AT392000B - Faerbemittel fuer keratinische fasern, insbesondere menschliche haare, und verfahren zur faerbung keratinischer fasern unter verwendung dieser mittel - Google Patents

Faerbemittel fuer keratinische fasern, insbesondere menschliche haare, und verfahren zur faerbung keratinischer fasern unter verwendung dieser mittel Download PDF

Info

Publication number: AT392000B
Authority: AT; Austria
Prior art keywords: nitro; methyl; fibers; group; hair
Prior art date: 1981-01-14

Application number

AT0011182A

Other languages

German (de)

English (en)

Other versions

ATA11182A (de

Inventor

Andree Bugaut

Alex Junino

Jean-Jacques Vandenboosche

Original Assignee

Oreal

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

1981-01-14

Filing date

1982-01-13

Publication date

1990-12-27

1982-01-13 Application filed by Oreal filed Critical Oreal

1990-07-15 Publication of ATA11182A publication Critical patent/ATA11182A/de

1990-12-27 Application granted granted Critical

1990-12-27 Publication of AT392000B publication Critical patent/AT392000B/de

Links

239000003795 chemical substances by application Substances 0.000 title claims description 38
239000003086 colorant Substances 0.000 title claims description 33
239000000835 fiber Substances 0.000 title claims description 28
238000000034 method Methods 0.000 title claims description 11
238000004040 coloring Methods 0.000 title description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 56
239000000203 mixture Substances 0.000 claims description 43
150000001875 compounds Chemical class 0.000 claims description 34
239000000975 dye Substances 0.000 claims description 26
125000000217 alkyl group Chemical group 0.000 claims description 21
102000011782 Keratins Human genes 0.000 claims description 15
108010076876 Keratins Proteins 0.000 claims description 15
-1 glycol ethers Chemical class 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
238000004043 dyeing Methods 0.000 claims description 13
229910052739 hydrogen Inorganic materials 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
150000003839 salts Chemical class 0.000 claims description 12
230000001476 alcoholic effect Effects 0.000 claims description 11
230000003647 oxidation Effects 0.000 claims description 11
238000007254 oxidation reaction Methods 0.000 claims description 10
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
239000002537 cosmetic Substances 0.000 claims description 7
230000003113 alkalizing effect Effects 0.000 claims description 6
125000003277 amino group Chemical group 0.000 claims description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
239000002243 precursor Substances 0.000 claims description 6
230000008569 process Effects 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 4
239000000982 direct dye Substances 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
150000002431 hydrogen Chemical group 0.000 claims description 4
239000007800 oxidant agent Substances 0.000 claims description 4
239000011347 resin Substances 0.000 claims description 4
229920005989 resin Polymers 0.000 claims description 4
239000002453 shampoo Substances 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
125000004103 aminoalkyl group Chemical group 0.000 claims description 3
150000001555 benzenes Chemical class 0.000 claims description 3
239000000872 buffer Substances 0.000 claims description 3
239000003638 chemical reducing agent Substances 0.000 claims description 3
238000009967 direct dyeing Methods 0.000 claims description 3
150000002334 glycols Chemical class 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
FYTRVVJHEWUARG-UHFFFAOYSA-N n-(2-aminophenyl)nitramide Chemical compound NC1=CC=CC=C1N[N+]([O-])=O FYTRVVJHEWUARG-UHFFFAOYSA-N 0.000 claims description 3
239000002304 perfume Substances 0.000 claims description 3
229920005862 polyol Polymers 0.000 claims description 3
150000003077 polyols Chemical class 0.000 claims description 3
150000003254 radicals Chemical class 0.000 claims description 3
239000003352 sequestering agent Substances 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
239000002562 thickening agent Substances 0.000 claims description 3
239000002535 acidifier Substances 0.000 claims description 2
239000001000 anthraquinone dye Substances 0.000 claims description 2
239000000987 azo dye Substances 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
239000006210 lotion Substances 0.000 claims description 2
150000002828 nitro derivatives Chemical class 0.000 claims description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
101150009274 nhr-1 gene Proteins 0.000 claims 1
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239000000155 melt Substances 0.000 description 26
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238000001035 drying Methods 0.000 description 19
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238000012360 testing method Methods 0.000 description 12
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238000010992 reflux Methods 0.000 description 11
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238000001816 cooling Methods 0.000 description 10
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239000000126 substance Substances 0.000 description 8
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 8
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IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
239000003054 catalyst Substances 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
238000001953 recrystallisation Methods 0.000 description 7
OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 6
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 6
230000008878 coupling Effects 0.000 description 6
238000010168 coupling process Methods 0.000 description 6
238000005859 coupling reaction Methods 0.000 description 6
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
229920002134 Carboxymethyl cellulose Polymers 0.000 description 5
241001070941 Castanea Species 0.000 description 5
235000014036 Castanea Nutrition 0.000 description 5
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 5
238000009835 boiling Methods 0.000 description 5
239000001768 carboxy methyl cellulose Substances 0.000 description 5
235000010948 carboxy methyl cellulose Nutrition 0.000 description 5
239000008112 carboxymethyl-cellulose Substances 0.000 description 5
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
229910000041 hydrogen chloride Inorganic materials 0.000 description 5
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 5
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 4
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 4
QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 4
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
230000015556 catabolic process Effects 0.000 description 4
ALSTYHKOOCGGFT-UHFFFAOYSA-N cis-oleyl alcohol Natural products CCCCCCCCC=CCCCCCCCCO ALSTYHKOOCGGFT-UHFFFAOYSA-N 0.000 description 4
238000006731 degradation reaction Methods 0.000 description 4
239000007789 gas Substances 0.000 description 4
229910000037 hydrogen sulfide Inorganic materials 0.000 description 4
JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 4
229960005323 phenoxyethanol Drugs 0.000 description 4
238000005507 spraying Methods 0.000 description 4
MWGATWIBSKHFMR-UHFFFAOYSA-N 2-anilinoethanol Chemical compound OCCNC1=CC=CC=C1 MWGATWIBSKHFMR-UHFFFAOYSA-N 0.000 description 3
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 3
YRLORWPBJZEGBX-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazine Chemical compound C1=CC=C2NCCOC2=C1 YRLORWPBJZEGBX-UHFFFAOYSA-N 0.000 description 3
IOCXBXZBNOYTLQ-UHFFFAOYSA-N 3-nitrobenzene-1,2-diamine Chemical compound NC1=CC=CC([N+]([O-])=O)=C1N IOCXBXZBNOYTLQ-UHFFFAOYSA-N 0.000 description 3
YCGBOLMHJWHYDM-UHFFFAOYSA-N 4-methyl-6,7-dihydro-5h-cyclopenta[d]pyrimidin-2-amine Chemical compound CC1=NC(N)=NC2=C1CCC2 YCGBOLMHJWHYDM-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
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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 3
239000005639 Lauric acid Substances 0.000 description 3
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 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
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239000007864 aqueous solution Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
GUXKNOXLHZGZAT-UHFFFAOYSA-N 2-[3-amino-2-(2-hydroxyethyl)-4-nitrophenyl]ethanol Chemical compound OCCC1=C(C(=C(C=C1)[N+](=O)[O-])N)CCO GUXKNOXLHZGZAT-UHFFFAOYSA-N 0.000 description 2
PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
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QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
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239000005642 Oleic acid Substances 0.000 description 2
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
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206010070834 Sensitisation Diseases 0.000 description 2
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
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BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 2
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HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
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125000002091 cationic group Chemical group 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
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230000000052 comparative effect Effects 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
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125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
230000000694 effects Effects 0.000 description 2
DZGCGKFAPXFTNM-UHFFFAOYSA-N ethanol;hydron;chloride Chemical compound Cl.CCO DZGCGKFAPXFTNM-UHFFFAOYSA-N 0.000 description 2
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229910052500 inorganic mineral Inorganic materials 0.000 description 2
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
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125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
230000008313 sensitization Effects 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
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239000007921 spray Substances 0.000 description 2
239000010902 straw Substances 0.000 description 2
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OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
238000011282 treatment Methods 0.000 description 2
ANBZTKMYPDMODS-YPKPFQOOSA-N (z)-n,n-diethyloctadec-9-enamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(CC)CC ANBZTKMYPDMODS-YPKPFQOOSA-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
QFUSCYRJMXLNRB-UHFFFAOYSA-N 2,6-dinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O QFUSCYRJMXLNRB-UHFFFAOYSA-N 0.000 description 1
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
LDLCZOVUSADOIV-UHFFFAOYSA-N 2-bromoethanol Chemical compound OCCBr LDLCZOVUSADOIV-UHFFFAOYSA-N 0.000 description 1
ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 1
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-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
NPDACUSDTOMAMK-UHFFFAOYSA-N 4-Chlorotoluene Chemical compound CC1=CC=C(Cl)C=C1 NPDACUSDTOMAMK-UHFFFAOYSA-N 0.000 description 1
RAUWPNXIALNKQM-UHFFFAOYSA-N 4-nitro-1,2-phenylenediamine Chemical compound NC1=CC=C([N+]([O-])=O)C=C1N RAUWPNXIALNKQM-UHFFFAOYSA-N 0.000 description 1
TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-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
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
101100027097 Caenorhabditis elegans npp-15 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
241000251730 Chondrichthyes Species 0.000 description 1
241000640882 Condea Species 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
229920000084 Gum arabic Chemical class 0.000 description 1
QZXSMBBFBXPQHI-UHFFFAOYSA-N N-(dodecanoyl)ethanolamine Chemical compound CCCCCCCCCCCC(=O)NCCO QZXSMBBFBXPQHI-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000978776 Senegalia senegal Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Chemical class 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 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
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 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
239000000981 basic 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
229920002678 cellulose Chemical class 0.000 description 1
239000001913 cellulose Chemical class 0.000 description 1
235000010980 cellulose Nutrition 0.000 description 1
230000008859 change Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
239000013068 control sample Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
238000004042 decolorization Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
125000005594 diketone group Chemical group 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
238000011156 evaluation Methods 0.000 description 1
230000003203 everyday effect 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
125000005843 halogen group Chemical group 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
238000007689 inspection Methods 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000463 material 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
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
239000006083 mineral thickener Substances 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
XTTMNDFFWSZHCZ-UHFFFAOYSA-N n-(2-methoxyethyl)aniline Chemical compound COCCNC1=CC=CC=C1 XTTMNDFFWSZHCZ-UHFFFAOYSA-N 0.000 description 1
ZTQDYDIRBKMMQB-UHFFFAOYSA-N n-(4-aminophenyl)nitramide Chemical class NC1=CC=C(N[N+]([O-])=O)C=C1 ZTQDYDIRBKMMQB-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
WQMOWDRIXRBJBW-UHFFFAOYSA-N phenyl(piperidin-1-yl)diazene Chemical compound C1CCCCN1N=NC1=CC=CC=C1 WQMOWDRIXRBJBW-UHFFFAOYSA-N 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
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000000523 sample Substances 0.000 description 1
230000035945 sensitivity Effects 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
235000010265 sodium sulphite Nutrition 0.000 description 1
HLWRUJAIJJEZDL-UHFFFAOYSA-M sodium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC([O-])=O HLWRUJAIJJEZDL-UHFFFAOYSA-M 0.000 description 1
238000010186 staining Methods 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
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
230000008719 thickening Effects 0.000 description 1
238000012546 transfer Methods 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 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
230000003313 weakening effect Effects 0.000 description 1
230000002087 whitening effect Effects 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)

AT0011182A 1981-01-14 1982-01-13 Faerbemittel fuer keratinische fasern, insbesondere menschliche haare, und verfahren zur faerbung keratinischer fasern unter verwendung dieser mittel AT392000B (de)

Applications Claiming Priority (1)

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

Publications (2)

Publication Number	Publication Date
ATA11182A ATA11182A (de)	1990-07-15
AT392000B true AT392000B (de)	1990-12-27

Family

ID=19729560

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
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

Country Status (12)

Country	Link
JP (1)	JPS57139584A (fr)
AT (1)	AT392000B (fr)
BE (1)	BE891773A (fr)
BR (1)	BR8200142A (fr)
CA (1)	CA1175069A (fr)
CH (1)	CH651469A5 (fr)
DE (1)	DE3200787C2 (fr)
FR (1)	FR2497662B1 (fr)
GB (1)	GB2090853B (fr)
IT (1)	IT1172866B (fr)
LU (1)	LU83063A1 (fr)
MX (1)	MX156690A (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
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

Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB707618A (en) *	1951-02-07	1954-04-21	Unilever Ltd	Improvements in or relating to hair dyes
GB741334A (en) *	1953-06-01	1955-11-30	Unilever Ltd	Improvements in or relating to hair dyes

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU50461A1 (fr) *	1966-02-15	1967-08-16
US3743678A (en) *	1968-02-28	1973-07-03	Clairol Inc	Hair dyeing compositions
CA1024071A (fr) *	1972-08-09	1978-01-10	George Alperin	Teinture semi-permanente pour cheveux contenant un colorant nitro, une amine quaternaire et certaines amides d'acides gras n-oxyacilees

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 BE BE0/207048A patent/BE891773A/fr not_active IP Right Cessation
- 1982-01-13 GB GB8200899A patent/GB2090853B/en not_active Expired
- 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 JP JP57003983A patent/JPS57139584A/ja active Granted
- 1982-01-13 CA CA000394101A patent/CA1175069A/fr not_active Expired
- 1982-01-13 CH CH185/82A patent/CH651469A5/fr not_active IP Right Cessation

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB707618A (en) *	1951-02-07	1954-04-21	Unilever Ltd	Improvements in or relating to hair dyes
GB741334A (en) *	1953-06-01	1955-11-30	Unilever Ltd	Improvements in or relating to hair dyes

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, BD.83, 1975, 113 808 B *

Also Published As

Publication number	Publication date
FR2497662B1 (fr)	1985-11-22
JPS57139584A (en)	1982-08-28
IT1172866B (it)	1987-06-18
FR2497662A1 (fr)	1982-07-16
GB2090853A (en)	1982-07-21
ATA11182A (de)	1990-07-15
BR8200142A (pt)	1982-11-03
LU83063A1 (fr)	1982-09-10
MX156690A (es)	1988-09-27
DE3200787A1 (de)	1982-09-09
GB2090853B (en)	1985-02-27
DE3200787C2 (de)	1994-08-04
JPH0329828B2 (fr)	1991-04-25
CH651469A5 (fr)	1985-09-30
BE891773A (fr)	1982-07-13
CA1175069A (fr)	1984-09-25
IT8168731A0 (it)	1981-12-30

Legal Events

Date	Code	Title
1985-05-15	UEP	Publication of translation of european patent specification
1993-04-15	ELJ	Ceased due to non-payment of the annual fee
2001-10-15	EELA	Cancelled due to lapse of time

Publication	Publication Date	Title
DE2628641A1 (de)	1977-01-13	Glycerinierte kuppler
DE3019827A1 (de)	1980-11-27	Faerbende polymerisate, verfahren zu deren herstellung und deren verwendung in faerbemitteln
DE68904942T2 (de)	1993-06-03	Mindestens eine doppelte und eine einfache farbbase enthaltendes oxidationsfaerbemittel und verfahren zur faerbung mit diesem mittel.
DE69001413T2 (de)	1993-08-19	Einen indolfarbstoff und mindestens ein paraphenylendiamin mit einer sekundaeren aminogruppe enthaltende faerbemittel fuer keratinfasern und verfahren.
DE3025992C2 (fr)	1992-05-07
DE69500038T2 (de)	1997-01-23	Keratinische Fasern Oxydationsfärbemittel enthaltend einen Derivaten von Paraphenylenediamine und einen 6-Hydroxy 1,4-Benzoxazine
DE69417204T3 (de)	2008-06-26	Oxydative Haarfärbungszusammensetzung von einem Paraphenylendiamin und einem Meta-aminophenol, und Verfahren zur Anwendung
AT399276B (de)	1995-04-25	Färbemittel für keratinische fasern auf der basis von nitrobenzol-farbstoffen sowie färbeverfahren
DE3025991C2 (fr)	1989-05-18
DE3219406C2 (de)	1994-06-16	Nitro-paraphenylendiamin-Derivate, Verfahren zu deren Herstellung und Mittel zur Färbung keratinischer Fasern, die diese Derivate enthalten
DE3131409C2 (fr)	1989-01-12
DE3237004C2 (fr)	1992-02-13
DE2913995C2 (fr)	1989-08-31
AT401343B (de)	1996-08-26	Färbemittel für keratinfasern, insbesondere für humanhaare, auf basis eines 6-halogeno-4-nitrometaphenylendiamins und färbeverfahren für keratinfasern
AT392000B (de)	1990-12-27	Faerbemittel fuer keratinische fasern, insbesondere menschliche haare, und verfahren zur faerbung keratinischer fasern unter verwendung dieser mittel
EP0727203A1 (fr)	1996-08-21	Colorant d'oxydation pour cheveux
DE69700325T2 (de)	1999-11-04	Oxidationsfärbungsverfahren in zwei Stufen von keratinischen Fasern mit einem Mangansalz oder einem Komplex von Mangan und ein 1-Naphtol, substituiert in Lage 4 und eine Färbeset
DE3131366A1 (de)	1982-08-05	Haarfaerbemittel auf der basis von nitro-direktfarbstoffen und verfahren zur faerbung unter verwendung der genannten mittel
DE3442366A1 (de)	1985-06-13	Faerbemittel zum direktfaerben von keratinfasern und verfahren zum faerben von keratinfasern
DE3612665A1 (de)	1986-10-16	Nitroaminophenole, verfahren zu deren herstellung und diese verbindungen enthaltende faerbemittel
DE3131348C2 (fr)	1990-07-26
EP0895471B1 (fr)	2003-04-02	Agent et procede pour la coloration de fibres keratiniques
EP0132568A1 (fr)	1985-02-13	Dérivés de 1,4-diamino-5-chloro-2-nitrobenzène, procédé de leur production et agents pour la teinture des cheveux
AT400396B (de)	1995-12-27	Färbemittel zum direktfärben von keratinfasern, sowie färbeverfahren für keratinfasern
DE2913821A1 (de)	1979-10-18	Neue para-phenylendiamine, verfahren zu deren herstellung und diese enthaltende mittel