JP2006501248A5 - - Google Patents
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- JP2006501248A5 JP2006501248A5 JP2004532112A JP2004532112A JP2006501248A5 JP 2006501248 A5 JP2006501248 A5 JP 2006501248A5 JP 2004532112 A JP2004532112 A JP 2004532112A JP 2004532112 A JP2004532112 A JP 2004532112A JP 2006501248 A5 JP2006501248 A5 JP 2006501248A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- carbon atoms
- alkyl
- alkyl group
- carbon
- 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.)
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- 125000004432 carbon atom Chemical group C* 0.000 claims 53
- 125000000217 alkyl group Chemical group 0.000 claims 26
- 229910052799 carbon Inorganic materials 0.000 claims 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 10
- 150000001721 carbon Chemical group 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 5
- 125000003277 amino group Chemical group 0.000 claims 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 5
- 125000002091 cationic group Chemical group 0.000 claims 5
- 239000012954 diazonium Substances 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 claims 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 230000008878 coupling Effects 0.000 claims 4
- 238000010168 coupling process Methods 0.000 claims 4
- 238000005859 coupling reaction Methods 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 150000001343 alkyl silanes Chemical class 0.000 claims 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 2
- 125000003172 aldehyde group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 238000004040 coloring Methods 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 239000000463 material Substances 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004149 thio group Chemical group *S* 0.000 claims 2
- 125000004001 thioalkyl group Chemical group 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 claims 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 1
- 125000005157 alkyl carboxy group Chemical group 0.000 claims 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000004103 aminoalkyl group Chemical group 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 150000004982 aromatic amines Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000001989 diazonium salts Chemical class 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical group COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 239000011148 porous material Substances 0.000 claims 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000011593 sulfur Chemical group 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 125000004950 trifluoroalkyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405754 | 2002-09-02 | ||
| PCT/EP2003/009417 WO2004019897A1 (en) | 2002-09-02 | 2003-08-26 | Method of colouring porous material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006501248A JP2006501248A (ja) | 2006-01-12 |
| JP2006501248A5 true JP2006501248A5 (enExample) | 2006-10-05 |
Family
ID=31970507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004532112A Withdrawn JP2006501248A (ja) | 2002-09-02 | 2003-08-26 | 多孔質材料の着色方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7229479B2 (enExample) |
| EP (1) | EP1534226A1 (enExample) |
| JP (1) | JP2006501248A (enExample) |
| KR (1) | KR20050058415A (enExample) |
| CN (1) | CN1678285A (enExample) |
| AU (1) | AU2003258664A1 (enExample) |
| BR (1) | BR0313991A (enExample) |
| MX (1) | MXPA05002011A (enExample) |
| WO (1) | WO2004019897A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007500735A (ja) * | 2003-05-15 | 2007-01-18 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | キャップされたジアゾニウム化合物と毛髪の反応からなる毛髪の着色方法、及び関連する組成物及び化合物 |
| JP5274832B2 (ja) | 2004-04-08 | 2013-08-28 | チバ ホールディング インコーポレーテッド | 二硫化染料、それを含む組成物及び毛を染める方法 |
| BRPI0615644B1 (pt) | 2005-08-30 | 2017-06-06 | Ciba Specialty Chemicals Holding Inc | compostos corantes contendo um grupo tiol, método de tingimento de fibras contendo queratina, bem como composição |
| US7794509B2 (en) | 2006-06-13 | 2010-09-14 | Ciba Corporation | Tricationic dyes |
| US20090016975A1 (en) * | 2007-07-12 | 2009-01-15 | Robert Bianchini | Fade-resistant coloring composition containing an acid dye and a cationic conditioning agent for a keratin-containing substrate |
| US8097045B2 (en) | 2008-01-17 | 2012-01-17 | Basf Se | Polymeric hair dyes |
| US8257448B2 (en) | 2009-02-25 | 2012-09-04 | Basf Se | Hair dyeing composition |
| CN107753305A (zh) | 2009-02-25 | 2018-03-06 | 巴斯夫欧洲公司 | 毛发染色组合物 |
| MX2012000557A (es) | 2009-07-15 | 2012-03-07 | Basf Se | Tintes para el cabello polimeros. |
| ES2612475T3 (es) | 2010-08-17 | 2017-05-17 | Basf Se | Tintes capilares poliméricos de disulfuro o tiol |
| EP2705094B1 (en) | 2011-05-03 | 2021-12-15 | Basf Se | Disulfide dyes |
| FR2980199B1 (fr) * | 2011-09-15 | 2013-08-23 | Oreal | Composition tinctoriale comprenant une base d'oxydation para-aminophenol cationique |
| FR2994570B1 (fr) * | 2012-08-17 | 2014-08-01 | Oreal | Composition tinctoriale comprenant un derive o-alkyle de meta-phenylenediamine cationique |
| FR2996552B1 (fr) * | 2012-08-17 | 2016-10-14 | Oreal | Composition tinctoriale comprenant un derive o-alkyle substitue de meta-phenylenediamine cationique |
| FR2994571B1 (fr) * | 2012-08-17 | 2014-07-25 | Oreal | Composition tinctoriale comprenant un derive o-alkyle ramifie de meta-phenylenediamine cationique |
| WO2015059368A1 (fr) | 2013-09-02 | 2015-04-30 | L'oreal | Procede de coloration des fibres keratiniques a partir de colorants cationiques styryles disulfures, et composition comprenant lesdits colorants |
| GB201320636D0 (en) * | 2013-11-22 | 2014-01-08 | Medical Res Council | Compounds |
| ITUA20161586A1 (it) * | 2016-03-11 | 2017-09-11 | Beauty & Business S P A | Composizione per colorare la fibra cheratinica |
| CN113668263A (zh) * | 2021-09-27 | 2021-11-19 | 义乌市华越新材料科技有限公司 | 一种含野菊花提取物的纺织染料及染色方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1882556A (en) * | 1932-10-11 | Pbocess of fbepabxno azo dyestttffs | ||
| DE1617888A1 (de) * | 1967-03-14 | 1971-06-03 | Therachemie Chem Therapeut | Verfahren zum Faerben von menschlichen Haaren |
| DE3009833A1 (de) * | 1980-03-14 | 1981-10-01 | Henkel Kgaa | Verbessertes haarfaerbeverfahren mittels azo-entwicklungsfarbstoffen |
| FR2776289B1 (fr) * | 1998-03-20 | 2001-02-02 | Oreal | Composition de teinture d'oxydation contenant un coupleur cationique, procedes de teinture, nouveaux coupleurs cationiques |
| FR2779054B1 (fr) * | 1998-05-26 | 2001-06-29 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
| FR2794644B1 (fr) * | 1999-06-09 | 2004-04-16 | Oreal | Utilisation de sels d'arenediazonium et de copulants cationiques pour la teinture reactive de fibres keratiniques |
| AU1671202A (en) * | 2000-11-17 | 2002-05-27 | Clairol Inc | Novel coupler for use in oxidative hair dyeing |
| CA2424961A1 (en) * | 2000-11-17 | 2002-05-23 | P&G-Clairol, Inc. | Novel coupler for use in oxidative hair dyeing |
| AU2002219835B2 (en) * | 2000-11-17 | 2005-08-04 | P&G-Clairol, Inc. | Novel coupler for use in oxidative hair dyeing |
| MXPA03004377A (es) * | 2000-11-17 | 2005-01-25 | P & G Clariol Inc | Acoplador novedoso para utilizarse en el tenido oxidativo del cabello. |
| EP1365732A1 (en) * | 2001-03-08 | 2003-12-03 | Ciba SC Holding AG | Method of colouring porous material |
-
2003
- 2003-08-26 US US10/525,469 patent/US7229479B2/en not_active Expired - Fee Related
- 2003-08-26 AU AU2003258664A patent/AU2003258664A1/en not_active Abandoned
- 2003-08-26 EP EP03790920A patent/EP1534226A1/en not_active Withdrawn
- 2003-08-26 CN CNA038207001A patent/CN1678285A/zh active Pending
- 2003-08-26 WO PCT/EP2003/009417 patent/WO2004019897A1/en not_active Ceased
- 2003-08-26 JP JP2004532112A patent/JP2006501248A/ja not_active Withdrawn
- 2003-08-26 MX MXPA05002011A patent/MXPA05002011A/es active IP Right Grant
- 2003-08-26 KR KR1020057002931A patent/KR20050058415A/ko not_active Withdrawn
- 2003-08-26 BR BR0313991-3A patent/BR0313991A/pt not_active IP Right Cessation
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