CH255315A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH255315A CH255315A CH255315DA CH255315A CH 255315 A CH255315 A CH 255315A CH 255315D A CH255315D A CH 255315DA CH 255315 A CH255315 A CH 255315A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- dye
- new azo
- new
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Die vorliegende Erfindung bezieht. sich auf ein Verfahren zur Herstellung eines neuen Azofarbstoffes, gemäss welchem diazo- tiertes 2-Cyan-4-nitranilin mit dem Schwefel- säureester des N-ss-Oxyäthyl-N-ss'-p-tolyloxy- äthylaniline gekuppelt wird.
Der neue Farbstoff bildet ein grünlich- schwarzes Pulver, welches in heissem Wasser eine rötlichviolette Lösung und in Sch-#vefel- sä.ure eine stumpfe karmesinrote Lösung er gibt.
<I>Beispiel:</I> <B>16,3</B> Teile 2-Cyan-4-nitranilin werden gemäss der in Beispiel 1 des britischen Pa tentes Nr. 447561 beschriebenen Methode di- azotiert und die so erhaltene Lösung unter Rühren einer gekühlten Lösung von 35,7 Tei len des Natriumsalzes des N-ss-Oxyäthyl- '-ss'-p-tolyloxyäthylanilinschwefelsäureesters in 400 Teilen Wasser hinzugesetzt.
Nach be endeter Kupplung wird das Gemisch langsam mit 40%iger wässriger Natriumhydroxyd- Irisung so lange versetzt, und zwar unter Aufrechterhaltung einer Temperatur von weniger als 10 C durch Aussenkühlung, bis (las Gemisch eben lackmusal'kalisch reagiert. Hierauf wird während einer weiteren Stunde gerührt und der Farbstoff alsdann abfil- triert und bei 30-40 C getrocknet.
Der Farbstoff bildet ein grünlicbschwarzes Pul ver, welches in heissem Wasser unter Bildung einer rötlichvioletten Lösung und in Schwe felsäure unter Bildung einer stumpfen karmesinroten Lösung löslich ist. Er färbt. Celluloseacetatkunstseide und Polyamid fasern oder Polyamidgewebe in violetten Farbtönen von sehr guter Lichtechtheit, so fern das Auffärben aus einem neutralen Na triumchlorid oder Natriumsulfat enthalten den Färbebade erfolgt.
Process for the production of a new azo dye. The present invention relates. refers to a process for the production of a new azo dye, according to which diazotized 2-cyano-4-nitroaniline is coupled with the sulfuric acid ester of N-ß-oxyethyl-N-ß-p-tolyloxy-ethylaniline.
The new dye forms a greenish-black powder, which gives a reddish-purple solution in hot water and a dull crimson-red solution in shear acid.
<I> Example: </I> <B> 16.3 </B> parts of 2-cyano-4-nitroaniline are azotized according to the method described in Example 1 of British Patent No. 447561, and the solution thus obtained while stirring, a cooled solution of 35.7 parts of the sodium salt of N-ßs-oxyethyl- '-ss'-p-tolyloxyethylaniline sulfuric acid ester in 400 parts of water is added.
After the coupling is complete, 40% aqueous sodium hydroxide iridescence is slowly added to the mixture, while maintaining a temperature of less than 10 ° C. by external cooling, until the mixture reacts like a litmus. This is followed by a further hour stirred and the dye is then filtered off and dried at 30.degree.-40.degree.
The dye forms a greenish-black powder which is soluble in hot water to form a reddish-purple solution and in sulfuric acid to form a dull crimson solution. He colors. Cellulose acetate rayon and polyamide fibers or polyamide fabric in violet shades of very good lightfastness, as long as the dye is made from a neutral sodium chloride or sodium sulfate containing the dye bath.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB255315X | 1944-08-28 | ||
CH249376T | 1945-08-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH255315A true CH255315A (en) | 1948-06-15 |
Family
ID=25729349
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH255315D CH255315A (en) | 1944-08-28 | 1945-08-28 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH255315A (en) |
-
1945
- 1945-08-28 CH CH255315D patent/CH255315A/en unknown
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