GB362513A - Process for the manufacture of azo dyestuffs - Google Patents

Process for the manufacture of azo dyestuffs

Info

Publication number
GB362513A
GB362513A GB26688/30A GB2668830A GB362513A GB 362513 A GB362513 A GB 362513A GB 26688/30 A GB26688/30 A GB 26688/30A GB 2668830 A GB2668830 A GB 2668830A GB 362513 A GB362513 A GB 362513A
Authority
GB
United Kingdom
Prior art keywords
aminonaphthol
acid
sulphonic
disulphonic acid
amino
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
GB26688/30A
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
Publication of GB362513A publication Critical patent/GB362513A/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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/50Tetrazo dyes
    • C09B35/56Tetrazo dyes of the type

Landscapes

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

Abstract

Tetrakisazo dyes are made by tetrazotizing a benzidine disulphonic acid or dicarboxylic acid or a derivative thereof, coupling with two molecular parts of a middle component or with one molecular part each of two different middle components, again tetrazotizing and coupling with two molecular parts of similar or dissimilar N-alkylated or aralkylated 2 : 8-aminonaphthols substituted by one or two sulphonic acid groups or derivatives thereof or alternatively with one molecular part of one such component and one molecular part of a 2 : 8-aminonaphthol disulphonic acid or a derivative thereof. They yield deep printings on silk fast to water and sublimation. In examples the following dyestuffs are described: benzidine-o-disulphonic acid \sQ 1-methyl - 3-amino-4-methoxybenzene (2 mols.) \sQ 2 : 8-aminonaphthol-3 : 6-disulphonic acid (1 mol.) and n-butyl-2-amino-8-naphthol-6-sulphonic acid or hydroxyethyl-2-amino-8-naphthol-6-sulphonic acid (1 mol.) or aminoethyl - 2 : 8 - aminonaphthol - 3 : 6 disulphonic acid (2 mols.). Specification 319,407, [Class 2 (iii), Dyes &c.], is referred to. The N-alkyl-2 : 8-aminonaphthol sulphonic acids referred to above are prepared by boiling the corresponding aminonaphthol sulphonic acids with bisulphite and the corresponding alkylamines according to Bucherer's reaction.
GB26688/30A 1929-09-07 1930-09-06 Process for the manufacture of azo dyestuffs Expired GB362513A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE362513X 1929-09-07

Publications (1)

Publication Number Publication Date
GB362513A true GB362513A (en) 1931-12-07

Family

ID=6305937

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26688/30A Expired GB362513A (en) 1929-09-07 1930-09-06 Process for the manufacture of azo dyestuffs

Country Status (1)

Country Link
GB (1) GB362513A (en)

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