CH653549A5 - Compositions tinctoriales pour cheveux a base de paraphenylenediamine et d'orthoaminophenol et leur utilisation. - Google Patents
Compositions tinctoriales pour cheveux a base de paraphenylenediamine et d'orthoaminophenol et leur utilisation. Download PDFInfo
- Publication number
- CH653549A5 CH653549A5 CH5256/80A CH525680A CH653549A5 CH 653549 A5 CH653549 A5 CH 653549A5 CH 5256/80 A CH5256/80 A CH 5256/80A CH 525680 A CH525680 A CH 525680A CH 653549 A5 CH653549 A5 CH 653549A5
- Authority
- CH
- Switzerland
- Prior art keywords
- hair
- paraphenylenediamine
- orthoaminophenol
- dye
- weight
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 123
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 title claims description 72
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 title claims description 56
- 239000000975 dye Substances 0.000 claims description 73
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 64
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 37
- 230000015572 biosynthetic process Effects 0.000 claims description 18
- 238000004040 coloring Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 238000004043 dyeing Methods 0.000 claims description 12
- 230000003647 oxidation Effects 0.000 claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000000982 direct dye Substances 0.000 claims description 4
- 239000007800 oxidant agent Substances 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- VRDIULHPQTYCLN-UHFFFAOYSA-N Prothionamide Chemical compound CCCC1=CC(C(N)=S)=CC=N1 VRDIULHPQTYCLN-UHFFFAOYSA-N 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 150000001555 benzenes Chemical class 0.000 claims description 2
- 239000000872 buffer Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000002304 perfume Substances 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims 1
- 239000001005 nitro dye Substances 0.000 claims 1
- 230000000149 penetrating effect Effects 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 48
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 45
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 41
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 36
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 24
- 229910021529 ammonia Inorganic materials 0.000 description 24
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 21
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 21
- 230000001590 oxidative effect Effects 0.000 description 19
- 239000002585 base Substances 0.000 description 18
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 17
- ALSTYHKOOCGGFT-UHFFFAOYSA-N cis-oleyl alcohol Natural products CCCCCCCCC=CCCCCCCCCO ALSTYHKOOCGGFT-UHFFFAOYSA-N 0.000 description 17
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 12
- 239000006210 lotion Substances 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 10
- 239000002609 medium Substances 0.000 description 10
- 244000060011 Cocos nucifera Species 0.000 description 9
- 235000013162 Cocos nucifera Nutrition 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 8
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 8
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- 238000004587 chromatography analysis Methods 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- 238000009833 condensation Methods 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 4
- 241001070941 Castanea Species 0.000 description 4
- 235000014036 Castanea Nutrition 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 description 4
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 4
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000012458 free base Substances 0.000 description 4
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 4
- -1 (paraamino) anilino Chemical group 0.000 description 3
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 3
- 239000005695 Ammonium acetate Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 235000019257 ammonium acetate Nutrition 0.000 description 3
- 229940043376 ammonium acetate Drugs 0.000 description 3
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 3
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 3
- 239000006071 cream Substances 0.000 description 3
- 229960004418 trolamine Drugs 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- WVCHIGAIXREVNS-UHFFFAOYSA-N 2-hydroxy-1,4-naphthoquinone Chemical compound C1=CC=C2C(O)=CC(=O)C(=O)C2=C1 WVCHIGAIXREVNS-UHFFFAOYSA-N 0.000 description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000118 hair dye Substances 0.000 description 2
- CSFWPUWCSPOLJW-UHFFFAOYSA-N hydroxynaphthoquinone Natural products C1=CC=C2C(=O)C(O)=CC(=O)C2=C1 CSFWPUWCSPOLJW-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229960005323 phenoxyethanol Drugs 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical class CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- ZCSHACFHMFHFKK-UHFFFAOYSA-N 2-methyl-1,3,5-trinitrobenzene;2,4,6-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)C1NC([N+]([O-])=O)NC([N+]([O-])=O)N1.CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O ZCSHACFHMFHFKK-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- 240000009226 Corylus americana Species 0.000 description 1
- 235000001543 Corylus americana Nutrition 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000084 Gum arabic Chemical class 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000000205 acacia gum Chemical class 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000011162 ammonium carbonates Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000002610 basifying agent Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000001913 cellulose Chemical class 0.000 description 1
- 229920002678 cellulose Chemical class 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- PMRPLIMEJYCXCT-UHFFFAOYSA-N hydrogen peroxide;lead Chemical compound [Pb].OO PMRPLIMEJYCXCT-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/413—Indoanilines; Indophenol; Indoamines
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7917889A FR2460664A1 (fr) | 1979-07-10 | 1979-07-10 | Compositions tinctoriales pour cheveux a base de paraphenylenediamine et d'orthoaminophenol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH653549A5 true CH653549A5 (fr) | 1986-01-15 |
Family
ID=9227724
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH5256/80A CH653549A5 (fr) | 1979-07-10 | 1980-07-09 | Compositions tinctoriales pour cheveux a base de paraphenylenediamine et d'orthoaminophenol et leur utilisation. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4370142A (en, 2012) |
| JP (1) | JPS5615205A (en, 2012) |
| AR (1) | AR221769A1 (en, 2012) |
| AT (1) | AT377913B (en, 2012) |
| BE (1) | BE884233A (en, 2012) |
| BR (1) | BR8004265A (en, 2012) |
| CA (1) | CA1167052A (en, 2012) |
| CH (1) | CH653549A5 (en, 2012) |
| DE (1) | DE3025992A1 (en, 2012) |
| FR (1) | FR2460664A1 (en, 2012) |
| GB (1) | GB2054664B (en, 2012) |
| IT (1) | IT1130492B (en, 2012) |
| NL (1) | NL8003963A (en, 2012) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU85853A1 (fr) * | 1985-04-16 | 1986-11-05 | Oreal | Nouveaux nitroaminophenols,leur procede de preparation et leur utilisation en teinture des fibres keratiniques,nouveaux nitroaminobenzenes intermediaires et leur utilisation en teinture des fibres keratiniques |
| JPS6267012A (ja) * | 1985-09-17 | 1987-03-26 | Hoou Kk | 染毛剤 |
| JPH0253715A (ja) * | 1988-08-18 | 1990-02-22 | Hoyu Co Ltd | 自動酸化型一剤式染毛剤 |
| US5344464A (en) * | 1988-09-08 | 1994-09-06 | L'oreal | Oxidation dye composition containing at least one double base in combination with at least one single base and dyeing process making use of it |
| FR2635976B1 (fr) * | 1988-09-08 | 1994-01-21 | Oreal | Composition tinctoriale d'oxydation contenant au moins une base double associee a au moins une base simple et procede de teinture la mettant en oeuvre |
| FR2638453B1 (fr) * | 1988-10-28 | 1991-06-07 | Oreal | Ortho-aminophenols 5-substitues, procede pour les preparer et leur utilisation pour la teinture d'oxydation des fibres keratiniques |
| JP2523419B2 (ja) * | 1991-08-30 | 1996-08-07 | 花王株式会社 | ケラチン質繊維処理剤組成物 |
| FR2726185B1 (fr) * | 1994-11-02 | 1997-04-25 | Oreal | Composition tinctoriale a base de colorants d'oxydation et procede de teinture mettant en oeuvre cette composition |
| US6743264B2 (en) | 2002-02-14 | 2004-06-01 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Two step permanent coloring of hair |
| US7060111B2 (en) * | 2003-07-03 | 2006-06-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Method for providing more vibrant, natural and long-lasting color to hair |
| US7074244B2 (en) * | 2003-07-03 | 2006-07-11 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Hair dyeing method including an aligning step |
| JP4865987B2 (ja) * | 2003-10-06 | 2012-02-01 | 花王株式会社 | 染毛剤組成物 |
| USD509410S1 (en) * | 2004-01-28 | 2005-09-13 | Villeroy & Boch Ag | Tray stand |
| FR2923387B1 (fr) * | 2007-11-09 | 2010-01-15 | Oreal | Composition comprenant un derive de cellulose modifie, un polymere non ionique et des colorants d'oxydation, procede de teinture et utilisation |
| DE102014216942A1 (de) * | 2014-08-26 | 2016-03-03 | Henkel Ag & Co. Kgaa | Multitonale Einschritt-Färbungen mit verdickter Vorbehandlungslösung I |
| DE102014216941A1 (de) * | 2014-08-26 | 2016-03-03 | Henkel Ag & Co. Kgaa | Multitonale Einschritt-Färbungen mit schaumartiger Vorbehandlungslösung |
| WO2020142521A1 (en) * | 2018-12-31 | 2020-07-09 | L'oreal | Hair coloring compositions and methods of use |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE103505C (en, 2012) * | ||||
| DE1144879B (de) * | 1959-12-17 | 1963-03-07 | Schwarzkopf Fa Hans | Verfahren zum Faerben von Haaren |
| US3649159A (en) * | 1968-06-03 | 1972-03-14 | Fmc Corp | Hair coloring method using a peroxydiphosphate oxidant |
| JPS505539A (en, 2012) * | 1973-05-19 | 1975-01-21 | ||
| US4104021A (en) * | 1976-05-28 | 1978-08-01 | Combe Incorporated | Process for dyeing hair in which the depth of shade is gradually increased in successive treatments |
| PH13324A (en) * | 1976-05-28 | 1980-03-13 | Combe Inc | Process for dyeing hair in which the depth of shade is gradually increased in successive treatments |
| FR2421608A1 (fr) * | 1978-04-06 | 1979-11-02 | Oreal | Composition destinee a la teinture des cheveux contenant des precurseurs de colorants par oxydation de type para et de type ortho |
| FR2430932A1 (fr) * | 1978-07-12 | 1980-02-08 | Oreal | Metaphenylenediamines et compositions tinctoriales les contenant |
-
1979
- 1979-07-10 FR FR7917889A patent/FR2460664A1/fr active Granted
-
1980
- 1980-06-30 AT AT0342080A patent/AT377913B/de not_active IP Right Cessation
- 1980-07-08 AR AR281686A patent/AR221769A1/es active
- 1980-07-08 US US06/167,149 patent/US4370142A/en not_active Expired - Lifetime
- 1980-07-09 NL NL8003963A patent/NL8003963A/nl not_active Application Discontinuation
- 1980-07-09 GB GB8022429A patent/GB2054664B/en not_active Expired
- 1980-07-09 CH CH5256/80A patent/CH653549A5/fr not_active IP Right Cessation
- 1980-07-09 JP JP9377480A patent/JPS5615205A/ja active Granted
- 1980-07-09 BE BE0/201336A patent/BE884233A/fr not_active IP Right Cessation
- 1980-07-09 BR BR8004265A patent/BR8004265A/pt unknown
- 1980-07-09 IT IT68089/80A patent/IT1130492B/it active
- 1980-07-09 CA CA000355805A patent/CA1167052A/fr not_active Expired
- 1980-07-09 DE DE19803025992 patent/DE3025992A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2460664B1 (en, 2012) | 1983-08-19 |
| GB2054664A (en) | 1981-02-18 |
| DE3025992C2 (en, 2012) | 1992-05-07 |
| IT8068089A0 (it) | 1980-07-09 |
| DE3025992A1 (de) | 1981-01-29 |
| BE884233A (fr) | 1981-01-09 |
| AR221769A1 (es) | 1981-03-13 |
| AT377913B (de) | 1985-05-28 |
| FR2460664A1 (fr) | 1981-01-30 |
| CA1167052A (fr) | 1984-05-08 |
| ATA342080A (de) | 1984-10-15 |
| US4370142A (en) | 1983-01-25 |
| NL8003963A (nl) | 1981-01-13 |
| BR8004265A (pt) | 1981-01-27 |
| GB2054664B (en) | 1983-09-01 |
| IT1130492B (it) | 1986-06-11 |
| JPS5615205A (en) | 1981-02-14 |
| JPH0214323B2 (en, 2012) | 1990-04-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1304202C (fr) | Procede de teinture des fibres keratiniques avec le 5, 6-dihydroxyindole associe a un iodure et une composition de peroxyde d'hydrogene a ph alcalin | |
| CA2214021C (fr) | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique | |
| CA2214022C (fr) | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique | |
| EP0953334B1 (fr) | Composition de teinture pour fibres kératiniques avec un colorant direct cationique et un polymère substantif | |
| CA2230717C (fr) | Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique | |
| EP0943320B1 (fr) | Procédé de teinture d'oxidation et composition de teinture d'oxidation pour fibres kératiniques comprenant un polymère amphiphile cationique | |
| CH653549A5 (fr) | Compositions tinctoriales pour cheveux a base de paraphenylenediamine et d'orthoaminophenol et leur utilisation. | |
| BE1001329A3 (fr) | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a des derives d'indole et composition tinctoriale mise en oeuvre | |
| CH672731A5 (en, 2012) | ||
| CA1151069A (fr) | Compositions tinctoriales pour cheveux contenant, comme coupleur, le diamino-2,4 butoxybenzene et/ou ses sels | |
| FR2722687A1 (fr) | Utilisation de gomme de guar dans des compositionsnon rincees pour la teinture des fibres keratiniques et procede de teinture | |
| CA1151070A (fr) | Compositions tinctoriales pour cheveux contenant, en tant que coupleur, au moins un diamino-2,4 alkylbenzene | |
| LU87113A1 (fr) | Procede de teinture des fibres keratiniques et composition de teinture mettant en oeuvre du 5,6-dihydroxyindole,un colorant quinonique et iodure | |
| CH657607A5 (fr) | Derives nitres de la serie benzenique, leur procede de preparation et leur utilisation en teinture des fibres keratiniques. | |
| EP0459901A1 (fr) | Procédé de teinture des fibres kératiniques avec le 2,6-diméthyl 1,4-diamino benzène et/ou le 2,3-diméthyl 1,4-diamino benzène et/ou le 2,6-diéthyl 1,4-diamino benzène en milieu acide et compositions mises en oeuvre | |
| FR2713924A1 (fr) | Procédé de coloration d'oxydation des fibres kératiniques humaines à l'aide de vapeur d'eau. | |
| CA1158561A (fr) | Composition tinctoriale pour cheveux a base de paraphenylene diamines | |
| EP0658094B1 (fr) | Composition de teinture d'oxydation des fibres keratiniques comprenant un para-aminophenol, un meta-aminophenol et un ortho-aminophenol, et procede de teinture utilisant une telle composition | |
| CA1188880A (fr) | Utilisation de derives alkyles de l'hydroquinone comme agent anti-oxydant dans des compositions tinctoriales d'oxydation | |
| LU84122A1 (fr) | Composition a base de colorants quinoniques destinee a etre utilisee pour la teinture des cheveux,procede de conservation de colorants quinoniques et utilisation pour la teinture des cheveux | |
| CH649703A5 (fr) | Compositions tinctoriales contenant des derives d'amino-3 nitro-4 anisole, leur utilisation en teinture des fibres keratiniques et composes utilises ainsi que leur procede de preparation. | |
| EP0710476B1 (fr) | Composition tinctoriale à base de colorants d'oxydation et procédé de teinture mettant en oeuvre cette composition | |
| FR2474490A1 (fr) | Nouveau derive de la 1,4-benzoquinonimine, composition tinctoriale pour cheveux et procede de teinture des cheveux le mettant en oeuvre | |
| EP1502579A1 (fr) | Composition de teinture de fibres keratiniques comprenant un colorant direct azodiazine particulier et procedes de coloration la mettant en oeuvre | |
| FR2858218A1 (fr) | Composition de teinture de fibres keratiniques comprenant un cololrant direct azodiazine particulier non amine en position 7 et procedes de coloration la mettant en oeuvre |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |