JPS57141455A - Reactive monoazo compound and dyeing by using the same - Google Patents

Reactive monoazo compound and dyeing by using the same

Info

Publication number
JPS57141455A
JPS57141455A JP2616881A JP2616881A JPS57141455A JP S57141455 A JPS57141455 A JP S57141455A JP 2616881 A JP2616881 A JP 2616881A JP 2616881 A JP2616881 A JP 2616881A JP S57141455 A JPS57141455 A JP S57141455A
Authority
JP
Japan
Prior art keywords
dyeing
sulfatoethylsulfone
aminobenzene
same
monoazo compound
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.)
Pending
Application number
JP2616881A
Other languages
Japanese (ja)
Inventor
Junji Toda
Masayoshi Kojima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
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 Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP2616881A priority Critical patent/JPS57141455A/en
Publication of JPS57141455A publication Critical patent/JPS57141455A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:Reactive monoazo compounds of formulaIwherein X is H, methyl, methoxy, chlorine, SO3H.
USE: Dyes which dye natural or man-made fibers such as wool, silk, polyamide, cotton, viscose rayon, regenerated cellulose fibers and leather rose. The dyes exhibits high degrees of exhaustion and fixation, and are excellent in fastnesses to chlorination, light and washing.
PREPARATION: Cyanuric chloride is condensed with the monoazo compound of formula II and a compd. of formula III in any order to produce the desired compound. Examples of the compds. of formula III are 1-aminobenzene-2-β-sulfatoethylsulfone and 1-aminobenzene-3-β-sulfatoethylsulfone.
COPYRIGHT: (C)1982,JPO&Japio
JP2616881A 1981-02-26 1981-02-26 Reactive monoazo compound and dyeing by using the same Pending JPS57141455A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2616881A JPS57141455A (en) 1981-02-26 1981-02-26 Reactive monoazo compound and dyeing by using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2616881A JPS57141455A (en) 1981-02-26 1981-02-26 Reactive monoazo compound and dyeing by using the same

Publications (1)

Publication Number Publication Date
JPS57141455A true JPS57141455A (en) 1982-09-01

Family

ID=12186011

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2616881A Pending JPS57141455A (en) 1981-02-26 1981-02-26 Reactive monoazo compound and dyeing by using the same

Country Status (1)

Country Link
JP (1) JPS57141455A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7282070B2 (en) 2005-05-10 2007-10-16 Everlight Usa, Inc. Reactive dye composition and the use thereof
EP2009065A1 (en) 2007-06-29 2008-12-31 Everlight USA, Inc. Reactive dyestuffs with alkylthio group and beta-sulfatoethylsulfone group
US7704286B2 (en) 2005-08-31 2010-04-27 Everlight Usa, Inc. Reactive dyestuff composition and their use

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7282070B2 (en) 2005-05-10 2007-10-16 Everlight Usa, Inc. Reactive dye composition and the use thereof
US7704286B2 (en) 2005-08-31 2010-04-27 Everlight Usa, Inc. Reactive dyestuff composition and their use
EP2009065A1 (en) 2007-06-29 2008-12-31 Everlight USA, Inc. Reactive dyestuffs with alkylthio group and beta-sulfatoethylsulfone group

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