CH211023A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH211023A CH211023A CH211023DA CH211023A CH 211023 A CH211023 A CH 211023A CH 211023D A CH211023D A CH 211023DA CH 211023 A CH211023 A CH 211023A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- brown
- 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 Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 4- (4'-Methyl)-phenoxyacetylamino-2.5-diäth- oxy-l-aminobenzol mit dem 2-Oxy-2'-(4"- chlor)-phenyl-5.6-pseudonaphthazimid ver einigt.
Der neue Farbstoff bildet ein braunes, in Wasser unlösliches Pulver. Auf geeigneten Substraten, wie z. B. Baumwolle, hergestellt, färbt er diese in echten braunen Tönen. <I>Beispiel:</I> 34,4 Teile des 4-(4'-11Iethyl)-phenoxy- acetylamino -<B>2.5</B> - diäthoxy -1- aminobenzols werden wie üblich diazotiert und in eine Lösung von 29,5 Teilen 2-Oxy-2'-(4"-chlor)- phenyl-5.6-pseudonaphthazimid, 40 Teilen 30%iger Natriumhydroxydlösung, 15 Tei- len Soda in 1000 Teilen Wasser eingetragen.
Der gebildete Farbstoff fällt sofort aus. Der braune Niederschlag wird filtriert und getrocknet.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained when diazotized 4- (4'-methyl) -phenoxyacetylamino-2.5-diet-oxy-l-aminobenzene with the 2-oxy-2 '- (4 "- chlorine) - phenyl-5.6-pseudonaphthazimide united.
The new dye forms a brown powder that is insoluble in water. On suitable substrates, such as. B. Cotton, he dyes them in real brown tones. <I> Example: </I> 34.4 parts of 4- (4'-11Iethyl) -phenoxy-acetylamino - <B> 2.5 </B> - diethoxy -1-aminobenzene are diazotized as usual and converted into a solution of 29.5 parts of 2-oxy-2 '- (4 "-chlor) - phenyl-5,6-pseudonaphthazimide, 40 parts of 30% strength sodium hydroxide solution, 15 parts of soda in 1000 parts of water were added.
The dye formed precipitates immediately. The brown precipitate is filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH208952T | 1937-06-30 | ||
CH211023T | 1937-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH211023A true CH211023A (en) | 1940-08-15 |
Family
ID=25724639
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH211023D CH211023A (en) | 1937-06-30 | 1937-06-30 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH211023A (en) |
-
1937
- 1937-06-30 CH CH211023D patent/CH211023A/en unknown
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