GB532261A - Manufacture of azo-dyestuffs - Google Patents

Manufacture of azo-dyestuffs

Info

Publication number
GB532261A
GB532261A GB21081/39A GB2108139A GB532261A GB 532261 A GB532261 A GB 532261A GB 21081/39 A GB21081/39 A GB 21081/39A GB 2108139 A GB2108139 A GB 2108139A GB 532261 A GB532261 A GB 532261A
Authority
GB
United Kingdom
Prior art keywords
acid
nitro
dyestuffs
aminophenol
resorcinol
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
GB21081/39A
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 GB532261A publication Critical patent/GB532261A/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
    • C09B35/38Trisazo dyes ot the type
    • C09B35/40Trisazo dyes ot the type the component K being a dihydroxy or polyhydroxy compound

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Abstract

532,261. Dyes ; dyeing. SOC. OF CHEMICAL INDUSTRY IN BASLE. July 20, 1939, Nos. 21081 and 21082. Convention dates, July 22, 1938 and July 1, 1939. Sample furnished. [Classes 2 (iii) and 15 (ii)] Trisazo dyes are made by combining a dihydroxy compound of the aryl series which is capable of coupling twice, on the one hand with a diazotized amine of the general formula where V is a lake-forming group, e.g. a hydroxyl, carboxyl or alkoxy group, X is hydrogen or a non-solubilizing group, and Y, Z, may be hydrogen or any substituents, and on the other hand with a diazoazo compound obtained by coupling a tetrazotized diaminodiphenyl on one side only with an o-hydroxybenzoic acid. Specified substituents X are nitro or sulphonamide groups and halogen atoms, while Y and Z may be sulphonic, carboxyl, nitro or alkyl groups or halogen atoms. The products dye fibres containing cellulose or regenerated cellulose chiefly in brown shades. The dyeings or prints may be treated with copper compounds, in the dye bath or on the fibre, or the dyestuffs may be partially metallized, and the resulting dyeings treated with metallizing agents, especially agents yielding copper, as described in Specification 516,076. In examples, dyestuffs are made from (1) benzidine, salicylic acid or o-cresotinic acid, resorcinol, and 1-hydroxy-2- amino-4-chloro-sulphamido-, or nitro-benzene or 4 - nitro - 2 - aminophenol - 6 - sulphonic acid, and (2)3:3'-dimethyl (or dimethoxy)-4:4<SP>1</SP>-diaminodiphenyl, salicylic acid or o-cresotinic acid, resorcinol, and 4-nitro-2-aminophenol or its 6-sulphonic acid or 4-sulphamido-2-aminophenol. In an example of the dyeing process, cotton is dyed with one of the dyestuffs of example (1) in a bath containing sodium carbonate, to which glauber's salt is added, and later on copper sulphate and tartaric acid. Specifications 12932/15, 101601, [both in Class 2 (iii)] and 455,274 also are referred to A sample has been furnished under Sect. 2 (5) of a dyestuff made from benzidine, salicylic acid, resorcinol and 4-chloro-2-aminophenoxyacetic acid. The Specification as open to inspection under Sect. 91 comprises also the conversion of the dyestuffs into completely metallized products by treating them in substance with agents yielding metals, e.g. with chromium, iron, cobalt, nickel, and copper compounds. The products are, as a rule, sparingly soluble or insoluble, and may be dyed by the process of Specification 458,501. This subject-matter does not appear in the Specification as accepted.
GB21081/39A 1938-07-22 1939-07-20 Manufacture of azo-dyestuffs Expired GB532261A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH532261X 1938-07-22

Publications (1)

Publication Number Publication Date
GB532261A true GB532261A (en) 1941-01-21

Family

ID=4518524

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21081/39A Expired GB532261A (en) 1938-07-22 1939-07-20 Manufacture of azo-dyestuffs

Country Status (1)

Country Link
GB (1) GB532261A (en)

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