MA31848B1 - Colorants réactifs, leurs procédés de préparation et leur utilisation - Google Patents
Colorants réactifs, leurs procédés de préparation et leur utilisationInfo
- Publication number
- MA31848B1 MA31848B1 MA32835A MA32835A MA31848B1 MA 31848 B1 MA31848 B1 MA 31848B1 MA 32835 A MA32835 A MA 32835A MA 32835 A MA32835 A MA 32835A MA 31848 B1 MA31848 B1 MA 31848B1
- Authority
- MA
- Morocco
- Prior art keywords
- substituted
- group
- alkyl
- radical
- unsubstituted
- Prior art date
Links
- 238000004040 coloring Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- -1 sulfo, carboxyl Chemical group 0.000 abstract 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 239000002657 fibrous material Substances 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- APVPOHHVBBYQAV-UHFFFAOYSA-N n-(4-aminophenyl)sulfonyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 APVPOHHVBBYQAV-UHFFFAOYSA-N 0.000 abstract 1
- 239000000985 reactive dye Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/503—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
- C09B62/5033—Dioxazine dyes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/503—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an esterified or non-esterified hydroxyalkyl sulfonyl or mercaptoalkyl sulfonyl group, a quaternised or non-quaternised aminoalkyl sulfonyl group, a heterylmercapto alkyl sulfonyl group, a vinyl sulfonyl or a substituted vinyl sulfonyl group, or a thiophene-dioxide group
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/465—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/004—Mixtures of two or more reactive dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Color Printing (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Detergent Compositions (AREA)
Abstract
La présente invention a pour objet des colorants réactifs de formule (1) dans laquelle qi représente un atome d'hydrogène, un halogène ou un radical de formule (2a) ou (2b), r1, r2 et r3 représentent indépendamment un atome d'hydrogène ou un alkyle en c1-c4 qui est non substitué ou substitué par un groupe hydroxyle, sulfo, carboxyle ou sulfato, et r1 dans la formule (1) et r1 dans la formule (2a) ont des significations identiques ou différentes et r2 dans la formule (1) et r2 dans la formule (2a) ont des significations différentes ou identiques, (r4)0-1 et (r5)0-1 représentent indépendamment l'un de l'autre des substituants identiques ou différents 0 ou 1 choisis dans le groupe constitué par un alkyle en c1-c4, un alcoxy en c1-c4, un halogène et un sulfo, a représente un atome d'hydrogène ou un alkyle en c1-c4 qui est non substitué ou substitué par un groupe hydroxyle, sulfo, carboxyle ou sulfato, un phényle qui est non substitué ou substitué par un alkyle en c1-c4, un alcoxy en c1-c4, un alcanoylamino en c2-c4, un groupe hydroxyle, carboxyle, carbamoyle, sulfo ou halogène, un phényl-c1-c2-alkylène qui est non substitué ou substitué dans le cycle phényle par un alkyle en c1-c4, un alcoxy en c1-c4, un alcanoylamino en c2-c4, un groupe hydroxyle, carboxyle, sulfo, carbamoyle ou halogène, un cycloalkyle en c5-c7 qui est non substitué ou substitué par un alkyle en c1-c4, b représente un radical alkylène en c2-c12 qui peut être interrompu par 1, 2 ou 3 éléments du groupe constitué par -nh-, -n(ch3)- ou -o- et est non substitué ou substitué par un groupe hydroxyle, sulfo, sulfato, cyano ou carboxyle, un radical cycloalkylène en c5-c7 ou un radical alkylène en c1-c2-cycloalkylène en c5-c7 qui est non substitué ou substitué dans le cycle cycloalkyle par un radical alkyle en c1-c4, alkylènephénylène en c1-c2 ou un radical phénylène qui sont non substitués ou substitués dans le cycle phényle par un alkyle en c1-c4, un alcoxy en c1-c4, un alcanoylamino en c2-c4, un groupe sulfo, halogène ou carboxyle, v1 etv2 représentent indépendamment un halogène, t représente un radical répondant à la formule -co-(ch2)m-so2-y (3a), -co-ch(hai)-ch2-hai (3b) ou -co-c(hai) = ch2 (3c), hal représente un halogène, x représente un groupe hydroxyle ou y, y représente un groupe vinyle ou un radical -ch2-ch2-u et u représente un groupe qui peut être séparé dans des conditions alcalines, et m représente le chiffre 2, 3 ou 4. Ces colorants sont adaptés pour colorer des matériaux fibreux très différents, en particulier des matériaux en fibre cellulosique, et pour produire des teintures présentant de bonnes propriétés générales
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07119331 | 2007-10-25 | ||
| PCT/EP2008/063373 WO2009053238A2 (fr) | 2007-10-25 | 2008-10-07 | Colorants réactifs, leurs procédés de préparation et leur utilisation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31848B1 true MA31848B1 (fr) | 2010-11-01 |
Family
ID=39874128
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA32835A MA31848B1 (fr) | 2007-10-25 | 2010-05-14 | Colorants réactifs, leurs procédés de préparation et leur utilisation |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US7905928B2 (fr) |
| EP (1) | EP2201071B1 (fr) |
| JP (1) | JP5416703B2 (fr) |
| KR (1) | KR101538622B1 (fr) |
| CN (1) | CN101835849B (fr) |
| AT (1) | ATE541899T1 (fr) |
| BR (1) | BRPI0818211B8 (fr) |
| CO (1) | CO6311011A2 (fr) |
| DO (1) | DOP2010000120A (fr) |
| ES (1) | ES2379671T3 (fr) |
| HN (1) | HN2010000751A (fr) |
| MA (1) | MA31848B1 (fr) |
| MX (1) | MX2010002804A (fr) |
| MY (1) | MY149741A (fr) |
| PT (1) | PT2201071E (fr) |
| SV (1) | SV2010003549A (fr) |
| TW (1) | TWI468471B (fr) |
| WO (1) | WO2009053238A2 (fr) |
| ZA (1) | ZA201001879B (fr) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102321390B (zh) * | 2011-09-07 | 2013-11-06 | 上海雅运纺织化工股份有限公司 | 三原色活性染料组合物及其在纤维上的染色应用 |
| EP3162859A1 (fr) | 2015-11-02 | 2017-05-03 | DyStar Colours Distribution GmbH | Mélanges de colorants réactifs aux fibres exempts de métaux lourds, bleus et bleus marine |
| BR112020016325B8 (pt) | 2018-02-16 | 2023-05-16 | Huntsman Adv Mat Switzerland | Processo para curtimento e tingimento simultâneos de material fibroso contendo colágeno, couro ou imitação de couro, e seu uso |
| CN116333512A (zh) * | 2022-12-12 | 2023-06-27 | 湖北丽源科技股份有限公司 | 一种蓝色毛用活性染料及其制备方法和应用 |
| CN115873419A (zh) * | 2022-12-30 | 2023-03-31 | 宿迁虹光化学工业有限公司 | 一种活性染料合成方法及其应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1225789B (de) | 1957-08-17 | 1966-09-29 | Hoechst Ag | Verfahren zur Herstellung von wasserloeslichen Farbstoffen |
| EP0112797A1 (fr) * | 1982-11-26 | 1984-07-04 | Ciba-Geigy Ag | Procédé de teinture ou d'impression, avec des colorants réactifs, de matières fibreuses contenant de la cellulose |
| DE3625347A1 (de) * | 1985-09-19 | 1987-03-26 | Hoechst Ag | Wasserloesliche triphendioxazin-verbindungen, verfahren zu ihrer herstellung und ihre verwendung als farbstoffe |
| US4841049A (en) * | 1986-09-12 | 1989-06-20 | Ciba-Geigy Corporation | Reactive dyes of the dioxazine series |
| TW422871B (en) * | 1995-04-25 | 2001-02-21 | Ciba Sc Holding Ag | Reactive dyes from the dioxazine series, their preparation and use |
| TW506993B (en) * | 1999-03-15 | 2002-10-21 | Ciba Sc Holding Ag | Reactive dyes, processes for their preparation and process for dyeing or printing a fibre material |
| JP2001139835A (ja) | 1999-09-16 | 2001-05-22 | Ciba Specialty Chem Holding Inc | アクリロイルアミノ置換染料の付加生成物、その調製法及び用途 |
-
2008
- 2008-10-07 KR KR1020107011439A patent/KR101538622B1/ko active IP Right Grant
- 2008-10-07 JP JP2010530393A patent/JP5416703B2/ja active Active
- 2008-10-07 US US12/739,079 patent/US7905928B2/en active Active
- 2008-10-07 EP EP08842856A patent/EP2201071B1/fr active Active
- 2008-10-07 ES ES08842856T patent/ES2379671T3/es active Active
- 2008-10-07 PT PT08842856T patent/PT2201071E/pt unknown
- 2008-10-07 WO PCT/EP2008/063373 patent/WO2009053238A2/fr active Application Filing
- 2008-10-07 AT AT08842856T patent/ATE541899T1/de active
- 2008-10-07 BR BRPI0818211A patent/BRPI0818211B8/pt active IP Right Grant
- 2008-10-07 MX MX2010002804A patent/MX2010002804A/es active IP Right Grant
- 2008-10-07 MY MYPI2010001006A patent/MY149741A/en unknown
- 2008-10-07 CN CN200880113594.XA patent/CN101835849B/zh active Active
- 2008-10-23 TW TW97140602A patent/TWI468471B/zh active
-
2010
- 2010-03-09 CO CO10027697A patent/CO6311011A2/es active IP Right Grant
- 2010-03-16 ZA ZA2010/01879A patent/ZA201001879B/en unknown
- 2010-04-21 HN HN2010000751A patent/HN2010000751A/es unknown
- 2010-04-22 DO DO2010000120A patent/DOP2010000120A/es unknown
- 2010-04-23 SV SV2010003549A patent/SV2010003549A/es unknown
- 2010-05-14 MA MA32835A patent/MA31848B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP5416703B2 (ja) | 2014-02-12 |
| CO6311011A2 (es) | 2011-08-22 |
| MX2010002804A (es) | 2010-03-31 |
| HN2010000751A (es) | 2013-09-23 |
| ATE541899T1 (de) | 2012-02-15 |
| TW200930764A (en) | 2009-07-16 |
| JP2011500928A (ja) | 2011-01-06 |
| US20100251490A1 (en) | 2010-10-07 |
| SV2010003549A (es) | 2011-08-09 |
| EP2201071B1 (fr) | 2012-01-18 |
| WO2009053238A3 (fr) | 2009-12-17 |
| DOP2010000120A (es) | 2012-05-31 |
| RU2010120807A (ru) | 2011-11-27 |
| BRPI0818211B8 (pt) | 2023-05-16 |
| BRPI0818211B1 (pt) | 2017-07-11 |
| WO2009053238A2 (fr) | 2009-04-30 |
| MY149741A (en) | 2013-10-14 |
| CN101835849A (zh) | 2010-09-15 |
| KR101538622B1 (ko) | 2015-07-29 |
| EP2201071A2 (fr) | 2010-06-30 |
| CN101835849B (zh) | 2014-03-19 |
| ES2379671T3 (es) | 2012-04-30 |
| TWI468471B (zh) | 2015-01-11 |
| PT2201071E (pt) | 2012-04-03 |
| ZA201001879B (en) | 2010-11-24 |
| US7905928B2 (en) | 2011-03-15 |
| KR20100075659A (ko) | 2010-07-02 |
| BRPI0818211A2 (fr) | 2009-04-30 |
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