ZA200108983B - Oxidation dyeing composition for keratinous fibres and dyeing method using the same. - Google Patents
Oxidation dyeing composition for keratinous fibres and dyeing method using the same. Download PDFInfo
- Publication number
- ZA200108983B ZA200108983B ZA200108983A ZA200108983A ZA200108983B ZA 200108983 B ZA200108983 B ZA 200108983B ZA 200108983 A ZA200108983 A ZA 200108983A ZA 200108983 A ZA200108983 A ZA 200108983A ZA 200108983 B ZA200108983 B ZA 200108983B
- Authority
- ZA
- South Africa
- Prior art keywords
- para
- phenylenediamine
- amino
- bis
- methyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 43
- 238000004043 dyeing Methods 0.000 title claims description 23
- 230000003647 oxidation Effects 0.000 title claims description 18
- 238000007254 oxidation reaction Methods 0.000 title claims description 18
- 238000000034 method Methods 0.000 title claims description 6
- -1 alkylene radical Chemical class 0.000 claims description 65
- 150000003254 radicals Chemical class 0.000 claims description 44
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 125000000623 heterocyclic group Chemical group 0.000 claims description 36
- 229910052757 nitrogen Inorganic materials 0.000 claims description 35
- 239000002253 acid Substances 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 31
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 23
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 150000005840 aryl radicals Chemical class 0.000 claims description 18
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical class NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Chemical group 0.000 claims description 6
- WNYJRJRHKRZXEO-UHFFFAOYSA-N 2-propan-2-ylbenzene-1,4-diamine Chemical compound CC(C)C1=CC(N)=CC=C1N WNYJRJRHKRZXEO-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 230000001590 oxidative effect Effects 0.000 claims description 5
- 239000001301 oxygen Chemical group 0.000 claims description 5
- GZVVXXLYQIFVCA-UHFFFAOYSA-N 2,3-dimethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=CC=C1N GZVVXXLYQIFVCA-UHFFFAOYSA-N 0.000 claims description 4
- KEEQZNSCYCPKOJ-UHFFFAOYSA-N 2,6-diethylbenzene-1,4-diamine Chemical compound CCC1=CC(N)=CC(CC)=C1N KEEQZNSCYCPKOJ-UHFFFAOYSA-N 0.000 claims description 4
- MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 claims description 4
- BLIZPKXNRQDIID-UHFFFAOYSA-N 2-methyl-4-(2-methylazepan-1-yl)aniline Chemical compound CC1CCCCCN1C1=CC=C(N)C(C)=C1 BLIZPKXNRQDIID-UHFFFAOYSA-N 0.000 claims description 4
- UZQJQJNKYMSTCP-UHFFFAOYSA-N 4-(4-methylpiperidin-1-yl)aniline Chemical compound C1CC(C)CCN1C1=CC=C(N)C=C1 UZQJQJNKYMSTCP-UHFFFAOYSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical group O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- JUJVNTRWJQHLEI-UHFFFAOYSA-N 2-[1-(4-aminophenyl)piperidin-2-yl]ethanol Chemical compound C1=CC(N)=CC=C1N1C(CCO)CCCC1 JUJVNTRWJQHLEI-UHFFFAOYSA-N 0.000 claims description 3
- PBKSTGOYDKJISC-UHFFFAOYSA-N 4-(2,7-dimethylazepan-1-yl)aniline Chemical compound CC1CCCCC(C)N1C1=CC=C(N)C=C1 PBKSTGOYDKJISC-UHFFFAOYSA-N 0.000 claims description 3
- NUDWEEWTZMRVEQ-UHFFFAOYSA-N [2-amino-5-(3-hydroxyazepan-1-yl)phenyl]urea Chemical compound C1=C(N)C(NC(=O)N)=CC(N2CC(O)CCCC2)=C1 NUDWEEWTZMRVEQ-UHFFFAOYSA-N 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- NKNCGBHPGCHYCQ-UHFFFAOYSA-N (2,5-diaminophenyl)methanol Chemical compound NC1=CC=C(N)C(CO)=C1 NKNCGBHPGCHYCQ-UHFFFAOYSA-N 0.000 claims description 2
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical compound O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 claims description 2
- OPVLNFDJMGKVLT-UHFFFAOYSA-N 1,2,2-trimethyl-4-trimethylsilyloxy-3,4-dihydroquinolin-6-amine Chemical compound C1=C(N)C=C2C(O[Si](C)(C)C)CC(C)(C)N(C)C2=C1 OPVLNFDJMGKVLT-UHFFFAOYSA-N 0.000 claims description 2
- DMOJFMSIAIUEBK-UHFFFAOYSA-N 1-(4-amino-3-methylphenyl)-5-methylpyrrolidin-3-ol Chemical compound CC1CC(O)CN1C1=CC=C(N)C(C)=C1 DMOJFMSIAIUEBK-UHFFFAOYSA-N 0.000 claims description 2
- GWNVVNCBLQDFMB-UHFFFAOYSA-N 1-N-[2-[2-(2-phenylmethoxyethoxy)ethoxy]ethyl]-2-propan-2-ylbenzene-1,4-diamine Chemical compound C(C1=CC=CC=C1)OCCOCCOCCNC1=C(C=C(C=C1)N)C(C)C GWNVVNCBLQDFMB-UHFFFAOYSA-N 0.000 claims description 2
- BWAPJIHJXDYDPW-UHFFFAOYSA-N 2,5-dimethyl-p-phenylenediamine Chemical compound CC1=CC(N)=C(C)C=C1N BWAPJIHJXDYDPW-UHFFFAOYSA-N 0.000 claims description 2
- XKXRQLPWQOIVCY-UHFFFAOYSA-N 2-(5-amino-6-methyl-2,3-dihydroindol-1-yl)ethanol Chemical compound C1=C(N)C(C)=CC2=C1CCN2CCO XKXRQLPWQOIVCY-UHFFFAOYSA-N 0.000 claims description 2
- OMTAKASKFZRZNT-UHFFFAOYSA-N 2-(6-amino-2,2,4-trimethyl-3,4-dihydroquinolin-1-yl)ethylurea Chemical compound C1=C(N)C=C2C(C)CC(C)(C)N(CCNC(N)=O)C2=C1 OMTAKASKFZRZNT-UHFFFAOYSA-N 0.000 claims description 2
- ZNMLQKPOMKCZJB-UHFFFAOYSA-N 2-(6-amino-3,4-dihydro-2h-quinolin-1-yl)ethanethiol Chemical compound SCCN1CCCC2=CC(N)=CC=C21 ZNMLQKPOMKCZJB-UHFFFAOYSA-N 0.000 claims description 2
- FFNRMTIRPOBSCZ-UHFFFAOYSA-N 2-[2-(6-amino-2,2-dimethyl-3,4-dihydroquinolin-1-yl)ethoxy]ethanol Chemical compound NC1=CC=C2N(CCOCCO)C(C)(C)CCC2=C1 FFNRMTIRPOBSCZ-UHFFFAOYSA-N 0.000 claims description 2
- RUMWFEBHCCEJOL-UHFFFAOYSA-N 2-[2-[2-(5-amino-2,3-dihydroindol-1-yl)ethoxy]ethoxy]ethanol Chemical compound NC1=CC=C2N(CCOCCOCCO)CCC2=C1 RUMWFEBHCCEJOL-UHFFFAOYSA-N 0.000 claims description 2
- WLZBCQIGDVVETM-UHFFFAOYSA-N 2-[2-[2-[2-(4-amino-2-propan-2-ylanilino)ethoxy]ethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCOCCNC1=C(C=C(C=C1)N)C(C)C WLZBCQIGDVVETM-UHFFFAOYSA-N 0.000 claims description 2
- SBNGOHZRTZAFKP-UHFFFAOYSA-N 2-[2-[2-[2-[6-amino-4-(hydroxymethyl)-2,2-dimethyl-7-propan-2-yl-3,4-dihydroquinolin-1-yl]ethoxy]ethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCOCCN1C(C)(C)CC(CO)C2=C1C=C(C(C)C)C(N)=C2 SBNGOHZRTZAFKP-UHFFFAOYSA-N 0.000 claims description 2
- FXFTWEVIIHVHDS-UHFFFAOYSA-N 2-fluorobenzene-1,4-diamine Chemical compound NC1=CC=C(N)C(F)=C1 FXFTWEVIIHVHDS-UHFFFAOYSA-N 0.000 claims description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 2
- DEVIZNZNRWPPRE-UHFFFAOYSA-N 3-[6-amino-4-(hydroxymethyl)-2,2-dimethyl-7-propan-2-yl-3,4-dihydroquinolin-1-yl]propan-1-ol Chemical compound OCCCN1C(C)(C)CC(CO)C2=C1C=C(C(C)C)C(N)=C2 DEVIZNZNRWPPRE-UHFFFAOYSA-N 0.000 claims description 2
- WLZJOYOSPWZDLH-UHFFFAOYSA-N 4-(2,7-dimethylazepan-1-yl)-2-methylsulfanylaniline Chemical compound C1=C(N)C(SC)=CC(N2C(CCCCC2C)C)=C1 WLZJOYOSPWZDLH-UHFFFAOYSA-N 0.000 claims description 2
- POKISONDDBRXBK-UHFFFAOYSA-N 4-n,4-n,2-trimethylbenzene-1,4-diamine Chemical compound CN(C)C1=CC=C(N)C(C)=C1 POKISONDDBRXBK-UHFFFAOYSA-N 0.000 claims description 2
- XBTWVJKPQPQTDW-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(C)=C1 XBTWVJKPQPQTDW-UHFFFAOYSA-N 0.000 claims description 2
- QNGVNLMMEQUVQK-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C=C1 QNGVNLMMEQUVQK-UHFFFAOYSA-N 0.000 claims description 2
- UOWYGPTYSRURDP-UHFFFAOYSA-N 4-n,4-n-dipropylbenzene-1,4-diamine Chemical compound CCCN(CCC)C1=CC=C(N)C=C1 UOWYGPTYSRURDP-UHFFFAOYSA-N 0.000 claims description 2
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 claims description 2
- FBTMLRHNYWHNHH-UHFFFAOYSA-N 6-amino-1,2,2,4,7-pentamethyl-3,4-dihydroquinolin-3-ol Chemical compound CC1=C(N)C=C2C(C)C(O)C(C)(C)N(C)C2=C1 FBTMLRHNYWHNHH-UHFFFAOYSA-N 0.000 claims description 2
- PVJVEVHSSDDJHI-UHFFFAOYSA-N 6-amino-1-bromo-2,2-dimethyl-7-propan-2-yloxy-3,4-dihydroquinoline-4-thiol Chemical compound BrN1C(C)(C)CC(S)C2=C1C=C(OC(C)C)C(N)=C2 PVJVEVHSSDDJHI-UHFFFAOYSA-N 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 claims description 2
- MLPIMVDKFGMEDX-UHFFFAOYSA-N NC=1C=C2CC(C(N(C2=CC1C)CCC(C(O)OCCOCCOCCOCC)O)(C)C)C Chemical compound NC=1C=C2CC(C(N(C2=CC1C)CCC(C(O)OCCOCCOCCOCC)O)(C)C)C MLPIMVDKFGMEDX-UHFFFAOYSA-N 0.000 claims description 2
- LWSFYBCRKVQVIT-UHFFFAOYSA-N OCCOCCOCCOCCNC1=C(C=C(C=C1)N)OC(C)C Chemical compound OCCOCCOCCOCCNC1=C(C=C(C=C1)N)OC(C)C LWSFYBCRKVQVIT-UHFFFAOYSA-N 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 2
- 125000005110 aryl thio group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- QPMLSUSACCOBDK-UHFFFAOYSA-N diazepane Chemical class C1CCNNCC1 QPMLSUSACCOBDK-UHFFFAOYSA-N 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- UVEZPRNQGOLAPH-UHFFFAOYSA-N n-[1-(4-amino-3-methylphenyl)pyrrolidin-3-yl]methanesulfonamide Chemical compound C1=C(N)C(C)=CC(N2CC(CC2)NS(C)(=O)=O)=C1 UVEZPRNQGOLAPH-UHFFFAOYSA-N 0.000 claims description 2
- LHMKPCGWIKJVFN-UHFFFAOYSA-N n-[1-(4-amino-3-phenoxyphenyl)pyrrolidin-3-yl]methanesulfonamide Chemical compound C1C(NS(=O)(=O)C)CCN1C1=CC=C(N)C(OC=2C=CC=CC=2)=C1 LHMKPCGWIKJVFN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N ortho-methyl aniline Natural products CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 claims description 2
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 claims description 2
- 125000005499 phosphonyl group Chemical group 0.000 claims description 2
- 150000004885 piperazines Chemical class 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 125000004585 polycyclic heterocycle group Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical compound [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims description 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 125000004964 sulfoalkyl group Chemical group 0.000 claims description 2
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 125000004001 thioalkyl group Chemical group 0.000 claims description 2
- 125000004950 trifluoroalkyl group Chemical group 0.000 claims description 2
- 239000002585 base Substances 0.000 claims 6
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 1
- WSMJTXVQAZYLAV-UHFFFAOYSA-N 1-methylindol-4-ol Chemical compound C1=CC=C2N(C)C=CC2=C1O WSMJTXVQAZYLAV-UHFFFAOYSA-N 0.000 claims 1
- KSWSJJMINLWJDI-UHFFFAOYSA-N 1-methylindole-2,7-diamine Chemical compound C1=CC(N)=C2N(C)C(N)=CC2=C1 KSWSJJMINLWJDI-UHFFFAOYSA-N 0.000 claims 1
- KQGOJGSMIRVVJL-UHFFFAOYSA-N 1-n-methyl-4-n-[4-[4-(methylamino)anilino]butyl]benzene-1,4-diamine Chemical compound C1=CC(NC)=CC=C1NCCCCNC1=CC=C(NC)C=C1 KQGOJGSMIRVVJL-UHFFFAOYSA-N 0.000 claims 1
- XAWPKHNOFIWWNZ-UHFFFAOYSA-N 1h-indol-6-ol Chemical compound OC1=CC=C2C=CNC2=C1 XAWPKHNOFIWWNZ-UHFFFAOYSA-N 0.000 claims 1
- FFBGMHQWMQGPBB-UHFFFAOYSA-N 2-(5-amino-2,3-dihydroindol-1-yl)ethanethiol Chemical compound NC1=CC=C2N(CCS)CCC2=C1 FFBGMHQWMQGPBB-UHFFFAOYSA-N 0.000 claims 1
- TZDKSSYMXFUTIJ-UHFFFAOYSA-N 2-(5-amino-3-methyl-2,3-dihydroindol-1-yl)ethanol Chemical compound C1=C(N)C=C2C(C)CN(CCO)C2=C1 TZDKSSYMXFUTIJ-UHFFFAOYSA-N 0.000 claims 1
- YEASAHKXQJHZPL-UHFFFAOYSA-N 2-[1-(4-amino-3-methylphenyl)pyrrolidin-3-yl]oxyethanol Chemical compound C1=C(N)C(C)=CC(N2CC(CC2)OCCO)=C1 YEASAHKXQJHZPL-UHFFFAOYSA-N 0.000 claims 1
- STAVIAALKQJNMR-UHFFFAOYSA-N 2-[2-(6-amino-2,2,3-trimethyl-3,4-dihydroquinolin-1-yl)ethoxy]ethanol Chemical compound NC1=CC=C2N(CCOCCO)C(C)(C)C(C)CC2=C1 STAVIAALKQJNMR-UHFFFAOYSA-N 0.000 claims 1
- KCCKRHSIGCKPDU-UHFFFAOYSA-N 2-[2-[2-(6-amino-2,2,3-trimethyl-7-propan-2-yl-3,4-dihydroquinolin-1-yl)ethoxy]ethoxy]ethanol Chemical compound OCCOCCOCCN1C(C)(C)C(C)CC2=C1C=C(C(C)C)C(N)=C2 KCCKRHSIGCKPDU-UHFFFAOYSA-N 0.000 claims 1
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- 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
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0002858A FR2805738B1 (fr) | 2000-03-06 | 2000-03-06 | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200108983B true ZA200108983B (en) | 2002-09-11 |
Family
ID=8847770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200108983A ZA200108983B (en) | 2000-03-06 | 2001-10-31 | Oxidation dyeing composition for keratinous fibres and dyeing method using the same. |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1181004A1 (hu) |
| JP (1) | JP2003525889A (hu) |
| KR (1) | KR20010113913A (hu) |
| CN (1) | CN1372457A (hu) |
| AU (1) | AU752948B2 (hu) |
| BR (1) | BR0105561A (hu) |
| CA (1) | CA2373099A1 (hu) |
| CZ (1) | CZ20014324A3 (hu) |
| FR (1) | FR2805738B1 (hu) |
| HU (1) | HUP0202007A2 (hu) |
| PL (1) | PL352292A1 (hu) |
| WO (1) | WO2001066072A1 (hu) |
| ZA (1) | ZA200108983B (hu) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2822373B1 (fr) * | 2001-03-21 | 2005-12-02 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des derives de paraphenylenediamine a groupement pyrrolidinyle |
| FR2822374B1 (fr) * | 2001-03-21 | 2004-07-09 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des derives de paraphenylenediamine a groupement pyrrolidinyle |
| FR2848436A1 (fr) * | 2002-12-13 | 2004-06-18 | Oreal | Composition tinctoriale comprenant une paraphenylenediamine tertiaire cationique et un paraaminophenol, procedes et utilisations |
| CN100404016C (zh) * | 2003-03-11 | 2008-07-23 | 章华东 | 一种焗油染发剂和加工方法 |
| AU2006300478B2 (en) * | 2005-10-05 | 2010-06-17 | Mitsubishi Tanabe Pharma Corporation | Dermatitis treating agent |
| FR2984316B1 (fr) * | 2011-12-16 | 2017-08-11 | Oreal | Coupleur de structure 7-amino-indole, composition tinctoriale en comprenant, procedes et utilisations. |
| CN114555048A (zh) * | 2019-06-28 | 2022-05-27 | 莱雅公司 | 用于角蛋白纤维的氧化染色的美容组合物 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2707488B1 (fr) * | 1993-07-13 | 1995-09-22 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un para-aminophénol, un méta-aminophénol et une paraphénylènediamine et/ou une bis-phénylalkylènediamine. |
| FR2717383B1 (fr) * | 1994-03-21 | 1996-04-19 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et un polymère substantif cationique ou amphotère et utilisation. |
| EP0917531B1 (de) * | 1996-07-03 | 2002-01-09 | Hans Schwarzkopf GmbH & Co. KG | Piperazin-derivate und oxidationsfärbemittel |
| DE19707545A1 (de) * | 1997-02-26 | 1998-08-27 | Henkel Kgaa | Neue Diazacycloheptan-Derivate und deren Verwendung |
| US5851237A (en) * | 1997-07-14 | 1998-12-22 | Anderson; James S. | Oxidative hair dye compositions and methods containing 1--(4-aminophenyl) pyrrolidines |
| JPH11158048A (ja) * | 1997-12-01 | 1999-06-15 | Fuji Photo Film Co Ltd | ジアルキルアニリン化合物を配合する染毛剤組成物 |
| US5993491A (en) * | 1998-05-13 | 1999-11-30 | Bristol-Myers Squibb Company | Oxidative hair dye compositions and methods containing 1-(4-aminophenyl)-2-pyrrolidinemethanols |
-
2000
- 2000-03-06 FR FR0002858A patent/FR2805738B1/fr not_active Expired - Fee Related
-
2001
- 2001-03-06 BR BR0105561-5A patent/BR0105561A/pt not_active IP Right Cessation
- 2001-03-06 WO PCT/FR2001/000663 patent/WO2001066072A1/fr not_active Application Discontinuation
- 2001-03-06 JP JP2001564725A patent/JP2003525889A/ja active Pending
- 2001-03-06 HU HU0202007A patent/HUP0202007A2/hu unknown
- 2001-03-06 KR KR1020017014180A patent/KR20010113913A/ko not_active Application Discontinuation
- 2001-03-06 EP EP01913934A patent/EP1181004A1/fr not_active Withdrawn
- 2001-03-06 AU AU39341/01A patent/AU752948B2/en not_active Ceased
- 2001-03-06 CZ CZ20014324A patent/CZ20014324A3/cs unknown
- 2001-03-06 CN CN01801178A patent/CN1372457A/zh active Pending
- 2001-03-06 CA CA002373099A patent/CA2373099A1/fr not_active Abandoned
- 2001-03-06 PL PL01352292A patent/PL352292A1/xx unknown
- 2001-10-31 ZA ZA200108983A patent/ZA200108983B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003525889A (ja) | 2003-09-02 |
| EP1181004A1 (fr) | 2002-02-27 |
| CN1372457A (zh) | 2002-10-02 |
| KR20010113913A (ko) | 2001-12-28 |
| CZ20014324A3 (cs) | 2002-07-17 |
| CA2373099A1 (fr) | 2001-09-13 |
| FR2805738A1 (fr) | 2001-09-07 |
| BR0105561A (pt) | 2002-03-19 |
| WO2001066072A1 (fr) | 2001-09-13 |
| FR2805738B1 (fr) | 2003-03-14 |
| AU3934101A (en) | 2001-09-17 |
| HUP0202007A2 (hu) | 2002-11-28 |
| PL352292A1 (en) | 2003-08-11 |
| AU752948B2 (en) | 2002-10-03 |
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