CH133693A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH133693A CH133693A CH133693DA CH133693A CH 133693 A CH133693 A CH 133693A CH 133693D A CH133693D A CH 133693DA CH 133693 A CH133693 A CH 133693A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- acid
- red
- naphtholcarboxylic
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Es wurde gefunden, dass die 2.6-Naphtol- carbonsäure bei der Kombination mit Diazo- verbindungen wertvolle Azofarbstoffe liefert, welche sich vor denen aus 2.3-Naphtholcar- bonsäure durch leichtere Löslichkeit und gegenüber denjenigen aus 2.6-Naphtholsulfo- säure vielfach durch grössere Farbstärke aus zeichnen.
Vorliegendes Patent bezieht sich nun auf die Darstellung eines Azofarbstoffes durch Kupplung von diazotier ter p-Chlorarrilin-o- sulfosäure mit 2.6-Naphtholcarbonsäure.
Trocken ist der neue Azofarbstoff ein rotbraunes Pulver, löslich in konzentrierter Schwefelsäure mit rötlicher Farbe. Er färbt Wolle in gelbroten Tönen.
<I>Beispiel:</I> 207,5 Teile p-Chloranilin-o-sulfosäure wer den in der üblichen Weise diazotiert. Die Diazolösung vermischt man mit einer wässeri gen Lösung von 210 Teilen 2.6-naphtholcar- bonsaurem Natrium, der man die zur Ab stumpfung der freien Mineralsäure nötige Menge von essigsaurere Natrium zugefügt hat. Zum Schluss wird sodaalkalisch gearacht und in sodaalkalischer Lösung zu Ende ge kuppelt. Der Farbstoff wird durch Aussalzen abgeschieden.
Process for the preparation of an azo dye. It has been found that 2.6-naphtholecarboxylic acid, when combined with diazo compounds, provides valuable azo dyes which are distinguished from those from 2,3-naphtholcarboxylic acid by easier solubility and compared to those from 2,6-naphtholsulfonic acid in many cases by greater color strength .
The present patent now relates to the preparation of an azo dye by coupling diazotized p-chlorarriline-o-sulfonic acid with 2,6-naphtholcarboxylic acid.
When dry, the new azo dye is a red-brown powder, soluble in concentrated sulfuric acid with a reddish color. He dyes wool in yellow-red tones.
<I> Example: </I> 207.5 parts of p-chloroaniline-o-sulfonic acid are diazotized in the usual way. The diazo solution is mixed with an aqueous solution of 210 parts of 2,6-naphtholcarbonsaurem sodium, to which one has added the amount of acetic acid sodium necessary to blunt the free mineral acid. Finally, it is made soda-alkaline and coupled to the end in a soda-alkaline solution. The dye is deposited by salting out.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE133693X | 1926-10-05 | ||
CH129001T | 1927-09-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH133693A true CH133693A (en) | 1929-06-15 |
Family
ID=25711191
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH133693D CH133693A (en) | 1926-10-05 | 1927-09-30 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH133693A (en) |
-
1927
- 1927-09-30 CH CH133693D patent/CH133693A/en unknown
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