CH163008A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH163008A CH163008A CH163008DA CH163008A CH 163008 A CH163008 A CH 163008A CH 163008D A CH163008D A CH 163008DA CH 163008 A CH163008 A CH 163008A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- 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
- C09B29/02—Monoazo dyes prepared by diazotising and coupling from diazotised o-amino-hydroxy compounds
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 5-Nitro-2-amino-l-phenol mit [1-(uo-Ogäthyl)'- amino]-2-methogy-5-methylbenzol vereinigt.
Der neue Farbstoff bildet ein violettes Pulver, das in Wasser unlöslich ist, sich aber in Essigsäureäthylester mit rotvioletter Farbe löst. Er färbt nach geeigneter Verpastung Acetatseide in rotvioletten Tönen, die sich durch ihre Reinheit auszeichnen.
<I>Beispiel:</I> 15,4 Teile 5-Nitro-2-amino-l-phenol wer den mit 300 Teilen Wasser vermahlen und die erhaltene Suspension mit 25 Teilen kon zentrierter Salzsäure und 7 Teilen Natrium nitrit diazotiert. Die so erhaltene Diazo- lösung vereinigt man mit einer Lösung von 18,1 Teilen [1-(cv-Ogäthyl)-amino]-2-meth- ogy-5-methylbenzol in verdünnter Salzsäure. Der nach längerem Rühren ausgeschiedene Farbstoff wird filtriert und gewaschen.
Process for the preparation of a new azo dye .. It has been found that a new azo dye is obtained if diazotized 5-nitro-2-amino-1-phenol with [1- (uo-Ogäthyl) '- amino] -2-methogy -5-methylbenzene combined.
The new dye forms a purple powder, which is insoluble in water, but dissolves in ethyl acetate with a red-purple color. After suitable pasting, it dyes acetate silk in red-violet tones, which are characterized by their purity.
<I> Example: </I> 15.4 parts of 5-nitro-2-amino-1-phenol are ground with 300 parts of water and the suspension obtained is diazotized with 25 parts of concentrated hydrochloric acid and 7 parts of sodium nitrite. The diazo solution thus obtained is combined with a solution of 18.1 parts of [1- (cv-Ogäthyl) -amino] -2-methoxy-5-methylbenzene in dilute hydrochloric acid. The dye which separates out after prolonged stirring is filtered and washed.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH163008T | 1932-07-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH163008A true CH163008A (en) | 1933-07-31 |
Family
ID=4416122
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH163008D CH163008A (en) | 1932-07-08 | 1932-07-08 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH163008A (en) |
-
1932
- 1932-07-08 CH CH163008D patent/CH163008A/en unknown
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