JP2006527744A5 - - Google Patents
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- Publication number
- JP2006527744A5 JP2006527744A5 JP2006516303A JP2006516303A JP2006527744A5 JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5 JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5
- Authority
- JP
- Japan
- Prior art keywords
- dye
- composition according
- optionally substituted
- group
- cationic
- 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
- 239000000203 mixture Substances 0.000 claims 19
- 125000002091 cationic group Chemical group 0.000 claims 6
- 125000005647 linker group Chemical group 0.000 claims 5
- 102000011782 Keratins Human genes 0.000 claims 3
- 108010076876 Keratins Proteins 0.000 claims 3
- 238000010521 absorption reaction Methods 0.000 claims 3
- 238000004043 dyeing Methods 0.000 claims 3
- 239000000835 fiber Substances 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 239000007800 oxidant agent Substances 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 230000001590 oxidative effect Effects 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-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
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 150000001450 anions Chemical class 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
- 125000003118 aryl group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 1
- -1 azomethine Natural products 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000007857 hydrazones Chemical class 0.000 claims 1
- 229940097275 indigo Drugs 0.000 claims 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 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
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229950000688 phenothiazine Drugs 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 125000005649 substituted arylene group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical group NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 claims 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 1
- 0 CN(C)C=CN(C)*N=Nc(cc1)ccc1Nc1nc(NCCOC)nc(Nc(cc2)ccc2Nc(cc2)ccc2N=NC2=[N+]CCN2C)n1 Chemical compound CN(C)C=CN(C)*N=Nc(cc1)ccc1Nc1nc(NCCOC)nc(Nc(cc2)ccc2Nc(cc2)ccc2N=NC2=[N+]CCN2C)n1 0.000 description 1
- CCYLOTMMRSLCAL-HRGRZTPGSA-O C[C@H](C1)/C(/NC(C=C2)=CCC2/N=N/c2[n+](C)cc[n]2C)=C/CC/C(/Nc(cc2)ccc2NC2C=CC(/N=N/c3[n+2]cc[n]3C)=CC2)=N\C1N(CCO)CCO Chemical compound C[C@H](C1)/C(/NC(C=C2)=CCC2/N=N/c2[n+](C)cc[n]2C)=C/CC/C(/Nc(cc2)ccc2NC2C=CC(/N=N/c3[n+2]cc[n]3C)=CC2)=N\C1N(CCO)CCO CCYLOTMMRSLCAL-HRGRZTPGSA-O 0.000 description 1
- UZRAMPDQILKSGI-UHFFFAOYSA-P C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(NCCC[n]3cncc3)n2)[nH+]cc1 Chemical compound C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(NCCC[n]3cncc3)n2)[nH+]cc1 UZRAMPDQILKSGI-UHFFFAOYSA-P 0.000 description 1
- VUTPQCLYLXXRAM-UHFFFAOYSA-P C[n]1c(NNc(cc2)ccc2Nc(cc2)ccc2Nc2nc(NC(C=C3)=CCC3/N=N/c3[n+](C)cc[n]3C)nc(NCCCCCCO)n2)[nH+]cc1 Chemical compound C[n]1c(NNc(cc2)ccc2Nc(cc2)ccc2Nc2nc(NC(C=C3)=CCC3/N=N/c3[n+](C)cc[n]3C)nc(NCCCCCCO)n2)[nH+]cc1 VUTPQCLYLXXRAM-UHFFFAOYSA-P 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR03/07186 | 2003-06-16 | ||
| FR0307186A FR2855967B1 (fr) | 2003-06-16 | 2003-06-16 | Composition tinctoriale eclaircissante comprenant au moins un colorant direct cationique a chromophores mixtes |
| PCT/FR2004/001517 WO2004112738A1 (fr) | 2003-06-16 | 2004-06-16 | Composition tinctoriale eclaircissante comprenant au moins un colorant direct cationique a chromophores mixtes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006527744A JP2006527744A (ja) | 2006-12-07 |
| JP2006527744A5 true JP2006527744A5 (enExample) | 2007-08-02 |
| JP4728230B2 JP4728230B2 (ja) | 2011-07-20 |
Family
ID=33484445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006516303A Expired - Fee Related JP4728230B2 (ja) | 2003-06-16 | 2004-06-16 | 混合発色団を有する少なくとも一つのカチオン性直接染料を含む明色化染色組成物 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1648402A1 (enExample) |
| JP (1) | JP4728230B2 (enExample) |
| KR (1) | KR20060021898A (enExample) |
| CN (1) | CN1835730B (enExample) |
| BR (1) | BRPI0411495A (enExample) |
| FR (1) | FR2855967B1 (enExample) |
| MX (1) | MXPA05013749A (enExample) |
| WO (1) | WO2004112738A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| 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 |
| FR2895904B1 (fr) * | 2006-01-12 | 2008-02-29 | Oreal | Utilisation pour la coloration avec effet eclaircissant des matieres keratiniques d'une composition comprenant un colorant fluorescent de type cyanine |
| JP2008105976A (ja) * | 2006-10-24 | 2008-05-08 | Shinichiro Isobe | 化粧用組成物 |
| EP3271025A1 (en) | 2015-03-19 | 2018-01-24 | Noxell Corporation | Method of coloring hair with direct dye compounds |
| CN107750154A (zh) * | 2015-03-19 | 2018-03-02 | 诺赛尔股份有限公司 | 用于使用阳离子直接染料对毛发进行染色的组合物 |
| WO2016149430A1 (en) * | 2015-03-19 | 2016-09-22 | The Procter & Gamble Company | Compositions for dyeing hair with cationic direct dyes |
| EP3271026A1 (en) * | 2015-03-19 | 2018-01-24 | Noxell Corporation | Method of coloring hair with direct dye compounds |
| US10034823B2 (en) | 2016-09-16 | 2018-07-31 | Noxell Corporation | Method of coloring hair with washfast blue imidazolium direct dye compounds |
| US9918919B1 (en) | 2016-09-16 | 2018-03-20 | Noxell Corporation | Method of coloring hair with washfast yellow imidazolium direct dye compounds |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0714954B1 (de) * | 1994-11-03 | 2002-09-25 | Ciba SC Holding AG | Kationische Imidazolazofarbstoffe |
| FR2773991B1 (fr) * | 1998-01-26 | 2000-05-26 | Oreal | Utilisation a titre d'agent protecteur des fibres keratiniques de polymeres de polyammonium quaternaire heterocyclique et compositions cosmetiques |
| JP2002080332A (ja) * | 2000-03-17 | 2002-03-19 | Kao Corp | 染毛剤組成物 |
| JP2001261535A (ja) * | 2000-03-17 | 2001-09-26 | Kao Corp | 毛髪用染色剤組成物 |
| EP1133975B1 (en) * | 2000-03-17 | 2008-02-13 | Kao Corporation | Use of a compound for dyeing hair |
| WO2002030374A1 (en) * | 2000-10-12 | 2002-04-18 | Ciba Specialty Chemicals Holding Inc. | Method of dyeing keratin-containing fibres |
| FR2822697B1 (fr) * | 2001-04-02 | 2003-07-25 | Oreal | Nouvelle composition tinctoriale pour la teinture des fibres keratiniques comprenant un colorant azoique cationique particulier |
| FR2822693B1 (fr) * | 2001-04-02 | 2003-06-27 | Oreal | Nouvelle composition tinctoriale pour la teinture des fibres keratiniques comprenant un colorant azoique cationique particulier |
| FR2822698B1 (fr) * | 2001-04-03 | 2006-04-21 | Oreal | Nouvelle composition tinctoriale pour la teinture des fibres keratiniques comprenant un colorant monoazoique dicationique |
| FR2825625B1 (fr) * | 2001-06-12 | 2005-06-17 | Oreal | Utilisation de composes dicationiques en teinture des fibres keratiniques humaines et compositions les contenant |
| WO2003006554A1 (en) * | 2001-07-11 | 2003-01-23 | Ciba Specialty Chemicals Holding Inc. | A method of coloring hair using cationic dyes |
-
2003
- 2003-06-16 FR FR0307186A patent/FR2855967B1/fr not_active Expired - Fee Related
-
2004
- 2004-06-16 JP JP2006516303A patent/JP4728230B2/ja not_active Expired - Fee Related
- 2004-06-16 MX MXPA05013749A patent/MXPA05013749A/es active IP Right Grant
- 2004-06-16 CN CN2004800235158A patent/CN1835730B/zh not_active Expired - Fee Related
- 2004-06-16 EP EP04767378A patent/EP1648402A1/fr not_active Withdrawn
- 2004-06-16 BR BRPI0411495-7A patent/BRPI0411495A/pt not_active Application Discontinuation
- 2004-06-16 KR KR1020057024229A patent/KR20060021898A/ko not_active Ceased
- 2004-06-16 WO PCT/FR2004/001517 patent/WO2004112738A1/fr not_active Ceased
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