GB456768A - Process for the manufacture of polyazo dyestuffs - Google Patents

Process for the manufacture of polyazo dyestuffs

Info

Publication number
GB456768A
GB456768A GB14271/35A GB1427135A GB456768A GB 456768 A GB456768 A GB 456768A GB 14271/35 A GB14271/35 A GB 14271/35A GB 1427135 A GB1427135 A GB 1427135A GB 456768 A GB456768 A GB 456768A
Authority
GB
United Kingdom
Prior art keywords
acid
mol
nitroaniline
sulphonic
acids
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
GB14271/35A
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 GB14271/35A priority Critical patent/GB456768A/en
Publication of GB456768A publication Critical patent/GB456768A/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
    • C09B35/52Tetrazo dyes of the type

Landscapes

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

Abstract

Polyazo dyes are made by coupling 1 mol. of a naphthol sulphonic acid capable of coupling both in an acid and in an alkaline medium, in either order, with 1 mol of a tetrazodiphenyl and 1 mol. of a diazo compound, one of the couplings being effected in an acid and the other in an alkaline medium, combining the diazo disazo compound obtained with 1 mol. of resorcinol or a derivative thereof, and causing the trisazo dyestuff to react in an alkaline medium with 1 mol. of a monodiazo compound or at the same time or successively with 2 mols. of the same or different monodiazo compounds. Instead of the tetrazodiphenyl a diazo compound of the benzene series containing a group which is convertible into an amino group may be used. They yield brown to blackish brown shades on leather fast to acids and alkalies. In the examples the following dyes are described: (1) sulphanilic acid --> (alk.) H acid \sM (acid) benzidine --> resorcinol \sx p-nitroaniline; (2) 4-nitroaniline-2-sulphonic acid is used instead of sulphanilic acid in (1); this component and the p-nitroaniline may also be substituted by aniline disulphonic acids, naphthionic acid, naphthylamine disulphonic acids, chloraniline sulphonic acids, anisidine sulphonic acids, aminoazobenzene mono- or disulphonic acids, etc.; (3) sulphanilic acid (1 mol.) and p-nitroaniline (1 mol.) are used as end components in (1); p-nitraniline disulphonic acids, substituted anilines and aniline sulphonic acids, picramic acid and 1 : 3-diamino-4-nitrobenzene may also be used; (4) sulphanilic acid --> (alk.) J acid \sM (acid) benzidine --> resorcinol \sx 4-nitroaniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); p-aminobenzoic acid, 1-hydroxy-4-aminobenzene-2-carboxylic acid &c. may also be used as components; (5) sulphanilic acid --> (acid) J acid \sM (alk.) benzidine --> resorcinol \sx 4-nitraniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); (6) sulphanilic acid --> (alk.) J acid \sM (acid) p-nitroaniline (reduced) --> resorcinol \sx 4-nitraniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); (7) H acid is used instead of J acid. Further similar combinations are specified in a table. Other double coupling components mentioned are 1-amino-8-naphthol-4 - sulphonic acid, phenyl J acid and 2 : 5-dihydroxynaphthalene - 7 - sulphonic acid and other diaminodiphenyls are m-nitrobenzidine and benzidine-m-disulphonic acid.
GB14271/35A 1935-05-15 1935-05-15 Process for the manufacture of polyazo dyestuffs Expired GB456768A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB14271/35A GB456768A (en) 1935-05-15 1935-05-15 Process for the manufacture of polyazo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB14271/35A GB456768A (en) 1935-05-15 1935-05-15 Process for the manufacture of polyazo dyestuffs

Publications (1)

Publication Number Publication Date
GB456768A true GB456768A (en) 1936-11-16

Family

ID=10038137

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14271/35A Expired GB456768A (en) 1935-05-15 1935-05-15 Process for the manufacture of polyazo dyestuffs

Country Status (1)

Country Link
GB (1) GB456768A (en)

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