GB361489A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB361489A GB361489A GB2845230A GB2845230A GB361489A GB 361489 A GB361489 A GB 361489A GB 2845230 A GB2845230 A GB 2845230A GB 2845230 A GB2845230 A GB 2845230A GB 361489 A GB361489 A GB 361489A
- Authority
- GB
- United Kingdom
- Prior art keywords
- azo
- dyeings
- navy blue
- diaminoazo
- compound
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/36—Trisazo dyes of the type
- C09B35/362—D is benzene
Abstract
Azo dyes; lakes; azo dyes, forming on the material; cellulose esters, dyeing.--Azo dyestuffs giving navy blue to black dyeings on acetate silk and cellulose esters in general are produced in substance, on a substratum or on the fibre by coupling with 2 : 3-oxynaphthoic acid (2 mols.) a tetrazo compound of a diaminoazo compound of the general formula-- <FORM:0361489/IV/1> in which R is an aromatic residue, substituted or not, with the NH2 group in pposition to the azo group. The diaminoazo compounds are obtainable by coupling a diazotized aromatic p-nitramine or p-monoacetyldiamine with a -amino-ar-tetrahydronaphthalene and reducing or hydrolysing the product. The following examples are specified: (1) Acetate silk is treated for \ba3/4\be hr. at 70-75 DEG C. in a bath containing the hydrochloride of 4-aminobenzene - azo-4<1>-amino - ar - tetrahydronaphthalene, hydrochloric acid and sodium acetate, subjected to tetrazotization of the diamine at 10-15 DEG C., and developed at 60-70 DEG C. with 2 : 3-oxynaphthoic acid to obtain a vivid navy blue readily dischargeable dyeing. (2) The 2-chloro derivative of the diaminoazo compound in (1) similarly gives more reddish dyeings. (3) The 2-methoxy derivative similarly gives greenish navy blue dyeings. (4) The 2-methyl derivative similarly gives navy blue dyeings. Specification 330,591, [Class 2 (iii), Dyes &c.], is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2845230A GB361489A (en) | 1930-09-23 | 1930-09-23 | Manufacture of azo-dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2845230A GB361489A (en) | 1930-09-23 | 1930-09-23 | Manufacture of azo-dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB361489A true GB361489A (en) | 1931-11-26 |
Family
ID=10275840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2845230A Expired GB361489A (en) | 1930-09-23 | 1930-09-23 | Manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB361489A (en) |
-
1930
- 1930-09-23 GB GB2845230A patent/GB361489A/en not_active Expired
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