SE445970B - Harfergningsmedel pa basis av oxidationsfergemnen - Google Patents
Harfergningsmedel pa basis av oxidationsfergemnenInfo
- Publication number
- SE445970B SE445970B SE7714800A SE7714800A SE445970B SE 445970 B SE445970 B SE 445970B SE 7714800 A SE7714800 A SE 7714800A SE 7714800 A SE7714800 A SE 7714800A SE 445970 B SE445970 B SE 445970B
- Authority
- SE
- Sweden
- Prior art keywords
- coupling
- diamino
- hair
- weight
- component
- Prior art date
Links
- 239000000126 substance Substances 0.000 title claims description 10
- 230000003647 oxidation Effects 0.000 title description 2
- 238000007254 oxidation reaction Methods 0.000 title description 2
- 238000010168 coupling process Methods 0.000 claims description 23
- 238000005859 coupling reaction Methods 0.000 claims description 23
- 230000008878 coupling Effects 0.000 claims description 22
- 239000000118 hair dye Substances 0.000 claims description 15
- 239000000975 dye Substances 0.000 claims description 14
- 210000004209 hair Anatomy 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 7
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 claims description 6
- XQDNFAMOIPNVES-UHFFFAOYSA-N 3,5-Dimethoxyphenol Chemical compound COC1=CC(O)=CC(OC)=C1 XQDNFAMOIPNVES-UHFFFAOYSA-N 0.000 claims description 4
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 claims description 3
- DBIJZEYNEPBLGA-UHFFFAOYSA-N 2,4-diamino-3-chlorophenol Chemical compound NC1=CC=C(O)C(N)=C1Cl DBIJZEYNEPBLGA-UHFFFAOYSA-N 0.000 claims description 2
- WSVFDPKNANXQKM-UHFFFAOYSA-N 2,4-diamino-6-methylphenol Chemical compound CC1=CC(N)=CC(N)=C1O WSVFDPKNANXQKM-UHFFFAOYSA-N 0.000 claims description 2
- DDQAFFLMUSVRSQ-UHFFFAOYSA-N 5-(methylamino)benzene-1,3-diol Chemical compound CNC1=CC(O)=CC(O)=C1 DDQAFFLMUSVRSQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- ZMXYNJXDULEQCK-UHFFFAOYSA-N 2-amino-p-cresol Chemical compound CC1=CC=C(O)C(N)=C1 ZMXYNJXDULEQCK-UHFFFAOYSA-N 0.000 claims 1
- ZYSOYLBBCYWEMB-UHFFFAOYSA-N 7-aminonaphthalen-1-ol Chemical compound C1=CC=C(O)C2=CC(N)=CC=C21 ZYSOYLBBCYWEMB-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 239000002085 irritant Substances 0.000 claims 1
- 231100000021 irritant Toxicity 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 13
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 9
- -1 for example Chemical class 0.000 description 9
- 239000007800 oxidant agent Substances 0.000 description 8
- 239000006071 cream Substances 0.000 description 7
- 238000004043 dyeing Methods 0.000 description 5
- 238000005691 oxidative coupling reaction Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 235000019646 color tone Nutrition 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000037308 hair color Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 3
- 229960001755 resorcinol Drugs 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- 230000002110 toxicologic effect Effects 0.000 description 3
- 231100000027 toxicology Toxicity 0.000 description 3
- VPMMJSPGZSFEAH-UHFFFAOYSA-N 2,4-diaminophenol;hydrochloride Chemical compound [Cl-].NC1=CC=C(O)C([NH3+])=C1 VPMMJSPGZSFEAH-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000004061 bleaching Methods 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
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003599 detergent 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
- 239000004615 ingredient Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 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
- 159000000000 sodium salts Chemical group 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- YBLFXCPZOBQIIN-UHFFFAOYSA-N 3-methoxybenzene-1,2-diamine;sulfuric acid Chemical compound OS(O)(=O)=O.COC1=CC=CC(N)=C1N YBLFXCPZOBQIIN-UHFFFAOYSA-N 0.000 description 1
- FDJQHYWUHGBBTO-UHFFFAOYSA-N 4-methoxybenzene-1,3-diamine;sulfuric acid Chemical compound OS(O)(=O)=O.COC1=CC=C(N)C=C1N FDJQHYWUHGBBTO-UHFFFAOYSA-N 0.000 description 1
- ZLHGTHCCYUEAIK-UHFFFAOYSA-N 5,7-dibromo-2-(5,7-dibromo-3-hydroxy-1H-indol-2-yl)indol-3-one Chemical compound [O-]c1c([nH]c2c(Br)cc(Br)cc12)C1=[NH+]c2c(cc(Br)cc2Br)C1=O ZLHGTHCCYUEAIK-UHFFFAOYSA-N 0.000 description 1
- VDBJCDWTNCKRTF-UHFFFAOYSA-N 6'-hydroxyspiro[2-benzofuran-3,9'-9ah-xanthene]-1,3'-dione Chemical compound O1C(=O)C2=CC=CC=C2C21C1C=CC(=O)C=C1OC1=CC(O)=CC=C21 VDBJCDWTNCKRTF-UHFFFAOYSA-N 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 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
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000008859 change Effects 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
- 238000004040 coloring Methods 0.000 description 1
- NKLPQNGYXWVELD-UHFFFAOYSA-M coomassie brilliant blue Chemical compound [Na+].C1=CC(OCC)=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=C1 NKLPQNGYXWVELD-UHFFFAOYSA-M 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- SKKIWNWLPWAHTF-UHFFFAOYSA-L disodium;5-(4-acetamidoanilino)-8-amino-9,10-dioxoanthracene-1,2-disulfonate Chemical compound [Na+].[Na+].C1=CC(NC(=O)C)=CC=C1NC1=CC=C(N)C2=C1C(=O)C(C=CC(=C1S([O-])(=O)=O)S([O-])(=O)=O)=C1C2=O SKKIWNWLPWAHTF-UHFFFAOYSA-L 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
- 238000001035 drying Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 231100000640 hair analysis Toxicity 0.000 description 1
- 230000003700 hair damage Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000005259 measurement Methods 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
- 150000007522 mineralic acids 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
- 230000001590 oxidative effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- MQEFDQWUCTUJCP-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine;sulfuric acid Chemical compound OS(O)(=O)=O.NC1=NC(N)=C(N)C(N)=N1 MQEFDQWUCTUJCP-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- BADRBIXUSUCBEG-UHFFFAOYSA-M sodium;2-[(4-amino-3-methyl-9,10-dioxoanthracen-1-yl)amino]-5-methylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1NC1=CC(C)=C(N)C2=C1C(=O)C1=CC=CC=C1C2=O BADRBIXUSUCBEG-UHFFFAOYSA-M 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 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
- A61K8/415—Aminophenols
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/347—Phenols
-
- 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
-
- 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
- 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)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2702118A DE2702118C3 (de) | 1977-01-20 | 1977-01-20 | Haarfärbemittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE7714800L SE7714800L (sv) | 1978-07-21 |
| SE445970B true SE445970B (sv) | 1986-08-04 |
Family
ID=5999057
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7714800A SE445970B (sv) | 1977-01-20 | 1977-12-27 | Harfergningsmedel pa basis av oxidationsfergemnen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4213758A (is") |
| AT (1) | AT362070B (is") |
| BE (1) | BE863079R (is") |
| CH (1) | CH604709A5 (is") |
| DE (1) | DE2702118C3 (is") |
| DK (1) | DK148894C (is") |
| FR (1) | FR2377801A2 (is") |
| GB (1) | GB1572983A (is") |
| IT (1) | IT1111155B (is") |
| NL (1) | NL7711952A (is") |
| SE (1) | SE445970B (is") |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2833989A1 (de) * | 1978-08-03 | 1980-02-21 | Wella Ag | Mittel zum faerben von haaren |
| DE3011191A1 (de) * | 1980-03-22 | 1981-10-01 | Henkel KGaA, 4000 Düsseldorf | Neue kupplerkomponenten fuer oxidationshaarfarben, deren herstellung und verwendung sowie diese enthaltende haarfaerbemittel |
| DE3233541A1 (de) * | 1982-09-10 | 1984-03-15 | Henkel KGaA, 4000 Düsseldorf | Haarfaerbemittel |
| GB2159828B (en) * | 1984-04-20 | 1987-10-21 | Shiseido Co Ltd | Naphthalene derivatives and hair dye compositions containing them |
| DE3508265A1 (de) * | 1985-03-08 | 1986-09-11 | Ruetgerswerke Ag | Haarfaerbemittel |
| DE3627922A1 (de) * | 1986-08-18 | 1988-03-03 | Henkel Kgaa | Neue tetraaminopyrimidin-derivate und deren verwendung in haarfaerbemitteln |
| DE19735866C1 (de) * | 1997-08-19 | 1998-10-15 | Goldwell Gmbh | Haarfärbemittel |
| FR2772613B1 (fr) | 1997-12-19 | 2003-05-09 | Oreal | Utilisation du phloroglucinol dans une composition cosmetique |
| FR2776186B1 (fr) * | 1998-03-20 | 2001-01-26 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| DE102004008918A1 (de) * | 2004-02-24 | 2005-09-08 | Wella Ag | (3,5-Diaminophenyl)(2,4-dihydroxy-phenyl)methanon und dessen Säureaddukte, Verfahren zur deren Herstellung und die Verwendung diese Verbindungen zur Färbung von Fasern |
| FR2974510B1 (fr) * | 2011-04-29 | 2013-04-12 | Oreal | Composition de coloration mettant en oeuvre un coupleur derive de phenol en milieu riche en corps gras, procedes et dispositif |
| EP2830579B1 (en) | 2012-03-27 | 2020-02-26 | Noxell Corporation | Hair colorant compositions comprising 3-amino 2,6 dimethylphenol, methods, and kits comprising the compositions |
| CN104168876B (zh) | 2012-03-27 | 2017-11-03 | 诺赛尔股份有限公司 | 包含3‑氨基‑2,6‑二甲基苯酚和1,4‑苯二胺型显色剂的毛发着色剂组合物、方法以及包含所述组合物的套盒 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3184387A (en) * | 1955-11-25 | 1965-05-18 | Oreal | Process for dyeing hair with substituted 2, 4-diaminophenols |
| DE1096552B (de) * | 1955-11-25 | 1961-01-05 | Monsavon L Oreal Soc | Mittel zum Faerben von lebenden Haaren |
| US3488138A (en) * | 1962-10-18 | 1970-01-06 | Clairol Inc | Stabilized nitro-aminobenzene dyeing compositions |
| US3415608A (en) * | 1968-01-26 | 1968-12-10 | Lowenstein Dyes & Cosmetics In | Stabilized oxidation dye compositions |
| LU56722A1 (is") * | 1968-08-14 | 1970-02-16 | ||
| US4003699A (en) * | 1974-11-22 | 1977-01-18 | Henkel & Cie G.M.B.H. | Oxidation hair dyes based upon tetraaminopyrimidine developers |
-
1977
- 1977-01-20 DE DE2702118A patent/DE2702118C3/de not_active Expired
- 1977-10-31 NL NL7711952A patent/NL7711952A/xx not_active Application Discontinuation
- 1977-12-06 CH CH1490577A patent/CH604709A5/xx not_active IP Right Cessation
- 1977-12-27 SE SE7714800A patent/SE445970B/sv not_active IP Right Cessation
- 1977-12-27 DK DK580977A patent/DK148894C/da not_active IP Right Cessation
-
1978
- 1978-01-10 US US05/868,304 patent/US4213758A/en not_active Expired - Lifetime
- 1978-01-18 IT IT19348/78A patent/IT1111155B/it active
- 1978-01-19 BE BE184450A patent/BE863079R/xx not_active IP Right Cessation
- 1978-01-19 AT AT38478A patent/AT362070B/de not_active IP Right Cessation
- 1978-01-19 GB GB2138/78A patent/GB1572983A/en not_active Expired
- 1978-01-20 FR FR7801667A patent/FR2377801A2/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DK148894B (da) | 1985-11-11 |
| IT7819348A0 (it) | 1978-01-18 |
| CH604709A5 (is") | 1978-09-15 |
| DE2702118B2 (de) | 1980-08-07 |
| GB1572983A (en) | 1980-08-13 |
| ATA38478A (de) | 1980-09-15 |
| NL7711952A (nl) | 1978-07-24 |
| DE2702118A1 (de) | 1978-08-03 |
| DE2702118C3 (de) | 1981-06-04 |
| AT362070B (de) | 1981-04-27 |
| US4213758A (en) | 1980-07-22 |
| DK148894C (da) | 1986-04-14 |
| FR2377801A2 (fr) | 1978-08-18 |
| DK580977A (da) | 1978-07-21 |
| SE7714800L (sv) | 1978-07-21 |
| IT1111155B (it) | 1986-01-13 |
| BE863079R (fr) | 1978-07-19 |
| FR2377801B2 (is") | 1981-12-31 |
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