NO845010L - Haarfarvningspreparat - Google Patents
HaarfarvningspreparatInfo
- Publication number
- NO845010L NO845010L NO845010A NO845010A NO845010L NO 845010 L NO845010 L NO 845010L NO 845010 A NO845010 A NO 845010A NO 845010 A NO845010 A NO 845010A NO 845010 L NO845010 L NO 845010L
- Authority
- NO
- Norway
- Prior art keywords
- phenylenediamine
- product
- methyl
- hydroxyethyl
- ethyl
- Prior art date
Links
- 239000000047 product Substances 0.000 claims description 97
- 239000000203 mixture Substances 0.000 claims description 57
- 230000003647 oxidation Effects 0.000 claims description 34
- 238000007254 oxidation reaction Methods 0.000 claims description 34
- 239000007800 oxidant agent Substances 0.000 claims description 17
- 230000001590 oxidative effect Effects 0.000 claims description 12
- 239000000118 hair dye Substances 0.000 claims description 11
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000004040 coloring Methods 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- JLEBZTSKNDQWIO-UHFFFAOYSA-N 2-(4-amino-2-methylanilino)ethanol Chemical compound CC1=CC(N)=CC=C1NCCO JLEBZTSKNDQWIO-UHFFFAOYSA-N 0.000 claims description 4
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 4
- 230000003113 alkalizing effect Effects 0.000 claims description 4
- 150000001450 anions Chemical group 0.000 claims description 4
- RBUQOUQQUQCSAU-UHFFFAOYSA-N 2-(4-aminoanilino)ethanol Chemical compound NC1=CC=C(NCCO)C=C1 RBUQOUQQUQCSAU-UHFFFAOYSA-N 0.000 claims description 3
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 claims description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 2
- VJPLXQSOOXFJIN-UHFFFAOYSA-N 1-n,4-n,2-triethylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(NCC)C(CC)=C1 VJPLXQSOOXFJIN-UHFFFAOYSA-N 0.000 claims description 2
- ZEMODTUZIWTRPF-UHFFFAOYSA-N 1-n,4-n-diethylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(NCC)C=C1 ZEMODTUZIWTRPF-UHFFFAOYSA-N 0.000 claims description 2
- AJRMZGCRNAVPFB-UHFFFAOYSA-N 1-n,5-dimethylbenzene-1,2,4-triamine Chemical compound CNC1=CC(C)=C(N)C=C1N AJRMZGCRNAVPFB-UHFFFAOYSA-N 0.000 claims description 2
- MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 claims description 2
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 claims description 2
- YJQCPPZYIKJFNQ-UHFFFAOYSA-N 2-(4-amino-3-methylanilino)ethanol Chemical compound CC1=CC(NCCO)=CC=C1N YJQCPPZYIKJFNQ-UHFFFAOYSA-N 0.000 claims description 2
- WFXLRLQSHRNHCE-UHFFFAOYSA-N 2-(4-amino-n-ethylanilino)ethanol Chemical compound OCCN(CC)C1=CC=C(N)C=C1 WFXLRLQSHRNHCE-UHFFFAOYSA-N 0.000 claims description 2
- WSGWDXQKCFQMAK-UHFFFAOYSA-N 2-butylbenzene-1,4-diamine Chemical compound CCCCC1=CC(N)=CC=C1N WSGWDXQKCFQMAK-UHFFFAOYSA-N 0.000 claims description 2
- SIEIFSKZDMFTSW-UHFFFAOYSA-N 2-chloro-4-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C(Cl)=C1 SIEIFSKZDMFTSW-UHFFFAOYSA-N 0.000 claims description 2
- ZSIMBMYNZHSZGJ-UHFFFAOYSA-N 2-ethylbenzene-1,4-diamine Chemical compound CCC1=CC(N)=CC=C1N ZSIMBMYNZHSZGJ-UHFFFAOYSA-N 0.000 claims description 2
- MMQPGHVKPBDZLV-UHFFFAOYSA-N 2-methoxy-1-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C=C1OC MMQPGHVKPBDZLV-UHFFFAOYSA-N 0.000 claims description 2
- NAFFHKHTPPSYMZ-UHFFFAOYSA-N 2-methoxy-4-n-methylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C(OC)=C1 NAFFHKHTPPSYMZ-UHFFFAOYSA-N 0.000 claims description 2
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 2
- WNYJRJRHKRZXEO-UHFFFAOYSA-N 2-propan-2-ylbenzene-1,4-diamine Chemical compound CC(C)C1=CC(N)=CC=C1N WNYJRJRHKRZXEO-UHFFFAOYSA-N 0.000 claims description 2
- YFHBPZJUEOCAMK-UHFFFAOYSA-N 2-propylbenzene-1,4-diamine Chemical compound CCCC1=CC(N)=CC=C1N YFHBPZJUEOCAMK-UHFFFAOYSA-N 0.000 claims description 2
- XOBAIYPLCUTNFV-UHFFFAOYSA-N 4-n,2-dimethylbenzene-1,4-diamine Chemical compound CNC1=CC=C(N)C(C)=C1 XOBAIYPLCUTNFV-UHFFFAOYSA-N 0.000 claims description 2
- NMELCDHMSQSBFE-UHFFFAOYSA-N 4-n,5-dimethylbenzene-1,2,4-triamine Chemical compound CNC1=CC(N)=C(N)C=C1C NMELCDHMSQSBFE-UHFFFAOYSA-N 0.000 claims description 2
- 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 description 2
- SKIBELYSXFYZPS-UHFFFAOYSA-N 4-n-ethylbenzene-1,4-diamine Chemical compound CCNC1=CC=C(N)C=C1 SKIBELYSXFYZPS-UHFFFAOYSA-N 0.000 claims description 2
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 claims description 2
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 claims description 2
- 229960001922 sodium perborate Drugs 0.000 claims description 2
- 229940045872 sodium percarbonate Drugs 0.000 claims description 2
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 claims description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims description 2
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical group OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims description 2
- FCDKGTXZKZEBPA-UHFFFAOYSA-N 2-[4-(2-hydroxyethylamino)anilino]ethanol Chemical compound OCCNC1=CC=C(NCCO)C=C1 FCDKGTXZKZEBPA-UHFFFAOYSA-N 0.000 claims 1
- DTWYHUJRSXQSHT-UHFFFAOYSA-N 3-[4-amino-n-(2,3-dihydroxypropyl)anilino]propane-1,2-diol Chemical compound NC1=CC=C(N(CC(O)CO)CC(O)CO)C=C1 DTWYHUJRSXQSHT-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- -1 aliphatic hydrocarbon radical Chemical class 0.000 description 18
- 239000000975 dye Substances 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 230000003750 conditioning effect Effects 0.000 description 7
- 239000000543 intermediate Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 229910052736 halogen Chemical group 0.000 description 4
- 150000002367 halogens Chemical group 0.000 description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000002431 hydrogen Chemical group 0.000 description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- QWYUSINUEXGRFZ-UHFFFAOYSA-N 1-n-ethyl-4-n-propylbenzene-1,4-diamine Chemical compound CCCNC1=CC=C(NCC)C=C1 QWYUSINUEXGRFZ-UHFFFAOYSA-N 0.000 description 1
- MWXIHZYOTSENGV-UHFFFAOYSA-N 2-(1,4-diaminocyclohexa-2,4-dien-1-yl)ethanol Chemical compound NC1=CCC(N)(CCO)C=C1 MWXIHZYOTSENGV-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- UAUJQMZIJSDNFP-UHFFFAOYSA-N 2-[4-(2-hydroxyethylamino)-3-methylanilino]ethanol Chemical compound CC1=CC(NCCO)=CC=C1NCCO UAUJQMZIJSDNFP-UHFFFAOYSA-N 0.000 description 1
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 125000005644 linolenyl group Chemical group 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002891 organic anions Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000979 synthetic dye Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- WPPGURUIRLDHAB-UHFFFAOYSA-M triethyl(hexadecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CC WPPGURUIRLDHAB-UHFFFAOYSA-M 0.000 description 1
- 230000003442 weekly effect Effects 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
- A61Q5/12—Preparations containing hair conditioners
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/22—Peroxides; Oxygen; Ozone
-
- 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
- A61K8/416—Quaternary ammonium compounds
-
- 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
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/88—Two- or multipart kits
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Inorganic Chemistry (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Dental Preparations (AREA)
- Golf Clubs (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB838333431A GB8333431D0 (en) | 1983-12-15 | 1983-12-15 | Hair treatment composition |
Publications (1)
Publication Number | Publication Date |
---|---|
NO845010L true NO845010L (no) | 1985-06-17 |
Family
ID=10553331
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO845010A NO845010L (no) | 1983-12-15 | 1984-12-13 | Haarfarvningspreparat |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0146350A3 (fr) |
DK (1) | DK602484A (fr) |
FI (1) | FI844856L (fr) |
GB (1) | GB8333431D0 (fr) |
NO (1) | NO845010L (fr) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4716037A (en) * | 1986-02-24 | 1987-12-29 | S. C. Johnson & Son, Inc. | Method of eliminating the corrosivity of hair conditioning compositions |
DE4301663C1 (de) * | 1993-01-22 | 1994-02-24 | Goldwell Ag | Haarfärbemittel |
US5376146A (en) * | 1993-08-26 | 1994-12-27 | Bristol-Myers Squibb Company | Two-part aqueous composition for coloring hair, which forms a gel on mixing of the two parts |
BR9713645A (pt) | 1996-12-31 | 2000-04-11 | American Medical Research Inc | Produto de pele tendo propriedade contìnuas anti-microbial, anti-viral, anti-séptico e de cicatrização. |
FR2769309B1 (fr) * | 1997-10-08 | 2001-06-15 | Oreal | Composition de teinture d'oxydation des fibres keratiniques comprenant un derive d'aminoacide en tant que base d'oxydation et nouveaux derives d'aminoacides |
GB9908062D0 (en) * | 1999-04-08 | 1999-06-02 | Unilever Plc | Hair treatment composition |
US6770103B2 (en) * | 2001-03-19 | 2004-08-03 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Method and composition for the gradual permanent coloring of hair |
US6726729B2 (en) * | 2001-12-28 | 2004-04-27 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates in a shampoo base |
US6758867B2 (en) | 2001-12-28 | 2004-07-06 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates in a shampoo base |
US6709468B2 (en) | 2002-03-07 | 2004-03-23 | Unilever Home & Personal Care Usa | Gradual permanent coloring of hair using dye intermediates in alkaline water which contains quaternary ammonium compounds |
US6736860B2 (en) | 2002-03-12 | 2004-05-18 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates dissolved in alkaline water with fatty alcohol |
US6743265B2 (en) | 2002-03-13 | 2004-06-01 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Gradual permanent coloring of hair using dye intermediates dissolved in alkaline water with a gelling agent |
US7074244B2 (en) | 2003-07-03 | 2006-07-11 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Hair dyeing method including an aligning step |
US7060111B2 (en) * | 2003-07-03 | 2006-06-13 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Method for providing more vibrant, natural and long-lasting color to hair |
WO2005018589A1 (fr) * | 2003-08-22 | 2005-03-03 | Unilever Plc | Preparation de coloration capillaire |
EP2076237A1 (fr) * | 2006-10-25 | 2009-07-08 | L'Oreal | Composition utilisée pour colorer par oxydation des fibres kératiniques comprenant au moins un sel d'ammonium particulier dérivé de 18mea et méthode de coloration comprenant l'utilisation de ladite composition |
FR2907669B1 (fr) * | 2006-10-25 | 2008-12-26 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant au moins un sel d'ammonium particulier derive du 18mea et procede de coloration a partir de la composition. |
CA2671454C (fr) * | 2006-12-01 | 2014-10-14 | Alberto-Culver Company | Procede permettant d'inhiber l'affadissement et d'ameliorer l'intensite des cheveux colores |
EP2225003B1 (fr) * | 2007-07-03 | 2017-10-11 | L'Oréal | Procédés et trousses pour la teinture capillaire permanente |
US8088176B2 (en) | 2008-08-29 | 2012-01-03 | L'oreal | Methods and kits for permanently coloring hair using a developer composition containing an oxidizer composition and a shampoo |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1052622A (fr) * | 1952-03-20 | 1954-01-26 | & Tech Modernes Lab | Procédé pour la teinture des poils et cheveux et préparation pour la mise en oeuvre de ce procédé |
FR1476584A (fr) * | 1965-10-12 | 1967-04-14 | Chemisches Lab Fritz Walter La | Colorants capillaires cation-actif de consistance notamment liquide, crémeuse ou du type gel |
BE736388A (fr) * | 1968-07-25 | 1970-01-22 | ||
FR2045991A7 (en) * | 1969-06-11 | 1971-03-05 | Gillette Co | Hair tinting preparations with reduced - amounts of peroxide |
US4402700A (en) * | 1976-02-09 | 1983-09-06 | Clairol Incorporated | Composition for coloring hair containing an oxidizing agent and certain quaternary amines |
US4096243A (en) * | 1976-02-09 | 1978-06-20 | Clairol Incorporated | Composition for lightening hair containing an oxidizing agent and certain quaternary amines |
-
1983
- 1983-12-15 GB GB838333431A patent/GB8333431D0/en active Pending
-
1984
- 1984-12-10 FI FI844856A patent/FI844856L/fi not_active Application Discontinuation
- 1984-12-13 NO NO845010A patent/NO845010L/no unknown
- 1984-12-13 EP EP84308692A patent/EP0146350A3/fr not_active Withdrawn
- 1984-12-14 DK DK602484A patent/DK602484A/da not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
FI844856L (fi) | 1985-06-16 |
EP0146350A3 (fr) | 1986-06-04 |
DK602484D0 (da) | 1984-12-14 |
GB8333431D0 (en) | 1984-01-25 |
FI844856A0 (fi) | 1984-12-10 |
DK602484A (da) | 1985-06-16 |
EP0146350A2 (fr) | 1985-06-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO845010L (no) | Haarfarvningspreparat | |
AU762113B2 (en) | Two-part hair dye compositions containing polyether polyurethanes and conditioning agents | |
US7465323B2 (en) | High carbonate oxidative dye compositions | |
US4402700A (en) | Composition for coloring hair containing an oxidizing agent and certain quaternary amines | |
US5104413A (en) | Hair dye composition | |
US3488138A (en) | Stabilized nitro-aminobenzene dyeing compositions | |
NO151394B (no) | Fremgangsmaate til kondisjonering og lysgjoering eller farging av menneskehaar | |
CZ291831B6 (cs) | Prostředek k přímému použití pro oxidační barvení keratinových vláken, způsob a souprava pro barvení keratinových vláken | |
US5741337A (en) | Process for the oxidative dyeing of keratinous fibres with a composition which contains an oxidation dye precursor, a coupler, and an oxidant at an acidic pH | |
JP2000503327A (ja) | ケラチン繊維上においてメタメリー効果を発現する染色剤 | |
US4322212A (en) | Oxidation hair dyes comprising substituted benzotriazoles | |
US4532127A (en) | Composition for lightening or coloring hair containing an oxidizing agent and certain quaternary amines | |
JPH08175939A (ja) | 少なくとも2の特定のパラ−フェニレンジアミン誘導体を含むケラチン繊維の酸化染色のための組成物 | |
JP2582235B2 (ja) | 2−(β−ヒドロキシエチル)−パラ−フェニレンジアミン、2−メチルレゾルシノール及び3−アミノフェノールからなるケラチン繊維の酸化染料組成物及びそれを用いた染色方法 | |
JPH04117322A (ja) | 酸化毛染剤及び毛染法 | |
JPH039085B2 (fr) | ||
JPS5949204B2 (ja) | 毛髪染色,調節組成物 | |
PL202183B1 (pl) | Kompozycje do utleniającego farbowania włókien keratynowych | |
EP0002828B1 (fr) | Composition pour la teinture des cheveux | |
JPH0789832A (ja) | 染毛組成物 | |
US4725283A (en) | Dyeing compositions for keratinic fibres, based on halogenated meta-phenylenediamines | |
JPH0234321B2 (fr) | ||
JPH0892047A (ja) | ヘアダイ組成物 | |
US4668237A (en) | Dye composition containing 5-nitrovanillin and its use for dyeing keratinic fibres, and especially human hair | |
JPH09157141A (ja) | 酸化染毛剤 |