GB198634A - The manufacture of new azodyestuffs - Google Patents

The manufacture of new azodyestuffs

Info

Publication number
GB198634A
GB198634A GB1427323A GB1427323A GB198634A GB 198634 A GB198634 A GB 198634A GB 1427323 A GB1427323 A GB 1427323A GB 1427323 A GB1427323 A GB 1427323A GB 198634 A GB198634 A GB 198634A
Authority
GB
United Kingdom
Prior art keywords
group
naphthylamine
hydroxy
acid
sulphonic
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
GB1427323A
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Priority to GB1427323A priority Critical patent/GB198634A/en
Publication of GB198634A publication Critical patent/GB198634A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02—Disazo dyes
    • C09B35/039—Disazo dyes characterised by the tetrazo component
    • C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl

Landscapes

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

Abstract

Disazo dyes are prepared by coupling the tetrazo compound from 4 : 41-diaminodiphenyl-3 : 31-dicarboxylic acid on the one hand with an aryl-2-naphthylamine, and on the other with an azo dye component which contains a sulphonic or carboxylic group, or two hydroxy or two amino groups, or one hydroxy and one amino group or a hydroxy group in conjunction with the CH2.CO group of the acetoaceticanilide or of the pyrazolones. The products dye cotton in red to blue shades which by after-treatment with metallic salts, for example copper or vanadium salts, become deeper and fast to light and washing. In an example, the tetrazo compound is coupled with phenyl-2-naphthylamine and 1-amino-8-naphthol-4-sulphonic acid. The dyeing properties are also given of the corresponding dyestuffs in which the 1 : 8 : 4-acid is replaced by methyl-2-naphthylamine-7-sulphonic acid, 1-naphthol-5-sulphonic acid, resorcin, or 1-o-oxyphenyl-3-methyl-5-pyrazolone.
GB1427323A 1922-01-31 1922-01-31 The manufacture of new azodyestuffs Expired GB198634A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1427323A GB198634A (en) 1922-01-31 1922-01-31 The manufacture of new azodyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1427323A GB198634A (en) 1922-01-31 1922-01-31 The manufacture of new azodyestuffs

Publications (1)

Publication Number Publication Date
GB198634A true GB198634A (en) 1923-05-31

Family

ID=10038169

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1427323A Expired GB198634A (en) 1922-01-31 1922-01-31 The manufacture of new azodyestuffs

Country Status (1)

Country Link
GB (1) GB198634A (en)

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