GB609301A - Manufacture of disazo-dyestuffs - Google Patents

Manufacture of disazo-dyestuffs

Info

Publication number
GB609301A
GB609301A GB2413/42A GB241342A GB609301A GB 609301 A GB609301 A GB 609301A GB 2413/42 A GB2413/42 A GB 2413/42A GB 241342 A GB241342 A GB 241342A GB 609301 A GB609301 A GB 609301A
Authority
GB
United Kingdom
Prior art keywords
acid
mols
cotton
hydroxide solution
aqueous
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
GB2413/42A
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
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Publication of GB609301A publication Critical patent/GB609301A/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
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/08Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
    • 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
    • C09B41/00Special methods of performing the coupling reaction
    • C09B41/001Special methods of performing the coupling reaction characterised by the coupling medium

Landscapes

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

Abstract

Disazo dyes are obtained by coupling tetrazotised 3 : 31 - dihydroxy - 4 : 41 - diaminodiphenyl with 2 mols. of the same or different coupling components (other than a 1-hydroxynaphthalenesulphonic acid carrying an auxochromic group in 8-position) in a medium rendered alkaline with a hydroxide of an alkali metal, e.g. sodium or potassium, or of an alkaline earth metal, e.g. calcium, magnesium, strontium or barium, or of ammonium. Specified coupling components are 2 : 5 : 7- and 2 : 8 : 6-aminonaphtholsulphonic acids, 2 : 6-naphtholsulphonic acid and 2 : 3 : 6-naphtholdisulphonic acid. The products are suitable for dyeing cellulose fibres, e.g. of cotton or regenerated cellulose, or animal fibres, e.g. wool, silk or leather and may be treated in substance, in the dyebath or on the fibre, with agents yielding metal, e.g. copper, chromium, iron, nickel or cobalt. The metal compounds produced in substance may be incorporated in nitrocellulose lacquers, artificial resins and spinning masses. In examples, tetrazotised 3 : 31 - dihydroxy - 4 : 41 - diaminodiphenyl is coupled (1) in aqueous potassium hydroxide solution, (2) in aqueous calcium hydroxide solution with 2 : 5 : 7-aminonaphtholsulphonic acid (2 mols.) to obtain a product giving fast blue after-coppered dyeings on cotton, (3) in aqueous potassium hydroxide solution with 2 : 3 : 6-naphtholdisulphonic acid (2 mols.) to obtain a similar product, (4) in aqueous calcium hydroxide solution with 2 : 8 : 6-aminonaphtholsulphonic acid (2 mols.) to obtain a similar product. In an example of the dyeing process, wetted-out cotton is introduced into an aqueous dyebath at 50 DEG C. containing the dyestuff obtained in (1) above and sodium carbonate, the temperature is raised to 95 DEG C. and, after addition of Glauber salt, is so maintained for 1 hour; the temperature is then allowed to fall to 80 DEG C. and sodium copper tartrate added, whereupon coppering is effected for 1/2 hour at 80-90 DEG C. and the cotton is rinsed and, if desired, soaped. Specifications 455,274 and 609,302 are referred to.
GB2413/42A 1941-02-18 1942-02-24 Manufacture of disazo-dyestuffs Expired GB609301A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH609301X 1941-02-18

Publications (1)

Publication Number Publication Date
GB609301A true GB609301A (en) 1948-09-29

Family

ID=4523289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2413/42A Expired GB609301A (en) 1941-02-18 1942-02-24 Manufacture of disazo-dyestuffs

Country Status (5)

Country Link
BE (1) BE444533A (en)
DE (1) DE745094C (en)
FR (1) FR889850A (en)
GB (1) GB609301A (en)
NL (1) NL60554C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH437589A (en) * 1963-11-08 1967-06-15 Durand & Huguenin Ag Process for the preparation of water-soluble, metallizable disazo dyes

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB102881A (en) * 1916-05-13 1917-01-04 Oliver Imray Manufacture of New, Direct-dyeing Ortho-oxy-azo-dyestuffs.

Also Published As

Publication number Publication date
BE444533A (en)
DE745094C (en) 1944-06-10
NL60554C (en)
FR889850A (en) 1944-01-20

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