CH674461A5 - - Google Patents
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- Publication number
- CH674461A5 CH674461A5 CH4466/87A CH446687A CH674461A5 CH 674461 A5 CH674461 A5 CH 674461A5 CH 4466/87 A CH4466/87 A CH 4466/87A CH 446687 A CH446687 A CH 446687A CH 674461 A5 CH674461 A5 CH 674461A5
- Authority
- CH
- Switzerland
- Prior art keywords
- group
- composition
- dihydroxyindole
- hydrogen atom
- hair
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 135
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 82
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 51
- 238000000034 method Methods 0.000 claims description 38
- -1 amine salts Chemical class 0.000 claims description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 23
- 150000002475 indoles Chemical class 0.000 claims description 22
- 239000000243 solution Substances 0.000 claims description 22
- 235000019441 ethanol Nutrition 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 238000004043 dyeing Methods 0.000 claims description 15
- 239000002904 solvent Substances 0.000 claims description 14
- 239000000835 fiber Substances 0.000 claims description 12
- 229940054051 antipsychotic indole derivative Drugs 0.000 claims description 10
- 239000002537 cosmetic Substances 0.000 claims description 9
- 102000011782 Keratins Human genes 0.000 claims description 8
- 108010076876 Keratins Proteins 0.000 claims description 8
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 8
- 239000003513 alkali Substances 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-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
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- 239000002562 thickening agent Substances 0.000 claims description 4
- JHFAEUICJHBVHB-UHFFFAOYSA-N 1h-indol-2-ol Chemical compound C1=CC=C2NC(O)=CC2=C1 JHFAEUICJHBVHB-UHFFFAOYSA-N 0.000 claims description 3
- QGJCWKNNWOVPTJ-UHFFFAOYSA-N 2-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2NC(C)=CC2=C1 QGJCWKNNWOVPTJ-UHFFFAOYSA-N 0.000 claims description 3
- ZUTZCXDHPIACCR-UHFFFAOYSA-N 3-methyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=CNC2=C1 ZUTZCXDHPIACCR-UHFFFAOYSA-N 0.000 claims description 3
- YFTGOBNOJKXZJC-UHFFFAOYSA-N 5,6-dihydroxyindole-2-carboxylic acid Chemical compound OC1=C(O)C=C2NC(C(=O)O)=CC2=C1 YFTGOBNOJKXZJC-UHFFFAOYSA-N 0.000 claims description 3
- RWEBZZKCIMKUTO-UHFFFAOYSA-N 5-methoxy-1h-indol-6-ol Chemical compound C1=C(O)C(OC)=CC2=C1NC=C2 RWEBZZKCIMKUTO-UHFFFAOYSA-N 0.000 claims description 3
- WZARGPVIAOAKMH-UHFFFAOYSA-N 6-methoxy-1h-indol-5-ol Chemical compound C1=C(O)C(OC)=CC2=C1C=CN2 WZARGPVIAOAKMH-UHFFFAOYSA-N 0.000 claims description 3
- 239000002535 acidifier Substances 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 3
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- 150000007522 mineralic acids Chemical class 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 235000005985 organic acids Nutrition 0.000 claims description 3
- 239000011877 solvent mixture Substances 0.000 claims description 3
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 3
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims description 2
- HMTUVSJLXALWIU-UHFFFAOYSA-N 2,3-dimethyl-1h-indole-5,6-diol Chemical compound OC1=C(O)C=C2C(C)=C(C)NC2=C1 HMTUVSJLXALWIU-UHFFFAOYSA-N 0.000 claims description 2
- HXCHORPNRVSDCD-UHFFFAOYSA-N 5h-[1,3]dioxolo[4,5-f]indole Chemical compound C1=C2OCOC2=CC2=C1NC=C2 HXCHORPNRVSDCD-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- KVXNKFYSHAUJIA-UHFFFAOYSA-N acetic acid;ethoxyethane Chemical compound CC(O)=O.CCOCC KVXNKFYSHAUJIA-UHFFFAOYSA-N 0.000 claims description 2
- 230000003113 alkalizing effect Effects 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001099 ammonium carbonate Substances 0.000 claims description 2
- 235000011162 ammonium carbonates Nutrition 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000006071 cream Substances 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- LOEPZYUWYZWRJE-UHFFFAOYSA-N ethyl 5,6-dihydroxy-1h-indole-2-carboxylate Chemical compound OC1=C(O)C=C2NC(C(=O)OCC)=CC2=C1 LOEPZYUWYZWRJE-UHFFFAOYSA-N 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 150000004679 hydroxides Chemical class 0.000 claims description 2
- 239000004310 lactic acid Substances 0.000 claims description 2
- 235000014655 lactic acid Nutrition 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000011975 tartaric acid Substances 0.000 claims description 2
- 235000002906 tartaric acid Nutrition 0.000 claims description 2
- YQQFWHXOWCVOEC-UHFFFAOYSA-N trimethyl-[(5-trimethylsilyloxy-1h-indol-6-yl)oxy]silane Chemical compound C1=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=CC2=C1NC=C2 YQQFWHXOWCVOEC-UHFFFAOYSA-N 0.000 claims description 2
- FSYSJTXGNHBKHU-UHFFFAOYSA-N (6-hydroxy-1h-indol-5-yl) acetate Chemical compound C1=C(O)C(OC(=O)C)=CC2=C1NC=C2 FSYSJTXGNHBKHU-UHFFFAOYSA-N 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims 2
- PGNRLPTYNKQQDY-UHFFFAOYSA-N 2,3-dihydroxyindole Chemical compound C1=CC=C2C(O)=C(O)NC2=C1 PGNRLPTYNKQQDY-UHFFFAOYSA-N 0.000 claims 1
- 235000011054 acetic acid Nutrition 0.000 claims 1
- 239000002280 amphoteric surfactant Substances 0.000 claims 1
- 235000015165 citric acid Nutrition 0.000 claims 1
- 235000011167 hydrochloric acid Nutrition 0.000 claims 1
- 229910001511 metal iodide Inorganic materials 0.000 claims 1
- 235000011007 phosphoric acid Nutrition 0.000 claims 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Inorganic materials [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 41
- 238000004040 coloring Methods 0.000 description 16
- SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 description 12
- 239000002609 medium Substances 0.000 description 12
- 230000002269 spontaneous effect Effects 0.000 description 11
- 229930182470 glycoside Natural products 0.000 description 9
- 229920002907 Guar gum Polymers 0.000 description 8
- 229920013806 TRITON CG-110 Polymers 0.000 description 8
- 239000000665 guar gum Substances 0.000 description 8
- 235000010417 guar gum Nutrition 0.000 description 8
- 229960002154 guar gum Drugs 0.000 description 8
- 229920013683 Celanese Polymers 0.000 description 7
- 239000000975 dye Substances 0.000 description 6
- 229940107816 ammonium iodide Drugs 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000000230 xanthan gum Substances 0.000 description 3
- 235000010493 xanthan gum Nutrition 0.000 description 3
- 229920001285 xanthan gum Polymers 0.000 description 3
- 229940082509 xanthan gum Drugs 0.000 description 3
- 241001070941 Castanea Species 0.000 description 2
- 235000014036 Castanea Nutrition 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- 230000000593 degrading effect Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Inorganic materials [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- JBYZCUOEVLMOEL-UHFFFAOYSA-N (6-hydroxy-1H-indol-2-yl) acetate Chemical compound C(C)(=O)OC=1NC2=CC(=CC=C2C=1)O JBYZCUOEVLMOEL-UHFFFAOYSA-N 0.000 description 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- HKRNZAJWONCZDK-UHFFFAOYSA-N 2,3-dimethyl-1h-indole-5,6-diol;hydrobromide Chemical compound Br.OC1=C(O)C=C2C(C)=C(C)NC2=C1 HKRNZAJWONCZDK-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- SBZBDWBZQAABFX-UHFFFAOYSA-N 7-(2-amino-2-carboxyethyl)-2-[7-(2-amino-2-carboxyethyl)-5-oxo-1,4-benzothiazin-2-yl]-5-hydroxy-4H-1,4-benzothiazine-3-carboxylic acid Chemical compound NC(Cc1cc(O)c2NC(C(O)=O)=C(Sc2c1)c1cnc2c(cc(CC(N)C(O)=O)cc2=O)s1)C(O)=O SBZBDWBZQAABFX-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 229920000084 Gum arabic Polymers 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
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 239000001785 acacia senegal l. willd gum Substances 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 1
- 229910001619 alkaline earth metal iodide Inorganic materials 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
- 239000012298 atmosphere 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
- 229920001222 biopolymer Polymers 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 150000002193 fatty amides Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 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
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003352 sequestering agent 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
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 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
- A61K8/49—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
- 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 |
|---|---|---|---|
| LU86668A LU86668A1 (fr) | 1986-11-17 | 1986-11-17 | Procede de teinture des fibres keratiniques avec des derives d'indole associes avec un iodure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH674461A5 true CH674461A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-06-15 |
Family
ID=19730812
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH4466/87A CH674461A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1986-11-17 | 1987-11-17 |
Country Status (18)
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5492541A (en) * | 1985-08-02 | 1996-02-20 | Clairol Incorporated | Dye compositions containing 5,6-dihydroxy indoles and a foam generator |
| LU86899A1 (fr) * | 1987-05-25 | 1989-01-19 | Oreal | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre |
| LU86947A1 (fr) * | 1987-07-17 | 1989-03-08 | Oreal | Procede de teinture des fibres keratiniques,en particulier humaines,avec le 5-(hydroxy ou-methoxy)6-hydroxyindole |
| JP2566808B2 (ja) * | 1988-03-15 | 1996-12-25 | 花王株式会社 | 染毛剤組成物及び染毛方法 |
| LU87196A1 (fr) | 1988-04-12 | 1989-11-14 | Oreal | Procede de conservation du pouvoir tinctorial du 5,6-dihydroxyindole en milieu aqueux,composition et procede de teinture |
| US5346509A (en) * | 1988-05-12 | 1994-09-13 | Clairol Incorporated | Process for dyeing hair by the sequential treatment of hair with metal ion-containing composition and with a dye composition containing 5,6-dihydroxyindole-2-carboxylic acid and certain derivatives thereof |
| 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 |
| LU87338A1 (fr) * | 1988-09-12 | 1990-04-06 | Oreal | Utilisation de derives d'indole pour la teinture de matieres keratiniques,compositions tinctoriales,composes nouveaux et procede de teinture |
| US5354870A (en) * | 1988-09-12 | 1994-10-11 | L'oreal | Indole derivatives for dyeing keratin materials |
| LU87403A1 (fr) * | 1988-12-06 | 1990-07-10 | Oreal | Procede de teinture de fibres keratiniques avec un hydroxyindole,associe a un derive quinonique |
| LU87429A1 (fr) * | 1989-01-17 | 1990-07-24 | Oreal | Produit a base de particules de polymere comportant des pigments melaniques,son procede de preparation et son utilisation,en particulier en cosmetique |
| US5080890A (en) * | 1989-11-16 | 1992-01-14 | Loumar Cosmetics K.K. | Permanent waving lotion and a process for permanent waving of hair |
| FR2659228B1 (fr) * | 1990-03-08 | 1994-10-14 | Oreal | Procede de teinture des fibres keratiniques avec des 6 ou 7-monohydroxy-indoles a ph acide et compositions mises en óoeuvre. |
| US6238439B1 (en) | 1990-06-21 | 2001-05-29 | L'oreal | Method for dyeing keratinous fibers with indole compounds, compositions and devices for implementation |
| FR2664304B1 (fr) * | 1990-07-05 | 1992-10-09 | Oreal | Procede de teinture des fibres keratiniques avec le 4-hydroxyindole a ph acide et compositions mises en óoeuvre. |
| US5273550A (en) * | 1991-09-26 | 1993-12-28 | Clairol Incorporated | Process and kit for dyeing hair |
| GB9217444D0 (en) * | 1992-08-17 | 1992-09-30 | Unilever Plc | Compounds compositions and methods for producing pigmentation in hair or skin |
| FR2722687A1 (fr) * | 1994-07-22 | 1996-01-26 | Oreal | Utilisation de gomme de guar dans des compositionsnon rincees pour la teinture des fibres keratiniques et procede de teinture |
| US5958084A (en) * | 1996-01-22 | 1999-09-28 | Kao Corporation | Oxyalkylenized xanthane gum thickeners in permanent hair dyeing compositions and processes |
| GB9626711D0 (en) * | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair colouring compositions |
| GB9626675D0 (en) * | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair coloring compositions |
| GB9626713D0 (en) * | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair colouring compositions |
| GB9626712D0 (en) * | 1996-12-23 | 1997-02-12 | Procter & Gamble | Hair colouring compositions |
| US6432147B1 (en) | 1996-12-23 | 2002-08-13 | The Procter & Gamble Company | Hair coloring compositions |
| US6309426B1 (en) | 1996-12-23 | 2001-10-30 | The Procter & Gamble Company | Hair coloring compositions |
| US6398821B1 (en) | 1996-12-23 | 2002-06-04 | The Procter & Gamble Company | Hair coloring compositions |
| DE102005048183A1 (de) * | 2005-10-06 | 2007-04-12 | Henkel Kgaa | Verfahren zur oxidativen Färbung keratinhaltiger Fasern |
| JP5828996B2 (ja) * | 2008-12-26 | 2015-12-09 | ホーユー株式会社 | 毛髪化粧料組成物 |
| FR2958161B1 (fr) * | 2010-04-02 | 2012-04-27 | Oreal | Procede de traitement des cheveux mettant en oeuvre une emulsion directe comprenant un agent oxydant et une emulsion directe contenant un agent alcalin |
| EP2797886A2 (fr) * | 2011-12-30 | 2014-11-05 | Ecole Nationale Superieure de Chimie de Clermont Ferrand | Composes anti-douleur |
| CN110200823A (zh) * | 2019-06-12 | 2019-09-06 | 四川大学 | 一种基于苯硼酸的染发剂及其制备和使用方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1677508A (en) * | 1925-07-11 | 1928-07-17 | Inecto Inc | Art of dyeing fibers |
| BE564450A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1957-02-02 | |||
| BE549801A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1959-07-24 | |||
| DE2028818A1 (de) * | 1969-06-11 | 1970-12-17 | The Gillette Co,, Boston, Mass. (V.St.A,) | Verfahren zum Färben von Menschenhaar |
| US3976639A (en) * | 1970-11-04 | 1976-08-24 | Hoffmann-La Roche Inc. | Intermediates for indoles |
| FR2390158A1 (fr) * | 1977-05-10 | 1978-12-08 | Oreal | Compositions liquides de colorants de la famille des indoles destinees a la teinture des cheveux |
| CA1201067A (en) * | 1982-12-07 | 1986-02-25 | Keith Brown | Hair dyeing process and composition |
| GB2132342B (en) * | 1982-12-14 | 1986-03-19 | Land Combustion Ltd | Discrimination between flames of different fuels |
| LU86256A1 (fr) * | 1986-01-20 | 1988-01-20 | Oreal | Procede de teinture des fibres keratiniques avec du 5,6-dihydroxyindole associe avec un iodure |
| LU86346A1 (fr) * | 1986-03-06 | 1987-11-11 | Oreal | Compositions tinctoriales pour fibres keratiniques a base de derives d'indole et composes nouveaux |
-
1986
- 1986-11-17 LU LU86668A patent/LU86668A1/fr unknown
-
1987
- 1987-11-13 PT PT86127A patent/PT86127B/pt not_active IP Right Cessation
- 1987-11-16 IT IT67975/87A patent/IT1218693B/it active
- 1987-11-16 ES ES878703263A patent/ES2010731A6/es not_active Expired
- 1987-11-16 JP JP62287585A patent/JP2537919B2/ja not_active Expired - Lifetime
- 1987-11-17 GB GB8726839A patent/GB2197885B/en not_active Expired - Lifetime
- 1987-11-17 ZA ZA878600A patent/ZA878600B/xx unknown
- 1987-11-17 NL NL8702746A patent/NL8702746A/nl not_active Application Discontinuation
- 1987-11-17 CA CA000552007A patent/CA1295254C/fr not_active Expired - Lifetime
- 1987-11-17 US US07/121,890 patent/US4885006A/en not_active Expired - Fee Related
- 1987-11-17 FR FR878715866A patent/FR2606636B1/fr not_active Expired - Lifetime
- 1987-11-17 AU AU81298/87A patent/AU608786B2/en not_active Ceased
- 1987-11-17 BE BE8701300A patent/BE1000620A4/fr not_active IP Right Cessation
- 1987-11-17 BR BR8706192A patent/BR8706192A/pt unknown
- 1987-11-17 CH CH4466/87A patent/CH674461A5/fr not_active IP Right Cessation
- 1987-11-17 DE DE19873739028 patent/DE3739028A1/de active Granted
- 1987-11-17 CN CN198787107844A patent/CN87107844A/zh active Pending
- 1987-11-17 GR GR871752A patent/GR871752B/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2010731A6 (es) | 1989-12-01 |
| US4885006A (en) | 1989-12-05 |
| JP2537919B2 (ja) | 1996-09-25 |
| ZA878600B (en) | 1989-07-26 |
| IT8767975A0 (it) | 1987-11-16 |
| GB2197885B (en) | 1990-11-21 |
| PT86127A (fr) | 1987-12-01 |
| LU86668A1 (fr) | 1988-06-13 |
| BR8706192A (pt) | 1988-06-21 |
| DE3739028C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-04-12 |
| GB8726839D0 (en) | 1987-12-23 |
| AU608786B2 (en) | 1991-04-18 |
| GB2197885A (en) | 1988-06-02 |
| IT1218693B (it) | 1990-04-19 |
| BE1000620A4 (fr) | 1989-02-21 |
| PT86127B (pt) | 1990-11-20 |
| CA1295254C (fr) | 1992-02-04 |
| CN87107844A (zh) | 1988-07-13 |
| DE3739028A1 (de) | 1988-05-19 |
| FR2606636A1 (fr) | 1988-05-20 |
| JPS63170309A (ja) | 1988-07-14 |
| NL8702746A (nl) | 1988-06-16 |
| FR2606636B1 (fr) | 1990-08-31 |
| AU8129887A (en) | 1988-05-19 |
| GR871752B (en) | 1988-03-17 |
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Legal Events
| Date | Code | Title | Description |
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| PL | Patent ceased | ||
| PL | Patent ceased |