GB419599A - Improvements in the manufacture and production of azo dyestuffs - Google Patents

Improvements in the manufacture and production of azo dyestuffs

Info

Publication number
GB419599A
GB419599A GB1361233A GB1361233A GB419599A GB 419599 A GB419599 A GB 419599A GB 1361233 A GB1361233 A GB 1361233A GB 1361233 A GB1361233 A GB 1361233A GB 419599 A GB419599 A GB 419599A
Authority
GB
United Kingdom
Prior art keywords
wool
shades
orange
oxyquinaldine
coupled
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
GB1361233A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1361233A priority Critical patent/GB419599A/en
Publication of GB419599A publication Critical patent/GB419599A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/16Monoazo compounds containing chromium

Landscapes

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

Abstract

Monazo-, disazo-, and polyazo dyes are prepared by coupling 8-oxyquinaldine or its derivatives (including 8-oxyquinophthalone) with diazo or tetrazo compounds of any kind and selecting the components so that the dyestuffs contain at least one sulphonic acid group and if desired, after-treating the dyestuffs with agents supplying metals, preferably chromium. The dyestuffs may be used with advantage for dyeing in neutral baths containing chromium salts; they may be employed as substantive dyes for cotton, acid wool dyes and in some cases as lake dyestuffs. Suitable diazo compounds are aniline and its halogen, sulpho, nitro and alkoxy derivatives, benzidine, naphthylamine and substituted derivatives thereof. In examples: (1) 3.6-disulphoaniline is diazotised and coupled with 8-oxyquinophthalone (prepared by melting 8 - oxyquinaldine with phthalic acid anhydride at about 170 DEG C.); the product yields red-orange dyeings on wool turning to orange shades on treatment with bichromate (alternatively dyeing on chromemordanted wool yields orange dyeings); (2) 1 - oxy - 2 - amino - 4 - chlorbenzene - 6 - sulphonic acid is diazotised and coupled with 8-oxyquinaldine; wool is dyed yellow-brown shades which by after-treatment with bichromate or dyeing on chrome-mordanted fibre turn to brown shades; (3) 1-naphthylamine-4-sulphonic acid is diazotised and coupled with 8-oxyquinaldine; wool is dyed brown shades changed to red-brown by after-treatment with bichromate or by dyeing on chrome-mordanted wool; (4) 1 - amino - 3 - chlorbenze - 6 - sulphonic acid is diazotised and coupled with 8-oxyquinaldine; it dyes wool orange shades scarcely changed by treatment with bichromate or by dyeing on chrome-mordanted wool; on boiling with chromium formate a red-orange dye for wool or leather is obtained; the foregoing diazo body can be replaced by those from 1 - amino - 2 - chlorbenze - 5 - sulphonic acid, 1 - amino - 4 - chlorbenze - 2 - or 3 - sulphonic acids to give similar shades; (5) the diazo body from 1-amino-2,5-dichlorbenzene is coupled with 8-oxyquinaldine-5-sulphonic acid; it dyes wool red shades changed by after-treatment with bichromate or by dyeing on chrome-mordanted wool to orange shades; (6) the diazo body from 2-nitro-4<1>.4<1>-diaminodiphenyl is coupled with 8-oxyquinaldine-5-sulphonic acid; wool is dyed blue-red shades changed by after-chroming or by dyeing on chrome-mordanted wool to red-orange; cotton is dyed blue-red shades changed to orange by after-treatment with copper sulphate; (7) diazotised metanilic p acid is coupled with 8-oxy quinaldine; wool is dyed orange shades shades scarcely changed by after-chroming; (8) diazobenzene is coupled with 8-oxyquinaldine-5-sulphonic; wool is dyed yellow-red shades changed to orange by after-treatment with bichromate. Reference is also made to 8 - oxy - 5 - chloro - or - 5 - methylquinaldines as coupling components and 8 - oxyquinaldine and its derivatives in general may be prepared according to the method described in Specification 395,063. Specification 406,778 also is referred to.
GB1361233A 1933-05-10 1933-05-10 Improvements in the manufacture and production of azo dyestuffs Expired GB419599A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1361233A GB419599A (en) 1933-05-10 1933-05-10 Improvements in the manufacture and production of azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1361233A GB419599A (en) 1933-05-10 1933-05-10 Improvements in the manufacture and production of azo dyestuffs

Publications (1)

Publication Number Publication Date
GB419599A true GB419599A (en) 1934-11-12

Family

ID=10026195

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1361233A Expired GB419599A (en) 1933-05-10 1933-05-10 Improvements in the manufacture and production of azo dyestuffs

Country Status (1)

Country Link
GB (1) GB419599A (en)

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