Reactive dyes for cellulose. An unexpected hydrolysis product of a triazinyl reactive dye with a 3–carboxypyridine (nicotinic acid) leaving group
Author:
Affiliation:
1. Fine Chemicals Research Centre, ICI Colours and Fine Chemicals, PO Box No 42, Hexagon House, Blackley, Manchester M9 3DA
Publisher
Wiley
Subject
Polymers and Plastics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1478-4408.1990.tb01259.x
Reference34 articles.
1. ICI French P 1 271 347 (1959).
2. ICI Belgian P 628 855 (1962); 628 854 (1963).
3. Ciba German P 1 210 407; 1 544 431 (1961).
4. ICI BP 946 998 (1961); 1 005 240 (1963).
5. Acna Swiss P 447 433 (1965).
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1. Assessment of the application of cathodic stripping voltammetry to the analysis of diazo reactive dyes and their hydrolysis products;Dyes and Pigments;2001-09
2. The influence of temperature on the kinetics of concurrent hydrolysis and methanolysis reactions of a monochlorotriazine reactive dye;Dyes and Pigments;2000-07
3. Polarographic and voltammetric determination of selected triazine-based azo dyes with different reactive groups;Analytica Chimica Acta;1996-02
4. Neutral‐fixing reactive dyes for cotton. Part 1 —synthesis and application of quaternised S ‐triazinyl reactive dyes;Journal of the Society of Dyers and Colourists;1992-04
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