GB609301A - Manufacture of disazo-dyestuffs - Google Patents
Manufacture of disazo-dyestuffsInfo
- Publication number
- GB609301A GB609301A GB2413/42A GB241342A GB609301A GB 609301 A GB609301 A GB 609301A GB 2413/42 A GB2413/42 A GB 2413/42A GB 241342 A GB241342 A GB 241342A GB 609301 A GB609301 A GB 609301A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- mols
- cotton
- hydroxide solution
- aqueous
- 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
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
-
- 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
- C09B41/00—Special methods of performing the coupling reaction
- C09B41/001—Special methods of performing the coupling reaction characterised by the coupling medium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Coloring (AREA)
Abstract
Disazo dyes are obtained by coupling tetrazotised 3 : 31 - dihydroxy - 4 : 41 - diaminodiphenyl with 2 mols. of the same or different coupling components (other than a 1-hydroxynaphthalenesulphonic acid carrying an auxochromic group in 8-position) in a medium rendered alkaline with a hydroxide of an alkali metal, e.g. sodium or potassium, or of an alkaline earth metal, e.g. calcium, magnesium, strontium or barium, or of ammonium. Specified coupling components are 2 : 5 : 7- and 2 : 8 : 6-aminonaphtholsulphonic acids, 2 : 6-naphtholsulphonic acid and 2 : 3 : 6-naphtholdisulphonic acid. The products are suitable for dyeing cellulose fibres, e.g. of cotton or regenerated cellulose, or animal fibres, e.g. wool, silk or leather and may be treated in substance, in the dyebath or on the fibre, with agents yielding metal, e.g. copper, chromium, iron, nickel or cobalt. The metal compounds produced in substance may be incorporated in nitrocellulose lacquers, artificial resins and spinning masses. In examples, tetrazotised 3 : 31 - dihydroxy - 4 : 41 - diaminodiphenyl is coupled (1) in aqueous potassium hydroxide solution, (2) in aqueous calcium hydroxide solution with 2 : 5 : 7-aminonaphtholsulphonic acid (2 mols.) to obtain a product giving fast blue after-coppered dyeings on cotton, (3) in aqueous potassium hydroxide solution with 2 : 3 : 6-naphtholdisulphonic acid (2 mols.) to obtain a similar product, (4) in aqueous calcium hydroxide solution with 2 : 8 : 6-aminonaphtholsulphonic acid (2 mols.) to obtain a similar product. In an example of the dyeing process, wetted-out cotton is introduced into an aqueous dyebath at 50 DEG C. containing the dyestuff obtained in (1) above and sodium carbonate, the temperature is raised to 95 DEG C. and, after addition of Glauber salt, is so maintained for 1 hour; the temperature is then allowed to fall to 80 DEG C. and sodium copper tartrate added, whereupon coppering is effected for 1/2 hour at 80-90 DEG C. and the cotton is rinsed and, if desired, soaped. Specifications 455,274 and 609,302 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH609301X | 1941-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB609301A true GB609301A (en) | 1948-09-29 |
Family
ID=4523289
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2413/42A Expired GB609301A (en) | 1941-02-18 | 1942-02-24 | Manufacture of disazo-dyestuffs |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE444533A (en) |
DE (1) | DE745094C (en) |
FR (1) | FR889850A (en) |
GB (1) | GB609301A (en) |
NL (1) | NL60554C (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH437589A (en) * | 1963-11-08 | 1967-06-15 | Durand & Huguenin Ag | Process for the preparation of water-soluble, metallizable disazo dyes |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB102881A (en) * | 1916-05-13 | 1917-01-04 | Oliver Imray | Manufacture of New, Direct-dyeing Ortho-oxy-azo-dyestuffs. |
-
0
- NL NL60554D patent/NL60554C/xx active
- BE BE444533D patent/BE444533A/xx unknown
-
1942
- 1942-02-13 FR FR889850D patent/FR889850A/en not_active Expired
- 1942-02-14 DE DEG104866D patent/DE745094C/en not_active Expired
- 1942-02-24 GB GB2413/42A patent/GB609301A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE444533A (en) | |
DE745094C (en) | 1944-06-10 |
NL60554C (en) | |
FR889850A (en) | 1944-01-20 |
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