JPH06508856A - クリーム状のキャリヤー物質を主薬とする酸化毛髪染色剤および毛髪の染色方法 - Google Patents
クリーム状のキャリヤー物質を主薬とする酸化毛髪染色剤および毛髪の染色方法Info
- Publication number
- JPH06508856A JPH06508856A JP5519803A JP51980393A JPH06508856A JP H06508856 A JPH06508856 A JP H06508856A JP 5519803 A JP5519803 A JP 5519803A JP 51980393 A JP51980393 A JP 51980393A JP H06508856 A JPH06508856 A JP H06508856A
- Authority
- JP
- Japan
- Prior art keywords
- hair
- drug
- weight
- dye
- amino
- 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.)
- Granted
Links
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- 239000000126 substance Substances 0.000 title claims description 27
- 238000004043 dyeing Methods 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 4
- 239000000975 dye Substances 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 26
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 22
- 229940079593 drug Drugs 0.000 claims description 16
- 239000003814 drug Substances 0.000 claims description 16
- -1 glycerin fatty acid ester Chemical class 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 239000006071 cream Substances 0.000 claims description 13
- 235000011187 glycerol Nutrition 0.000 claims description 13
- 230000001590 oxidative effect Effects 0.000 claims description 11
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 239000003995 emulsifying agent Substances 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 9
- 150000002191 fatty alcohols Chemical class 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 4
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- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 150000005690 diesters Chemical class 0.000 claims description 4
- 229960001755 resorcinol Drugs 0.000 claims description 4
- ICVRBKCRXNVOJC-UHFFFAOYSA-N 1-amino-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2NC ICVRBKCRXNVOJC-UHFFFAOYSA-N 0.000 claims description 3
- 229940018563 3-aminophenol Drugs 0.000 claims description 3
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 claims description 2
- 229940075142 2,5-diaminotoluene Drugs 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
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000000982 direct dye Substances 0.000 claims description 2
- OJLOUXPPKZRTHK-UHFFFAOYSA-N dodecan-1-ol;sodium Chemical compound [Na].CCCCCCCCCCCCO OJLOUXPPKZRTHK-UHFFFAOYSA-N 0.000 claims description 2
- 230000001747 exhibiting effect Effects 0.000 claims 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 claims description 2
- JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 claims 3
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 claims 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims 2
- GGNQRNBDZQJCCN-UHFFFAOYSA-N hydroxyhydroquinone Natural products OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 claims 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 1
- GRLQBYQELUWBIO-UHFFFAOYSA-N 4,6-dichlorobenzene-1,3-diol Chemical compound OC1=CC(O)=C(Cl)C=C1Cl GRLQBYQELUWBIO-UHFFFAOYSA-N 0.000 claims 1
- BOTGCZBEERTTDQ-UHFFFAOYSA-N 4-Methoxy-1-naphthol Chemical compound C1=CC=C2C(OC)=CC=C(O)C2=C1 BOTGCZBEERTTDQ-UHFFFAOYSA-N 0.000 claims 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 claims 1
- 239000003245 coal Substances 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 11
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 10
- 239000007864 aqueous solution Substances 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000012876 carrier material Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 5
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 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 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000003118 aryl group Chemical group 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
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229940100608 glycol distearate Drugs 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229940114930 potassium stearate Drugs 0.000 description 3
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- GUQPDKHHVFLXHS-UHFFFAOYSA-M sodium;2-(2-dodecoxyethoxy)ethyl sulfate Chemical group [Na+].CCCCCCCCCCCCOCCOCCOS([O-])(=O)=O GUQPDKHHVFLXHS-UHFFFAOYSA-M 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- HVYWMOMLDIMFJA-UHFFFAOYSA-N 3-cholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 HVYWMOMLDIMFJA-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
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical class CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
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- 235000010265 sodium sulphite Nutrition 0.000 description 2
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- NKNCGBHPGCHYCQ-UHFFFAOYSA-N (2,5-diaminophenyl)methanol Chemical compound NC1=CC=C(N)C(CO)=C1 NKNCGBHPGCHYCQ-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
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- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 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
- 229940099259 vaseline Drugs 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- 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
- A61K8/37—Esters of carboxylic acids
- A61K8/375—Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
-
- 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
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene 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
- A61Q5/10—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)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims (9)
- 1.毛髪の酸化染色のための薬剤で、クリーム状のキャリヤー物質と、その中に 溶解された染料混合物とから構成されるものにおいて、(A)10〜30重量% の少なくとも1種の、10〜24の炭素原子を有する脂肪アルコール、 (B)0.2〜6.0重量%の少なくとも1種の、下記の式のジエステルR1− CO−O−(CH2−CH2−O)n−CO−R2(I)上式において、nは1 、2または3を示し、並びにR1およびR2は、12〜20の炭素原子を有する 同一または異なったアルキル残基を示し、(C)0.5〜20重量%の、10〜 24の炭素原子を有するグリセリン脂肪酸エステル、 (D)0.1〜10重量%の、非イオン性および/またはアニオン性および/ま たは両性乳化剤、 を含有すること、および (E)4.5〜12.5のpH値を示すことを特徴とする、毛髪酸化染色用薬剤 。
- 2.前記薬剤が、前記式(I)のジエステルとして、エチレングリコールジステ アレートを含有することを特徴とする請求項1記載の薬剤。
- 3.前記薬剤が、グリセリン脂肪酸エステルとして、グリセリンモノ−ジステア レートを含有することを特徴とする請求項1または2記載の薬剤。
- 4.前記薬剤が、グリセリンモノ−ジステアレートを0.5〜10.0重量%の 量で含有することを特徴とする請求項3記載の薬剤。
- 5.前記成分(D)の乳化剤の主要量が、ナトリウムラウリルアルコールジグリ コールエーテルスルフェートであることを特徴とする請求項1〜4いずれか1項 記載の薬剤。
- 6.前記染料混合物が、発色物質である1−ナフト−ル、4−メトキシ−1−ナ フトール、レゾルシン、4−クロロレゾルシン、4,6−ジクロロレゾルシン、 2−メチルレゾルシン、3−アミノフェノール、3−アミノ−6−メチルフェノ ール、4−ヒドロキシ−1,2−メチレンジオキシベンゼン、4−ヒドロキシイ ンドール、2,4−ジヒドロキシアニソールおよび2,4−ジヒドロキシフェノ キシエタノールの少なくとも1種を含有することを特徴とする請求項1〜5いず れか1項記載の薬剤。
- 7.前記染料混合物が、顕色剤物質である2,5−ジアミノトルエン、3−メチ ル−4−アミノフェノール、1,4−ジアミノベンゼン、2−(2′−ヒドロキ シエチル)−1,4−ジアミノベンゼン、テトラアミノピリミジンおよび4−ア ミノフェノールの少なくとも1種を含有することを特徴とする請求項1〜6いず れか1項記載の薬剤。
- 8.前記染料混合物が、直接性染料であるダイアモンドフクシン(C.I.42 510)、レザールビーHF(C.I.42520)、2−アミノ−4,6−ジ ニトロフェノール、2−ニトロ−4−(2′−ヒドロキシエチルアミノ)アニリ ン、2−N−2′,3′−ジヒドロキシプロピルアミノ−5−(N−メチル,N −ヒドロキシエチル)アミノ−ニトロベンゼン、2−アミノ−4−ニトロフェノ ール、アシッドブラウン4(C.I.14805)、アシッドブル−135(C .I.13385)、ディスパースバイオレット4(C.I.61105)、デ ィスパースブルー1(C.I.64500)、ディスパースレッド15(C.I .60710)、ディスパースバイオレット1(C.I.61100)、1,4 ,5,8−テトラアミノアントラキノンおよび1,4−ジアミノアントラキノン の少なくとも1種を含有することを特徴とする請求項1〜7いずれか1項記載の 薬剤。
- 9.毛髪を染色するための方法であって、前記請求項1〜8記載の毛髪染色剤を 使用する直前に、1種の酸化作用物質、特に過酸化水素を含有する液体状または クリーム伏の酸化剤と混合し、引き続いて毛髪処理に充分な量のこの混合物を毛 髪に塗布して約15〜約50℃で10〜45分間、毛髪に作用させ、毛髪を水で 濯いだ後に乾燥させることを特徴とする、毛髪の染色方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4216381A DE4216381A1 (de) | 1992-05-18 | 1992-05-18 | Oxidationshaarfärbemittel auf der Basis einer cremeförmigen Trägermasse und Verfahren zum Färben von Haaren |
DE4216381.1 | 1992-05-18 | ||
PCT/EP1993/000848 WO1993023006A1 (de) | 1992-05-18 | 1993-04-06 | Oxidationshaarfärbemittel auf der basis einer cremeförmigen trägermasse und verfahren zum färben von haaren |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06508856A true JPH06508856A (ja) | 1994-10-06 |
JP3431150B2 JP3431150B2 (ja) | 2003-07-28 |
Family
ID=6459147
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51980393A Expired - Lifetime JP3431150B2 (ja) | 1992-05-18 | 1993-04-06 | クリーム状のキャリヤー物質を主薬とする酸化毛髪染色剤および毛髪の染色方法 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5480459A (ja) |
EP (1) | EP0594811B1 (ja) |
JP (1) | JP3431150B2 (ja) |
BR (1) | BR9305527A (ja) |
DE (2) | DE4216381A1 (ja) |
ES (1) | ES2050646T3 (ja) |
WO (1) | WO1993023006A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003040748A (ja) * | 2001-07-06 | 2003-02-13 | Wella Ag | 酸化毛髪染色剤 |
JP2010254633A (ja) * | 2009-04-27 | 2010-11-11 | Nakano Seiyaku Kk | 2剤式酸化染毛・脱色剤用第1剤 |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2729565A1 (fr) * | 1995-01-20 | 1996-07-26 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
DE19719504C1 (de) * | 1997-05-12 | 1998-12-10 | Henkel Kgaa | Verfahren zur Herstellung von Haarfärbemitteln |
DE19755491C1 (de) | 1997-12-13 | 1999-05-12 | Henkel Kgaa | Mikrodispersionsverfahren zur Herstellung von Haarfärbepräparaten mit erhöhter Viskosität |
DE19901886C2 (de) * | 1999-01-19 | 2001-02-22 | Goldwell Gmbh | Verfahren zur Herstellung eines Haarfärbemittels |
DE19919089A1 (de) * | 1999-04-27 | 2000-11-23 | Cognis Deutschland Gmbh | Haarfärbepräparate |
DE19927076A1 (de) * | 1999-06-15 | 2000-12-21 | Cognis Deutschland Gmbh | Haarfärbepräparate |
FR2827761B1 (fr) * | 2001-07-27 | 2005-09-02 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant un alcool gras mono- ou poly-glycerole et un polyol particulier |
KR100465974B1 (ko) * | 2002-07-24 | 2005-01-13 | 주식회사 태평양 | 모발염색용 조성물 |
DE10359539A1 (de) | 2003-12-17 | 2005-07-14 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Pflegendes Oxidationsmittel in Tube |
DE10359557A1 (de) * | 2003-12-17 | 2005-07-14 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Oxidationsfärbemittel in Tube |
DE10359538A1 (de) | 2003-12-17 | 2005-07-14 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Tönungsmittel in Tuben |
FR2883736B1 (fr) † | 2005-03-31 | 2007-05-25 | Oreal | Composition colorante comprenant un ester d'acide gras et procede de coloration de fibres keratiniques la mettant en oeuvre |
US7578854B2 (en) * | 2005-03-31 | 2009-08-25 | L'oreal S.A. | Dye composition comprising at least one fatty acid ester and process for dyeing keratin fibers using the same |
US7569078B2 (en) * | 2005-03-31 | 2009-08-04 | L'oreal S.A. | Dye composition comprising at least one cellulose and process for dyeing keratin fibers using the dye composition |
US7651533B2 (en) | 2005-03-31 | 2010-01-26 | Oreal | Dye composition with a reduced content of starting materials, process for dyeing keratin fibers using the same and device therefor |
US7575605B2 (en) * | 2005-03-31 | 2009-08-18 | L'oreal S.A. | Dye composition comprising at least one glycerol ester and a process for dyeing keratin fibers using the composition |
FR2883738B1 (fr) * | 2005-03-31 | 2007-05-18 | Oreal | Composition colorante comprenant un polymere associatif non ionique, procede de coloration de fibres keratiniques la mettant en oeuvre |
US7442214B2 (en) * | 2005-03-31 | 2008-10-28 | L'oreal S.A. | Dye composition comprising at least one non-ionic associative polymer and process for dyeing keratin fibers using same |
US7550015B2 (en) * | 2005-03-31 | 2009-06-23 | L'oreal S.A. | Dye composition with a reduced content of starting materials, and process for dyeing keratin fibers using the same |
FR2883735B1 (fr) * | 2005-03-31 | 2009-06-12 | Oreal | Composition colorante a teneur diminuee en matieres premieres, procede de coloration de fibres keratiniques la mettant en oeuvre et dispositif |
EP2476407A1 (en) | 2011-01-18 | 2012-07-18 | The Procter & Gamble Company | Methods for preparing hair coloring compositions |
EP2476405A1 (en) | 2011-01-18 | 2012-07-18 | The Procter & Gamble Company | Hair coloring compositions with a non-ammonia alkalizing agent |
WO2019185127A1 (en) | 2018-03-27 | 2019-10-03 | Hct - Hair Cosmetic Technology Ag | Two component hair treatment kit comprising a hair coloring cream and a developer composition comprising a specific tensioactive compound |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2421607A1 (fr) * | 1978-04-06 | 1979-11-02 | Oreal | Procede de teinture des fibres keratiniques en deux temps par variation de ph |
FR2421608A1 (fr) * | 1978-04-06 | 1979-11-02 | Oreal | Composition destinee a la teinture des cheveux contenant des precurseurs de colorants par oxydation de type para et de type ortho |
DE3131006A1 (de) * | 1981-08-05 | 1983-02-24 | Henkel Kgaa | "cremegrundlage" |
DE3423589A1 (de) * | 1984-06-27 | 1986-01-09 | Wella Ag, 6100 Darmstadt | Oxidationshaarfaerbemittel auf basis einer niedrigviskosen traegermasse |
DE3423933A1 (de) * | 1984-06-29 | 1986-01-09 | Wella Ag, 6100 Darmstadt | 2-alkylsufonyl-1,4-diaminobenzole, verfahren zu ihrer herstellung sowie oxidationshaarfaerbemittel mit einem gehalt an diesen verbindungen |
DE3834142A1 (de) * | 1988-10-07 | 1990-04-12 | Wella Ag | Lagerstabiles cremefoermiges oxidationshaarfaerbemittel mit hohem farbstoff/elektrolyt-gehalt |
DE3836241A1 (de) * | 1988-10-25 | 1990-04-26 | Wella Ag | Konservierte haar- und koerperbehandlungsmittel sowie verwendung einer konservierungsstoff-kombination |
US5106609A (en) * | 1990-05-01 | 1992-04-21 | The Procter & Gamble Company | Vehicle systems for use in cosmetic compositions |
DE4017718A1 (de) * | 1990-06-01 | 1991-12-05 | Wella Ag | Oxidationshaarfaerbemittel aus einer emulsionsfoermigen farbstofftraegermasse und einer emulsionsfoermigen, oxidationsmittelhaltigen zusammensetzung und verfahren zum oxidativen faerben von haaren |
DE4123941A1 (de) * | 1991-07-19 | 1993-01-21 | Wella Ag | Verfahren zur oxidativen faerbung von haaren |
-
1992
- 1992-05-18 DE DE4216381A patent/DE4216381A1/de not_active Withdrawn
-
1993
- 1993-04-06 DE DE59302901T patent/DE59302901D1/de not_active Expired - Lifetime
- 1993-04-06 JP JP51980393A patent/JP3431150B2/ja not_active Expired - Lifetime
- 1993-04-06 EP EP93908916A patent/EP0594811B1/de not_active Expired - Lifetime
- 1993-04-06 US US08/150,210 patent/US5480459A/en not_active Expired - Lifetime
- 1993-04-06 WO PCT/EP1993/000848 patent/WO1993023006A1/de active IP Right Grant
- 1993-04-06 BR BR9305527A patent/BR9305527A/pt not_active IP Right Cessation
- 1993-04-06 ES ES93908916T patent/ES2050646T3/es not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003040748A (ja) * | 2001-07-06 | 2003-02-13 | Wella Ag | 酸化毛髪染色剤 |
JP2010254633A (ja) * | 2009-04-27 | 2010-11-11 | Nakano Seiyaku Kk | 2剤式酸化染毛・脱色剤用第1剤 |
Also Published As
Publication number | Publication date |
---|---|
ES2050646T3 (es) | 1996-10-16 |
DE59302901D1 (de) | 1996-07-18 |
WO1993023006A1 (de) | 1993-11-25 |
EP0594811A1 (de) | 1994-05-04 |
ES2050646T1 (es) | 1994-06-01 |
JP3431150B2 (ja) | 2003-07-28 |
US5480459A (en) | 1996-01-02 |
EP0594811B1 (de) | 1996-06-12 |
DE4216381A1 (de) | 1993-11-25 |
BR9305527A (pt) | 1994-09-27 |
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