SK1112000A3 - Oxidation dyes, their use and method for coloring of human hairs - Google Patents

Oxidation dyes, their use and method for coloring of human hairs Download PDF

Info

Publication number: SK1112000A3
Authority: SK; Slovakia
Prior art keywords: methyl; amino; oxidative; aminophenol; hydrogen
Prior art date: 1997-07-31

Application number

SK111-2000A

Other languages

English (en)

Slovak (sk)

Inventor

Horst Hoeffkes

Dieter Schrader

Hiroshi Tanaka

Original Assignee

Henkel Kgaa

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1997-07-31

Filing date

1998-07-22

Publication date

2000-07-11

1998-07-22 Application filed by Henkel Kgaa filed Critical Henkel Kgaa

2000-07-11 Publication of SK1112000A3 publication Critical patent/SK1112000A3/sk

Links

239000000975 dye Substances 0.000 title claims abstract description 42
238000007254 oxidation reaction Methods 0.000 title claims abstract description 41
210000004209 hair Anatomy 0.000 title claims abstract description 34
230000003647 oxidation Effects 0.000 title claims abstract description 32
238000004040 coloring Methods 0.000 title claims description 19
238000000034 method Methods 0.000 title claims description 13
230000008878 coupling Effects 0.000 claims abstract description 33
238000010168 coupling process Methods 0.000 claims abstract description 33
238000005859 coupling reaction Methods 0.000 claims abstract description 33
150000003839 salts Chemical class 0.000 claims abstract description 20
150000001875 compounds Chemical class 0.000 claims abstract description 14
VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical class C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 claims abstract description 14
239000001257 hydrogen Substances 0.000 claims abstract description 12
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
150000002431 hydrogen Chemical class 0.000 claims abstract description 6
150000007522 mineralic acids Chemical class 0.000 claims abstract description 4
150000001768 cations Chemical class 0.000 claims abstract description 3
125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims abstract 2
239000000203 mixture Substances 0.000 claims description 43
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 33
230000001590 oxidative effect Effects 0.000 claims description 28
OQWWMUWGSBRNMA-UHFFFAOYSA-N 1-(2,4-diaminophenoxy)ethanol Chemical compound CC(O)OC1=CC=C(N)C=C1N OQWWMUWGSBRNMA-UHFFFAOYSA-N 0.000 claims description 23
229940113489 2,4-diaminophenoxyethanol Drugs 0.000 claims description 23
DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 18
239000003086 colorant Substances 0.000 claims description 16
OIPPWFOQEKKFEE-UHFFFAOYSA-N orcinol Chemical compound CC1=CC(O)=CC(O)=C1 OIPPWFOQEKKFEE-UHFFFAOYSA-N 0.000 claims description 14
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 12
238000004043 dyeing Methods 0.000 claims description 12
ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 11
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 11
239000002243 precursor Substances 0.000 claims description 11
MWKPYVXITDAZLL-UHFFFAOYSA-N 4-[3-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1N MWKPYVXITDAZLL-UHFFFAOYSA-N 0.000 claims description 9
JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 9
ASHGTJPOSUFTGB-UHFFFAOYSA-N 3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 claims description 8
102000011782 Keratins Human genes 0.000 claims description 7
108010076876 Keratins Proteins 0.000 claims description 7
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
239000000835 fiber Substances 0.000 claims description 6
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 6
XYRDGCCCBJITBH-UHFFFAOYSA-N 3-amino-2-chloro-6-methylphenol Chemical compound CC1=CC=C(N)C(Cl)=C1O XYRDGCCCBJITBH-UHFFFAOYSA-N 0.000 claims description 5
229940018563 3-aminophenol Drugs 0.000 claims description 5
WDQMXRWYXILWPT-UHFFFAOYSA-N 5-amino-4-chloro-2-methylphenol Chemical compound CC1=CC(Cl)=C(N)C=C1O WDQMXRWYXILWPT-UHFFFAOYSA-N 0.000 claims description 5
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 4
SYRZWFBWUASJJI-UHFFFAOYSA-N 3-amino-2,4-dichlorophenol Chemical compound NC1=C(Cl)C=CC(O)=C1Cl SYRZWFBWUASJJI-UHFFFAOYSA-N 0.000 claims description 4
GHVHDYYKJYXFGU-UHFFFAOYSA-N Beta-Orcinol Chemical compound CC1=CC(O)=C(C)C(O)=C1 GHVHDYYKJYXFGU-UHFFFAOYSA-N 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 claims description 4
229940018564 m-phenylenediamine Drugs 0.000 claims description 4
ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 claims description 4
WLFXSECCHULRRO-UHFFFAOYSA-N pyridine-2,6-diol Chemical compound OC1=CC=CC(O)=N1 WLFXSECCHULRRO-UHFFFAOYSA-N 0.000 claims description 4
OREUKLHWMRALGC-UHFFFAOYSA-N 1-methyl-2,3-dihydroindole-5,6-diol Chemical compound OC1=C(O)C=C2N(C)CCC2=C1 OREUKLHWMRALGC-UHFFFAOYSA-N 0.000 claims description 3
150000007524 organic acids Chemical class 0.000 claims description 3
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239000008365 aqueous carrier Substances 0.000 claims description 2
DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 claims description 2
239000000126 substance Substances 0.000 abstract description 9
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
-1 heterocyclic hydrazones Chemical class 0.000 description 21
125000004432 carbon atom Chemical group C* 0.000 description 20
239000000047 product Substances 0.000 description 16
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125000000217 alkyl group Chemical group 0.000 description 14
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OSVNQUBJWRJOER-UHFFFAOYSA-N Resorcinin Natural products CC(C)CCCCCCCCC1=C(O)C=C(CCCC(C)C)C=C1O OSVNQUBJWRJOER-UHFFFAOYSA-N 0.000 description 11
235000014113 dietary fatty acids Nutrition 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
239000000982 direct dye Substances 0.000 description 10
239000004094 surface-active agent Substances 0.000 description 10
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150000004665 fatty acids Chemical class 0.000 description 8
241001070941 Castanea Species 0.000 description 7
235000014036 Castanea Nutrition 0.000 description 7
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238000010186 staining Methods 0.000 description 7
ATCBPVDYYNJHSG-UHFFFAOYSA-N 6-methoxy-2-n-methylpyridine-2,3-diamine Chemical compound CNC1=NC(OC)=CC=C1N ATCBPVDYYNJHSG-UHFFFAOYSA-N 0.000 description 6
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
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150000002191 fatty alcohols Chemical class 0.000 description 6
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 5
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IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
125000002252 acyl group Chemical group 0.000 description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
238000009826 distribution Methods 0.000 description 5
239000007800 oxidant agent Substances 0.000 description 5
239000002453 shampoo Substances 0.000 description 5
BXBOXUNPNIJELB-UHFFFAOYSA-N 2,6-dimethoxypyridine-3,5-diamine Chemical compound COC1=NC(OC)=C(N)C=C1N BXBOXUNPNIJELB-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
244000208060 Lawsonia inermis Species 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
239000003093 cationic surfactant Substances 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
230000037308 hair color Effects 0.000 description 4
239000002563 ionic surfactant Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
239000001294 propane Substances 0.000 description 4
TXMQOPNBBITFNX-UHFFFAOYSA-N 2,3-dihydro-1h-indole-5,6-diol;hydrobromide Chemical compound Br.C1=C(O)C(O)=CC2=C1NCC2 TXMQOPNBBITFNX-UHFFFAOYSA-N 0.000 description 3
DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 3
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108010009736 Protein Hydrolysates Proteins 0.000 description 3
244000269722 Thea sinensis Species 0.000 description 3
150000001340 alkali metals Chemical class 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000010949 copper Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000009472 formulation Methods 0.000 description 3
235000011187 glycerol Nutrition 0.000 description 3
239000000118 hair dye Substances 0.000 description 3
150000002476 indolines Chemical class 0.000 description 3
229910021645 metal ion Inorganic materials 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
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ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 3
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OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003605 opacifier Substances 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
238000005691 oxidative coupling reaction Methods 0.000 description 1
229940101267 panthenol Drugs 0.000 description 1
229940055726 pantothenic acid Drugs 0.000 description 1
235000019161 pantothenic acid Nutrition 0.000 description 1
239000011713 pantothenic acid Substances 0.000 description 1
235000020957 pantothenol Nutrition 0.000 description 1
239000011619 pantothenol Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000002304 perfume Substances 0.000 description 1
108040007629 peroxidase activity proteins Proteins 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical group 0.000 description 1
QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
BTSZTGGZJQFALU-UHFFFAOYSA-N piroctone olamine Chemical compound NCCO.CC(C)(C)CC(C)CC1=CC(C)=CC(=O)N1O BTSZTGGZJQFALU-UHFFFAOYSA-N 0.000 description 1
229940081510 piroctone olamine Drugs 0.000 description 1
239000000419 plant extract Substances 0.000 description 1
229920001521 polyalkylene glycol ether Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
150000003142 primary aromatic amines Chemical class 0.000 description 1
239000003380 propellant Substances 0.000 description 1
235000018102 proteins Nutrition 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
ABYXFACYSGVHCW-UHFFFAOYSA-N pyridine-3,5-diamine Chemical compound NC1=CN=CC(N)=C1 ABYXFACYSGVHCW-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 1
229960002026 pyrithione Drugs 0.000 description 1
DQAKJEWZWDQURW-UHFFFAOYSA-N pyrrolidonecarboxylic acid Chemical class OC(=O)N1CCCC1=O DQAKJEWZWDQURW-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000002994 raw material Substances 0.000 description 1
235000002020 sage Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
210000004761 scalp Anatomy 0.000 description 1
HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
239000000344 soap Substances 0.000 description 1
229940057950 sodium laureth sulfate Drugs 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229940001941 soy protein Drugs 0.000 description 1
239000008347 soybean phospholipid Substances 0.000 description 1
239000012177 spermaceti Substances 0.000 description 1
229940084106 spermaceti Drugs 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
230000008961 swelling Effects 0.000 description 1
229920001864 tannin Polymers 0.000 description 1
239000001648 tannin Substances 0.000 description 1
235000018553 tannin Nutrition 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
NWKBFCIAPOSTKG-UHFFFAOYSA-M trimethyl-[3-[(3-methyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(=O)C1N=NC1=CC=CC([N+](C)(C)C)=C1 NWKBFCIAPOSTKG-UHFFFAOYSA-M 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
239000001993 wax Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
235000009529 zinc sulphate Nutrition 0.000 description 1
239000011686 zinc sulphate Substances 0.000 description 1
244000089265 zong er cha Species 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/63—Steroids; Derivatives thereof
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Photoreceptors In Electrophotography (AREA)
Indole Compounds (AREA)

SK111-2000A 1997-07-31 1998-07-22 Oxidation dyes, their use and method for coloring of human hairs SK1112000A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19732975A DE19732975A1 (de)	1997-07-31	1997-07-31	Färbemittel
PCT/EP1998/004604 WO1999006016A1 (fr)	1997-07-31	1998-07-22	Colorants

Publications (1)

Publication Number	Publication Date
SK1112000A3 true SK1112000A3 (en)	2000-07-11

Family

ID=7837471

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK111-2000A SK1112000A3 (en)	1997-07-31	1998-07-22	Oxidation dyes, their use and method for coloring of human hairs

Country Status (24)

Country	Link
US (1)	US6090161A (fr)
EP (1)	EP1001734B1 (fr)
JP (1)	JP2001511436A (fr)
KR (1)	KR20010022386A (fr)
CN (1)	CN1166354C (fr)
AR (1)	AR010936A1 (fr)
AT (1)	ATE276726T1 (fr)
AU (1)	AU734004B2 (fr)
BR (1)	BR9810854A (fr)
CA (1)	CA2297888A1 (fr)
CO (1)	CO4980864A1 (fr)
DE (2)	DE19732975A1 (fr)
EA (1)	EA002660B1 (fr)
EE (1)	EE200000061A (fr)
HR (1)	HRP20000044A2 (fr)
HU (1)	HUP0004794A3 (fr)
ID (1)	ID24296A (fr)
IS (1)	IS5364A (fr)
NZ (1)	NZ503087A (fr)
PL (1)	PL338382A1 (fr)
SK (1)	SK1112000A3 (fr)
TR (1)	TR200000271T2 (fr)
WO (1)	WO1999006016A1 (fr)
YU (1)	YU4200A (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6569211B2 (en)	1991-11-19	2003-05-27	Henkel Kommanditgesellschaft Auf Aktien	5,6-dihydroxyindolines as additives for hair dyeing preparations
FR2773478B1 (fr) *	1998-01-13	2000-02-25	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
HUP0102869A2 (hu) *	1998-06-23	2002-02-28	Henkel Kommanditgesellschaft Auf Aktien	Keratin szálak színezésére szolgáló festőanyag
JP4471051B2 (ja) *	1999-06-22	2010-06-02	ライオン株式会社	染毛剤組成物及びその製造方法
WO2001097756A2 (fr)	2000-06-20	2001-12-27	Henkel Kommanditgesellschaft Auf Aktien	Nouveaux composants copulants pour colorants d'oxydation
FR2814947B1 (fr) *	2000-10-09	2003-01-31	Oreal	Composition tinctoriale favorisant la pigmentation naturelle procede d'obtention et utilisation pour la coloration de la peau et/ou des fibres keratiniques
US6953486B2 (en)	2000-10-09	2005-10-11	L'oreal	Dyeing composition, method for obtaining the same and use for coloring the skin and/or keratinous fibres
FR2853230B1 (fr) *	2003-04-01	2005-06-17	Oreal	Composition de coloration pour matieres keratiniques humaines comprenant un colorant auto-oxydable, procede et utilisation
WO2006060569A2 (fr) *	2004-12-02	2006-06-08	The Procter & Gamble Company	Compositions de teintures capillaires eclaircissantes pour cheveux renforces par des polymeres
FR2915882A1 (fr) *	2007-05-09	2008-11-14	Oreal	Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine et un colorant particulier
WO2024162252A1 (fr)	2023-01-30	2024-08-08	花王株式会社	Méthode de coloration des cheveux

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4013494A (en) *	1974-06-17	1977-03-22	Minnesota Mining And Manufacturing Company	Tube forming method
DE3723354A1 (de) *	1987-07-15	1989-01-26	Henkel Kgaa	Sulfatierte hydroxy-mischether, verfahren zu ihrer herstellung und ihre verwendung
DE3725030A1 (de) *	1987-07-29	1989-02-09	Henkel Kgaa	Oberflaechenaktive hydroxysulfonate
US5180396A (en) *	1987-12-18	1993-01-19	L'oreal	Process for dyeing keratinous fibres with oxidation dyes combined with indole derivatives and dyeing composition employed
LU87086A1 (fr) *	1987-12-18	1989-07-07	Oreal	Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes au 5,6-dihydroxyindole et a un iodure et composition tinctoriale mise en oeuvre
LU87336A1 (fr) *	1988-09-12	1990-04-06	Oreal	Procede de teinture des fibres keratiniques avec un monohydroxyindole associe a un iodure et compositions mises en oeuvre
DE3926344A1 (de) *	1989-08-09	1991-02-28	Henkel Kgaa	Verfahren zur herstellung von hellfarbigen oelsaeuresulfonaten
DE4016177A1 (de) *	1990-05-19	1991-11-21	Henkel Kgaa	Oxidationsfaerbemittel fuer keratinfasern
FR2662701B1 (fr) *	1990-05-31	1997-07-18	Oreal	Composition tinctoriale a base de 5,6-dihydroxyindolines et procede de teinture des fibres keratiniques.
DE4137971A1 (de) *	1991-11-19	1993-05-27	Henkel Kgaa	5,6-dihydroxyindoline als additiv zu haarfaerberezepturen
DE4208297A1 (de) *	1992-03-16	1993-09-23	Henkel Kgaa	Faerben von keratinischen fasern mit indolinen unter metallkatalyse
US5413612A (en) *	1992-04-29	1995-05-09	Clairol Incorporated	Composition and method for dyeing hair with indolic compounds in the presence of a chlorite oxidant
CA2134461A1 (fr) *	1992-04-29	1993-11-11	Gottfried Wenke	Compositions de colorant capillaires a base de 5,6-dihydroxyindole et d'un oxydant de type chlorite, et methodes pour son utilisation
FR2692782B1 (fr) *	1992-06-25	1995-06-23	Oreal	Procede de teinture des fibres keratiniques avec des derives indoliques ou indoliniques, du peroxyde d'hydrogene et une peroxydase.
US5350424A (en) *	1992-10-13	1994-09-27	Combe Incorporated	Dyestuff composition for the gradual dyeing of hair by atmospheric oxidation and process using the same
US5792220A (en) *	1997-05-16	1998-08-11	Bristol-Myers Squibb Company	Dyeing hair with melanin procursors in the presence of iodate and peroxide

1997
- 1997-07-31 DE DE19732975A patent/DE19732975A1/de not_active Withdrawn
1998
- 1998-07-22 CN CNB988077809A patent/CN1166354C/zh not_active Expired - Fee Related
- 1998-07-22 DE DE59812004T patent/DE59812004D1/de not_active Expired - Lifetime
- 1998-07-22 BR BR9810854-9A patent/BR9810854A/pt not_active IP Right Cessation
- 1998-07-22 EP EP98942598A patent/EP1001734B1/fr not_active Expired - Lifetime
- 1998-07-22 EE EEP200000061A patent/EE200000061A/xx unknown
- 1998-07-22 NZ NZ503087A patent/NZ503087A/xx not_active IP Right Cessation
- 1998-07-22 JP JP2000504831A patent/JP2001511436A/ja active Pending
- 1998-07-22 YU YU4200A patent/YU4200A/sh unknown
- 1998-07-22 AU AU90677/98A patent/AU734004B2/en not_active Ceased
- 1998-07-22 HR HR20000044A patent/HRP20000044A2/hr not_active Application Discontinuation
- 1998-07-22 AT AT98942598T patent/ATE276726T1/de active
- 1998-07-22 HU HU0004794A patent/HUP0004794A3/hu unknown
- 1998-07-22 TR TR2000/00271T patent/TR200000271T2/xx unknown
- 1998-07-22 EA EA200000609A patent/EA002660B1/ru not_active IP Right Cessation
- 1998-07-22 KR KR1020007000965A patent/KR20010022386A/ko not_active Withdrawn
- 1998-07-22 PL PL98338382A patent/PL338382A1/xx unknown
- 1998-07-22 ID IDW20000169A patent/ID24296A/id unknown
- 1998-07-22 WO PCT/EP1998/004604 patent/WO1999006016A1/fr active IP Right Grant
- 1998-07-22 CA CA002297888A patent/CA2297888A1/fr not_active Abandoned
- 1998-07-22 SK SK111-2000A patent/SK1112000A3/sk unknown
- 1998-07-28 CO CO98042936A patent/CO4980864A1/es unknown
- 1998-07-31 AR ARP980103800A patent/AR010936A1/es not_active Application Discontinuation
- 1998-07-31 US US09/127,422 patent/US6090161A/en not_active Expired - Lifetime
2000
- 2000-01-27 IS IS5364A patent/IS5364A/is unknown

Also Published As

Publication number	Publication date
KR20010022386A (ko)	2001-03-15
AR010936A1 (es)	2000-07-12
CN1265578A (zh)	2000-09-06
EP1001734B1 (fr)	2004-09-22
ATE276726T1 (de)	2004-10-15
WO1999006016A1 (fr)	1999-02-11
DE19732975A1 (de)	1999-02-04
NZ503087A (en)	2001-01-26
PL338382A1 (en)	2000-10-23
EA200000609A1 (ru)	2000-12-25
EA002660B1 (ru)	2002-08-29
HUP0004794A2 (hu)	2001-05-28
BR9810854A (pt)	2000-07-25
HRP20000044A2 (en)	2001-02-28
AU734004B2 (en)	2001-05-31
CA2297888A1 (fr)	1999-02-11
AU9067798A (en)	1999-02-22
ID24296A (id)	2000-07-13
CN1166354C (zh)	2004-09-15
EP1001734A1 (fr)	2000-05-24
DE59812004D1 (de)	2004-10-28
JP2001511436A (ja)	2001-08-14
CO4980864A1 (es)	2000-11-27
US6090161A (en)	2000-07-18
TR200000271T2 (tr)	2000-09-21
YU4200A (sh)	2002-09-19
EE200000061A (et)	2000-10-16
HUP0004794A3 (en)	2002-11-28
HK1029523A1 (en)	2001-04-06
IS5364A (is)	2000-01-27

Publication	Publication Date	Title
JP4140806B2 (ja)	2008-08-27	ケラチン繊維用の染色製剤
HUP0001491A2 (hu)	2000-09-28	Új 1,4-diazacikloheptán-származékok és ezeknek az alkalmazása oxidációs hajfestő szerekben
EP1239817B1 (fr)	2006-04-19	Utilisation de composes de methylquinolinium pour colorer des fibres keratiniques
SK1112000A3 (en)	2000-07-11	Oxidation dyes, their use and method for coloring of human hairs
CZ274698A3 (cs)	1999-03-17	Použití aminofenolových derivátů a oxidační barvicí prostředky
EP0873746A2 (fr)	1998-10-28	Agent de teinture pour les fibres kératiniques
DE19859750A1 (de)	2000-06-29	Mittel zum Färben von keratinhaltigen Fasern
WO2000038631A1 (fr)	2000-07-06	Agents permettant de colorer les fibres de keratine
JP2003506386A (ja)	2003-02-18	ケラチン繊維染色製剤
US6743263B1 (en)	2004-06-01	Method for coloring keratin fibers
EP0832640B1 (fr)	2008-04-30	Composition de teinture d'oxydation des fibres kératiniques
EP1037592B2 (fr)	2015-08-19	Nouvelles combinaisons d'agents de developpement pour colorants d'oxydation
SK9152000A3 (en)	2000-11-07	Novel p-aminophenol derivatives, an oxidative colorant containing them and the use thereof
EP1139991B1 (fr)	2002-08-28	Agent pour la coloration de fibres keratiniques
EP1194116B1 (fr)	2005-05-04	Agent de coloration de fibres contenant de la keratine
DE19859809A1 (de)	2000-06-29	Mittel zum Färben von keratinhaltigen Fasern
DE19826457A1 (de)	1999-12-16	Neue 2,4-Diaminophenolderivate und deren Verwendung
EP0979064B1 (fr)	2004-07-28	Colorants d'oxydation
CZ2000353A3 (cs)	2000-07-12	Oxidační prostředek pro barvení
MXPA00000989A (en)	2001-05-07	Dyes
DE19826456A1 (de)	1999-12-16	Neue 3,4-Diaminophenolderivate und deren Verwendung
DE19746249A1 (de)	1999-04-22	Neue Aminophenol-Derivate und deren Verwendung
CZ374099A3 (cs)	2000-04-12	Použití nenasycených aldehydů
CZ20004874A3 (cs)	2001-06-13	Prostředek pro barvení keratinových látek