GB490965A - Manufacture of azo-dyestuffs - Google Patents

Manufacture of azo-dyestuffs

Info

Publication number
GB490965A
GB490965A GB14857/37A GB1485737A GB490965A GB 490965 A GB490965 A GB 490965A GB 14857/37 A GB14857/37 A GB 14857/37A GB 1485737 A GB1485737 A GB 1485737A GB 490965 A GB490965 A GB 490965A
Authority
GB
United Kingdom
Prior art keywords
acid
amino
nitrobenzene
hydroxy
oxy
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
GB14857/37A
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.)
Durand and Huguenin AG
Original Assignee
Durand and Huguenin 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 Durand and Huguenin AG filed Critical Durand and Huguenin AG
Publication of GB490965A publication Critical patent/GB490965A/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
    • C09B33/00Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
    • C09B33/02Disazo dyes
    • C09B33/08Disazo dyes in which the coupling component is a hydroxy-amino compound
    • C09B33/10Disazo dyes in which the coupling component is a hydroxy-amino compound in which the coupling component is an amino naphthol

Landscapes

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

Abstract

Mordant dyeing disazo dyes are made by coupling J acid first in a weak acid medium and then in an alkaline medium with two molecular proportions of diazotized o-aminophenols or o-aminonaphthols at least one of them having a hydroxy group and a carboxy group in o-position to one another. They may be used for chrome printing and are of particular value in the form of their complex metal compounds, being suitable for dyeing and mordant printing on cotton, silk, and regenerated cellulose, e.g. by the processes described in Specifications 26460/12, 318,469, [both in Class 2 (iii)], 319,457, [Class 15 (ii)], and 435,701. The metal compounds may be obtained according to the process described in Specification 26460/12. Di-and trivalent metal compounds, e.g. iron compounds may be used and more than one metal may be introduced into the dyestuff. In examples, the dyestuffs 2 - amino - 1 - hydroxybenzene - 6 - carboxylic acid --> (acid) J acid \sM (alkaline) 1-amino-2-oxy-3-nitrobenzene-5-sulphonic acid; 2-amino-4-sulpho - 1 -hydroxybenzene-6-carboxylic acid --> (acid) J acid \sM (alkaline) picramic acid or 2 - amino - 4 - sulpho - 1 - hydroxybenzene-6-carboxylic acid or 1-amino-2-oxy-3-nitrobenzene-5-sulphonic acid are boiled with an agent yielding chromium, e.g. chromium acetate or sulphate. The products yield greyish shades when printed on cotton. Specifications 8575/03, 1581/04, [both in Class 2], 29567/13, [Class 2 (iii)], 351,400, and 357,543 also are referred to. The Specification as open to inspection under Sect. 91 states that of the two diazo compounds which are coupled as above with J acid at least one must be derived from an o-aminiphenol or o-aminonaphthol and at least one must contain the usual mordant groups such as the salicylic group. In examples and a table, dyes from the following additional components are specified: (acid coupling) p-aminosalicylic acid, p-amino-o-sulphosalicylic acid, 1 - amino - 2 - oxy - 3 - nitrobenzene - 5-sulphonic acid, 3 - amino - 4 - sulphobenzene azosalicylic acid, o - amino - p - chlorsalicylic acid, 1 - hydroxy - 2 - amino - 6 - nitrobenzene-4 - sulphonic acid, 1 - hydroxy - 2 - amino - 4-chlorobenzene-6-sulphonic acid; (alkaline coupling) 1 - amino - 2 - oxy - 3- or 4-nitro - 5-chlorobenzene, p-aminosalicylic acid, 1-oxy-2-amino - 4 - chlorbenzene - 6 - sulphonic acid, 1 - hydroxy - 2 - amino - 6 - methyl - 4 - nitrobenzene, 5 - nitro - 2 - aminophenol, 1 - hydroxy - 2 - amino - 4 - methyl - 6 - nitrobenzene, 1 - hydroxy - 2 - amino - 4 - nitrobenzene-6 - sulphonic acid. Chromium lactate and copper sulphate are also specified as agents yielding metal. Some of the chromium compounds may be boiled with caustic soda to give more soluble products. This subject-matter does not appear in the Specification as accepted.
GB14857/37A 1936-05-28 1937-05-28 Manufacture of azo-dyestuffs Expired GB490965A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE490965X 1936-05-28

Publications (1)

Publication Number Publication Date
GB490965A true GB490965A (en) 1938-08-24

Family

ID=6544192

Family Applications (1)

Application Number Title Priority Date Filing Date
GB14857/37A Expired GB490965A (en) 1936-05-28 1937-05-28 Manufacture of azo-dyestuffs

Country Status (1)

Country Link
GB (1) GB490965A (en)

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