11 AT AT00403471T patent/ATE383183T1/en active
- 2000-12-14 AU AU72283/00A patent/AU751648B2/en not_active Ceased
- 2000-12-21 CA CA002329839A patent/CA2329839C/en not_active Expired - Fee Related
- 2000-12-22 BR BRPI0006588-9B1A patent/BR0006588B1/en active IP Right Grant
- 2000-12-27 AR ARP000106934A patent/AR027909A1/en not_active Application Discontinuation
- 2000-12-28 PL PL344853A patent/PL200242B1/en not_active IP Right Cessation
- 2000-12-28 RU RU2000133186/14A patent/RU2207840C2/en not_active IP Right Cessation
- 2000-12-29 CN CNB00137270XA patent/CN100536815C/en not_active Expired - Lifetime
- 2000-12-30 KR KR10-2000-0087148A patent/KR100416825B1/en not_active IP Right Cessation
-
2001
- 2001-01-02 US US09/750,716 patent/US20010023514A1/en not_active Abandoned
- 2001-01-04 JP JP2001000249A patent/JP4025020B2/en not_active Expired - Lifetime
-
2004
- 2004-10-07 US US10/959,486 patent/US20050076458A1/en not_active Abandoned
-
2007
- 2007-07-23 JP JP2007190780A patent/JP2007262101A/en not_active Withdrawn
-
2009
- 2009-02-23 US US12/390,879 patent/US7771492B2/en not_active Expired - Fee Related
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