ES2190234T3 - Colorantes reactivos, su obtencion y uso. - Google Patents
Colorantes reactivos, su obtencion y uso.Info
- Publication number
- ES2190234T3 ES2190234T3 ES99936477T ES99936477T ES2190234T3 ES 2190234 T3 ES2190234 T3 ES 2190234T3 ES 99936477 T ES99936477 T ES 99936477T ES 99936477 T ES99936477 T ES 99936477T ES 2190234 T3 ES2190234 T3 ES 2190234T3
- Authority
- ES
- Spain
- Prior art keywords
- fiber
- reactive group
- beta
- sulfatoethylsulfonyl
- obtaining
- 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.)
- Expired - Lifetime
Links
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
- C09B62/465—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
- C09B62/47—Azo dyes
- C09B62/475—Disazo or polyazo 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
- C09B62/4401—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 with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system
- C09B62/4403—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 with two or more reactive groups at least one of them being directly attached to a heterocyclic system and at least one of them being directly attached to a non-heterocyclic system the heterocyclic system being a triazine ring
- C09B62/4411—Azo dyes
- C09B62/4415—Disazo or polyazo 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
- C09B62/507—Azo dyes
- C09B62/513—Disazo or polyazo 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
- 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
- C09B67/0046—Mixtures of two or more azo dyes
- C09B67/0055—Mixtures of two or more disazo dyes
- C09B67/0057—Mixtures of two or more reactive disazo dyes
Abstract
Compuestos de la fórmula (1) **(Fórmula)** en la que K1 y K2 en cada caso con independencia entre sí significan un resto de la fórmula **(Fórmula)** en las que (R4)0-3 significa de 0 a 3 restos iguales o distintos, elegidos entre alquilo C1-C4; alcoxi C1-C4; alcoxi C1-C4 sustituido en la parte alquilo por hidroxi, alcoxi C1-C4 o sulfato; halógeno; carboxi; hidroxi; amino; Nmono- o N, N-di-(alquil C1-C2)amino; alcanoilamino C2-C4; ureido, sulfo; (alquil C1-C4)sulfonilo; (alquil C1-C4)sulfonilamino y el resto reactivo de la fórmula (2e) **(Fórmula)** en la que X significa halógeno, 3-carboxipiridin-1-ilo o 3-carbamoilpiridin-1-ilo, T, con independencia de su aparición, tiene el significado de X o significa hidroxi, alcoxi C1-C4, fenoxi, alquiltio C1-C4, morfolino, amino eventualmente sustituido por restos no reactivos con las fibras o un resto reactivo con las fibras de las fórmulas (3a), (3b), (3c), (3d), (3e) o (3f) **(Fórmula)** R1 y R1alpha con independencia entre sí significan en cada caso hidrógeno o alquilo C1-C4, R2 significa hidrógeno; alquilo C1-C4 eventualmente sustituido por hidroxi, sulfo, sulfato, carboxi o ciano; o un resto -alk(R3)-SO2-Y, R3 significa hidrógeno, hidroxi, sulfo, sulfato, carboxi, ciano, halógeno, (alcoxi C1-C4)carbonilo, alcanoiloxi C1-C4, carbamoílo o el grupo -SO2-Y, alk y alk1, con independencia entre sí, significan alquileno C1-C6, ¿arylen¿ significa un resto fenileno o naftileno sin sustituir o sustituido por sulfo, carboxi, alquilo C1-C4, alcoxi C1-C4 o halógeno, Y1 significa un grupo -CH(Hal)-CH2-Hal o -C(Hal)=CH2 y Hal significa cloro o bromo, Q es un resto -O- o -NR1-, en el que R1 tiene el significado definido anteriormente, W es un grupo -SO2-NR2-, -CONR2- o -NR2CO-, m es el número 0 ó 1 e Y significa vinilo o un resto -CH2-CH2-U y U significa un grupo eliminable en medio básico, (R4alpha)0-2 significa de 0 a 2 restos iguales o distintos, elegidos entre alquilo C1-C4, alcoxi C1-C4, fenoxi, halógeno, sulfo e hidroxi; R5 significa hidrógeno o alquilo C1-C4, R5a con independencia de su aparición tiene el significado de R5 o bien significa alcanoílo C2-C4, hidroxialquilo C1-C4, sulfatoalquilo C1-C4, (alcoxi C1-C4)-alquilo o fenilo eventualmente sustituido por metilo, metoxi, cloro o sulfo; R6 significa hidrógeno, alquilo C1-C4 o fenilo; (R7)0-2 significa de 0 a 2 sustituyentes iguales o distintos, elegidos entre hidroxi y el resto reactivo con las fibras de la fórmula (2a) -SO2-Y (2a) en el que Y tiene el significado definido anteriormente, R8 significa hidrógeno o alquilo C1-C4 eventualmente sustituido por hidroxi, alcoxi C1-C4, sulfato, sulfo, halógeno o ciano; R9 con independencia de su aparición tiene el mismo significado que R8 o es alcanoílo C2-C4 o benzoílo, o bien -NR8R9 significa un resto reactivo con las fibras de la fórmula (2e) indicada anteriormente; R10 y R10alpha con independencia entre sí significan en cada caso carbamoílo, sulfometilo o ciano; R11 significa hidrógeno o alquilo C1-C4, que está eventualmente sustituido por un resto de la fórmula (2e) ya definida anteriormente; R12 y R13 con independencia entre sí significan en cada caso hidrógeno o alquilo C1-C12 eventualmente sustituido por hidroxi, alcoxi C1-C4, fenoxi, sulfato, sulfo, carboxi, amino o N-mono- o N, N-di-(alquil C1-C4)amino (que a su vez puede estar sustituido en la parte alquilo por hidroxi, alcoxi C1-C4, fenoxi, sulfato, sulfo, carboxi o un resto reactivo con las fibras de la fórmula (2e) indicada anteriormente) y/o eventualmente interrumpido por -O-, excepto en el caso del metilo; R14 significa metilo o carboxi; R15 significa hidroxi o amino; (R16)0-3 significa de 0 a 3 restos iguales o distintos, elegidos entre sulfo, halógeno, hidroxi, alcoxi C1-C4 y alquilo C1-C4; (R17)0-2 significa de 0 a 2 restos iguales o distintos, elegidos entre alquilo C1-C4, alcoxi C1-C4, alcoxi C1-C4 que está sustituido en la parte alquilo por hidroxi, alcoxi C1-C4 o sulfato; alcanoilamino C2-C4, ureido, halógeno y sulfo; K significa un resto de las fórmulas (4a), (4b), (4c), (4d), (4e), (4f), (4g) o (4h) o (4j), (4k) o (4l) indicadas anteriormente y con preferencia un resto de la fórmula (4e); D significa un resto fenilo o 1- o 2-naftilo que lleva de 1 a 3 restos iguales o distintos, elegidos entre sulfo, alquilo C1-C4, alcoxi C1-C4, halógeno y un resto reactivo con las fibras de las fórmulas (2a), (2b), (2c) o (2d) -SO2-Y (2a), -CONR2-(CH2)n-SO2-Y (2b), -NH-CO-CH(Hal)-CH2-Hal (2c) o -NH-CO-C(Hal)=CH2 (2d) en las que n significa un número entero de 1 a 6 y R2, Hal e Y tienen los significados definidos anteriormente; Da es el resto de un cromóforo monoazoico o diazoico; y X e Y tienen en cada caso el significado definido antes; pero por lo menos uno de los restos K1 y K2 lleva un grupo reactivo con las fibras.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP98810659 | 1998-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2190234T3 true ES2190234T3 (es) | 2003-07-16 |
Family
ID=8236188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES99936477T Expired - Lifetime ES2190234T3 (es) | 1998-07-13 | 1999-07-05 | Colorantes reactivos, su obtencion y uso. |
Country Status (8)
Country | Link |
---|---|
US (1) | US6518408B1 (es) |
EP (1) | EP1095105B1 (es) |
JP (1) | JP2003518141A (es) |
AT (1) | ATE231903T1 (es) |
AU (1) | AU5156499A (es) |
DE (1) | DE59904172D1 (es) |
ES (1) | ES2190234T3 (es) |
WO (1) | WO2000004099A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4641194B2 (ja) * | 2005-02-01 | 2011-03-02 | 日本化薬株式会社 | アゾ化合物、インク組成物、記録方法及び着色体 |
JP6198349B2 (ja) * | 2013-08-01 | 2017-09-20 | 日本化薬株式会社 | 黒色用トリスアゾ化合物、それを含む黒色用染料組成物およびその使用 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2807260C2 (de) | 1978-02-21 | 1986-10-09 | Hoechst Ag, 6230 Frankfurt | Wasserlösliche Farbstoffe, Verfahren zu deren Herstellung, ihre Verwendung als faserreaktive Farbstoffe zum Färben und Bedrucken von Fasermaterialien |
TW225549B (es) | 1992-04-14 | 1994-06-21 | Bayer Ag | |
DE4309554A1 (de) | 1993-03-24 | 1994-09-29 | Bayer Ag | Faserreaktive Azofarbstoffe |
-
1999
- 1999-07-05 EP EP99936477A patent/EP1095105B1/de not_active Expired - Lifetime
- 1999-07-05 DE DE59904172T patent/DE59904172D1/de not_active Expired - Fee Related
- 1999-07-05 AT AT99936477T patent/ATE231903T1/de not_active IP Right Cessation
- 1999-07-05 ES ES99936477T patent/ES2190234T3/es not_active Expired - Lifetime
- 1999-07-05 WO PCT/EP1999/004647 patent/WO2000004099A1/de active IP Right Grant
- 1999-07-05 AU AU51564/99A patent/AU5156499A/en not_active Abandoned
- 1999-07-05 US US09/743,694 patent/US6518408B1/en not_active Expired - Fee Related
- 1999-07-05 JP JP2000560199A patent/JP2003518141A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP1095105A1 (de) | 2001-05-02 |
WO2000004099A1 (de) | 2000-01-27 |
ATE231903T1 (de) | 2003-02-15 |
DE59904172D1 (de) | 2003-03-06 |
US6518408B1 (en) | 2003-02-11 |
AU5156499A (en) | 2000-02-07 |
JP2003518141A (ja) | 2003-06-03 |
EP1095105B1 (de) | 2003-01-29 |
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