GB476428A - Manufacture and application of new azo dyestuffs - Google Patents

Manufacture and application of new azo dyestuffs

Info

Publication number
GB476428A
GB476428A GB1568836A GB1568836A GB476428A GB 476428 A GB476428 A GB 476428A GB 1568836 A GB1568836 A GB 1568836A GB 1568836 A GB1568836 A GB 1568836A GB 476428 A GB476428 A GB 476428A
Authority
GB
United Kingdom
Prior art keywords
acid
dyeing
naphthol
fur
aminonaphthol
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
Application number
GB1568836A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB1568836A priority Critical patent/GB476428A/en
Publication of GB476428A publication Critical patent/GB476428A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/24Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28Amino naphthols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Monoazo dyes; acid wool and mordant dyes, dyeing with.--Monoazo dyes, suitable for dyeing furs, pelts or hair, are obtained by coupling diazotized 4-nitro-4<1>-aminodiphenylamine-2-sulphonic acid with an aminonaphthol, free from sulphonic or carboxylic acid groups or with an N-alkyl-, N-hydroxyalkyl-, N-aryl or N-acylderivative thereof. The dyeings are red, red-violet and violet to brown shades of good solidity, evenness and fastness to light and rubbing. The materials may be subjected before dyeing, to the usual "killing" treatment with soda ash, ammonia, lime or caustic soda, followed, after neutralizing with acid, by a "chrome-tannage," e.g. with chrome alum, an alkali bichromate or basic chromium sulphate and, if necessary, neutralization with sodium bicarbonate; they may be further treated with agents such as hypochlorites or phosphates to increase the dyeing capacity of the hair fibres. Examples are given of the manufacture of the dyestuffs with the use, as coupling component, of (1) 1 : 5-aminonaphthol (coupled alkaline), (2) 1 : 5-aminonaphthol (coupled acid), (3) 2 : 7-aminonaphthol (coupled alkaline). In examples of the dyeing process (a) a chrome-tanned long-haired white rabbit fur is entered into a bath at 40 DEG C. containing the dyestuff of (1) above, the temperature is raised during 20 minutes to 75 DEG C., and so maintained for 100 minutes with an addition of acetic acid after the first 30 minutes and of formic acid after a further 30 minutes; the fur is then removed, dried and drummed in sawdust; (b) a chrome-tanned shorn white rabbit fur is entered into a bath at 40 DEG C. containing the dyestuff, 4-nitro-4<1>-aminodiphenylamine - 2 - sulphonic acid --> (alkaline) 1-b -hydroxyethylamino-5-naphthol, dyeing is effected as in (a) at a temperature of 55--60 DEG C., and the fur is then removed, dried and drummed as in (a). A table is also given showing the shades obtainable on fur with the use of the dyestuffs having as coupling components, 1-dimethylamino-5-naphthol, 1-acetylamino - 5 - naphthol, 1 - acetylamino-7-naphthol and 2-phenylamino-7-naphthol (all coupled alkaline). Specification 23026/07, [Class 2], is referred to.
GB1568836A 1936-06-04 1936-06-04 Manufacture and application of new azo dyestuffs Expired GB476428A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1568836A GB476428A (en) 1936-06-04 1936-06-04 Manufacture and application of new azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1568836A GB476428A (en) 1936-06-04 1936-06-04 Manufacture and application of new azo dyestuffs

Publications (1)

Publication Number Publication Date
GB476428A true GB476428A (en) 1937-12-06

Family

ID=10063642

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1568836A Expired GB476428A (en) 1936-06-04 1936-06-04 Manufacture and application of new azo dyestuffs

Country Status (1)

Country Link
GB (1) GB476428A (en)

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