GB482240A - Primary trisazo-dyestuffs derived from resorcinol, their copper compounds and process for their manufacture - Google Patents
Primary trisazo-dyestuffs derived from resorcinol, their copper compounds and process for their manufactureInfo
- Publication number
- GB482240A GB482240A GB17943/37A GB1794337A GB482240A GB 482240 A GB482240 A GB 482240A GB 17943/37 A GB17943/37 A GB 17943/37A GB 1794337 A GB1794337 A GB 1794337A GB 482240 A GB482240 A GB 482240A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphonic acid
- nitroaniline
- nitro
- aminodiphenylamine
- mol
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/18—Trisazo or higher polyazo dyes
- C09B33/24—Trisazo dyes of the type
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Primary trisazo dyes are made by combining resorcinol in an alkaline solution, firstly with a diazotized negatively substituted o-aminophenol of the benzene series (1 mol.), secondly with a nitrodiazo compound (1 mol.) and finally with a diazotized nitroaminodiphenylamine sulphonic acid (1 mol.). The copper compounds of the dyes are made by treating with a copper salt in substance, in the dye-bath or by after-treatment of the dyeings. The dyes and their copper compounds yield clear neutral brown shades on silk and leather. In examples dyes from the following components are described (1) (i) 2 - nitro - 6 - amino - 1 - phenol - 4 - sulphonic acid or the isomeric 4 : 6 : 1 : 2-compound, picramic acid, (ii) p-nitroaniline, 2-chlor-4-nitroaniline, 4-nitroaniline-2-sulphonic acid, 2 - nitroaniline - 4 - sulphonic acid, 4-nitro-41-aminodiphenylamine-2-sulphonic acid, (iii) 4-nitro - 41 - aminodiphenylamine - 2 - sulphonic acid; the copper compound is made by treating with aqueous copper sulphate; (2) (i) 3-amino-2 - hydroxybenzene - 1 - carboxylic - 5 - sulphonic acid, (ii) 4-nitroaniline-2-sulphonic acid or p-nitroaniline, (iii) 4-nitro-41-aminodiphenylamine-2-sulphonic acid; the copper compound is made by heating with qqueous copper sulphate and sodium acetate. Other diazo components specified are (i) 4- or 5-nitro-2-aminophenol, 3-amino-2-hydroxybenzoic acid, 4 : 6-dinitro-2-aminophenol, (ii) o- and m-nitroaniline and nitroaminodiphenylaminesulphonic acids, (iii) 2-nitro-41-aminodiphenylamine-4-sulphonic acid. Specification 447,775 is referred to. The Specification as open to inspection under Sect. 91 comprises the use of the following diazo compounds in the order stated (i) a negatively substituted o-aminophenol, (ii) any desired diazo component, (iii) an aminodiphenylamine sulphonic acid and refers to the treatment of the dyes with a metal salt, e.g. of chromium, aluminium, titanium, vanadium, manganese, iron, cobalt and nickel singly or mixed. The conversion of the dyestuffs described in German Specification 629,743 into metal compounds is mentioned. Such dyes are made by coupling resorcinol in any order with a diazotized 4-aminodiphenylamine-2-sulphonic acid (1 mol.), diazotized 2-amino-6-nitro-1-phenol-4-sulphonic acid or 4 : 6-dinitro-2-aminophenol (1 mol.) or a mixture of these two diazo compounds and finally with a diazo compound of the benzene series (1 mol.). This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH482240X | 1936-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB482240A true GB482240A (en) | 1938-03-25 |
Family
ID=4516344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17943/37A Expired GB482240A (en) | 1936-07-13 | 1937-06-28 | Primary trisazo-dyestuffs derived from resorcinol, their copper compounds and process for their manufacture |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB482240A (en) |
-
1937
- 1937-06-28 GB GB17943/37A patent/GB482240A/en not_active Expired
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