LU83063A1 - Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines,nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation - Google Patents
Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines,nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation Download PDFInfo
- Publication number
- LU83063A1 LU83063A1 LU83063A LU83063A LU83063A1 LU 83063 A1 LU83063 A1 LU 83063A1 LU 83063 A LU83063 A LU 83063A LU 83063 A LU83063 A LU 83063A LU 83063 A1 LU83063 A1 LU 83063A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- methyl
- nitro
- hydrogen
- preparation
- dye
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 91
- 239000000835 fiber Substances 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 10
- 230000008569 process Effects 0.000 title claims description 9
- 238000002360 preparation method Methods 0.000 title description 56
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 51
- 239000000975 dye Substances 0.000 claims description 49
- 150000001875 compounds Chemical class 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
- 102000011782 Keratins Human genes 0.000 claims description 16
- 108010076876 Keratins Proteins 0.000 claims description 16
- -1 N, N-diethylamino-ethyl Chemical group 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 238000004040 coloring Methods 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 230000003647 oxidation Effects 0.000 claims description 13
- 238000007254 oxidation reaction Methods 0.000 claims description 13
- 238000004043 dyeing Methods 0.000 claims description 12
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 239000002243 precursor Substances 0.000 claims description 7
- 239000002537 cosmetic Substances 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
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- 125000003277 amino group Chemical group 0.000 claims description 4
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- 229920005989 resin Polymers 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000002562 thickening agent Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 239000002610 basifying agent Substances 0.000 claims description 3
- 150000001555 benzenes Chemical class 0.000 claims description 3
- 239000000982 direct dye Substances 0.000 claims description 3
- 238000009967 direct dyeing Methods 0.000 claims description 3
- 239000006210 lotion Substances 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- FYTRVVJHEWUARG-UHFFFAOYSA-N n-(2-aminophenyl)nitramide Chemical class NC1=CC=CC=C1N[N+]([O-])=O FYTRVVJHEWUARG-UHFFFAOYSA-N 0.000 claims description 2
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- 239000000155 melt Substances 0.000 description 24
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- 238000010992 reflux Methods 0.000 description 10
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- VLVCWODDMDGANW-UHFFFAOYSA-N 4-methyl-n-phenylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=CC=C1 VLVCWODDMDGANW-UHFFFAOYSA-N 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 9
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- 239000011734 sodium Substances 0.000 description 8
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- 238000009835 boiling Methods 0.000 description 6
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 6
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- IOCXBXZBNOYTLQ-UHFFFAOYSA-N 3-nitrobenzene-1,2-diamine Chemical class NC1=CC=CC([N+]([O-])=O)=C1N IOCXBXZBNOYTLQ-UHFFFAOYSA-N 0.000 description 4
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- BPPMIQPXQVIZNJ-UHFFFAOYSA-N 2-chloro-1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1Cl BPPMIQPXQVIZNJ-UHFFFAOYSA-N 0.000 description 1
- GUXQOHMLFVAZAH-UHFFFAOYSA-N 2-ethyl-n,n-dihydroxyaniline Chemical compound CCC1=CC=CC=C1N(O)O GUXQOHMLFVAZAH-UHFFFAOYSA-N 0.000 description 1
- HVNUPXQONRHUOX-UHFFFAOYSA-N 2-methoxy-5-methyl-1,3-dinitrobenzene Chemical compound COC1=C([N+]([O-])=O)C=C(C)C=C1[N+]([O-])=O HVNUPXQONRHUOX-UHFFFAOYSA-N 0.000 description 1
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 1
- FCMRHMPITHLLLA-UHFFFAOYSA-N 2-methyl-6-nitroaniline Chemical compound CC1=CC=CC([N+]([O-])=O)=C1N FCMRHMPITHLLLA-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
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 description 1
- WGEZJWMZNGUEHR-UHFFFAOYSA-N 3-amino-4-nitrophenol Chemical compound NC1=CC(O)=CC=C1[N+]([O-])=O WGEZJWMZNGUEHR-UHFFFAOYSA-N 0.000 description 1
- DZIJEXQVMORGQX-UHFFFAOYSA-N 3-methyl-5-nitroaniline Chemical compound CC1=CC(N)=CC([N+]([O-])=O)=C1 DZIJEXQVMORGQX-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- ZYZQSCWSPFLAFM-UHFFFAOYSA-N 4-amino-2-chlorophenol Chemical compound NC1=CC=C(O)C(Cl)=C1 ZYZQSCWSPFLAFM-UHFFFAOYSA-N 0.000 description 1
- ANHZPHIPRWOGCD-UHFFFAOYSA-N 4-amino-2-methyl-5-nitrophenol Chemical compound CC1=CC(N)=C([N+]([O-])=O)C=C1O ANHZPHIPRWOGCD-UHFFFAOYSA-N 0.000 description 1
- PNLPXABQLXSICH-UHFFFAOYSA-N 4-amino-3-chlorophenol Chemical compound NC1=CC=C(O)C=C1Cl PNLPXABQLXSICH-UHFFFAOYSA-N 0.000 description 1
- IQXUIDYRTHQTET-UHFFFAOYSA-N 4-amino-3-nitrophenol Chemical compound NC1=CC=C(O)C=C1[N+]([O-])=O IQXUIDYRTHQTET-UHFFFAOYSA-N 0.000 description 1
- JTTMYKSFKOOQLP-UHFFFAOYSA-N 4-hydroxydiphenylamine Chemical compound C1=CC(O)=CC=C1NC1=CC=CC=C1 JTTMYKSFKOOQLP-UHFFFAOYSA-N 0.000 description 1
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 1
- BTJYWJVLRHNVAP-UHFFFAOYSA-N 5,6-dimethylbenzimidazol-1-amine Chemical compound C1=C(C)C(C)=CC2=C1N(N)C=N2 BTJYWJVLRHNVAP-UHFFFAOYSA-N 0.000 description 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-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
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 101100517284 Caenorhabditis elegans nsun-1 gene Proteins 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-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 Polymers 0.000 description 1
- MPPMXVWRCNRDOE-UHFFFAOYSA-N N,3-dimethyl-5-nitroaniline Chemical compound CNc1cc(C)cc(c1)[N+]([O-])=O MPPMXVWRCNRDOE-UHFFFAOYSA-N 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
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 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
- 239000000443 aerosol Substances 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- MMCPOSDMTGQNKG-UHFFFAOYSA-N anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 1
- 125000004421 aryl sulphonamide group Chemical group 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
- 239000000987 azo dye 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
- HLKZFSVWBQSKKH-UHFFFAOYSA-N but-3-enoic acid;1-ethenylpyrrolidin-2-one Chemical compound OC(=O)CC=C.C=CN1CCCC1=O HLKZFSVWBQSKKH-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- KCLZXXMMEDEBMF-UHFFFAOYSA-N ethyl n-(3-hydroxyphenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(O)=C1 KCLZXXMMEDEBMF-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000006870 function Effects 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
- 230000037308 hair color Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 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
- 239000002198 insoluble material Substances 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
- 239000007788 liquid Substances 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- HEFFCQILGLLHQC-UHFFFAOYSA-N n,4-dimethyl-n-phenylbenzenesulfonamide Chemical compound C=1C=C(C)C=CC=1S(=O)(=O)N(C)C1=CC=CC=C1 HEFFCQILGLLHQC-UHFFFAOYSA-N 0.000 description 1
- QCIFLGSATTWUQJ-UHFFFAOYSA-N n,4-dimethylaniline Chemical compound CNC1=CC=C(C)C=C1 QCIFLGSATTWUQJ-UHFFFAOYSA-N 0.000 description 1
- CDZOGLJOFWFVOZ-UHFFFAOYSA-N n-propylaniline Chemical compound CCCNC1=CC=CC=C1 CDZOGLJOFWFVOZ-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 239000001005 nitro dye 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
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 235000015424 sodium Nutrition 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
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/418—Amines containing nitro groups
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- 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
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)
- Coloring (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU83063A LU83063A1 (fr) | 1981-01-14 | 1981-01-14 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines,nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
| IT68731/81A IT1172866B (it) | 1981-01-14 | 1981-12-30 | Composizione tintoria per fibre che ratiniche a base di 3-nitro-ortofenilendiammine impiegate e procedimento per la loro preparazione |
| BR8200142A BR8200142A (pt) | 1981-01-14 | 1982-01-12 | Composicao tintorial para fibras queratinicas processo para coloracao de fibras queratinicas e derivados de nitroortofenilenodiamina |
| AT0011182A AT392000B (de) | 1981-01-14 | 1982-01-13 | Faerbemittel fuer keratinische fasern, insbesondere menschliche haare, und verfahren zur faerbung keratinischer fasern unter verwendung dieser mittel |
| BE0/207048A BE891773A (fr) | 1981-01-14 | 1982-01-13 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines, nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
| CA000394101A CA1175069A (fr) | 1981-01-14 | 1982-01-13 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines, nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
| CH185/82A CH651469A5 (fr) | 1981-01-14 | 1982-01-13 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines, nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation. |
| JP57003983A JPS57139584A (en) | 1981-01-14 | 1982-01-13 | Dyeing composition and dyeing method using same |
| DE3200787A DE3200787C2 (de) | 1981-01-14 | 1982-01-13 | Nitro-orthophenylendiamin-derivate, Verfahren zur Herstellung sowie deren Verwendung in Mitteln zum Färben menschlicher Haare |
| MX190962A MX156690A (es) | 1981-01-14 | 1982-01-13 | Composicion tintorea a base de 3-nitroortofenile nilenodiaminas para tenir carbello humano |
| FR8200472A FR2497662B1 (fr) | 1981-01-14 | 1982-01-13 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines, nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
| GB8200899A GB2090853B (en) | 1981-01-14 | 1982-01-13 | Dyeing compositions for keratin fibres based on 3-nitro-ortho-phenylenediamines and certain 3-nitro-ortho-phenylenediamines used therein |
| US07/764,958 US5186717A (en) | 1981-01-14 | 1991-09-25 | Dyeing compositions for keratin fibres, based on 3-nitro-ortho-phenylenediamines, and certain 3-nitro-ortho-phenylenediamines used therein |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU83063A LU83063A1 (fr) | 1981-01-14 | 1981-01-14 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines,nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
| LU83063 | 1981-01-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU83063A1 true LU83063A1 (fr) | 1982-09-10 |
Family
ID=19729560
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU83063A LU83063A1 (fr) | 1981-01-14 | 1981-01-14 | Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines,nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS57139584A (ja) |
| AT (1) | AT392000B (ja) |
| BE (1) | BE891773A (ja) |
| BR (1) | BR8200142A (ja) |
| CA (1) | CA1175069A (ja) |
| CH (1) | CH651469A5 (ja) |
| DE (1) | DE3200787C2 (ja) |
| FR (1) | FR2497662B1 (ja) |
| GB (1) | GB2090853B (ja) |
| IT (1) | IT1172866B (ja) |
| LU (1) | LU83063A1 (ja) |
| MX (1) | MX156690A (ja) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU83686A1 (fr) * | 1981-10-08 | 1983-06-08 | Oreal | Composition tinctoriale pour fibres keratiniques a base de colorants nitres benzeniques |
| JPS6032851A (ja) * | 1983-08-01 | 1985-02-20 | Konishiroku Photo Ind Co Ltd | 発色剤と還元剤との酸化縮合色素の製造方法 |
| LU86308A1 (fr) * | 1986-02-14 | 1987-09-10 | Oreal | Composition tinctoriale pour fibres keratiniques a base de 2-nitrometaphenylenediamines,procede de preparation de ces composes et nouvelles 2-nitro-metaphenylenediamines utilisees |
| LU86309A1 (fr) * | 1986-02-14 | 1987-09-10 | Oreal | Composition pour fibres keratiniques et en particulier pour cheveux humains,a base de nitroanilines halogenes,procede de teinture utilisant ladite composition tinctoriale et nouvelles 2-nitroanilines halogenees utilisees |
| DE3714775A1 (de) * | 1987-05-04 | 1988-11-24 | Wella Ag | Verwendung von 2,6-dinitro-anilinderivaten in haarfaerbemitteln und neue 2,6-dinitro-anilinderivate |
| LU86951A1 (fr) * | 1987-07-27 | 1989-03-08 | Oreal | 2-nitro metaphenylenediamines substituees,leur procede de preparation et leur utilisation en teinture des fibres keratiniques et en particulier des cheveux humains |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE928909C (de) * | 1951-02-07 | 1955-06-13 | Kleinol Produktion G M B H | Verfahren zum Faerben von tierischen Fasern, insbesondere von menschlichen Haaren, ohne Zuhilfenahme von Oxydationsmitteln |
| GB741334A (en) * | 1953-06-01 | 1955-11-30 | Unilever Ltd | Improvements in or relating to hair dyes |
| LU50461A1 (ja) * | 1966-02-15 | 1967-08-16 | ||
| US3743678A (en) * | 1968-02-28 | 1973-07-03 | Clairol Inc | Hair dyeing compositions |
| CA1024071A (en) * | 1972-08-09 | 1978-01-10 | George Alperin | Semi-permanent hair dye composition comprising a nitro-dye, a quaternary amine and certain n-oxyalkylated fatty acid amide |
-
1981
- 1981-01-14 LU LU83063A patent/LU83063A1/fr unknown
- 1981-12-30 IT IT68731/81A patent/IT1172866B/it active
-
1982
- 1982-01-12 BR BR8200142A patent/BR8200142A/pt unknown
- 1982-01-13 FR FR8200472A patent/FR2497662B1/fr not_active Expired
- 1982-01-13 MX MX190962A patent/MX156690A/es unknown
- 1982-01-13 CA CA000394101A patent/CA1175069A/fr not_active Expired
- 1982-01-13 JP JP57003983A patent/JPS57139584A/ja active Granted
- 1982-01-13 BE BE0/207048A patent/BE891773A/fr not_active IP Right Cessation
- 1982-01-13 CH CH185/82A patent/CH651469A5/fr not_active IP Right Cessation
- 1982-01-13 AT AT0011182A patent/AT392000B/de not_active IP Right Cessation
- 1982-01-13 DE DE3200787A patent/DE3200787C2/de not_active Expired - Fee Related
- 1982-01-13 GB GB8200899A patent/GB2090853B/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB2090853A (en) | 1982-07-21 |
| AT392000B (de) | 1990-12-27 |
| MX156690A (es) | 1988-09-27 |
| JPH0329828B2 (ja) | 1991-04-25 |
| BR8200142A (pt) | 1982-11-03 |
| BE891773A (fr) | 1982-07-13 |
| GB2090853B (en) | 1985-02-27 |
| FR2497662B1 (fr) | 1985-11-22 |
| IT1172866B (it) | 1987-06-18 |
| DE3200787C2 (de) | 1994-08-04 |
| CA1175069A (fr) | 1984-09-25 |
| FR2497662A1 (fr) | 1982-07-16 |
| ATA11182A (de) | 1990-07-15 |
| IT8168731A0 (it) | 1981-12-30 |
| JPS57139584A (en) | 1982-08-28 |
| DE3200787A1 (de) | 1982-09-09 |
| CH651469A5 (fr) | 1985-09-30 |
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