CH191738A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH191738A CH191738A CH191738DA CH191738A CH 191738 A CH191738 A CH 191738A CH 191738D A CH191738D A CH 191738DA CH 191738 A CH191738 A CH 191738A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- weight
- parts
- preparation
- azo dye
- Prior art date
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Description
Verfahren zur Herstellung eines Azofarbstoffes. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man Aminotetrazol dianotiert, sauer mit 2-Amino- 5-rraphthol-7-arrlfonsäure vereinigt und 2 Mol des so erhältlichen Monoazofarbstoffes mit 1 Mol tetrazotierten 4 . 4'- Diamino - 3 .
3'- di- methoxydiphenyl zu dem Farbstoff der Kon stitution
EMI0001.0015
Der neue Farbstoff färbt Baumwolle in grünstichig dunkelblauen Tönen, die durch Nachkupfern licht- und waschecht werden.
<I>Beispiel:</I> 9 Gewichtsteile 2 - amino - 5 - naphthol - 7- sulfonsaures Natrium werden in 120 Gewichts teilen Wasser gelöst, und die Lösung wird mit Salzsäure bis zur kongosauren Reaktion versetzt.
In die saure Suspension der Amino- naphtholsulfonsäui-e lässt man eine aus 3 Ge wichtsteilen Aminotetrazol (kristallwasser haltig) und 2 Gewichtsteilen Natriumnitrit in 100 Gewichtsteilen Wasser und 5 Ge wichtsteilen konz. Salzsäure bereitete Diazo- lösung auf einmal zufliessen; die Kupplung setzt sofort ein, und nach einiger Zeit erhält man eine klare, orangegelbe Lösung. Bald darauf beginnt der Farbstoff auszukristalli sieren. Durch Zugabe von Kochsalz wird dessen Abscheidung vervollständigt.
Der in üblicher Weise isolierte Farbstoff wird in 100 Gewichtsteilen Wasser durch Zugabe von 10-15 Gewichtsteilen Soda in Lösung gebracht. Sodann lässt man die aus 3,6 Gewichtsteilen Dianisidin mit 2 Gewichts teilen Natriumnitrit in üblicher Weise berei tete Tetrazolösung einfliessen. Pyridinzusatz beschleunigt die Kupplung. Der fertig gebil dete Farbstoff der vorgenannten Formel wird durch Aussalzen und Abpressen isoliert. Auf Baumwolle erzeugt der Farbstoff grünstichig dunkelblaue Töne, die durch Nachkupfern licht- und waschecht werden.
Process for the preparation of an azo dye. The present patent relates to a process for the preparation of an azo dye, characterized in that aminotetrazole is dianotized, acidically combined with 2-amino-5-raphthol-7-arulfonic acid and 2 mol of the monoazo dye obtainable in this way with 1 mol of tetrazotized 4. 4'- diamino - 3.
3'-dimethoxydiphenyl to the dye of the constitution
EMI0001.0015
The new dye dyes cotton in greenish dark blue tones, which are made light- and wash-fast by re-coppering.
<I> Example: </I> 9 parts by weight of 2-amino-5-naphthol-7-sulphonic acid sodium are dissolved in 120 parts by weight of water, and the solution is mixed with hydrochloric acid until the Congo acid reaction occurs.
In the acidic suspension of the amino naphtholsulfonsäui-e one leaves from 3 parts by weight of aminotetrazole (containing water of crystallization) and 2 parts by weight of sodium nitrite in 100 parts by weight of water and 5 parts by weight of conc. Hydrochloric acid prepared diazo solution flow in at once; the coupling sets in immediately and after a while a clear, orange-yellow solution is obtained. Soon afterwards the dye begins to crystallize out. Its separation is completed by adding common salt.
The dye, isolated in the usual way, is brought into solution in 100 parts by weight of water by adding 10-15 parts by weight of soda. The tetrazo solution prepared in the usual way from 3.6 parts by weight of dianisidine with 2 parts by weight of sodium nitrite is then allowed to flow in. Addition of pyridine accelerates the coupling. The finished gebil ended dye of the above formula is isolated by salting out and pressing. On cotton, the dye creates dark blue tones with a greenish tint, which can be made light and washable by re-coppering.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191738X | 1934-10-17 | ||
CH187121T | 1935-10-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH191738A true CH191738A (en) | 1937-06-30 |
Family
ID=25721481
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH191738D CH191738A (en) | 1934-10-17 | 1935-10-12 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH191738A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2817658A (en) * | 1954-12-03 | 1957-12-24 | Geigy Ag J R | Metallisable trisazo dyestuffs |
-
1935
- 1935-10-12 CH CH191738D patent/CH191738A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2817658A (en) * | 1954-12-03 | 1957-12-24 | Geigy Ag J R | Metallisable trisazo dyestuffs |
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