CH238518A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH238518A CH238518A CH238518DA CH238518A CH 238518 A CH238518 A CH 238518A CH 238518D A CH238518D A CH 238518DA CH 238518 A CH238518 A CH 238518A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- carboxylic acid
- new
- Prior art date
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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstofes. Es wurde gefunden, dass man einen neuen A zofarbstoff erhält, wenn man diazotiertes 1-Aminobenzol -2- carbonsäure-4-sulfo-(2'-car- bonsäure)-anilid mit Barbitursäure kuppelt.
Der neue Farbstoff bildet ein gelbes Pul ver, das Wolle aus saurem Bade grünstichig gelb färbt. Durch Nachchromieren erhält man ein farbstarkes grünstichiges Gelb mit guten Echtheiten.
Beispiel: Man löst 33,6 Teile 1-Aminobenzol-2-car- bonsäure-4-sulfo-(2'-carbonsäure)-anilid in 28 Teilen 30%iger Natriumhydroxydlösung und 150 Teilen Wasser und gibt 7 Teile Na triumnitrit zu. Diese Lösung giesst man bei 0-5 in eine Mischung von 52 Teilen 30 % iger Salzsäure und Eis. Nach einer Stunde ist die Diazotierung beendet.
Man giesst den Diazo- brei in eine mit Eis auf 5-8 gekühlte Lö sung von 12,8 Teilen Barbitursäure und 40 Teilen Natriumcarbonat in 300 Teilen Wasser. Nach vollständiger Kupplung wird der Farbstoff ausgesalzen, filtriert und ge trocknet.
Process for the preparation of a new azo dye. It has been found that a new azo dye is obtained when diazotized 1-aminobenzene -2-carboxylic acid-4-sulfo- (2'-carboxylic acid) anilide is coupled with barbituric acid.
The new dye forms a yellow powder that dyes wool from an acidic bath with a greenish yellow. Chromium-plating gives a strong greenish yellow with good fastness properties.
Example: 33.6 parts of 1-aminobenzene-2-carboxylic acid-4-sulfo- (2'-carboxylic acid) anilide are dissolved in 28 parts of 30% strength sodium hydroxide solution and 150 parts of water and 7 parts of sodium nitrite are added. This solution is poured at 0-5 into a mixture of 52 parts of 30% strength hydrochloric acid and ice. The diazotization is over after one hour.
The diazo slurry is poured into a solution, cooled to 5-8 with ice, of 12.8 parts of barbituric acid and 40 parts of sodium carbonate in 300 parts of water. After the coupling is complete, the dye is salted out, filtered and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH238518T | 1944-02-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH238518A true CH238518A (en) | 1945-07-31 |
Family
ID=4460659
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH238518D CH238518A (en) | 1944-02-23 | 1944-02-23 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH238518A (en) |
-
1944
- 1944-02-23 CH CH238518D patent/CH238518A/en unknown
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