CH141541A - Process for the preparation of a polyazo dye. - Google Patents
Process for the preparation of a polyazo dye.Info
- Publication number
- CH141541A CH141541A CH141541DA CH141541A CH 141541 A CH141541 A CH 141541A CH 141541D A CH141541D A CH 141541DA CH 141541 A CH141541 A CH 141541A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- green
- sulfonic acid
- diazotized
- dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Polyazofarbatoffes. Es wurde gefunden, dass man einen werte vollen grünen Direktfarbstoff erhält, wenn man 2 Mol. der diazotierten Aminoazover- bindung aus diazotierter 4-Toluidin-3-sulfo- säure und 1-Amino-2-äthoxynaplhtalin-6- sulfosäure auf 1 Mol. des Kondensations produktes aus 1 Mol. Cyanurchlorid, 2 Mol. 1 .
8 - Aminonaphtol - 3,. 6,- disulfosäure und 1 Mol. 4-Amino-4'-oxyazobenzol-3'-carbon- säure kuppelt.
Beispiel: Die in üblicher Weise aus 930 Gewichts teilen des Aminoazofarbstoffes aus diazotier- ter 4-Amino-l-methylbenzol-3-sulfosäure und 1-Amino-2-äthoxynaphtalin-6-sulfosäure her gestellte, abgeschiedene und mit Eiswasser verpastete Diazoverbindung fliesst bei 5 bis <B>1,0'</B> zu einer gut gerührten, zweckmässig mit Pyridin versetzten Lösung von 1213 Ge wichtsteilen des Kondensationsproduktes aus 1 Mol. Cyanurchlorid,
2 Mol. 1 .8-Amino- naphtol - 3 . 6 - disulfosäure und 1 Mol. 4- Amino-4'-oxyazobenzol-3'-carbonsäure. Die Kupplung setzt sofort unter Tiefgrünfärbung der Lösung ein und ist bald beendigt.
Der Farbstoff stellt in getrocknetem Zu stand ein dunkles, bronceglänzendes Pulver dar, das sich mit grüner Farbe in Wasser löst und aus dem Glaubersalz-Sodabad in kräf tigen, blaustichig-grünen Tönen von grosser Reinheit auf die pflanzliche Faser aufzieht. Die Färbungen besitzen eine sehr gute Licht echtheit.
Process for the preparation of a Polyazofarbatoffes. It has been found that a valuable full green direct dye is obtained if 2 moles of the diazotized aminoazo compound from diazotized 4-toluidine-3-sulfonic acid and 1-amino-2-ethoxynaplhtalin-6-sulfonic acid are added to 1 mole. of the condensation product from 1 mol. Cyanuric chloride, 2 mol. 1.
8 - aminonaphtol - 3 ,. 6, - disulfonic acid and 1 mol. 4-amino-4'-oxyazobenzene-3'-carboxylic acid couples.
Example: The diazo compound prepared in the usual way from 930 parts by weight of the aminoazo dye from diazotized 4-amino-1-methylbenzene-3-sulfonic acid and 1-amino-2-ethoxynaphthalene-6-sulfonic acid, deposited and pasted with ice water flows in 5 to <B> 1.0 '</B> to a well-stirred solution of 1213 parts by weight of the condensation product of 1 mol of cyanuric chloride, suitably mixed with pyridine,
2 mol. 1 .8-amino naphtol - 3. 6 - disulfonic acid and 1 mole. 4-amino-4'-oxyazobenzene-3'-carboxylic acid. The coupling starts immediately with a deep green coloration of the solution and is soon over.
When dried, the dye is a dark, bronze-shimmering powder that dissolves in water with a green color and is absorbed from the Glauber's salt soda bath in strong, bluish-green tones of great purity on the vegetable fiber. The colors have very good light fastness.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE141541X | 1927-11-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH141541A true CH141541A (en) | 1930-08-15 |
Family
ID=5668735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH141541D CH141541A (en) | 1927-11-22 | 1928-11-14 | Process for the preparation of a polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH141541A (en) |
-
1928
- 1928-11-14 CH CH141541D patent/CH141541A/en unknown
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