CH211026A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH211026A CH211026A CH211026DA CH211026A CH 211026 A CH211026 A CH 211026A CH 211026D A CH211026D A CH 211026DA CH 211026 A CH211026 A CH 211026A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- dye
- 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)
- 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 z.- - (4' -Methyl) -phenogyacetylamino - 2 . 5 - di- methoxy-l-aminobenzol mit dem 2-Ogy-2'- (2)-naphthyl-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> 31,6 Teile des 4-(4'-Methyl)-phenogy- acetylamin o - 2 . 5 - dimethogy -1-aminobenzols werden wie üblich diazotiert und in eine Lö sung von 31,1 Teilen 2-Ogy-2'-(2)-naphthyl- 5,6-pseudonaphthazimid, 40 Teilen 30%iger Natriumhydrogydlösung, 15 Teilen Soda und 1000 Teilen Wasser eingetragen. Der gebil dete 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 if diazotized z.- (4'-methyl) -phenogyacetylamino-2. 5 - dimethoxy-l-aminobenzene combined with the 2-Ogy-2'- (2) -naphthyl-5.6-pseudonaphthazimide.
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> 31.6 parts of 4- (4'-methyl) -phenogy-acetylamine o - 2. 5 - dimethogy -1-aminobenzols are diazotized as usual and in a solution of 31.1 parts of 2-Ogy-2 '- (2) -naphthyl-5,6-pseudonaphthazimide, 40 parts of 30% sodium hydrogen hydroxide solution, 15 parts of soda and 1000 parts of water entered. The formed dye 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 | ||
CH211026T | 1937-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH211026A true CH211026A (en) | 1940-08-15 |
Family
ID=25724642
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH211026D CH211026A (en) | 1937-06-30 | 1937-06-30 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH211026A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1209591B (en) * | 1957-06-18 | 1966-01-27 | Stin | Arrangement for triggering events on rail vehicles through magnetic influence from the route |
-
1937
- 1937-06-30 CH CH211026D patent/CH211026A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1209591B (en) * | 1957-06-18 | 1966-01-27 | Stin | Arrangement for triggering events on rail vehicles through magnetic influence from the route |
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