CH211024A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH211024A CH211024A CH211024DA CH211024A CH 211024 A CH211024 A CH 211024A CH 211024D A CH211024D A CH 211024DA CH 211024 A CH211024 A CH 211024A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- new
- red
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen azofarbstdfes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 2.5-Diehlor-l-aminobenzol mit dem 2-Oxy- 2'- (4"-chlor) -phenyl-5.6-pseudonaphthazimid vereinigt.
Der neue Farbstoff bildet ein rotbraunes, in Wasser unlösliches Pulver. Auf geeigne ten Substraten, wie z. B. Baumwolle, her gestellt, färbt er diese in echten rotbraunen Tönen.
Beispiel: 16.2 Teile des 2.5-Dichlor-l-aminobenzols werden wie üblich diazotiert und in eine Lösung von 29.5 Teilen 2-Oxy-2'-(4"-chlor)- phenyl-5.6-pseudonaphthazimid, 40 Teilen äül iger Natriumhydroxydlösung, 15 Teilen Soda in 1000 Teilen Wasser eingetragen. Der gebildete Farbstoff fällt sofort aus. Der rot braune Niederschlag wird filtriert und ge trocknet.
Process for the production of a new azo color. It has been found that a new azo dye is obtained when diazotized 2.5-diehlor-1-aminobenzene is combined with 2-oxy-2'- (4 "-chlor) -phenyl-5.6-pseudonaphthazimide.
The new dye forms a red-brown powder that is insoluble in water. On appro priate substrates such. B. Cotton, made ago, he dyes them in real red-brown tones.
Example: 16.2 parts of 2.5-dichloro-1-aminobenzene are diazotized as usual and poured into a solution of 29.5 parts of 2-oxy-2 '- (4 "-chlor) - phenyl-5.6-pseudonaphthazimide, 40 parts of aqueous sodium hydroxide solution, 15 Parts of soda are added to 1000 parts of water. The dye formed precipitates out immediately. The red-brown precipitate is filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH211024T | 1937-06-30 | ||
CH208952T | 1937-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH211024A true CH211024A (en) | 1940-08-15 |
Family
ID=25724640
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH211024D CH211024A (en) | 1937-06-30 | 1937-06-30 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH211024A (en) |
-
1937
- 1937-06-30 CH CH211024D patent/CH211024A/en unknown
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