GB439811A - Improvements in the manufacture and production of azo dyestuffs - Google Patents

Improvements in the manufacture and production of azo dyestuffs

Info

Publication number
GB439811A
GB439811A GB1764034A GB1764034A GB439811A GB 439811 A GB439811 A GB 439811A GB 1764034 A GB1764034 A GB 1764034A GB 1764034 A GB1764034 A GB 1764034A GB 439811 A GB439811 A GB 439811A
Authority
GB
United Kingdom
Prior art keywords
chromium
chlor
naphthol
nitro
disulphonic acid
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
GB1764034A
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 GB1764034A priority Critical patent/GB439811A/en
Publication of GB439811A publication Critical patent/GB439811A/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

Abstract

Chromium orthohydroxy azo dyestuffs are prepared by coupling diazotized 5-nitro-4-chlor-2-amino phenol with 1-naphthol-3 : 8-disulphonic acid or 1-naphthol-4 : 8-disulphonic acid and chrominating the azo dyestuffs thus obtained. It is stated that in contrast to known chromium compounds derived from 5-nitro-4-chlor-2-amino phenol and naphthalene disulphonic acids, the new compounds show an especially high levelling power. In examples: (1) 5-nitro-4-chlor-2-aminophenol --->1-naphthol 4 : 8-disulphonic acid, the dyestuff is then treated with a solution of chromium sulphate and salted out. The chromium compound yields on wool, deep, very level navy blue dyeings.; (2) 5-nitro-4-chlor-2-aminophenol ---> 1-naphthol-3 : 8-disulphonic acid, the dyestuff is then treated with a solution of chromium formate. It yields dark greenish blue dyeings. Specification 9264/06, [Class 2], is referred to.
GB1764034A 1934-06-14 1934-06-14 Improvements in the manufacture and production of azo dyestuffs Expired GB439811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1764034A GB439811A (en) 1934-06-14 1934-06-14 Improvements in the manufacture and production of azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1764034A GB439811A (en) 1934-06-14 1934-06-14 Improvements in the manufacture and production of azo dyestuffs

Publications (1)

Publication Number Publication Date
GB439811A true GB439811A (en) 1935-12-16

Family

ID=10098659

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1764034A Expired GB439811A (en) 1934-06-14 1934-06-14 Improvements in the manufacture and production of azo dyestuffs

Country Status (1)

Country Link
GB (1) GB439811A (en)

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