DE2628999C2 - Haarfärbemittel - Google Patents
HaarfärbemittelInfo
- Publication number
- DE2628999C2 DE2628999C2 DE2628999A DE2628999A DE2628999C2 DE 2628999 C2 DE2628999 C2 DE 2628999C2 DE 2628999 A DE2628999 A DE 2628999A DE 2628999 A DE2628999 A DE 2628999A DE 2628999 C2 DE2628999 C2 DE 2628999C2
- Authority
- DE
- Germany
- Prior art keywords
- udf54
- udf53
- hair dye
- carbon atoms
- diamino
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000000118 hair dye Substances 0.000 title claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000000126 substance Substances 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
- 239000000975 dye Substances 0.000 claims description 9
- 230000003647 oxidation Effects 0.000 claims description 9
- 238000007254 oxidation reaction Methods 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- WERSDZKEJFOKJJ-UHFFFAOYSA-N 4-methoxy-5-methylbenzene-1,3-diamine Chemical compound COC1=C(C)C=C(N)C=C1N WERSDZKEJFOKJJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000000982 direct dye Substances 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000000839 emulsion Substances 0.000 description 10
- -1 heterocyclic hydrazones Chemical class 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- 238000005691 oxidative coupling reaction Methods 0.000 description 6
- 238000004040 coloring Methods 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
- LQUBUCFMDWDLHL-UHFFFAOYSA-N 5-(2-methoxyethyl)benzene-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.COCCC1=CC(N)=CC(N)=C1 LQUBUCFMDWDLHL-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 230000037308 hair color Effects 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 3
- NNKPLDDESWSLES-UHFFFAOYSA-N 4-ethoxy-5-methylbenzene-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.CCOC1=C(C)C=C(N)C=C1N NNKPLDDESWSLES-UHFFFAOYSA-N 0.000 description 3
- WSGOOWHLGKOYFL-UHFFFAOYSA-N 4-methoxy-5-methylbenzene-1,3-diamine;dihydrochloride Chemical compound Cl.Cl.COC1=C(C)C=C(N)C=C1N WSGOOWHLGKOYFL-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 230000002110 toxicologic effect Effects 0.000 description 3
- 231100000027 toxicology Toxicity 0.000 description 3
- GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
- OOUYRFXOKGNRMR-UHFFFAOYSA-N 1-(2-methoxyethyl)-3,5-dinitrobenzene Chemical compound COCCC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 OOUYRFXOKGNRMR-UHFFFAOYSA-N 0.000 description 2
- XSFKCGABINPZRK-UHFFFAOYSA-N 4-aminopyrazol-3-one Chemical class NC1=CN=NC1=O XSFKCGABINPZRK-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 101100311330 Schizosaccharomyces pombe (strain 972 / ATCC 24843) uap56 gene Proteins 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 150000001860 citric acid derivatives Chemical class 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 150000003893 lactate salts Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 2
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 101150018444 sub2 gene Proteins 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- JUCSVQOEZGIMPJ-UHFFFAOYSA-N 2-ethoxy-1-methyl-3,5-dinitrobenzene Chemical compound CCOC1=C(C)C=C([N+]([O-])=O)C=C1[N+]([O-])=O JUCSVQOEZGIMPJ-UHFFFAOYSA-N 0.000 description 1
- XCHBHMOBNNBYAX-UHFFFAOYSA-N 2-methoxy-1-methyl-3,5-dinitrobenzene Chemical compound COC1=C(C)C=C([N+]([O-])=O)C=C1[N+]([O-])=O XCHBHMOBNNBYAX-UHFFFAOYSA-N 0.000 description 1
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 1
- CQLYXIUHVFRXLT-UHFFFAOYSA-N 2-methoxyethylbenzene Chemical compound COCCC1=CC=CC=C1 CQLYXIUHVFRXLT-UHFFFAOYSA-N 0.000 description 1
- MODIWXTUGZOVPP-UHFFFAOYSA-N 2-morpholin-4-ylpyrimidine-4,5,6-triamine Chemical compound NC1=C(N)C(N)=NC(N2CCOCC2)=N1 MODIWXTUGZOVPP-UHFFFAOYSA-N 0.000 description 1
- STMSOJGQPFGGLE-UHFFFAOYSA-N 2-n,2-n,4-n,4-n-tetramethylpyrimidine-2,4,5,6-tetramine Chemical compound CN(C)C1=NC(N)=C(N)C(N(C)C)=N1 STMSOJGQPFGGLE-UHFFFAOYSA-N 0.000 description 1
- GFKHZYMALAAJBX-UHFFFAOYSA-N 2-n,2-n-dimethylpyrimidine-2,4,5,6-tetramine Chemical compound CN(C)C1=NC(N)=C(N)C(N)=N1 GFKHZYMALAAJBX-UHFFFAOYSA-N 0.000 description 1
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000001049 brown dye Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- VFNGKCDDZUSWLR-UHFFFAOYSA-L disulfate(2-) Chemical compound [O-]S(=O)(=O)OS([O-])(=O)=O VFNGKCDDZUSWLR-UHFFFAOYSA-L 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000003700 hair damage Effects 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 150000004988 m-phenylenediamines Chemical class 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 229940055726 pantothenic acid Drugs 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 239000011713 pantothenic acid Substances 0.000 description 1
- 230000007903 penetration ability Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 159000000000 sodium salts Chemical group 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2628999A DE2628999C2 (de) | 1976-06-28 | 1976-06-28 | Haarfärbemittel |
| SE7706635A SE422410B (sv) | 1976-06-28 | 1977-06-07 | Harfergningsmedel pa basis av oxidationsfergemnen |
| NL7706257A NL7706257A (nl) | 1976-06-28 | 1977-06-07 | Haarverfmiddelen. |
| DK250777A DK158771C (da) | 1976-06-28 | 1977-06-07 | Haarfarvningsmiddel samt 3,5-diaminoalkylbenzener til brug ved haarfarvningsmidlet |
| US05/807,972 US4171203A (en) | 1976-06-28 | 1977-06-20 | Hair dye compositions containing 3,5-diamino-2-substituted-alkylbenzenes |
| IT24971/77A IT1080777B (it) | 1976-06-28 | 1977-06-23 | Tintura per capelli |
| GB26498/77A GB1581579A (en) | 1976-06-28 | 1977-06-24 | Hair dye compositions |
| JP7563577A JPS533427A (en) | 1976-06-28 | 1977-06-27 | Hairrdies |
| BE178808A BE856145A (fr) | 1976-06-28 | 1977-06-27 | Teintures pour cheveux contenant de nouveaux 3,5-diaminoalkylbenzenes substitues en positions 2-comme copulants |
| AT452577A AT348135B (de) | 1976-06-28 | 1977-06-27 | Haarfaerbemittel |
| FR7719866A FR2356413A1 (fr) | 1976-06-28 | 1977-06-28 | Teintures pour cheveux contenant de nouveaux 3,5-diaminoalkylbenzenes substitues en position 2- comme copulants |
| CH794077A CH632925A5 (de) | 1976-06-28 | 1977-06-28 | Haarfaerbemittel. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2628999A DE2628999C2 (de) | 1976-06-28 | 1976-06-28 | Haarfärbemittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2628999A1 DE2628999A1 (de) | 1978-01-05 |
| DE2628999C2 true DE2628999C2 (de) | 1987-03-26 |
Family
ID=5981658
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2628999A Expired DE2628999C2 (de) | 1976-06-28 | 1976-06-28 | Haarfärbemittel |
Country Status (12)
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2362116A1 (fr) * | 1976-08-20 | 1978-03-17 | Oreal | Metaphenylenediamines et compositions tinctoriales les contenant |
| DE2855917A1 (de) * | 1978-12-23 | 1980-07-10 | Wella Ag | Mittel und verfahren zur faerbung von haaren |
| FR2459042A1 (fr) * | 1979-06-18 | 1981-01-09 | Oreal | Nouvelles compositions tinctoriales pour cheveux contenant, comme coupleur le diamino-2,4 butoxybenzene et/ou ses sels |
| FR2461494A1 (fr) * | 1979-07-24 | 1981-02-06 | Oreal | Compositions tinctoriales pour cheveux contenant, en tant que coupleur, au moins un diamino-2,4 alkylbenzene |
| DE3011191A1 (de) * | 1980-03-22 | 1981-10-01 | Henkel KGaA, 4000 Düsseldorf | Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung und verwendung sowie diese enthaltende haarfaerbemittel |
| US5089257A (en) * | 1980-08-21 | 1992-02-18 | Henkel Kommanditgesellschaft Auf Aktien | Preparation for the simultaneous coloring, washing, and conditioning of human hair |
| US4566876A (en) * | 1983-03-10 | 1986-01-28 | Clairol Incorporated | Meta-phenylenediamine coupler compounds and oxidative hair dye compositions and methods using same |
| DE3430513A1 (de) * | 1984-08-18 | 1986-02-27 | Wella Ag, 6100 Darmstadt | Haarfaerbemittel mit diamino-tetrafluorethoxybenzolen sowie neue diamino-tetrafluorethoxybenzole |
| DE3622784A1 (de) * | 1986-07-07 | 1988-01-21 | Wella Ag | Neue 5-alkoxy-2,4-diamino-alkylbenzole sowie haarfaerbemittel mit 5-alkoxy-2,4-diamino-alkyl-benzolen |
| USRE34745E (en) * | 1986-10-30 | 1994-09-27 | The Dow Chemical Company | High purity process for the preparation of 4,6-diamino-1,3-benzenediol |
| USH726H (en) | 1987-01-09 | 1990-01-02 | Clairol Incorporated | 2,4-bis-aryloxy-m-phenylenediamines and their use as couplers in oxidation dye compositions |
| LU86905A1 (fr) * | 1987-05-29 | 1989-01-19 | Oreal | Nouvelles metaphenylenediamines,leur procede de preparation,composes intermediaires et utilisation de ces metaphenylenediamines en tant que coupleurs pour la teinture d'oxydation des fibres keratiniques et en particulier des cheveux humains |
| LU87396A1 (fr) * | 1988-11-22 | 1990-06-12 | Oreal | Nouvelles metaphenylenediamines trialcoxy-substituees,leur procede de preparation,et leur utilisation en tant que coupleurs pour la teinture d'oxydation des fibres keratiniques et en particulier des cheveux humains |
| FR2786092B1 (fr) * | 1998-11-20 | 2002-11-29 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| DE19959318A1 (de) * | 1999-12-09 | 2001-06-13 | Henkel Kgaa | Neue Farbstoffkombination |
| DE19959319A1 (de) * | 1999-12-09 | 2001-06-13 | Henkel Kgaa | Neue Farbstoffkombination |
| DE19959320A1 (de) * | 1999-12-09 | 2001-06-13 | Henkel Kgaa | Neue Farbstoffkombination |
| DE10034618A1 (de) * | 2000-07-17 | 2002-01-31 | Henkel Kgaa | Oxidationshaarfärbemittel |
| DE10114561A1 (de) * | 2001-03-24 | 2002-09-26 | Wella Ag | Verwendung von Mitteln enthaltend Kreatin, Kreatin und/oder deren Derivaten zur Verstärkung und Strukturverbesserung von keratinischen Fasern |
| DE10260822A1 (de) * | 2002-12-23 | 2004-07-01 | Henkel Kgaa | Neue Kupplerkomponenten |
| DE102004053653A1 (de) * | 2004-11-03 | 2006-05-04 | Henkel Kgaa | Oxidationsfärbemittel ohne Entwicklerkomponente |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1574337A (en) * | 1924-10-15 | 1926-02-23 | Bogert Marston Taylor | Dyestuff intermediates |
| US2548574A (en) * | 1947-02-27 | 1951-04-10 | Eastman Kodak Co | Sulfonamide substituted p-phenylenediamines containing o-alkoxy groups as silver halide photographic developers |
| BE625116A (US20110009641A1-20110113-C00273.png) * | 1961-11-22 | |||
| FR1426889A (fr) * | 1964-03-02 | 1966-02-04 | Oreal | Nouvelle solution tinctoriale pour cheveux |
| GB1077920A (en) * | 1964-12-18 | 1967-08-02 | Monsanto Chem Australia Ltd | Preparation of o-phenylenediamines |
| NL125337C (US20110009641A1-20110113-C00273.png) * | 1965-04-21 | |||
| US4031160A (en) * | 1965-05-06 | 1977-06-21 | Societe Anonyme Dite: L'oreal | 2-Amino-4-hydroxy-5-chloro toluene and the hydrochloride thereof |
| LU56102A1 (US20110009641A1-20110113-C00273.png) * | 1968-05-17 | 1970-01-14 | ||
| LU56722A1 (US20110009641A1-20110113-C00273.png) * | 1968-08-14 | 1970-02-16 | ||
| BE786710A (fr) * | 1971-10-04 | 1973-01-25 | Bristol Myers Co | Composition pour la teinture du cheveu avec |
| US4003699A (en) * | 1974-11-22 | 1977-01-18 | Henkel & Cie G.M.B.H. | Oxidation hair dyes based upon tetraaminopyrimidine developers |
| FR2315255A1 (fr) * | 1975-06-26 | 1977-01-21 | Oreal | Coupleurs glycoles |
-
1976
- 1976-06-28 DE DE2628999A patent/DE2628999C2/de not_active Expired
-
1977
- 1977-06-07 NL NL7706257A patent/NL7706257A/xx not_active Application Discontinuation
- 1977-06-07 SE SE7706635A patent/SE422410B/xx not_active IP Right Cessation
- 1977-06-07 DK DK250777A patent/DK158771C/da active
- 1977-06-20 US US05/807,972 patent/US4171203A/en not_active Expired - Lifetime
- 1977-06-23 IT IT24971/77A patent/IT1080777B/it active
- 1977-06-24 GB GB26498/77A patent/GB1581579A/en not_active Expired
- 1977-06-27 AT AT452577A patent/AT348135B/de not_active IP Right Cessation
- 1977-06-27 JP JP7563577A patent/JPS533427A/ja active Granted
- 1977-06-27 BE BE178808A patent/BE856145A/xx not_active IP Right Cessation
- 1977-06-28 FR FR7719866A patent/FR2356413A1/fr active Granted
- 1977-06-28 CH CH794077A patent/CH632925A5/de not_active IP Right Cessation
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| ATA452577A (de) | 1978-06-15 |
| IT1080777B (it) | 1985-05-16 |
| US4171203A (en) | 1979-10-16 |
| DE2628999A1 (de) | 1978-01-05 |
| JPS533427A (en) | 1978-01-13 |
| DK158771C (da) | 1990-12-03 |
| BE856145A (fr) | 1977-12-27 |
| JPS6154768B2 (US20110009641A1-20110113-C00273.png) | 1986-11-25 |
| AT348135B (de) | 1979-01-25 |
| SE422410B (sv) | 1982-03-08 |
| NL7706257A (nl) | 1977-12-30 |
| DK250777A (da) | 1977-12-29 |
| FR2356413B1 (US20110009641A1-20110113-C00273.png) | 1981-07-31 |
| FR2356413A1 (fr) | 1978-01-27 |
| GB1581579A (en) | 1980-12-17 |
| CH632925A5 (de) | 1982-11-15 |
| SE7706635L (sv) | 1977-12-29 |
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