LU85557A1 - Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant - Google Patents

Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant Download PDF

Info

Publication number: LU85557A1
Authority: LU; Luxembourg
Prior art keywords: composition according; composition; formula; compound; dye
Prior art date: 1984-09-27

Application number

LU85557A

Other languages

English (en)

French (fr)

Inventor

Grollier Jean-Francois

Cotteret Jean

Junino Alex

Genet Alain

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.)

1984-09-27

Filing date

1984-09-27

Publication date

1986-04-03

1984-09-27 Application filed by Oreal filed Critical Oreal

1984-09-27 Priority to LU85557A priority Critical patent/LU85557A1/fr

1985-09-06 Priority to FR8513243A priority patent/FR2570600B1/fr

1985-09-19 Priority to CA000491125A priority patent/CA1253082A/fr

1985-09-23 Priority to AT2765/85A priority patent/AT393220B/de

1985-09-24 Priority to AU47908/85A priority patent/AU576898B2/en

1985-09-25 Priority to NL8502619A priority patent/NL192248C/nl

1985-09-25 Priority to DK433985A priority patent/DK164635C/da

1985-09-26 Priority to BR8504753A priority patent/BR8504753A/pt

1985-09-26 Priority to IT8567821A priority patent/IT1206826B/it

1985-09-26 Priority to CH4174/85A priority patent/CH667385A5/fr

1985-09-26 Priority to US06/780,606 priority patent/US4690685A/en

1985-09-26 Priority to GR852357A priority patent/GR852357B/el

1985-09-26 Priority to DE19853534369 priority patent/DE3534369A1/de

1985-09-27 Priority to JP60212720A priority patent/JPS61171768A/ja

1985-09-27 Priority to GB08523819A priority patent/GB2164959B/en

1985-09-27 Priority to BE0/215648A priority patent/BE903333A/fr

1985-09-27 Priority to ZA857487A priority patent/ZA857487B/xx

1986-04-03 Publication of LU85557A1 publication Critical patent/LU85557A1/fr

Links

239000000203 mixture Substances 0.000 title claims description 90
239000000835 fiber Substances 0.000 title claims description 21
238000004043 dyeing Methods 0.000 title claims description 11
238000000034 method Methods 0.000 title claims description 10
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical class NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 title description 3
239000000975 dye Substances 0.000 claims description 43
150000001875 compounds Chemical class 0.000 claims description 32
-1 2-nitro-paraphenylene diamines Chemical class 0.000 claims description 26
102000011782 Keratins Human genes 0.000 claims description 16
108010076876 Keratins Proteins 0.000 claims description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 9
150000003839 salts Chemical class 0.000 claims description 9
239000003795 chemical substances by application Substances 0.000 claims description 8
239000000982 direct dye Substances 0.000 claims description 8
125000003277 amino group Chemical group 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 6
239000012458 free base Substances 0.000 claims description 6
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239000011707 mineral Substances 0.000 claims description 6
150000001412 amines Chemical group 0.000 claims description 5
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239000002585 base Substances 0.000 claims description 4
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125000000623 heterocyclic group Chemical group 0.000 claims description 4
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239000002243 precursor Substances 0.000 claims description 4
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
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LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
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239000000443 aerosol Substances 0.000 claims description 2
125000004103 aminoalkyl group Chemical group 0.000 claims description 2
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150000001555 benzenes Chemical class 0.000 claims description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 2
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239000007788 liquid Substances 0.000 claims description 2
239000001005 nitro dye Substances 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
239000007800 oxidant agent Substances 0.000 claims description 2
239000002304 perfume Substances 0.000 claims description 2
239000003755 preservative agent Substances 0.000 claims description 2
239000003352 sequestering agent Substances 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 1
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QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 claims 1
239000000987 azo dye Substances 0.000 claims 1
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150000002790 naphthalenes Chemical class 0.000 claims 1
239000003605 opacifier Substances 0.000 claims 1
230000001590 oxidative effect Effects 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 51
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 24
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
239000000047 product Substances 0.000 description 12
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
235000019441 ethanol Nutrition 0.000 description 7
HVHNMNGARPCGGD-UHFFFAOYSA-N 2-nitro-p-phenylenediamine Chemical class NC1=CC=C(N)C([N+]([O-])=O)=C1 HVHNMNGARPCGGD-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000004458 analytical method Methods 0.000 description 6
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238000001035 drying Methods 0.000 description 5
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PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
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125000004432 carbon atom Chemical group C* 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
230000003647 oxidation Effects 0.000 description 4
238000007254 oxidation reaction Methods 0.000 description 4
238000001953 recrystallisation Methods 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
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238000009835 boiling Methods 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
238000004040 coloring Methods 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
239000003921 oil Substances 0.000 description 3
235000019198 oils Nutrition 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
239000012429 reaction media Substances 0.000 description 3
WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
239000003240 coconut oil Chemical class 0.000 description 2
235000019864 coconut oil Nutrition 0.000 description 2
239000002537 cosmetic Substances 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000000605 extraction Methods 0.000 description 2
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150000004665 fatty acids Chemical class 0.000 description 2
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230000037308 hair color Effects 0.000 description 2
239000000118 hair dye Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
230000003381 solubilizing effect Effects 0.000 description 2
238000003756 stirring Methods 0.000 description 2
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
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SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
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GVBHRNIWBGTNQA-UHFFFAOYSA-N 2-methoxy-4-nitroaniline Chemical compound COC1=CC([N+]([O-])=O)=CC=C1N GVBHRNIWBGTNQA-UHFFFAOYSA-N 0.000 description 1
BEJQXBXPRXFJDP-UHFFFAOYSA-N 3-(3,3-dihydroxypropoxy)propane-1,1-diol Chemical compound OC(O)CCOCCC(O)O BEJQXBXPRXFJDP-UHFFFAOYSA-N 0.000 description 1
LAMUXTNQCICZQX-UHFFFAOYSA-N 3-chloropropan-1-ol Chemical compound OCCCCl LAMUXTNQCICZQX-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 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
CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
229920002907 Guar gum Chemical class 0.000 description 1
229920000084 Gum arabic Chemical class 0.000 description 1
GZGZVOLBULPDFD-UHFFFAOYSA-N HC Red No. 3 Chemical compound NC1=CC=C(NCCO)C([N+]([O-])=O)=C1 GZGZVOLBULPDFD-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
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235000021355 Stearic acid Nutrition 0.000 description 1
244000186561 Swietenia macrophylla Species 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
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
230000002378 acidificating effect Effects 0.000 description 1
239000002535 acidifier Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
239000012080 ambient air Substances 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000011162 ammonium carbonates Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant 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
ZPHQBFRCXUIIAZ-UHFFFAOYSA-N benzene;hydrochloride Chemical compound Cl.C1=CC=CC=C1 ZPHQBFRCXUIIAZ-UHFFFAOYSA-N 0.000 description 1
239000001045 blue dye Substances 0.000 description 1
150000003842 bromide salts Chemical class 0.000 description 1
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150000001735 carboxylic acids Chemical class 0.000 description 1
150000001767 cationic compounds Chemical class 0.000 description 1
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150000001805 chlorine compounds Chemical class 0.000 description 1
239000003086 colorant Substances 0.000 description 1
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230000005494 condensation Effects 0.000 description 1
238000000151 deposition Methods 0.000 description 1
229940028356 diethylene glycol monobutyl ether Drugs 0.000 description 1
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VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
VGYFVNQYBUPXCQ-UHFFFAOYSA-N ethene;2-methyloxirane Chemical compound C=C.CC1CO1 VGYFVNQYBUPXCQ-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000001914 filtration Methods 0.000 description 1
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238000004128 high performance liquid chromatography Methods 0.000 description 1
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150000004679 hydroxides Chemical class 0.000 description 1
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239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
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150000002462 imidazolines Chemical class 0.000 description 1
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239000006210 lotion Substances 0.000 description 1
159000000003 magnesium salts Chemical class 0.000 description 1
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239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical class C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229960005323 phenoxyethanol Drugs 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
150000004986 phenylenediamines Chemical class 0.000 description 1
229940067107 phenylethyl alcohol Drugs 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
235000010413 sodium alginate Nutrition 0.000 description 1
239000000661 sodium alginate Substances 0.000 description 1
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235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
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PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
238000009987 spinning Methods 0.000 description 1
239000008117 stearic acid Chemical class 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000725 suspension Substances 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
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
235000012431 wafers Nutrition 0.000 description 1
238000005406 washing Methods 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
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B51/00—Nitro or nitroso dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Veterinary Medicine (AREA)
Chemical Kinetics & Catalysis (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)
Coloring (AREA)

LU85557A 1984-09-27 1984-09-27 Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant LU85557A1 (fr)

Priority Applications (17)

Application Number	Priority Date	Filing Date	Title
LU85557A LU85557A1 (fr)	1984-09-27	1984-09-27	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
FR8513243A FR2570600B1 (fr)	1984-09-27	1985-09-06	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
CA000491125A CA1253082A (fr)	1984-09-27	1985-09-19	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
AT2765/85A AT393220B (de)	1984-09-27	1985-09-23	Faerbemittel fuer keratinfasern, insbesondere fuer menschliche haare, und verfahren zum faerben von keratinfasern, insbesondere von menschlichen haaren
AU47908/85A AU576898B2 (en)	1984-09-27	1985-09-24	Dyeing coimposition for keratinous fibres containing at least one co-solubilised n-substituted 2-nitro-para-phenylenediamine
NL8502619A NL192248C (nl)	1984-09-27	1985-09-25	Verfpreparaat voor keratinevezels, alsmede werkwijze voor het verven van keratinevezels.
DK433985A DK164635C (da)	1984-09-27	1985-09-25	Farvningsmiddel til keratinfibre og indfarvningsproces for disse under anvendelse af et saadant farvningsmiddel
BR8504753A BR8504753A (pt)	1984-09-27	1985-09-26	Composicao tintorial e processo de tingimento de fibras queratinicas
IT8567821A IT1206826B (it)	1984-09-27	1985-09-26	Composizione tintoria per fibre cheratiniche comprendente almeno una 2 nitro parafenilendiammina n sostituita cosolubilizzata e corrispondente procedimento per la tintura di fibre cheratiniche
CH4174/85A CH667385A5 (fr)	1984-09-27	1985-09-26	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant.
US06/780,606 US4690685A (en)	1984-09-27	1985-09-26	Dyeing composition for keratinous fibres containing at least one co-solubilized N-substituted 2-nitro-para-phenylenediamine
GR852357A GR852357B (pt)	1984-09-27	1985-09-26
DE19853534369 DE3534369A1 (de)	1984-09-27	1985-09-26	Faerbemittel fuer keratinfasern, das mindestens ein n-substituiertes 2-nitro-p-phenylendiamin enthaelt, und faerbeverfahren fuer keratinfasern
JP60212720A JPS61171768A (ja)	1984-09-27	1985-09-27	少くとも１種のｎ−置換された共可溶化性２−ニトロ−パラフエニレンジアミンを含むケラチン繊維のための染色組成物および相当するケラチン繊維の染色方法
GB08523819A GB2164959B (en)	1984-09-27	1985-09-27	Dyeing composition for keratinous fibres containing at least one co-solubilised n-substituted 2-nitro-para-phenylenediamine
BE0/215648A BE903333A (fr)	1984-09-27	1985-09-27	Compositions tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylene-diamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
ZA857487A ZA857487B (en)	1984-09-27	1985-09-27	Dyeing composition for keratinous fibres containing at least one co-solubilised n-substituted 2-nitro-para-phenylenediamine

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU85557		1984-09-27
LU85557A LU85557A1 (fr)	1984-09-27	1984-09-27	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant

Publications (1)

Publication Number	Publication Date
LU85557A1 true LU85557A1 (fr)	1986-04-03

Family

ID=19730328

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85557A LU85557A1 (fr)	1984-09-27	1984-09-27	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant

Country Status (17)

Country	Link
US (1)	US4690685A (pt)
JP (1)	JPS61171768A (pt)
AT (1)	AT393220B (pt)
AU (1)	AU576898B2 (pt)
BE (1)	BE903333A (pt)
BR (1)	BR8504753A (pt)
CA (1)	CA1253082A (pt)
CH (1)	CH667385A5 (pt)
DE (1)	DE3534369A1 (pt)
DK (1)	DK164635C (pt)
FR (1)	FR2570600B1 (pt)
GB (1)	GB2164959B (pt)
GR (1)	GR852357B (pt)
IT (1)	IT1206826B (pt)
LU (1)	LU85557A1 (pt)
NL (1)	NL192248C (pt)
ZA (1)	ZA857487B (pt)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
LU85541A1 (fr) *	1984-09-17	1986-04-03	Oreal	Nouveau colorant nitre benzenique,son procede de preparation et son utilisation en teinture de fibres keratiniques
DE3545994A1 (de) *	1985-12-23	1987-06-25	Wella Ag	4-bis(2'-hydroxyethyl)amino-1-(3'-hydroxypropyl)amino-2-nitro-benzol, verfahren zu dessen herstellung sowie mittel zum faerben von haaren
US5180399A (en) *	1987-05-25	1993-01-19	L'oreal	Process for dyeing keratinous fibres with oxidation bases combined with an iodide and dyeing composition employed
US4857071A (en) *	1987-08-21	1989-08-15	Clairol, Inc.	Novel hair dye and method of use
LU87097A1 (fr) *	1987-12-30	1989-07-07	Oreal	Procede de teinture des fibres keratiniques et composition de teinture mettant en oeuvre du 5,6-dihydroxyindole,un colorant direct nitre et un iodure
US5167669A (en) *	1989-07-21	1992-12-01	L'oreal	Composition for dyeing keratinous fibers employing an indole dye and at least one para-phenylenediamine containing a secondary amino group and process for use
US5171889A (en) *	1990-10-31	1992-12-15	Clairol Incorporated	Compositions containing nitroaniline dyes having a carbamide substituent group
FR2692572B1 (fr) *	1992-06-19	2001-08-31	Oreal	2-nitro p-phénylènediamines hydroxypropylées, leur procédé de préparation et leur utilisation en teinture des fibres kératiniques.
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
FR2954098A1 (fr) *	2009-12-23	2011-06-24	Oreal	Composition comprenant au moins un derive d'orthodiphenol un derive metallique particulier et un agent alcalinisant, pour colorer les fibres keratiniques
KR102164724B1 (ko) *	2020-04-20	2020-10-13	한국콜마주식회사	폼 타입의 반영구 염모제용 조성물

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT200263B (de) *	1953-06-01	1958-10-25	Unilever Nv	Mittel zum Färben von tierischen Fasern, insbesondere von menschlichem Haar
NL94968C (pt) *	1953-06-01
GB741334A (en) *	1953-06-01	1955-11-30	Unilever Ltd	Improvements in or relating to hair dyes
US2750327A (en) *	1953-06-01	1956-06-12	Lever Brothers Ltd	Process of dyeing animal fibers and dyes and dyeing compositions therefor
US3088978A (en) *	1960-09-12	1963-05-07	Walter H Brunner	Catalytic hydrogenation of 2, 4-dinitrophenylamines
US3088877A (en) *	1960-10-13	1963-05-07	Walter H Brunner	Method of dyeing keratinaceous materials with p-phenylene diamine compositions
US3088878A (en) *	1960-11-22	1963-05-07	Walter H Brunner	Method of dyeing keratinaceous materials with nitro-substituted para-phenylene diamine compositions
US3119867A (en) *	1962-01-26	1964-01-28	Clairol Inc	Amino, nitro-phenyl-biguanides and amino, nitro-phenyl; guanyl-ureas
FR1310072A (pt) *	1964-06-12	1963-03-04
FR1411124A (fr) *	1964-07-30	1965-09-17	Oreal	Nouveaux colorants pour la teinture des cheveux et leur procédé de préparation
US3274249A (en) *	1964-09-14	1966-09-20	Clairol Inc	Derivatives of 1, 4-diamino-2-nitro-benzenes
US3629330A (en) *	1965-05-24	1971-12-21	Clairol Inc	Components for hair dyeing compositions
US3646216A (en) *	1967-09-01	1972-02-29	Shulton Inc	N1-aminoalkyl derivatives of 2-nitro-p-phenylenediamine
US3632582A (en) *	1967-11-02	1972-01-04	Clairol Inc	Process for preparing nitro-p-phenylene-diamines
US3634478A (en) *	1969-09-18	1972-01-11	Clairol Inc	N-(cyanoalkyl)-nitrophenylene diamines
CA1019678A (en) *	1972-11-24	1977-10-25	George Alperin	Aqueous alkaline hair dye compositions
CA1101335A (en) *	1976-06-30	1981-05-19	Raymond Feinland	P-phenylene diamines and 1,2,4-benzenetriols as hair dye preparation
GB2082207B (en) *	1980-08-08	1984-03-07	Oreal	Hair-dryeing compositions based on nitro direct dyestuffs and a dyeing process using these compositions
LU83686A1 (fr) *	1981-10-08	1983-06-08	Oreal	Composition tinctoriale pour fibres keratiniques a base de colorants nitres benzeniques
FR2519251B1 (fr) *	1982-01-05	1985-11-22	Oreal	Composition tinctoriales a base de precurseurs de colorants d'oxydation et d'orthonitranilines n-substituees comprenant une alcanolamine et du bisulfite de sodium et leur utilisation en teinture des fibres keratiniques
LU85098A1 (fr) *	1983-11-21	1985-07-17	Oreal	Composition tinotoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants
LU85421A1 (fr) *	1984-06-20	1986-01-24	Oreal	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylene n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants
LU85541A1 (fr) *	1984-09-17	1986-04-03	Oreal	Nouveau colorant nitre benzenique,son procede de preparation et son utilisation en teinture de fibres keratiniques

1984
- 1984-09-27 LU LU85557A patent/LU85557A1/fr unknown
1985
- 1985-09-06 FR FR8513243A patent/FR2570600B1/fr not_active Expired
- 1985-09-19 CA CA000491125A patent/CA1253082A/fr not_active Expired
- 1985-09-23 AT AT2765/85A patent/AT393220B/de not_active IP Right Cessation
- 1985-09-24 AU AU47908/85A patent/AU576898B2/en not_active Expired
- 1985-09-25 DK DK433985A patent/DK164635C/da not_active IP Right Cessation
- 1985-09-25 NL NL8502619A patent/NL192248C/nl not_active IP Right Cessation
- 1985-09-26 CH CH4174/85A patent/CH667385A5/fr not_active IP Right Cessation
- 1985-09-26 GR GR852357A patent/GR852357B/el unknown
- 1985-09-26 BR BR8504753A patent/BR8504753A/pt unknown
- 1985-09-26 DE DE19853534369 patent/DE3534369A1/de active Granted
- 1985-09-26 US US06/780,606 patent/US4690685A/en not_active Expired - Lifetime
- 1985-09-26 IT IT8567821A patent/IT1206826B/it active
- 1985-09-27 GB GB08523819A patent/GB2164959B/en not_active Expired
- 1985-09-27 BE BE0/215648A patent/BE903333A/fr not_active IP Right Cessation
- 1985-09-27 JP JP60212720A patent/JPS61171768A/ja active Granted
- 1985-09-27 ZA ZA857487A patent/ZA857487B/xx unknown

Also Published As

Publication number	Publication date
DK164635C (da)	1992-12-14
GB8523819D0 (en)	1985-10-30
NL8502619A (nl)	1986-04-16
DE3534369A1 (de)	1986-04-03
AU4790885A (en)	1986-04-10
CH667385A5 (fr)	1988-10-14
GB2164959B (en)	1988-04-27
FR2570600B1 (fr)	1988-12-30
BE903333A (fr)	1986-03-27
IT8567821A0 (it)	1985-09-26
DK433985A (da)	1986-03-28
GB2164959A (en)	1986-04-03
DK433985D0 (da)	1985-09-25
JPS61171768A (ja)	1986-08-02
ZA857487B (en)	1986-06-25
NL192248B (nl)	1996-12-02
ATA276585A (de)	1991-02-15
DK164635B (da)	1992-07-27
GR852357B (pt)	1986-01-28
US4690685A (en)	1987-09-01
BR8504753A (pt)	1986-07-22
NL192248C (nl)	1997-04-03
IT1206826B (it)	1989-05-03
AU576898B2 (en)	1988-09-08
FR2570600A1 (fr)	1986-03-28
DE3534369C2 (pt)	1991-01-03
CA1253082A (fr)	1989-04-25
AT393220B (de)	1991-09-10
JPH039085B2 (pt)	1991-02-07

Publication	Publication Date	Title
CH666181A5 (fr)	1988-07-15	Compositions de teinture des fibres keratiniques contenant un colorant azoique.
CH640508A5 (fr)	1984-01-13	Metaphenylenediamines et compositions tinctoriales les contenant.
CH661501A5 (fr)	1987-07-31	Composes derivant du amino-3 propanol-2 utilisables pour la teinture des cheveux, leur procede de preparation, composition de teinture les contenant et procede de teinture de cheveux correspondant.
CH657607A5 (fr)	1986-09-15	Derives nitres de la serie benzenique, leur procede de preparation et leur utilisation en teinture des fibres keratiniques.
CA1341194C (fr)	2001-02-27	Composition de teinture de fibre keratinique contenant des bases d'oxydation dites "doubles" et des bases d'oxydation dites "simples", et procede de teinture la mettant en oeuvre
CA1252725A (fr)	1989-04-18	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
LU85557A1 (fr)	1986-04-03	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant
CA1180282A (fr)	1985-01-02	Composition tinctoriale pour fibres keratiniques a base de colorants nitres benzeniques
CA1251738A (fr)	1989-03-28	Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants
CH653007A5 (fr)	1985-12-13	Nitro-paraphenylenediamines chlorees et leur utilisation en teinture des fibres keratiniques.
CA1213889A (fr)	1986-11-12	Composition tinctoriale pour fibres keratiniques a base de nitro-anilines, nouvelles nitro-anilines et leur procede de preparation
CA1222462A (fr)	1987-06-02	Composition tinctoriale pour la coloration directe des fibres keratiniques, renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants
CH649569A5 (fr)	1985-05-31	Colorants nitres, leur procede de preparation et utilisation de ces colorants en teinture des fibres keratiniques.
FR2571364A1 (fr)	1986-04-11	Nouveau procede de preparation de nitroparaphenylenediamines n,n'-disubstituees, nouvelles oxazolidones utilisees dans ce procede, nouvelles nitroparaphenylenediamines n,n'-disubstituees obtenues selon ce procede et compositions tinctoriales contenant les nitroparaphenylenediamines n,n'-disubstituees obtenues selon ledit procede
FR2580279A1 (fr)	1986-10-17	Nouveaux nitroaminophenols, leur procede de preparation et leur utilisation en teinture des fibres keratiniques, nouveaux nitroaminobenzenes intermediaires et leur utilisation en teinture des fibres keratiniques
CH670086A5 (pt)	1989-05-12
CA1175069A (fr)	1984-09-25	Composition tinctoriale pour fibres keratiniques a base de nitro-3 orthophenylenediamines, nouvelles nitro-3 orthophenylenediamines utilisees et leurs procedes de preparation
CH640221A5 (fr)	1983-12-30	Paraphenylenediamines utilisables en teinture capillaire dite d'oxydation.
CH667588A5 (fr)	1988-10-31	Compositions de teinture pour fibres keratiniques a base de metaphenylenediamines halogenees.
CA1257611A (fr)	1989-07-18	Dinitro-2,4, hydroxyalkyl-6 anilines, leur procede de preparation et leur utilisation en teinture des fibres keratiniques, et en particulier des cheveux humains
BE894633A (fr)	1983-04-07	Composition tinctoriale pour fibres keratiniques a base de nitroanilines, nouvelles nitroanilines et leur procede de preparation
LU83730A7 (fr)	1983-09-01	Composition tinctoriale pour fibres keratiniques a base de nitro-anilines,nouvelles nitro-anilines et leur procede de preparation
CH669596A5 (pt)	1989-03-31
LU83315A1 (fr)	1983-03-24	Nouvelles nitro-paraphenylenediamines,leur procede de preparation et leur utilisation en teinture des fibres keratiniques
FR2512016A1 (fr)	1983-03-04	Procede de preparation de nitro-anilines, compositions tinctoriales pour cheveux les contenant et nitro-anilines nouvelles