CH222799A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH222799A CH222799A CH222799DA CH222799A CH 222799 A CH222799 A CH 222799A CH 222799D A CH222799D A CH 222799DA CH 222799 A CH222799 A CH 222799A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- amino
- 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 Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 1-Amino-2-oxy-4-nitrobenzol mit dem 1- Phenyl - 3 - methyl - 5 - pyrazolon, das aus 1 Amino- 2 - (4'-methyl)-phenylsulfon-5-sulfon- säure und Acetessigester erhältlich ist, ver einigt.
Der neue Farbstoff färbt Wolle aus sau rem Bade in orangen Tönen, die durch Nach- chromieren rein blaustichig rot werden.
<I>Beispiel:</I> Man löst 15,4 Teile 1-Amino-2-oxy-4- nitrobenzol in 30 Teilen Salzsäure von 30 und 100 Teilen Wasser. Man fügt so viel Eis zu, dass die Temperatur auf 0 fällt und diazotiert hierauf mit einer Lösung von 7 Teilen Natriumnitrit in 30 Teilen Wasser. Diesen Diazobrei giesst man in eine Lösung von 35 Teilen Natriumcarbonat und 40,8 Teile des Pyrazolous der Formel
EMI0001.0025
in 300 Teilen Wasser und etwas Eis. Nach .erfolgter Kupplung wird .der Farbstoff aus gesalzen, filtriert und getrocknet.
'Process for the production of a new azo dye. It has been found that a new azo dye is obtained if diazotized 1-amino-2-oxy-4-nitrobenzene is used with 1-phenyl - 3 - methyl - 5 - pyrazolone, which is obtained from 1 amino- 2 - (4'- methyl) -phenylsulfon-5-sulfonic acid and acetoacetic ester is available, united.
The new dye dyes wool from acidic baths in orange tones, which are given a purely bluish red tint when they are chromed.
<I> Example: </I> 15.4 parts of 1-amino-2-oxy-4-nitrobenzene are dissolved in 30 parts of hydrochloric acid in 30 and 100 parts of water. So much ice is added that the temperature falls to 0 and diazotization is then carried out with a solution of 7 parts of sodium nitrite in 30 parts of water. This diazo paste is poured into a solution of 35 parts of sodium carbonate and 40.8 parts of the pyrazolous of the formula
EMI0001.0025
in 300 parts of water and some ice. After coupling has taken place, the dye is salted out, filtered and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH222799T | 1941-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH222799A true CH222799A (en) | 1942-08-15 |
Family
ID=4452763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH222799D CH222799A (en) | 1941-09-20 | 1941-09-20 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH222799A (en) |
-
1941
- 1941-09-20 CH CH222799D patent/CH222799A/en unknown
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