CH165040A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH165040A CH165040A CH165040DA CH165040A CH 165040 A CH165040 A CH 165040A CH 165040D A CH165040D A CH 165040DA CH 165040 A CH165040 A CH 165040A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- new
- yellow
- 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)
- Paper (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>163008.</B> Verfahren zur Herstellung eines netten Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 5-Niti-o-2-.iinitio-l-phetiol mit (o-Oxi#*ithyl- anifin vereinigt.
Der neue Farbstoff bildet ein braunes Pulver, das in Wasser unlöslich ist, sich aber in Essigsi%tireäthylester mit gelbroter Farbe löst.<B>Er</B> färbt nach geeigneter Verpastung Acetatseide in gelbroten Tönen, die sich durch ihre Reinheit atiszeiehnen. <I>Beispiel:
</I> 15,4 Teile 5-Nitro-2-amiiio-l-phetiol wer- (len mit<B>300</B> Teilen Wasser verinahlen und die erhaltene Suspension mit<B>25</B> Teilen kon- zentrierter Salzsäure und<B>7</B> Teilen Natrium- nitrit diazotiert. Die so erhaltene Diazolösung vereinigt man mit einer Lösung von<B>13.7</B> Teilen w-Oxäthylanilin in verdünnter Salz säure.
Der nach längerem Rühren ausgeschie.- dene Farbstoff wird filtriert und gewaschen.
Additional patent to main patent no. <B> 163008. </B> Process for the production of a nice azo dye. It has been found that a new azo dye is obtained when diazotized 5-Niti-o-2-.iinitio-1-phetiol is combined with (o-Oxi # * ithylanifine.
The new dye forms a brown powder that is insoluble in water, but dissolves in ethyl acetate with a yellow-red color. <B> It </B>, when suitably pasted, dyes acetate silk in yellow-red shades, which are distinguished by their purity. <I> example:
15.4 parts of 5-nitro-2-amiiio-l-phetiol are ground with 300 parts of water and the suspension obtained is mixed with 25 parts of con - Centered hydrochloric acid and <B> 7 </B> parts of sodium nitrite diazotized The diazo solution thus obtained is combined with a solution of <B> 13.7 </B> parts of w-oxethylaniline in dilute hydrochloric acid.
The dye which separates out after prolonged stirring is filtered and washed.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH165040T | 1932-07-08 | ||
CH163008T | 1932-07-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH165040A true CH165040A (en) | 1933-10-31 |
Family
ID=25717685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH165040D CH165040A (en) | 1932-07-08 | 1932-07-08 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH165040A (en) |
-
1932
- 1932-07-08 CH CH165040D patent/CH165040A/en unknown
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