JP2006527743A5 - - Google Patents
Download PDFInfo
- 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- Withdrawn
Links
- 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 |
|---|---|---|---|---|
| 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 |
| 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 |
| JP5930969B2 (ja) | 2009-12-21 | 2016-06-08 | リビング プルーフ，インコーポレーテッド | 着色剤及びその使用方法 |
| CN106103597B (zh) * | 2014-03-07 | 2018-01-16 | 和光纯药工业株式会社 | 花青系着色组合物 |
| US20170209348A1 (en) * | 2014-06-24 | 2017-07-27 | Klox Technologies Inc. | Biophotonic compositions comprising halogen and uses thereof |
| JP6875286B2 (ja) * | 2015-03-19 | 2021-05-19 | ビーエイエスエフ・ソシエタス・エウロパエアＢａｓｆ Ｓｅ | カチオン性直接染料 |
| 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 |
|---|---|---|---|---|
| DE59510884D1 (de) * | 1994-11-03 | 2004-04-29 | Ciba Sc Holding Ag | Kationische Imidazolazofarbstoffe |
| 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 |
| US6843256B2 (en) * | 2000-03-09 | 2005-01-18 | Ciba Specialty Chemicals Corporation | Method of coloring hair using cationic dyes |
| 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 AT AT04767358T patent/ATE465781T1/de not_active IP Right Cessation
- 2004-06-16 BR BRPI0411496-5A patent/BRPI0411496A/pt not_active Application Discontinuation
- 2004-06-16 EP EP04767358A patent/EP1663400B1/fr not_active Expired - Lifetime
- 2004-06-16 JP JP2006516297A patent/JP2006527743A/ja not_active Withdrawn
- 2004-06-16 KR KR1020057024221A patent/KR20060020686A/ko not_active Ceased
- 2004-06-16 WO PCT/FR2004/001496 patent/WO2004112737A2/fr not_active Ceased
- 2004-06-16 CN CNA2004800235069A patent/CN1835729A/zh active Pending
- 2004-06-16 DE DE602004026887T patent/DE602004026887D1/de not_active Expired - Lifetime
- 2004-06-16 MX MXPA05013735A patent/MXPA05013735A/es active IP Right Grant
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7976585B2 (en) | Polymeric dyes | |
| KR101341856B1 (ko) | 트리아릴메탄 염료 | |
| KR101333719B1 (ko) | 양이온 올리고머성 아조 염료 | |
| KR101341855B1 (ko) | 옥사진 디설파이드 염료 | |
| JP2006527743A5 (https=) | ||
| KR101341861B1 (ko) | 스티릴 술피드 염료 | |
| KR101276213B1 (ko) | 설피드 염료의 혼합물 | |
| KR20080048501A (ko) | 크산텐 염료 | |
| KR20090015113A (ko) | 삼양이온성 염료 | |
| KR101341857B1 (ko) | 니트로설피드 염료 | |
| KR20080056213A (ko) | 티올 염료 | |
| KR20080038172A (ko) | 티올기 함유 염료 | |
| KR101047949B1 (ko) | 양이온성 염료, 그의 제조 방법 및 용도 | |
| MX2009001598A (es) | Colorantes derivados de tiol. | |
| JP2006527744A5 (https=) | ||
| KR100947753B1 (ko) | 양이온성 아조 화합물의 제조방법 | |
| Haucke et al. | Absorption and fluorescence of pyrylium salts | |
| JP2005336191A (ja) | 少なくとも１つのアミン官能基を有する化合物、顔料および化学的カップリング剤を含有するケラチン繊維の染色用組成物 | |
| DE19746137A1 (de) | Verwendung von Phenaziniumsalzen zum Färben von keratinhaltigen Fasern | |
| KR20060113953A (ko) | 캡핑된 디아조화 화합물 및 결합 성분을 사용한 착색 방법 | |
| JP2006527743A (ja) | 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 | |
| KR101269997B1 (ko) | 설피드 염료 | |
| JPS5967216A (ja) | 染毛剤 | |
| US20050273947A1 (en) | Composition for dyeing keratin fibers comprising at least one compound bearing at least one amine function, at least one pigment and at least one chemical coupling agent | |
| Maradiya et al. | Synthesis of novel azo dyes containing the thiophene moiety |