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GB610857A - Process for the production of chromable azo dyestuffs - Google Patents

Process for the production of chromable azo dyestuffs

Info

Publication number
GB610857A
GB610857A GB11664/46A GB1166446A GB610857A GB 610857 A GB610857 A GB 610857A GB 11664/46 A GB11664/46 A GB 11664/46A GB 1166446 A GB1166446 A GB 1166446A GB 610857 A GB610857 A GB 610857A
Authority
GB
United Kingdom
Prior art keywords
dichloro
class
chroming
sulphonic acid
production
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
GB11664/46A
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.)
Novartis AG
Original Assignee
JR Geigy 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 JR Geigy AG filed Critical JR Geigy AG
Publication of GB610857A publication Critical patent/GB610857A/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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

3 : 4 - Dichloro - 5 - nitro - 2 - aminophenol - 6 - sulphonic acid is obtainable by forming the benzoxazolone from 3 : 4 - dichloro - 2 - amino - phenol-6-sulphonic acid by means of phosgene, nitrating, and then opening the oxazolone ring with alkaline agents. Specifications 11196/06, [Class 2], 145,053, [Class 2 (iii)], and 460,561 are referred to.ALSO:Chromable azo dyestuffs, suitable for use in the metachrome dyeing process, are manufactured by coupling diazotized 4-chloro- or 3 : 4-dichloro-5-nitro-2-aminophenol-6-sulphonic acid with 5 : 8-dichloro-1-naphthol. Examples are given of the production of both dyestuffs, of which the first dyes wool from an acid bath in red-violet shades becoming bluish-grey on after-chroming, whilst the second dyes wool from an acid bath in blue-violet shades and yields greenish-blue dyeings by after-chroming or by the single-bath chroming process. Specifications 11196/06, [Class 2], 145,053, [Class 2 (iii)], and 460,561 are referred to.
GB11664/46A 1945-04-17 1946-04-16 Process for the production of chromable azo dyestuffs Expired GB610857A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH610857X 1945-04-17

Publications (1)

Publication Number Publication Date
GB610857A true GB610857A (en) 1948-10-21

Family

ID=4523390

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11664/46A Expired GB610857A (en) 1945-04-17 1946-04-16 Process for the production of chromable azo dyestuffs

Country Status (1)

Country Link
GB (1) GB610857A (en)

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