CH620826A5 - - Google Patents
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- Publication number
- CH620826A5 CH620826A5 CH462076A CH462076A CH620826A5 CH 620826 A5 CH620826 A5 CH 620826A5 CH 462076 A CH462076 A CH 462076A CH 462076 A CH462076 A CH 462076A CH 620826 A5 CH620826 A5 CH 620826A5
- Authority
- CH
- Switzerland
- Prior art keywords
- hair dye
- hair
- developer
- radical
- weight
- Prior art date
Links
- 239000000118 hair dye Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 230000003647 oxidation Effects 0.000 claims description 9
- 238000007254 oxidation reaction Methods 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000000982 direct dye Substances 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 description 8
- 238000004043 dyeing Methods 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- 238000005691 oxidative coupling reaction Methods 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- ASHGTJPOSUFTGB-UHFFFAOYSA-N 3-methoxyphenol Chemical compound COC1=CC=CC(O)=C1 ASHGTJPOSUFTGB-UHFFFAOYSA-N 0.000 description 5
- 239000006071 cream Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000037308 hair color Effects 0.000 description 3
- -1 heterocyclic hydrazones Chemical class 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 2
- NKTOLZVEWDHZMU-UHFFFAOYSA-N 2,5-xylenol Chemical compound CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 description 2
- TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 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
- 239000003086 colorant Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 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
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000011031 topaz Substances 0.000 description 2
- 229910052853 topaz Inorganic materials 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- JHRGJMLMFWJXOG-UHFFFAOYSA-N 1-phenylpyrazolidine-3,5-dione Chemical compound N1C(=O)CC(=O)N1C1=CC=CC=C1 JHRGJMLMFWJXOG-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- HFNLKCXGWUHDFM-UHFFFAOYSA-N 2-[[5-amino-2-(dimethylamino)-6-methoxypyrimidin-4-yl]amino]ethanol Chemical compound COC1=NC(N(C)C)=NC(NCCO)=C1N HFNLKCXGWUHDFM-UHFFFAOYSA-N 0.000 description 1
- RBUYKHJIMFQPOZ-UHFFFAOYSA-N 2-n-(2,3-dimethoxyphenyl)pyrimidine-2,4,5-triamine Chemical compound COC1=CC=CC(NC=2N=C(N)C(N)=CN=2)=C1OC RBUYKHJIMFQPOZ-UHFFFAOYSA-N 0.000 description 1
- SLIIXBZYBYDXEM-UHFFFAOYSA-N 2-n-benzyl-6-methoxypyrimidine-2,4,5-triamine Chemical compound NC1=C(N)C(OC)=NC(NCC=2C=CC=CC=2)=N1 SLIIXBZYBYDXEM-UHFFFAOYSA-N 0.000 description 1
- XSFKCGABINPZRK-UHFFFAOYSA-N 4-aminopyrazol-3-one Chemical class NC1=CN=NC1=O XSFKCGABINPZRK-UHFFFAOYSA-N 0.000 description 1
- FDTLVBPQBLBGGR-UHFFFAOYSA-N 4-n-[4-(dimethylamino)phenyl]-6-methoxypyrimidine-2,4,5-triamine Chemical compound COC1=NC(N)=NC(NC=2C=CC(=CC=2)N(C)C)=C1N FDTLVBPQBLBGGR-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
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 1
- LGRWZUOIFUJEKA-UHFFFAOYSA-N 6-butoxy-2-n,4-n-dimethylpyrimidine-2,4,5-triamine Chemical compound CCCCOC1=NC(NC)=NC(NC)=C1N LGRWZUOIFUJEKA-UHFFFAOYSA-N 0.000 description 1
- YJPPPLCDLDGFGW-UHFFFAOYSA-N 6-butoxypyrimidine-2,4,5-triamine Chemical compound CCCCOC1=NC(N)=NC(N)=C1N YJPPPLCDLDGFGW-UHFFFAOYSA-N 0.000 description 1
- UCTDXPJGVCWJDL-UHFFFAOYSA-N 6-ethoxy-2-n,2-n-dimethyl-4-n-phenylpyrimidine-2,4,5-triamine Chemical compound CCOC1=NC(N(C)C)=NC(NC=2C=CC=CC=2)=C1N UCTDXPJGVCWJDL-UHFFFAOYSA-N 0.000 description 1
- XJMSIPODWNIPEO-UHFFFAOYSA-N 6-ethoxy-2-piperidin-1-ylpyrimidine-4,5-diamine Chemical compound NC1=C(N)C(OCC)=NC(N2CCCCC2)=N1 XJMSIPODWNIPEO-UHFFFAOYSA-N 0.000 description 1
- DUMZZTDWQOJXJT-UHFFFAOYSA-N 6-methoxy-2-n,2-n,4-n,4-n-tetramethylpyrimidine-2,4,5-triamine Chemical compound COC1=NC(N(C)C)=NC(N(C)C)=C1N DUMZZTDWQOJXJT-UHFFFAOYSA-N 0.000 description 1
- RVAVXGQFODDNHN-UHFFFAOYSA-N 6-methoxy-2-n,2-n,4-n-trimethylpyrimidine-2,4,5-triamine Chemical compound CNC1=NC(N(C)C)=NC(OC)=C1N RVAVXGQFODDNHN-UHFFFAOYSA-N 0.000 description 1
- NXALJCSPNAEOCO-UHFFFAOYSA-N 6-methoxy-2-n,2-n-dimethyl-4-n-phenylpyrimidine-2,4,5-triamine Chemical compound COC1=NC(N(C)C)=NC(NC=2C=CC=CC=2)=C1N NXALJCSPNAEOCO-UHFFFAOYSA-N 0.000 description 1
- HSVDZSHDOZSPPS-UHFFFAOYSA-N 6-methoxy-2-n-methylpyrimidine-2,4,5-triamine Chemical compound CNC1=NC(N)=C(N)C(OC)=N1 HSVDZSHDOZSPPS-UHFFFAOYSA-N 0.000 description 1
- DEPZAQKDMUNUSY-UHFFFAOYSA-N 6-methoxy-2-piperidin-1-ylpyrimidine-4,5-diamine Chemical compound NC1=C(N)C(OC)=NC(N2CCCCC2)=N1 DEPZAQKDMUNUSY-UHFFFAOYSA-N 0.000 description 1
- BJNONTKPIUHGLZ-UHFFFAOYSA-N 6-propoxypyrimidine-2,4,5-triamine Chemical compound CCCOC1=NC(N)=NC(N)=C1N BJNONTKPIUHGLZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 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
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 230000007815 allergy Effects 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
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000002845 discoloration Methods 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
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 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
- 150000007522 mineralic acids Chemical class 0.000 description 1
- ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives 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
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 159000000000 sodium salts Chemical group 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 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
- 239000010981 turquoise Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2516117A DE2516117C2 (de) | 1975-04-12 | 1975-04-12 | Haarfärbemittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH620826A5 true CH620826A5 (cs) | 1980-12-31 |
Family
ID=5943758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH462076A CH620826A5 (cs) | 1975-04-12 | 1976-04-12 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4046503A (cs) |
| JP (1) | JPS51123837A (cs) |
| AT (1) | AT340061B (cs) |
| BE (1) | BE840641A (cs) |
| CH (1) | CH620826A5 (cs) |
| DE (1) | DE2516117C2 (cs) |
| FR (1) | FR2306681A1 (cs) |
| GB (1) | GB1522229A (cs) |
| IT (1) | IT1059608B (cs) |
| NL (1) | NL7602988A (cs) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2623564A1 (de) * | 1976-05-26 | 1977-12-15 | Henkel & Cie Gmbh | Haarfaerbemittel |
| US4169703A (en) * | 1978-08-03 | 1979-10-02 | Syntex (U.S.A.) Inc. | Oxidative red hair dye |
| DK0467026T3 (da) * | 1990-07-17 | 1993-05-10 | Goldwell Gmbh | Middel til farvning af hår og anvendelse af midlet |
| US7288124B2 (en) | 2004-09-08 | 2007-10-30 | L'oreal S.A. | Heteroaromatic binuclear black direct dyes |
| FR2874821B1 (fr) | 2004-09-08 | 2006-10-20 | Oreal | Nouveaux colorants directs noirs di-noyaux heteroaromatiques |
| DE102012218460A1 (de) | 2012-10-10 | 2014-04-10 | Henkel Ag & Co. Kgaa | Haarfärbemittel enthaltend Aminopyrimidinderivate |
| DE102012218459A1 (de) | 2012-10-10 | 2014-04-10 | Henkel Ag & Co. Kgaa | Haarfärbemittel enthaltend Aminopyrimidinderivate |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2355691A (en) * | 1942-11-21 | 1944-08-15 | Eastman Kodak Co | Pyrimidine couplers |
| US2350812A (en) * | 1942-11-21 | 1944-06-06 | Eastman Kodak Co | Diketopyrimidine coupler |
| BE490235A (cs) * | 1948-07-21 | |||
| US2584024A (en) * | 1948-08-21 | 1952-01-29 | Merck & Co Inc | 2,4,5-triamino-6-alkoxy pyrimidines and process of preparing same |
| US3200040A (en) * | 1961-03-22 | 1965-08-10 | Hans Schwarzkopf | Hair dye comprising diaminopyridines |
| DE1492175A1 (de) * | 1965-07-07 | 1970-02-12 | Schwarzkopf Gmbh Hans | Verfahren zum Faerben von lebenden Haaren |
| US3359168A (en) * | 1966-08-03 | 1967-12-19 | Warner Lambert Pharmaceutical | Dyeing hair with 2, 3, 6-triaminopyridine and salts thereof |
| CH483478A (de) * | 1967-06-14 | 1969-12-31 | Geigy Ag J R | Verfahren zur Herstellung von Cyclammoniumazofarbstoffen |
-
1975
- 1975-04-12 DE DE2516117A patent/DE2516117C2/de not_active Expired
-
1976
- 1976-03-22 NL NL7602988A patent/NL7602988A/xx not_active Application Discontinuation
- 1976-04-05 US US05/673,457 patent/US4046503A/en not_active Expired - Lifetime
- 1976-04-07 IT IT22008/76A patent/IT1059608B/it active
- 1976-04-09 GB GB14482/76A patent/GB1522229A/en not_active Expired
- 1976-04-09 JP JP51039481A patent/JPS51123837A/ja active Pending
- 1976-04-09 AT AT260676A patent/AT340061B/de not_active IP Right Cessation
- 1976-04-12 FR FR7610704A patent/FR2306681A1/fr active Granted
- 1976-04-12 BE BE166064A patent/BE840641A/xx not_active IP Right Cessation
- 1976-04-12 CH CH462076A patent/CH620826A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1522229A (en) | 1978-08-23 |
| DE2516117A1 (de) | 1976-10-21 |
| FR2306681B1 (cs) | 1981-05-08 |
| FR2306681A1 (fr) | 1976-11-05 |
| US4046503A (en) | 1977-09-06 |
| AT340061B (de) | 1977-11-25 |
| NL7602988A (nl) | 1976-10-14 |
| IT1059608B (it) | 1982-06-21 |
| ATA260676A (de) | 1977-03-15 |
| DE2516117C2 (de) | 1984-08-16 |
| JPS51123837A (en) | 1976-10-28 |
| BE840641A (fr) | 1976-10-12 |
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