CH234948A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH234948A CH234948A CH234948DA CH234948A CH 234948 A CH234948 A CH 234948A CH 234948D A CH234948D A CH 234948DA CH 234948 A CH234948 A CH 234948A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- new
- acid
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, .wenn man diazotiertes 4 - Amino - 3,2', 5'-trimethoxy - 6-chlordiphenyl mit 1-(4'-Chlor)-benzolsulfonylamino-8-oxy- naphthaIin-3,6-disulfonsäure vereinigt.
Der getrocknete neue Farbstoff bildet ein bordeauxrotes Pulver, das sich in konzen trierter Schwefelsäure mit blaugrüner Farbe löst und Wolle aus saurem Bade in sehr reinen stark rotsti.chig-violetten Tönen färbt. <I>Beispiel:
</I> @29'j5 Teile 4-Amino-3,2',5'-trimethoxy-6- chlordiphenyl werden mit Salzsäure und 6,9, Teilen Natriumnitrit diazotiert. Die erhal tene Diazolösung lässt man unter Kühlung in eine überschüssiges Natriumcarbonat ent haltende Lösung von 49,35 Teilen 1-(4' Chlor)-benzoIsulfonylamino-8-oxynaphthalin- 3,6-disulfonsäure unter Rühren einlaufen. Die Kupplung erfolgt rasch.
Nach Beendi gung der Kupplunig wird der zum Teil aus geschiedene Farbstoff durch Zusatz von Na- triumchlorid vollständig abgeschieden und filtriert.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained if diazotized 4-amino-3,2 ', 5'-trimethoxy-6-chlorodiphenyl with 1- (4'-chloro) -benzenesulfonylamino-8-oxynaphthaIine- 3,6-disulfonic acid combined.
The dried new dye forms a burgundy red powder that dissolves in concentrated sulfuric acid with a blue-green color and dyes wool from an acid bath in very pure, strongly reddish-violet shades. <I> example:
</I> @ 29'j5 parts of 4-amino-3,2 ', 5'-trimethoxy-6-chlorodiphenyl are diazotized with hydrochloric acid and 6.9 parts of sodium nitrite. The diazo solution obtained is allowed to run, with cooling, into a solution of 49.35 parts of 1- (4 'chloro) -benzoIsulphonylamino-8-oxynaphthalene-3,6-disulphonic acid containing excess sodium carbonate, while stirring. The coupling is quick.
After the coupling has ended, the dyestuff which has partly separated out is completely separated off by adding sodium chloride and filtered.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH234948T | 1940-10-17 | ||
CH233185T | 1940-10-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH234948A true CH234948A (en) | 1944-10-31 |
Family
ID=25727787
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH234948D CH234948A (en) | 1940-10-17 | 1940-10-17 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH234948A (en) |
-
1940
- 1940-10-17 CH CH234948D patent/CH234948A/en unknown
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