CH153704A - Process for the preparation of a substantive polyazo dye. - Google Patents
Process for the preparation of a substantive polyazo dye.Info
- Publication number
- CH153704A CH153704A CH153704DA CH153704A CH 153704 A CH153704 A CH 153704A CH 153704D A CH153704D A CH 153704DA CH 153704 A CH153704 A CH 153704A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- blue
- diazo compound
- preparation
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines substantiven Polyazofarbstotfes. Es wurde gefunden, dass man zu einem wertvollen substantiven Polyazofarbstoff ge langt, wenn man die Diazoverbindung von Metanilsäure mit 1-Naphtylamin-7-sulfosäure kuppelt, den so erhaltenen Farbstoff diazo- tiert, die Diazoverbindung mit 1-Amino-2- naphtolmethyläther-6-sulfosäure kuppelt,
den erhaltenen Disazofarbstoff abermals diazo- tiert und schliesslich seine Diazoverbindung in alkalischer Lösung unter Zusatz von Py- ridin mit dem Monoazofarbstoff vereinigt, welcher durch Kupplung von diazotierter Metanilsäure mit<B>9-.</B> 5-Aminonaphtol-7-mo@no- sulfosäure in saurer Lösung erhalten wird.
<I>Beispiel:</I> 17,3 Teile Metanilsäure werden diazotiert und in bekannter Weise mit 24,5 Teilen 1-naphtylamin-7-sulfosaurem Natron gekup pelt. Der erhaltene Farbstoff wird weiter diazotiert und mit 25,3 Teilen 1-Amino-2- naphtolmethyläther-6-.sulfosäure kombiniert. Man isoliert den Farbstoff und diazotiert nochmals weiter.
Der isolierte Diazokörper wird in eine mit Pyridin versetzte ammonia- kalische Lösung des Farbstoffes eingetragen, welcher durch saure Kupplung von 17,3 Tei len diazotierter Metanilsäure mit 24 Tei len 2.5-Aminonaphtol-7-monosulfosäure in saurer Lösung erhalten wurde. Nach be endeter Kupplung wird isoliert und ge trocknet.
Der erhaltene Farbstoff ist ein dunkel- bronziges Pulver, welches in Wasser mit blaugrüner, in konzentrierter Schwefelsäure mit blauer Farbe löslich ist. Er färbt auf Baumwolle ein Blaugrün von ausgezeichneter Lichtechtheit.
Method for the production of a substantive polyazo dye. It has been found that a valuable substantive polyazo dye is obtained if the diazo compound of metanilic acid is coupled with 1-naphthylamine-7-sulfonic acid, the dye thus obtained is diazo-tated and the diazo compound with 1-amino-2-naphthol methyl ether-6 -sulfonic acid couples,
the disazo dye obtained is diazotized again and finally its diazo compound is combined in an alkaline solution with the addition of pyridine with the monoazo dye, which is obtained by coupling diazotized metanilic acid with 5-aminonaphthol-7-mo @ nosulfonic acid is obtained in acidic solution.
<I> Example: </I> 17.3 parts of metanilic acid are diazotized and coupled in a known manner with 24.5 parts of 1-naphthylamine-7-sulphonic acid sodium. The dye obtained is further diazotized and combined with 25.3 parts of 1-amino-2-naphtholmethylether-6-sulfonic acid. The dye is isolated and diazotized again.
The isolated diazo body is introduced into an ammoniacal solution of the dye mixed with pyridine, which was obtained by acidic coupling of 17.3 parts of diazotized metanilic acid with 24 parts of 2,5-aminonaphthol-7-monosulphonic acid in acidic solution. After the coupling has ended, it is isolated and dried.
The dye obtained is a dark bronze powder which is soluble in water with a blue-green color and in concentrated sulfuric acid with a blue color. It dyes cotton a blue-green with excellent lightfastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE153704X | 1929-11-29 | ||
CH150308T | 1930-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH153704A true CH153704A (en) | 1932-03-31 |
Family
ID=25715626
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH153704D CH153704A (en) | 1929-11-29 | 1930-11-10 | Process for the preparation of a substantive polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH153704A (en) |
-
1930
- 1930-11-10 CH CH153704D patent/CH153704A/en unknown
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