CH192984A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH192984A CH192984A CH192984DA CH192984A CH 192984 A CH192984 A CH 192984A CH 192984D A CH192984D A CH 192984DA CH 192984 A CH192984 A CH 192984A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new
- new azo
- dye
- Prior art date
Links
Landscapes
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Gemäss der vorliegenden Erfindung erhält man einen neuen Azofarbstoff durch Kuppeln von diazotiertem p-Dodecylanilin mit 2-N-ss- hydroxyätbyl-N -n-butyryl-amin -8- naphtol-6- sulfonsäure in einem wässerigen alkalischen Medium.
<I>Beispiel:</I> 26,1 Teile p-Dodecylanilin werden in einem Gemisch von 200 Teilen Wasser und 100 Teilen l0o/oiger Salzsäure suspendiert und bei 5-10o C durch Zusetzen von 6,9 Teilen Natriumnitrit diazotiert. Die so er haltene Lösung der Diazoverbindung- wird einer eiskalten Lösung von 37,5 Teilen des Natriumsalzes der 2-N-ss-hydroxyäthyl-N-n- butyt#yl-amin-8-naphtol-6-sulfonsäure und 21 Teilen wasserfreiem Natriumkarbonat in 400 Teilen Wasser zugesetzt.
Der so gebildete neue Farbstoff wird abfiltriert, mit ein wenig schwachem Salzwasser gewaschen und ge trocknet. Der neue Farbstoff trocknet zu einem dunkelbraunen Pulver, welches sich im heissen Wasser zu einer rötlich braunen und in konzentrierter Schwefelsäure zu einer kar moisiuroten Lösung löst. Er färbt Wolle in rötlich braunen Tönen von sehr guter Halt barkeit beim Walken.
Process for the production of a new azo dye. According to the present invention, a new azo dye is obtained by coupling diazotized p-dodecylaniline with 2-N-β-hydroxyethyl-N-n-butyryl-amine -8-naphthol-6-sulfonic acid in an aqueous alkaline medium.
<I> Example: </I> 26.1 parts of p-dodecylaniline are suspended in a mixture of 200 parts of water and 100 parts of 10% hydrochloric acid and diazotized at 5-10 ° C. by adding 6.9 parts of sodium nitrite. The so he obtained solution of the diazo compound is an ice-cold solution of 37.5 parts of the sodium salt of 2-N-ss-hydroxyethyl-Nn-butyt # yl-amine-8-naphthol-6-sulfonic acid and 21 parts of anhydrous sodium carbonate in 400 Parts of water added.
The new dye thus formed is filtered off, washed with a little weak salt water and dried. The new dye dries to a dark brown powder, which dissolves in hot water to a reddish brown and in concentrated sulfuric acid to a caramelized solution. It dyes wool in reddish brown shades that are very durable when fulled.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB192984X | 1935-08-30 | ||
CH189409T | 1936-08-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192984A true CH192984A (en) | 1937-09-15 |
Family
ID=25721788
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192984D CH192984A (en) | 1935-08-30 | 1936-08-14 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192984A (en) |
-
1936
- 1936-08-14 CH CH192984D patent/CH192984A/en unknown
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