CH192853A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH192853A CH192853A CH192853DA CH192853A CH 192853 A CH192853 A CH 192853A CH 192853D A CH192853D A CH 192853DA CH 192853 A CH192853 A CH 192853A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- pure
- dye
- dioxypropyl
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Es wurde gefunden, dass man durch Kup peln von diazotiertern 2,4-Dinit.ranilin mit 4-Methoxy-3-(äthyl-@, r-dioxypropyl)-amino- acetanilid einen schwerlöslichen Azofarbstoff erhält, der sehr wertvolle Eigenschaften be sitzt. Er stellt ein dunkles, metallisch glän zendes Pulver dar, das sich in -Alkohol leicht mit blauer Farbe löst und Lacke oder Zellu- loseester in lichtechten, rein blauen Tönen anfärbt.
Die Textilfärbungen sind rein weiss ätzbar.
<I>Beispiel:</I> 183 Gt. 2,4-Dinitranilin werden in üb- lieber Weise mit einer Nitrosylschwefelsärire, entsprechend 69 Gt. Nitrit diazotiert. Die Diazoniumlösung wird auf Eis ausgetragen und mit 282 Gt. einer wässrigen Lösung von 4-Methoxy-3-(äthyl-@, r-dioxypropyl)-amino- acetanilid zur Kupplung gebracht.
Durch Abstumpfen der stark sauren Reaktion kann die Farbatoffbildung beschleunigt werden. Nach ihrer Beendigung wird der ausgeschie dene Farbstoff abgesaugt, neutral gewaschen und getrocknet. Er stellt ein dunkles, metal lisch glänzendes Pulver dar, das sich in Alkohol leicht mit blauer Farbe löst und Lacke oder Zelluloseester in lichtechten rein blauen Tönen anfärbt. Die Textilfärbungen sind rein weiss ätzbar.
Process for the preparation of an azo dye. It has been found that by coupling diazotized 2,4-Dinit.ranilin with 4-methoxy-3- (äthyl- @, r-dioxypropyl) aminoacetanilide, a sparingly soluble azo dye is obtained which has very valuable properties. It is a dark, metallic, glossy powder that easily dissolves in alcohol with a blue color and stains lacquer or cellulose esters in lightfast, pure blue tones.
The textile dyeings can be etched in pure white.
<I> Example: </I> 183 Gt. 2,4-Dinitraniline are in the usual way with a nitrosyl sulfuric acid, corresponding to 69 pbw. Diazotized nitrite. The diazonium solution is poured on ice and with 282 pbw. an aqueous solution of 4-methoxy-3- (äthyl- @, r-dioxypropyl) aminoacetanilide brought to the coupling.
Dye formation can be accelerated by dulling the strongly acidic reaction. When it has ended, the dyestuff excreted is filtered off with suction, washed neutral and dried. It is a dark, metallic, shiny powder that easily dissolves in alcohol with a blue color and colors paints or cellulose esters in lightfast, pure blue tones. The textile dyeings can be etched in pure white.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB192853X | 1935-08-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192853A true CH192853A (en) | 1937-09-15 |
Family
ID=10126856
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192853D CH192853A (en) | 1935-08-27 | 1936-08-13 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192853A (en) |
-
1936
- 1936-08-13 CH CH192853D patent/CH192853A/en unknown
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