JP2006527743A5 - - Google Patents
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- Publication number
- JP2006527743A5 JP2006527743A5 JP2006516297A JP2006516297A JP2006527743A5 JP 2006527743 A5 JP2006527743 A5 JP 2006527743A5 JP 2006516297 A JP2006516297 A JP 2006516297A JP 2006516297 A JP2006516297 A JP 2006516297A JP 2006527743 A5 JP2006527743 A5 JP 2006527743A5
- Authority
- JP
- Japan
- Prior art keywords
- dye
- composition according
- chromophore
- belongs
- range
- 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.)
- Withdrawn
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- 239000000203 mixture Substances 0.000 claims 25
- 125000005647 linker group Chemical group 0.000 claims 6
- 102000011782 Keratins Human genes 0.000 claims 3
- 108010076876 Keratins Proteins 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
- 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
- 238000010521 absorption reaction Methods 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
- 125000002091 cationic group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 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
- 239000007800 oxidant agent Substances 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
- 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
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000004040 coloring Methods 0.000 claims 1
- 238000010924 continuous production Methods 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
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 230000001590 oxidative effect Effects 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
- 239000012429 reaction media Substances 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 CC(*c(cc1)ccc1NCCNc(cc1)ccc1Nc(cc1)ccc1N=**c1[n+](*)cc[n]1*)Nc1[n+](*)cc[n]1I Chemical compound CC(*c(cc1)ccc1NCCNc(cc1)ccc1Nc(cc1)ccc1N=**c1[n+](*)cc[n]1*)Nc1[n+](*)cc[n]1I 0.000 description 2
- YILQVSSHPLYRPB-UHFFFAOYSA-P C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(N(CCO)CCO)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(N(CCO)CCO)n2)[nH+]cc1 YILQVSSHPLYRPB-UHFFFAOYSA-P 0.000 description 1
- RGDWIUDHQFHGCX-UHFFFAOYSA-P C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(NCCOC)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(NCCOC)n2)[nH+]cc1 RGDWIUDHQFHGCX-UHFFFAOYSA-P 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-O Cc1[nH+]cc[n]1C Chemical compound Cc1[nH+]cc[n]1C GIWQSPITLQVMSG-UHFFFAOYSA-O 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0307185A FR2855966B1 (fr) | 2003-06-16 | 2003-06-16 | Composition tinctoriale comprenant au moins un colorant direct a chromophores mixtes |
| PCT/FR2004/001496 WO2004112737A2 (fr) | 2003-06-16 | 2004-06-16 | Composition tinctoriale comprenant au moins un colorant direct a chromophores mixtes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006527743A JP2006527743A (ja) | 2006-12-07 |
| JP2006527743A5 true JP2006527743A5 (https=) | 2007-08-02 |
Family
ID=33484444
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006516297A Withdrawn JP2006527743A (ja) | 2003-06-16 | 2004-06-16 | 混合発色団を有する少なくとも一つの直接染料を含む染色組成物 |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1663400B1 (https=) |
| JP (1) | JP2006527743A (https=) |
| KR (1) | KR20060020686A (https=) |
| CN (1) | CN1835729A (https=) |
| AT (1) | ATE465781T1 (https=) |
| BR (1) | BRPI0411496A (https=) |
| DE (1) | DE602004026887D1 (https=) |
| FR (1) | FR2855966B1 (https=) |
| MX (1) | MXPA05013735A (https=) |
| WO (1) | WO2004112737A2 (https=) |
Families Citing this family (11)
| 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 |
| 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 |
| 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 |
| 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 |
| EP2516555B1 (en) * | 2009-12-21 | 2018-08-22 | Living Proof, Inc. | Coloring agents and methods of use thereof |
| KR20160130263A (ko) * | 2014-03-07 | 2016-11-10 | 와코 쥰야꾸 고교 가부시키가이샤 | 시아닌계 착색조성물 |
| JP2017519026A (ja) * | 2014-06-24 | 2017-07-13 | クロクス テクノロジーズ インコーポレイテッド | ハロゲンを含む生体光組成物およびその使用 |
| BR112017019798A2 (pt) * | 2015-03-19 | 2018-05-29 | Basf Se | compostos |
| CN105088821A (zh) * | 2015-09-08 | 2015-11-25 | 湖州吉昌丝绸有限公司 | 一种利用番茄红素对纯棉织物的染色方法 |
| JP2017114767A (ja) * | 2015-12-04 | 2017-06-29 | ロレアル | ケラチン繊維を染色するための組成物 |
| CN105596228B (zh) * | 2015-12-28 | 2018-11-02 | 肇庆迪彩日化科技有限公司 | 一种氧化型染色组合物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2215944T3 (es) * | 1994-11-03 | 2004-10-16 | Ciba Specialty Chemicals Holding Inc. | Colorantes imidazolazoicos cationicos. |
| FR2782450B1 (fr) * | 1998-08-19 | 2004-08-27 | Oreal | Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un agent tensio-actif anionique |
| DE60102904T2 (de) * | 2000-03-09 | 2005-03-31 | Ciba Specialty Chemicals Holding Inc. | Verfahren zur färbung von haaren unter verwendung von kationischen farbstoffen |
| 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 FR0307185A patent/FR2855966B1/fr not_active Expired - Fee Related
-
2004
- 2004-06-16 MX MXPA05013735A patent/MXPA05013735A/es active IP Right Grant
- 2004-06-16 JP JP2006516297A patent/JP2006527743A/ja not_active Withdrawn
- 2004-06-16 AT AT04767358T patent/ATE465781T1/de not_active IP Right Cessation
- 2004-06-16 KR KR1020057024221A patent/KR20060020686A/ko not_active Ceased
- 2004-06-16 BR BRPI0411496-5A patent/BRPI0411496A/pt not_active Application Discontinuation
- 2004-06-16 DE DE602004026887T patent/DE602004026887D1/de not_active Expired - Lifetime
- 2004-06-16 CN CNA2004800235069A patent/CN1835729A/zh active Pending
- 2004-06-16 EP EP04767358A patent/EP1663400B1/fr not_active Expired - Lifetime
- 2004-06-16 WO PCT/FR2004/001496 patent/WO2004112737A2/fr not_active Ceased
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