JP2002518424A5 - - Google Patents
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- Publication number
- JP2002518424A5 JP2002518424A5 JP2000555576A JP2000555576A JP2002518424A5 JP 2002518424 A5 JP2002518424 A5 JP 2002518424A5 JP 2000555576 A JP2000555576 A JP 2000555576A JP 2000555576 A JP2000555576 A JP 2000555576A JP 2002518424 A5 JP2002518424 A5 JP 2002518424A5
- Authority
- JP
- Japan
- Prior art keywords
- preparation according
- group
- hydrogen
- amino acid
- alkyl group
- 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
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- 239000000975 dye Substances 0.000 description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000002243 precursor Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 235000001014 amino acid Nutrition 0.000 description 5
- 150000001413 amino acids Chemical class 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 102000015636 Oligopeptides Human genes 0.000 description 4
- 108010038807 Oligopeptides Proteins 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 244000208060 Lawsonia inermis Species 0.000 description 3
- 150000001370 alpha-amino acid derivatives Chemical class 0.000 description 3
- 235000008206 alpha-amino acids Nutrition 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 150000002476 indolines Chemical class 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical group C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical class C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 description 2
- 239000004475 Arginine Substances 0.000 description 2
- GHVHDYYKJYXFGU-UHFFFAOYSA-N Beta-Orcinol Chemical compound CC1=CC(O)=C(C)C(O)=C1 GHVHDYYKJYXFGU-UHFFFAOYSA-N 0.000 description 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000982 direct dye Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 150000002475 indoles Chemical class 0.000 description 2
- VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical class C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- OIPPWFOQEKKFEE-UHFFFAOYSA-N orcinol Chemical compound CC1=CC(O)=CC(O)=C1 OIPPWFOQEKKFEE-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 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 description 1
- 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 description 1
- OREUKLHWMRALGC-UHFFFAOYSA-N 1-methyl-2,3-dihydroindole-5,6-diol Chemical compound OC1=C(O)C=C2N(C)CCC2=C1 OREUKLHWMRALGC-UHFFFAOYSA-N 0.000 description 1
- LGZSBRSLVPLNTM-UHFFFAOYSA-N 2-(4-amino-2-methyl-5-nitroanilino)ethanol Chemical compound CC1=CC(N)=C([N+]([O-])=O)C=C1NCCO LGZSBRSLVPLNTM-UHFFFAOYSA-N 0.000 description 1
- YESOPQNVGIQNEV-UHFFFAOYSA-N 2-(4-amino-2-nitroanilino)benzoic acid Chemical compound [O-][N+](=O)C1=CC(N)=CC=C1NC1=CC=CC=C1C(O)=O YESOPQNVGIQNEV-UHFFFAOYSA-N 0.000 description 1
- DBKXHYCKSFYSJU-UHFFFAOYSA-N 2-[(6-methyl-6-nitrocyclohexa-2,4-dien-1-yl)amino]ethanol Chemical compound [O-][N+](=O)C1(C)C=CC=CC1NCCO DBKXHYCKSFYSJU-UHFFFAOYSA-N 0.000 description 1
- NZKTVPCPQIEVQT-UHFFFAOYSA-N 2-[4-[(4-aminophenyl)diazenyl]-n-(2-hydroxyethyl)anilino]ethanol Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C(N(CCO)CCO)C=C1 NZKTVPCPQIEVQT-UHFFFAOYSA-N 0.000 description 1
- BMTSZVZQNMNPCT-UHFFFAOYSA-N 2-aminopyridin-3-ol Chemical compound NC1=NC=CC=C1O BMTSZVZQNMNPCT-UHFFFAOYSA-N 0.000 description 1
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 description 1
- XDHQHBSDKYPJRG-UHFFFAOYSA-N 3-[2-nitro-4-(trifluoromethyl)anilino]propane-1,2-diol Chemical compound OCC(O)CNC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O XDHQHBSDKYPJRG-UHFFFAOYSA-N 0.000 description 1
- XYRDGCCCBJITBH-UHFFFAOYSA-N 3-amino-2-chloro-6-methylphenol Chemical compound CC1=CC=C(N)C(Cl)=C1O XYRDGCCCBJITBH-UHFFFAOYSA-N 0.000 description 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- 229940018563 3-aminophenol Drugs 0.000 description 1
- VTXBLQLZQLHDIL-UHFFFAOYSA-N 4-(3-hydroxypropylamino)-3-nitrophenol Chemical compound OCCCNC1=CC=C(O)C=C1[N+]([O-])=O VTXBLQLZQLHDIL-UHFFFAOYSA-N 0.000 description 1
- UNBOSJFEZZJZLR-UHFFFAOYSA-N 4-(4-nitrophenylazo)aniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1 UNBOSJFEZZJZLR-UHFFFAOYSA-N 0.000 description 1
- XPLTXYDVYDWSSO-UHFFFAOYSA-N 4-(ethylamino)-3-nitrobenzoic acid Chemical compound CCNC1=CC=C(C(O)=O)C=C1[N+]([O-])=O XPLTXYDVYDWSSO-UHFFFAOYSA-N 0.000 description 1
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-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
- ZVDCYZVYRXZJQF-UHFFFAOYSA-N 6-nitro-1,2,3,4-tetrahydroquinoxaline Chemical compound N1CCNC2=CC([N+](=O)[O-])=CC=C21 ZVDCYZVYRXZJQF-UHFFFAOYSA-N 0.000 description 1
- TWLMSPNQBKSXOP-UHFFFAOYSA-N 6358-09-4 Chemical compound NC1=CC([N+]([O-])=O)=CC(Cl)=C1O TWLMSPNQBKSXOP-UHFFFAOYSA-N 0.000 description 1
- 235000017847 Anchusa officinalis Nutrition 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- MIWUTEVJIISHCP-UHFFFAOYSA-N HC Blue No. 2 Chemical compound OCCNC1=CC=C(N(CCO)CCO)C=C1[N+]([O-])=O MIWUTEVJIISHCP-UHFFFAOYSA-N 0.000 description 1
- GZGZVOLBULPDFD-UHFFFAOYSA-N HC Red No. 3 Chemical compound NC1=CC=C(NCCO)C([N+]([O-])=O)=C1 GZGZVOLBULPDFD-UHFFFAOYSA-N 0.000 description 1
- PNENOUKIPPERMY-UHFFFAOYSA-N HC Yellow No. 4 Chemical compound OCCNC1=CC=C([N+]([O-])=O)C=C1OCCO PNENOUKIPPERMY-UHFFFAOYSA-N 0.000 description 1
- 235000003325 Ilex Nutrition 0.000 description 1
- 241000209035 Ilex Species 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- VXOSJAYSAUDUOR-UHFFFAOYSA-N N-methyl-5,6-dihydroxyindole Chemical compound OC1=C(O)C=C2N(C)C=CC2=C1 VXOSJAYSAUDUOR-UHFFFAOYSA-N 0.000 description 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- 240000004050 Pentaglottis sempervirens Species 0.000 description 1
- 240000000513 Santalum album Species 0.000 description 1
- 235000008632 Santalum album Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000006468 Thea sinensis Nutrition 0.000 description 1
- RFQSMLBZXQOMKK-UHFFFAOYSA-N [3-[(4,8-diamino-6-bromo-1,5-dioxonaphthalen-2-yl)amino]phenyl]-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC(NC=2C(C3=C(N)C=C(Br)C(=O)C3=C(N)C=2)=O)=C1 RFQSMLBZXQOMKK-UHFFFAOYSA-N 0.000 description 1
- HSWXSHNPRUMJKI-UHFFFAOYSA-N [8-[(2-methoxyphenyl)hydrazinylidene]-7-oxonaphthalen-2-yl]-trimethylazanium;chloride Chemical compound [Cl-].COC1=CC=CC=C1N\N=C/1C2=CC([N+](C)(C)C)=CC=C2C=CC\1=O HSWXSHNPRUMJKI-UHFFFAOYSA-N 0.000 description 1
- CMPPYVDBIJWGCB-UHFFFAOYSA-N [8-[(4-amino-3-nitrophenyl)hydrazinylidene]-7-oxonaphthalen-2-yl]-trimethylazanium;chloride Chemical compound [Cl-].C12=CC([N+](C)(C)C)=CC=C2C=CC(=O)\C1=N\NC1=CC=C(N)C([N+]([O-])=O)=C1 CMPPYVDBIJWGCB-UHFFFAOYSA-N 0.000 description 1
- UXEAWNJALIUYRH-UHFFFAOYSA-N [8-[(4-aminophenyl)hydrazinylidene]-7-oxonaphthalen-2-yl]-trimethylazanium;chloride Chemical compound [Cl-].C12=CC([N+](C)(C)C)=CC=C2C=CC(=O)\C1=N/NC1=CC=C(N)C=C1 UXEAWNJALIUYRH-UHFFFAOYSA-N 0.000 description 1
- 229940054051 antipsychotic indole derivative Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000020279 black tea Nutrition 0.000 description 1
- 229940073669 ceteareth 20 Drugs 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000001041 indolyl group Chemical group 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
- 230000007935 neutral effect Effects 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- DWKARHJHPSUOBW-UHFFFAOYSA-N trimethyl-[3-[(2e)-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)hydrazinyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(O)=C1N=NC1=CC=CC([N+](C)(C)C)=C1 DWKARHJHPSUOBW-UHFFFAOYSA-N 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19827000A DE19827000A1 (de) | 1998-06-23 | 1998-06-23 | Färbemittel |
| US9392698P | 1998-07-23 | 1998-07-23 | |
| US19827000.3 | 1998-07-23 | ||
| US60/093,926 | 1998-07-23 | ||
| PCT/EP1999/004063 WO1999066890A1 (de) | 1998-06-23 | 1999-06-12 | Färbemittel zum färben von keratinfasern |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002518424A JP2002518424A (ja) | 2002-06-25 |
| JP2002518424A5 true JP2002518424A5 (enExample) | 2006-08-03 |
| JP4140806B2 JP4140806B2 (ja) | 2008-08-27 |
Family
ID=26046865
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000555576A Expired - Fee Related JP4140806B2 (ja) | 1998-06-23 | 1999-06-12 | ケラチン繊維用の染色製剤 |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US6537330B1 (enExample) |
| EP (1) | EP1098627B1 (enExample) |
| JP (1) | JP4140806B2 (enExample) |
| KR (1) | KR100681228B1 (enExample) |
| CN (1) | CN1216591C (enExample) |
| AT (1) | ATE258421T1 (enExample) |
| BR (1) | BR9911444A (enExample) |
| CA (1) | CA2335959C (enExample) |
| ES (1) | ES2215389T3 (enExample) |
| HU (1) | HUP0102869A2 (enExample) |
| ID (1) | ID27444A (enExample) |
| PL (1) | PL344746A1 (enExample) |
| TR (1) | TR200003566T2 (enExample) |
| WO (1) | WO1999066890A1 (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ID27444A (id) * | 1998-06-23 | 2001-04-12 | Henkel Ommanditgesellschaft Au | Zat pewarna |
| CN1196463C (zh) | 1999-12-20 | 2005-04-13 | 汉高两合股份公司 | 用于角蛋白纤维的固体染色剂 |
| DE10000460B4 (de) | 2000-01-07 | 2004-05-06 | Wella Aktiengesellschaft | Mittel und Verfahren zur Färbung von Haaren |
| DE10027975A1 (de) * | 2000-06-06 | 2001-12-13 | Henkel Kgaa | Verfahren zur oxidativen Färbung keratinischer Fasern |
| EP1286647B1 (de) * | 2000-06-06 | 2008-01-09 | Henkel Kommanditgesellschaft auf Aktien | Verfahren zur oxidativen färbung keratinischer fasern |
| DE10116759A1 (de) * | 2000-11-20 | 2002-05-23 | Henkel Kgaa | Grundlage für enzymatische Färbemittel |
| FR2818538B1 (fr) * | 2000-12-22 | 2003-02-07 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant au moins un 4,5 ou 3,4-diamino pyrazole ou un triamino pyrazole et au moins un compose carbonyle selectionne, et procede de teinture |
| JP4800502B2 (ja) * | 2001-04-23 | 2011-10-26 | 花王株式会社 | 染毛剤組成物 |
| JP5002091B2 (ja) * | 2001-04-23 | 2012-08-15 | 花王株式会社 | 染毛剤組成物 |
| DE10148841A1 (de) * | 2001-10-04 | 2003-04-10 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
| JP3984025B2 (ja) | 2001-11-07 | 2007-09-26 | 花王株式会社 | 染毛剤組成物 |
| DE10227238A1 (de) * | 2002-06-19 | 2004-01-15 | Wella Ag | Hochaffine kosmetische Mittel |
| US7807141B2 (en) | 2003-09-08 | 2010-10-05 | E.I. Du Pont De Nemours And Company | Peptide-based oral care surface reagents for personal care |
| US20050226839A1 (en) * | 2003-09-08 | 2005-10-13 | Xueying Huang | Pepetide-based body surface reagents for personal care |
| US7220405B2 (en) | 2003-09-08 | 2007-05-22 | E. I. Du Pont De Nemours And Company | Peptide-based conditioners and colorants for hair, skin, and nails |
| US7585495B2 (en) | 2003-09-08 | 2009-09-08 | E. I. Du Pont De Nemours And Company | Method for identifying shampoo-resistant hair-binding peptides and hair benefit agents therefrom |
| US20100311641A1 (en) * | 2003-09-08 | 2010-12-09 | E. I. Du Pont De Nemours And Company | Peptide-based body surface coloring reagents |
| US7285264B2 (en) * | 2003-09-08 | 2007-10-23 | E.I. Du Pont De Nemours And Company | Peptide-based body surface coloring reagents |
| US20050118124A1 (en) * | 2003-12-01 | 2005-06-02 | Reinhart Gale M. | Compositions for treating keratinous surfaces |
| JP4205602B2 (ja) * | 2004-02-02 | 2009-01-07 | ポーラ化成工業株式会社 | ２剤形態の染毛剤 |
| EP1723989A1 (en) * | 2005-02-18 | 2006-11-22 | L'oreal | Dye composition comprising at least one methine dye of particular structure and process for implementation thereof |
| DE102005013067A1 (de) * | 2005-03-18 | 2006-10-19 | Henkel Kgaa | Ammoniakfreies Oxidationsfärbemittel zur Färbung keratinhaltiger Fasern mit Luftsauerstoff als einzigem Oxidationsmittel |
| DE102005025494A1 (de) * | 2005-06-01 | 2006-12-14 | Henkel Kgaa | Mehrstufiges Färbeverfahren für keratinische Fasern |
| US7736633B2 (en) | 2005-09-28 | 2010-06-15 | E.I. Du Pont De Nemours And Company | Method for enhancing effects of colorants and conditioners |
| US7709601B2 (en) | 2005-12-15 | 2010-05-04 | E. I. Du Pont De Nemours And Company | Nylon binding peptides and methods of use |
| US7858581B2 (en) * | 2005-12-15 | 2010-12-28 | E. I. Du Pont De Nemours And Company | PMMA binding peptides and methods of use |
| US7632919B2 (en) * | 2005-12-15 | 2009-12-15 | E.I. Du Pont De Nemours And Company | Polystyrene binding peptides and methods of use |
| US7928076B2 (en) * | 2005-12-15 | 2011-04-19 | E. I. Du Pont De Nemours And Company | Polypropylene binding peptides and methods of use |
| US7906617B2 (en) | 2005-12-15 | 2011-03-15 | E. I. Du Pont De Nemours And Company | Polyethylene binding peptides and methods of use |
| US7700716B2 (en) * | 2005-12-15 | 2010-04-20 | E. I. Du Pont De Nemours And Company | Polytetrafluoroethylene binding peptides and methods of use |
| JP4992062B2 (ja) * | 2006-05-17 | 2012-08-08 | キム、スング−ホー | 骨伝導ヘッドセット |
| JP2007326810A (ja) * | 2006-06-07 | 2007-12-20 | Kao Corp | 一剤式染毛剤組成物 |
| JP5363700B2 (ja) * | 2006-06-07 | 2013-12-11 | 花王株式会社 | エアゾール型一剤式染毛剤組成物 |
| JP5363702B2 (ja) * | 2006-06-07 | 2013-12-11 | 花王株式会社 | 一剤式染毛剤組成物 |
| KR101441697B1 (ko) | 2006-06-07 | 2014-09-17 | 카오카부시키가이샤 | 일제식 염모제 조성물 |
| JP5363703B2 (ja) | 2006-06-07 | 2013-12-11 | 花王株式会社 | 一剤式染毛剤組成物 |
| BRPI0716024B1 (pt) * | 2006-08-10 | 2015-12-22 | Combe Inc | corante capilar de oxidação catalisada em contato com o ar. |
| CN1907253A (zh) * | 2006-08-23 | 2007-02-07 | 苏建华 | 用于毛发染色的含有氨基杂环化合物的组合物及染色方法 |
| DE102007027856A1 (de) * | 2007-06-13 | 2008-12-24 | Henkel Ag & Co. Kgaa | Oxidationsfärbemittel zur Färbung keratinhaltiger Fasern mit Luftsauerstoff als einzigem Oxidationsmittel |
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1999
- 1999-06-12 ID IDW20002571A patent/ID27444A/id unknown
- 1999-06-12 WO PCT/EP1999/004063 patent/WO1999066890A1/de not_active Ceased
- 1999-06-12 ES ES99929194T patent/ES2215389T3/es not_active Expired - Lifetime
- 1999-06-12 PL PL99344746A patent/PL344746A1/xx unknown
- 1999-06-12 EP EP99929194A patent/EP1098627B1/de not_active Expired - Lifetime
- 1999-06-12 JP JP2000555576A patent/JP4140806B2/ja not_active Expired - Fee Related
- 1999-06-12 HU HU0102869A patent/HUP0102869A2/hu unknown
- 1999-06-12 AT AT99929194T patent/ATE258421T1/de active
- 1999-06-12 TR TR2000/03566T patent/TR200003566T2/xx unknown
- 1999-06-12 BR BR9911444-5A patent/BR9911444A/pt not_active Application Discontinuation
- 1999-06-12 CA CA002335959A patent/CA2335959C/en not_active Expired - Fee Related
- 1999-06-12 CN CN998076317A patent/CN1216591C/zh not_active Expired - Fee Related
- 1999-06-12 KR KR1020007014558A patent/KR100681228B1/ko not_active Expired - Fee Related
- 1999-06-23 US US09/338,101 patent/US6537330B1/en not_active Expired - Lifetime
-
2003
- 2003-01-24 US US10/350,726 patent/US6818023B2/en not_active Expired - Fee Related
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