CH167383A - Process for the preparation of a fat-soluble azo dye. - Google Patents
Process for the preparation of a fat-soluble azo dye.Info
- Publication number
- CH167383A CH167383A CH167383DA CH167383A CH 167383 A CH167383 A CH 167383A CH 167383D A CH167383D A CH 167383DA CH 167383 A CH167383 A CH 167383A
- Authority
- CH
- Switzerland
- Prior art keywords
- fat
- preparation
- soluble azo
- azo dye
- parts
- Prior art date
Links
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
Verfahren zur Darstellung eines fettlöslichen Azofarbstoffes. Gemäss dem Hauptpatent erhält man einen iettlöslichen Azofarbstoff, wenn man 1-Di- (3 <B>-</B> methyl <B>-</B> 4<B>-</B> aminophenyl) <B>-</B> hexahydrobenzol tetrazotiert und die Tetrazoverbindung mit 4-Oxyphenyl-hexahydrobenzol kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff mit ähnlichen Eigen schaften, wenn man als Tetrazokomporlente das 1-Di-(3-methoxy-4-aininophenyl)-hexa- hydrobenzol wählt.
<I>Beispiel:</I> <B>29,5</B> Teile 1-Di-(3-methoxy-4-aminophenyl)- hexahydrobenzol von der Formel
EMI0001.0017
werden in<B>500</B> Teilen Wasser und<B>60</B> Teilen Salzsäure 20<B>0</B> B6 unter gelindem Erwärmen gelöst und bei<B>0-5 0 0</B> mit<B>13,
8</B> Teilen Natriumnitrit in wässeriger Lösung tetra- zotiert. Die klare Tetrazolösung läuft lang sam zu einer auf<B>0 0 C</B> gekühlten Suspension von<B>36</B> Teilen 4-Oxyphenylhexahydroberizol in 2000 Teilen Wasser und 14 Teilen Natrium- hydroxyd. Nach beendigter Kupplung wird der Farbstoff gepresst, bei etwa<B>50 0</B> C ge trocknet und darauf gemahlen. Er löst sich sehr leicht mit oranger Farbe in den übli chen organischen Lösungsmitteln, wie auch in Fetten, Ölen und Wachsen.
Die mit ihm erzielten Färbungen sind hervorragend licht- und sublimierecht.
Process for the preparation of a fat-soluble azo dye. According to the main patent, an ion-soluble azo dye is obtained if 1-di- (3-di- (3-B-methyl-4-aminophenyl) -amino-phenyl) is obtained / B> hexahydrobenzene tetrazotized and the tetrazo compound coupled with 4-oxyphenylhexahydrobenzene.
As has now been found further, a dye with similar properties is obtained if 1-di- (3-methoxy-4-aininophenyl) -hexa-hydrobenzene is chosen as the tetrazo component.
<I> Example: </I> <B> 29.5 </B> parts of 1-di- (3-methoxy-4-aminophenyl) -hexahydrobenzene of the formula
EMI0001.0017
are dissolved in <B> 500 </B> parts of water and <B> 60 </B> parts of hydrochloric acid 20 <B> 0 </B> B6 with gentle heating and at <B> 0-5 0 0 </ B > with <B> 13,
8 parts of sodium nitrite tetrazotized in an aqueous solution. The clear tetrazo solution slowly runs to a suspension, cooled to 0 ° C., of 36 parts of 4-oxyphenylhexahydroberizole in 2000 parts of water and 14 parts of sodium hydroxide. After coupling is complete, the dye is pressed, dried at about 50 ° C. and then ground. It dissolves very easily with an orange color in the usual organic solvents, as well as in fats, oils and waxes.
The colorations achieved with it are excellent lightfast and sublimation fast.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE167383X | 1931-11-30 | ||
CH163544T | 1932-10-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167383A true CH167383A (en) | 1934-02-15 |
Family
ID=25717807
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167383D CH167383A (en) | 1931-11-30 | 1932-10-18 | Process for the preparation of a fat-soluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167383A (en) |
-
1932
- 1932-10-18 CH CH167383D patent/CH167383A/en unknown
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