MX2010002804A - Tintes reactivos, procesos para su preparacion y su empleo. - Google Patents

Tintes reactivos, procesos para su preparacion y su empleo.

Info

Publication number
MX2010002804A
MX2010002804A MX2010002804A MX2010002804A MX2010002804A MX 2010002804 A MX2010002804 A MX 2010002804A MX 2010002804 A MX2010002804 A MX 2010002804A MX 2010002804 A MX2010002804 A MX 2010002804A MX 2010002804 A MX2010002804 A MX 2010002804A
Authority
MX
Mexico
Prior art keywords
sub
alkyl
unsubstituted
substituted
radical
Prior art date
Application number
MX2010002804A
Other languages
English (en)
Inventor
Athanassios Tzikas
Georg Roentgen
Thomas Verdugo
Original Assignee
Huntsman Adv Mat Switzerland
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Huntsman Adv Mat Switzerland filed Critical Huntsman Adv Mat Switzerland
Publication of MX2010002804A publication Critical patent/MX2010002804A/es

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
    • C09B62/503—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)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Color Printing (AREA)
  • Paints Or Removers (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Detergent Compositions (AREA)

Abstract

Tintes reactivos de la fórmula(1) (ver fórmula 1) en la cual Q1 es hidrógeno, halógeno o un radical de La fórmula (ver fórmula 2a, 2b) R1, R2 y R3 independientemente entre sí, son hidrógeno o C1-C4alquilo,que está insustituido o sustituido por hidroxilo, sulfo, carboxilo o sulfato, yR1 en la fórmula (1) yRien la fórmula (2a) tienen significados idénticos o diferentes, y R2 en la fórmula (1) y R2 en la fórmula (2a) tienen significados idénticos o diferentes. (R4)01 y (R5)01 independientemente entre sí son O o 1 sustituyentes,ident±cos o diferentes, del grupo que consiste de C1-C4alquilo, C1-C4alcoxilo, halógeno y sulfo, A es hidrógeno o C1-C4alquilo el cual está insustituido o sustituido por hidroxilo, sulfo, carboxilo o sulfato, fenilo el cual está insustituido o sustituido por C1-C4alquilo, C1-C4alcoxilo, C2-C4alkanoilamino, hidroxilo, carboxilo, carbamoilo, sulfo o halógeno, fenilo-C1-C2alquileno, el cual está insustituido o sustituido en el anillo fenilo por C1-C4alquilo, C1-C4alcoxiio, C2-C4alcanoilamino, hidroxilo, carboxilo, sulfo, carbamoilo o halógeno, o C5-C7cicloalquilo, el cual está insustituido o sustituido por C1-C4alquilo, B es un radical C2-C12alquilene el cual puede estar interrumpido por 1, 2 o 3 miembros, del grupo que consiste de -NH-, -N(CH3)- o -O- y esta ínsustituido o sustituido por hidroxilo, sulfo, sulfato, ciano o carboxilo, un radical C5-C7cicloalquileno o un radical C1-C2alquileno-C5-C7ciclo alquileno el cual está insustituido o sustituido en el anillo de cicloalquilo, por C1-C4alquilo, un radical C1-C2alquileno-fenileno o un radical fenileno los cuales están insustituidos o sustituidos en el anillo fenilo por C1-C4alquilo, C1-C4alcoxilo, C2-C4alcanoilamino, sulfo, halógeno o carboxilo, y1 y y2 independientemente entre sí son halógeno, T es un radical de la fórmula -CO- (CI2)-SO2-Y (3a), -CO-CH(Hal)-CH2-Hal (3b) o -CO-C(Ha1)CH2 (3c), Hal es halógeno, X es hidroxilo o Y, Y es vinil o a radical -CH2-CH2-U y U es un grupo el cual puede estar dividido bajo las condiciones alcalinas., y m es el número 2, 3 ó 4. son adecuados para teñir ampliamente diversos materiales de fibras, en particular materiales de fibras celulósicas y producir teñidos con buenas propiedades generales.
MX2010002804A 2007-10-25 2008-10-07 Tintes reactivos, procesos para su preparacion y su empleo. MX2010002804A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP07119331 2007-10-25
PCT/EP2008/063373 WO2009053238A2 (en) 2007-10-25 2008-10-07 Reactive dyes, processes for their preparation and their use

Publications (1)

Publication Number Publication Date
MX2010002804A true MX2010002804A (es) 2010-03-31

Family

ID=39874128

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2010002804A MX2010002804A (es) 2007-10-25 2008-10-07 Tintes reactivos, procesos para su preparacion y su empleo.

Country Status (19)

Country Link
US (1) US7905928B2 (es)
EP (1) EP2201071B1 (es)
JP (1) JP5416703B2 (es)
KR (1) KR101538622B1 (es)
CN (1) CN101835849B (es)
AT (1) ATE541899T1 (es)
BR (1) BRPI0818211B8 (es)
CO (1) CO6311011A2 (es)
DO (1) DOP2010000120A (es)
ES (1) ES2379671T3 (es)
HN (1) HN2010000751A (es)
MA (1) MA31848B1 (es)
MX (1) MX2010002804A (es)
MY (1) MY149741A (es)
PT (1) PT2201071E (es)
SV (1) SV2010003549A (es)
TW (1) TWI468471B (es)
WO (1) WO2009053238A2 (es)
ZA (1) ZA201001879B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
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 (en) 2015-11-02 2017-05-03 DyStar Colours Distribution GmbH Heavy metal free, blue and navy fibre-reactive dye mixtures
MA50851B1 (fr) 2018-02-16 2021-07-29 Huntsman Adv Mat Switzerland Procédé de tannage et de teinture simultanés de matériau fibreux contenant du collagène
CN116333512B (zh) * 2022-12-12 2024-10-01 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)

* Cited by examiner, † Cited by third party
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 (de) * 1982-11-26 1984-07-04 Ciba-Geigy Ag Verfahren zum Färben oder Bedrucken von cellulosehaltigem Fasermaterial mit Reaktivfarbstoffen
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

Also Published As

Publication number Publication date
KR101538622B1 (ko) 2015-07-29
DOP2010000120A (es) 2012-05-31
ES2379671T3 (es) 2012-04-30
PT2201071E (pt) 2012-04-03
BRPI0818211B1 (pt) 2017-07-11
EP2201071A2 (en) 2010-06-30
US7905928B2 (en) 2011-03-15
SV2010003549A (es) 2011-08-09
BRPI0818211B8 (pt) 2023-05-16
JP2011500928A (ja) 2011-01-06
CO6311011A2 (es) 2011-08-22
WO2009053238A2 (en) 2009-04-30
HN2010000751A (es) 2013-09-23
ATE541899T1 (de) 2012-02-15
RU2010120807A (ru) 2011-11-27
ZA201001879B (en) 2010-11-24
US20100251490A1 (en) 2010-10-07
KR20100075659A (ko) 2010-07-02
MA31848B1 (fr) 2010-11-01
JP5416703B2 (ja) 2014-02-12
MY149741A (en) 2013-10-14
BRPI0818211A2 (es) 2009-04-30
EP2201071B1 (en) 2012-01-18
WO2009053238A3 (en) 2009-12-17
TW200930764A (en) 2009-07-16
CN101835849B (zh) 2014-03-19
CN101835849A (zh) 2010-09-15
TWI468471B (zh) 2015-01-11

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