GB697136A - Manufacture of disazo- and polyazo-dyestuffs - Google Patents

Manufacture of disazo- and polyazo-dyestuffs

Info

Publication number
GB697136A
GB697136A GB15289/51A GB1528951A GB697136A GB 697136 A GB697136 A GB 697136A GB 15289/51 A GB15289/51 A GB 15289/51A GB 1528951 A GB1528951 A GB 1528951A GB 697136 A GB697136 A GB 697136A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
dyestuffs
quinolinol
phenyl
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
GB15289/51A
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.)
BASF Schweiz AG
Original Assignee
Ciba 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 Ciba AG filed Critical Ciba AG
Publication of GB697136A publication Critical patent/GB697136A/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
    • 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
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/04Disazo dyes characterised by the tetrazo component the tetrazo component being a benzene derivative

Landscapes

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

Abstract

The invention comprises the disazo and polyazo dyestuffs which are obtainable by coupling diazotized <FORM:0697136/IV (c)/1> (which may be substituted in the quinoline ring) (1) in an alkaline medium with a 1-naphthol-3-sulphonic acid containing a substituted amino group (e.g. arylamino or acylamino) in the 6- or 7-position; or (2) in an alkaline medium with a compound containing two residues of the type of (1) linked by a common amino group or by a bridge such as a urea or cyanuric residue, the second coupling position being occupied by the same or a different azo residue; or (3) in an acid medium with J acid, the product being coupled alkaline with a further diazo component. The aminoazo compounds of the above formula are made by coupling diazotized 5-amino-2-nitrobenzoic acid or 5-amino-2-acylaminobenzoic acid with the appropriate quinolinol and converting the 2-substituent into an amino group. The further diazo component in (3) may be a diazotized aniline-azo-salicylic acid. The disazo and polyazo dyestuffs may be used on animal p fibres such as wool, silk and leather. Those derived from J acid and its derivatives are suitable for dyeing and printing cotton, linen and regenerated cellulose. The dyestuffs may be metallized in the dyebath or on the fibre, e.g. by the methods of Specifications 455,274 and 619,969. In the examples the following dyestuffs are prepared: (1) 8 - quinolinol \sM 5 - amino - 2 - nitro - benzoic acid (reduced) --> N - phenyl - J acid, N - p - anisyl - J acid, N - (p - acetylamino - benzoyl) - J acid or N - phenyl - g - acid; 5 - amino - 2 - acetylaminobenzoic acid may also be used as diazo component, the acetylamino group being hydrolysed; (2) the monoazo intermediate of (1)-->(acid) J acid (alkaline)\sM cresidine\sM5-aminosalicylic acid; (3) the monoazo intermediate of (1)-->5 : 51-dihydroxy - 2 : 21 - dinaphthylamine - 7 : 71 - di - sulphonic acid\sMcresidine\sM5 - amino - salicylic acid; 8 : 81 - dihydroxy - 2 : 2 - di - naphthylamine-6 : 61-disulphonic acid or J acid urea may be used instead. In a further example cotton is dyed reddish blue with the product of (1) from N-phenyl-J acid, coppered in the dyebath or on the fibre. 8-Quinolinol-7-sulphonic acid and N-benzoyl-g -acid are also specified as components.
GB15289/51A 1950-06-28 1951-06-27 Manufacture of disazo- and polyazo-dyestuffs Expired GB697136A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH697136X 1950-06-28

Publications (1)

Publication Number Publication Date
GB697136A true GB697136A (en) 1953-09-16

Family

ID=4529710

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15289/51A Expired GB697136A (en) 1950-06-28 1951-06-27 Manufacture of disazo- and polyazo-dyestuffs

Country Status (1)

Country Link
GB (1) GB697136A (en)

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