JP2004203888A5 - - Google Patents
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- Publication number
- JP2004203888A5 JP2004203888A5 JP2003428262A JP2003428262A JP2004203888A5 JP 2004203888 A5 JP2004203888 A5 JP 2004203888A5 JP 2003428262 A JP2003428262 A JP 2003428262A JP 2003428262 A JP2003428262 A JP 2003428262A JP 2004203888 A5 JP2004203888 A5 JP 2004203888A5
- Authority
- JP
- Japan
- Prior art keywords
- bis
- azo
- ethyl
- methyl
- ethanediyl
- 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.)
- Pending
Links
- -1 triarylmethane Chemical compound 0.000 claims 27
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 16
- 239000000982 direct dye Substances 0.000 claims 16
- 229910052757 nitrogen Inorganic materials 0.000 claims 14
- FFJMLWSZNCJCSZ-UHFFFAOYSA-N n-methylmethanamine;hydrobromide Chemical compound Br.CNC FFJMLWSZNCJCSZ-UHFFFAOYSA-N 0.000 claims 12
- 238000004043 dyeing Methods 0.000 claims 9
- 239000000835 fiber Substances 0.000 claims 7
- 125000002091 cationic group Chemical group 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 102000011782 Keratins Human genes 0.000 claims 5
- 108010076876 Keratins Proteins 0.000 claims 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 3
- 230000002378 acidificating effect Effects 0.000 claims 3
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 230000007935 neutral effect Effects 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims 2
- 239000000975 dye Substances 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000005638 hydrazono group Chemical group 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- 230000001590 oxidative effect Effects 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Chemical group 0.000 claims 2
- RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 229910052698 phosphorus Chemical group 0.000 claims 2
- 239000011574 phosphorus Chemical group 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical group C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 claims 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims 1
- OMIVCRYZSXDGAB-UHFFFAOYSA-N 1,4-butanediyl Chemical group [CH2]CC[CH2] OMIVCRYZSXDGAB-UHFFFAOYSA-N 0.000 claims 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims 1
- USWVBZPHCSBUHH-UHFFFAOYSA-N 2-[2-[(2,6-dichloro-4-nitrophenyl)diazenyl]phenyl]ethyl-[4-[2-[2-[(2,6-dichloro-4-nitrophenyl)diazenyl]phenyl]ethyl-dimethylazaniumyl]butyl]-dimethylazanium Chemical compound C=1C=CC=C(N=NC=2C(=CC(=CC=2Cl)[N+]([O-])=O)Cl)C=1CC[N+](C)(C)CCCC[N+](C)(C)CCC1=CC=CC=C1N=NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl USWVBZPHCSBUHH-UHFFFAOYSA-N 0.000 claims 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 1
- DIKHIMPAUSPLRI-UHFFFAOYSA-N 3-[N-[2-(dimethylamino)ethyl]-4-[(3-phenyl-1,2,4-thiadiazol-5-yl)diazenyl]anilino]propanenitrile Chemical compound C1=CC(N(CCC#N)CCN(C)C)=CC=C1N=NC1=NC(C=2C=CC=CC=2)=NS1 DIKHIMPAUSPLRI-UHFFFAOYSA-N 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims 1
- REMCVESZARINCE-UHFFFAOYSA-L C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].ClC1=CC=2N(C3=CC=CC=C3SC2C=C1)CCN(CC[N+]1(CCN(CC1)C)C)C.ClC1=CC=2N(C3=CC=CC=C3SC2C=C1)CCN(C)CC[N+]1(CCN(CC1)C)C Chemical compound C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].ClC1=CC=2N(C3=CC=CC=C3SC2C=C1)CCN(CC[N+]1(CCN(CC1)C)C)C.ClC1=CC=2N(C3=CC=CC=C3SC2C=C1)CCN(C)CC[N+]1(CCN(CC1)C)C REMCVESZARINCE-UHFFFAOYSA-L 0.000 claims 1
- HHIBMZYEKPOCRP-UHFFFAOYSA-L C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].ClC1=CC=CC=2N(C3=CC=CC=C3SC12)CCN(CC[N+]1(CCN(CC1)C)C)C.ClC1=CC=CC=2N(C3=CC=CC=C3SC12)CCN(C)CC[N+]1(CCN(CC1)C)C Chemical compound C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].C1([N+](=O)[O-])=CC([N+](=O)[O-])=CC([N+](=O)[O-])=C1[O-].ClC1=CC=CC=2N(C3=CC=CC=C3SC12)CCN(CC[N+]1(CCN(CC1)C)C)C.ClC1=CC=CC=2N(C3=CC=CC=C3SC12)CCN(C)CC[N+]1(CCN(CC1)C)C HHIBMZYEKPOCRP-UHFFFAOYSA-L 0.000 claims 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 1
- 150000004056 anthraquinones Chemical class 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 229950000688 phenothiazine Drugs 0.000 claims 1
- 239000001007 phthalocyanine dye Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- 125000000165 tricyclic carbocycle group Chemical group 0.000 claims 1
- 239000001018 xanthene dye Substances 0.000 claims 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0216564A FR2848837B1 (fr) | 2002-12-23 | 2002-12-23 | Composition tinctoriale contenant un colorant direct polycationique particulier, procede de teinture, utilisation et dispositifs a plusieurs compartiments. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004203888A JP2004203888A (ja) | 2004-07-22 |
| JP2004203888A5 true JP2004203888A5 (enExample) | 2005-05-26 |
Family
ID=32406438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003428262A Pending JP2004203888A (ja) | 2002-12-23 | 2003-12-24 | 特定のポリカチオン性直接染料を含有する染色用組成物、染色方法、使用及び多区画染色具 |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP1433473B1 (enExample) |
| JP (1) | JP2004203888A (enExample) |
| AT (1) | ATE488217T1 (enExample) |
| DE (1) | DE60334968D1 (enExample) |
| ES (1) | ES2353744T3 (enExample) |
| FR (1) | FR2848837B1 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7485156B2 (en) | 2005-05-31 | 2009-02-03 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising at least one diamino-N,N-dihydropyrazolone derivative, at least one coupler and at least one associative polyurethane polymer |
| US7582121B2 (en) | 2005-05-31 | 2009-09-01 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising at least one diamino-N,N-dihydropyrazolone derivative, at least one coupler, and at least one heterocyclic direct dye |
| US7488355B2 (en) | 2005-05-31 | 2009-02-10 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising a diamino-N,N-dihydropyrazolone compound, a coupler, and a polyol |
| US7488356B2 (en) | 2005-05-31 | 2009-02-10 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising at least one diamino-N,N-dihydropyrazolone derivative, at least one coupler, and at least one surfactant |
| FR2925307B1 (fr) | 2007-12-21 | 2009-12-18 | Oreal | Procede de coloration directe eclaircissante ou d'oxydation en presence d'une amine organique particuliere et dispositif |
| FR2925323B1 (fr) | 2007-12-21 | 2009-12-18 | Oreal | Procede de coloration en presence d'un agent oxydant et d'une amine organique particuliere et dispositif |
| BRPI0910081A2 (pt) | 2008-12-19 | 2012-03-13 | L'oreal | Processo de clareamento das fibras queratínicas humanas, processo de coloração das fibras queratínicas humanas e dispositivos com vários compartimentos |
| FR2940103B1 (fr) | 2008-12-19 | 2011-06-10 | Oreal | Procede de coloration eclaircissante de matieres keratiniques mettant en oeuvre une emulsion comprenant un colorant et un agent alcalin et une composition oxydante |
| US7927381B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of an aqueous composition comprising at least one fatty substance, and device |
| EP2198831B1 (fr) | 2008-12-19 | 2017-05-10 | L'Oréal | Procédé d'éclaircissement ou de coloration directe éclaircissante ou d'oxydation en présence d'une amine organique et d'une base minérale et dispositif approprié |
| FR2940077B1 (fr) | 2008-12-19 | 2012-07-20 | Oreal | Procede de coloration eclaircissante de matieres keratiniques mettant en oeuvre une composition anhydre colorante comprenant un agent alcalin et une composition oxydante. |
| CN101822619B (zh) | 2008-12-19 | 2014-03-26 | 莱雅公司 | 在无机碱存在下着色或色泽变淡的方法以及试剂盒 |
| FR2940104B1 (fr) | 2008-12-19 | 2011-08-19 | Oreal | Procede de traitement des cheveux mettant en oeuvre une emulsion directe comprenant un agent oxydant et une composition contenant un agent alcalin |
| CN101780015A (zh) | 2008-12-19 | 2010-07-21 | 莱雅公司 | 使用无水组合物和单乙醇胺/碱性氨基酸混合物染色或色泽变淡人角蛋白纤维的方法,和用于该方法的合适设备 |
| BRPI0907294A2 (pt) | 2008-12-19 | 2013-05-07 | Oreal | processo de clareamento ou de coloraÇço das fibras queratÍnicas e dispositivo com vÁrios compartimentos |
| FR2942704B1 (fr) | 2009-03-04 | 2011-09-02 | Oreal | Dispositif de distribution d'une composition tinctoriale pour les fibres keratiniques et procede associe. |
| AU2010232729A1 (en) | 2009-03-31 | 2011-10-20 | Arqule, Inc. | Substituted indolo-pyridinone compounds |
| FR2949971B1 (fr) | 2009-09-17 | 2012-08-17 | Oreal | Procede d'eclaircissement ou de coloration en presence d'une composition anhydre particuliere et dispositif |
| FR2951080B1 (fr) | 2009-10-13 | 2012-01-20 | Oreal | Composition comprenant un corps gras et un acide organophosphonique ou l'un de ses sels, procede de coloration ou d'eclaircissement la mettant en oeuvre et dispositifs |
| FR2954113B1 (fr) | 2009-12-22 | 2013-03-08 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties ou plus, sous forme d'emulsion. |
| WO2011076647A2 (en) | 2009-12-22 | 2011-06-30 | L'oreal | Inverse emulsion for treating the hair comprising a particular fatty substance and an alkaline agent |
| FR2954121B1 (fr) | 2009-12-22 | 2016-03-25 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties, comprenant un corps gras particulier et une reductone. |
| FR2954101B1 (fr) | 2009-12-22 | 2012-05-11 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties ou plus, comprenant une composition alcaline en emulsion inverse. |
| FR2954127B1 (fr) | 2009-12-22 | 2015-10-30 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties, comprenant un corps gras et un agent sequestrant. |
| WO2011076646A2 (en) | 2009-12-22 | 2011-06-30 | L'oreal | Agent for dyeing and/or bleaching keratin fibres, comprising an inverse emulsion comprising an oxidizing agent |
| FR2954093B1 (fr) | 2009-12-22 | 2012-02-24 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques en deux parties ou plus sous forme d'emulsion et de dispersion |
| FR2954160B1 (fr) | 2009-12-22 | 2012-03-30 | Oreal | Composition de coloration ou d'eclaircissement comprenant un corps gras et un polymere amphotere |
| FR2954161B1 (fr) | 2009-12-23 | 2012-03-02 | Oreal | Procede de coloration ou d'eclaircissement de fibres keratiniques en presence d'alcane(s) lineaire(s) volatil(s) et dispositif |
| EP3360931B1 (en) * | 2010-03-15 | 2020-07-01 | Purdue Research Foundation | Higher order structured dyes with enhanced optical features |
| FR2958161B1 (fr) | 2010-04-02 | 2012-04-27 | Oreal | Procede de traitement des cheveux mettant en oeuvre une emulsion directe comprenant un agent oxydant et une emulsion directe contenant un agent alcalin |
| FR2959127B1 (fr) | 2010-04-22 | 2016-01-01 | Oreal | Emulsion inverse pour le traitement des cheveux comprenant un solvant particulier |
| FR2960773B1 (fr) | 2010-06-03 | 2015-12-11 | Oreal | Procedes de traitement cosmetique utilisant un revetement a base d'un polymere polyamide-polyether |
| JP2012007121A (ja) * | 2010-06-28 | 2012-01-12 | Sumitomo Chemical Co Ltd | 化合物及び着色組成物 |
| WO2015063122A1 (en) | 2013-10-30 | 2015-05-07 | L'oreal | Expanded dyeing composition comprising an inert gas, an oxidation dye and an oxyalkylenated nonionic surfactant |
| FR3037795B1 (fr) | 2015-06-25 | 2018-08-17 | L'oreal | Article de conditionnement comportant une enveloppe et une composition colorante, decolorante ou oxydante anhydre comprenant une argile fibreuse, et un compose choisi parmi un agent colorant et/ou un agent oxydant ; utilisation et procede pour colorer et/ou decolorer les fibres keratiniques |
| FR3059233B1 (fr) | 2016-11-28 | 2019-07-26 | L'oreal | Composition tinctoriale comprenant l'acide 12-hydroxystearique, une amine organique et un colorant |
| FR3097761B1 (fr) | 2019-06-27 | 2021-05-28 | Oreal | Composition comprenant l’acide 12-hydroxystéarique, une amine organique et un corps gras liquide |
| US12605326B2 (en) | 2019-12-24 | 2026-04-21 | L'oreal | Cosmetic composition comprising a polymer comprising at least one cationic (meth)acrylamide unit, a particular silicone and at least one surfactant |
| FR3113240B1 (fr) | 2020-08-10 | 2024-01-12 | Oreal | Composition comprenant au moins un silicone particulier, au moins un alcane et au moins une teinte directe et/ou au moins un pigment |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1259963A (fr) * | 1955-01-08 | 1961-05-05 | Rhone Poulenc Sa | Nouveaux dérivés de la phénothiazine et leurs procédés de préparation |
| US2945849A (en) * | 1957-03-04 | 1960-07-19 | Bayer Ag | Disazo compounds containing a quaternary ammonium group |
| NL131592C (enExample) * | 1966-07-25 | |||
| CH532117A (de) * | 1968-03-28 | 1972-12-31 | Ciba Geigy Ag | Farbstoffpräparate |
| CH505186A (de) * | 1967-05-29 | 1971-03-31 | Ciba Geigy Ag | Verfahren zur Herstellung neuer Disazofarbstoffe |
| HU172520B (hu) | 1975-06-27 | 1978-09-28 | Richter Gedeon Vegyeszet | Sposob poluchenija novykh proizvodnykh ksantenovoj kisloty |
| DE3821196A1 (de) * | 1988-06-23 | 1990-02-15 | Basf Ag | Basische rhodamin-farbstoffe |
| DE4005015C2 (de) * | 1989-02-23 | 2003-09-18 | Clariant Finance Bvi Ltd | Kationische Phthalocyaninfarbstoffe |
| DE4034060A1 (de) * | 1990-10-26 | 1992-04-30 | Basf Ag | Biskationische azofarbstoffe |
| FR2712294B1 (fr) * | 1993-11-10 | 1997-12-19 | Sandoz Sa | Phtalocyanines d'aluminium cationiques, leur préparation et leur utilisation comme colorants. |
| FR2786481B1 (fr) * | 1998-11-30 | 2002-09-13 | Oreal | Amino-di-anthraquinones cationiques, utilisation, compositions de teinture les renfermant et procedes de teinture |
| FR2788220B1 (fr) * | 1999-01-08 | 2001-02-16 | Oreal | Utilisation de composes nitres di-benzeniques cationiques en teinture des fibres keratiniques, compositions tinctoriales et procedes de teinture |
| DE19930927A1 (de) * | 1999-07-06 | 2001-01-11 | Henkel Kgaa | Neue Farbstoffe und Färbemittel |
-
2002
- 2002-12-23 FR FR0216564A patent/FR2848837B1/fr not_active Expired - Fee Related
-
2003
- 2003-12-23 DE DE60334968T patent/DE60334968D1/de not_active Expired - Lifetime
- 2003-12-23 EP EP03293291A patent/EP1433473B1/fr not_active Expired - Lifetime
- 2003-12-23 AT AT03293291T patent/ATE488217T1/de not_active IP Right Cessation
- 2003-12-23 ES ES03293291T patent/ES2353744T3/es not_active Expired - Lifetime
- 2003-12-24 JP JP2003428262A patent/JP2004203888A/ja active Pending
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