GB587110A - Manufacture of trisazo-dyestuffs - Google Patents

Manufacture of trisazo-dyestuffs

Info

Publication number
GB587110A
GB587110A GB13844/43A GB1384443A GB587110A GB 587110 A GB587110 A GB 587110A GB 13844/43 A GB13844/43 A GB 13844/43A GB 1384443 A GB1384443 A GB 1384443A GB 587110 A GB587110 A GB 587110A
Authority
GB
United Kingdom
Prior art keywords
diazotized
nitro
diazo
sulphonic acid
coupling
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
GB13844/43A
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 GB587110A publication Critical patent/GB587110A/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)
  • Coloring (AREA)

Abstract

Trisazo dyestuffs are manufactured by coupling 1 : 3-dihydroxynaphthalene with, in either order, on the one hand a diazo compound of the aryl series containing a lake-forming group (e.g. a hydroxy, carboxyl, alkoxy or alkoxy-carboxyl group) in o-position to the diazo group, and on the other hand a diazoazo compound obtained by unilateral coupling of a tetrazotized benzidine with an o-hydroxyaryl-carboxylic acid capable of coupling, and, if desired, treating the product in substance, in the dyebath or on the fibre with an agent yielding metal, e.g. chromium, cobalt, iron and especially copper. The products may be used for dyeing or printing animal fibres and especially cellulosic fibres such as cotton, linen and artificial silk and staple fibre of regenerated cellulose. The dyeings with the non-metallized dyestuffs may be after-metallized, advantageously by the single-bath process. In examples, the following diazo compounds are coupled with 1 : 3-dihydroxynaphthalene, which is then coupled with the diazoazo compound from tetrazotized benzidine and salicylic acid: (1) diazotized 2-aminophenol-4-sulphonamide; (2) diazotized 4-chloro- or 4-nitro-2-amino-phenol-6-sulphonic acid; (3) the diazo compound obtained by diazotizing 1 : 3 : 6-trichloro - 2 - aminobenzene - 4 - sulphonic acid and stirring with sodium acetate until the chlorine atom in the 1-position is replaced by a hydroxy group; (4) diazotized 6-nitro-2-aminophenol-4-sulphonic acid; (5) diazotized 2-aminophenol-6-carboxylic-4-sulphonic acid; (6) diazotized 5-nitro-2-aminophenol; (7) diazotized 4-nitro-2-aminobenzoic acid; (8) diazotized 1-amino-2-naphthol-4-sulphonic acid; (9) 6-nitro-1-diazo-2-naphthol-4-sulphonic acid; (10) diazotized 6-nitro-2-aminophenol-4-sulphonamide; (11) the diazo compound from the 2-amino-4-methyl-1-hydroxybenzene with bisulphite; (12) diazotized 2-aminophenol-4-sulphonic acid. In a further example, cotton is dyed with the product of (3) from a bath containing sodium carbonate and, in the later stages, Glauber salt, and is treated in the same bath with a solution of complex copper tartrate rendered weakly alkaline with sodium carbonate, yielding a brown shade. Specifications 455,274 and 532,261 are referred to. The Specification as open to inspection under Sect. 91 comprises also the manufacture of other dyestuffs (and their complex metal compounds) in which 1 : 3-dihydroxynaphthalene is used as a coupling component capable of coupling twice, including the diazo dyestuffs described in Specification 587,348. Reference is made to the use of diazo compounds not containing lake-forming groups, including those obtained by unilateral coupling of a tetrazotized diamine with any coupling component, and of diazo components obtained by coupling a diazo compound with a middle component. An additional example describes the manufacture of the dyestuffs 41-nitro-4-aminodiphenylamine-21-sulphonic acid --> 1 : 3-dihydroxynaphthalene \sM p-nitraniline or 41-nitro-4-amino-diphenylamine-21-sulphonic acid, which dye leather medium brown and reddish dark brown shades respectively. This subject-matter does not appear in the Specification as accepted.
GB13844/43A 1942-09-02 1943-08-25 Manufacture of trisazo-dyestuffs Expired GB587110A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH587110X 1942-09-02

Publications (1)

Publication Number Publication Date
GB587110A true GB587110A (en) 1947-04-15

Family

ID=4521870

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13844/43A Expired GB587110A (en) 1942-09-02 1943-08-25 Manufacture of trisazo-dyestuffs

Country Status (1)

Country Link
GB (1) GB587110A (en)

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