CH195541A - Process for the preparation of a water-soluble azo dye. - Google Patents
Process for the preparation of a water-soluble azo dye.Info
- Publication number
- CH195541A CH195541A CH195541DA CH195541A CH 195541 A CH195541 A CH 195541A CH 195541D A CH195541D A CH 195541DA CH 195541 A CH195541 A CH 195541A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- preparation
- soluble azo
- azo dye
- mole
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines wasserlöslichen Azofarbstoffes. Gegenstand ödes vorliegenden Zusatz patentes ist ein Verfahren zur Darstellung eines wasserlöslichen Azofarbstoffes, welches dadurch gekennzeichnet ist, dass man 1 Hol.
Phloroglucin mit 1 Mol. diazotierter 5- Aminoacenaphthen-$-sulfonsäure und 1 Mol. diazotierter 4-Amino-3-. 2'-.dimethyl-l. l'-azo- benzol-5 . 4'-@disulfonsäure vereinigt.
<I>Beispiel:</I> Die Suspension der aus 249 Gewichts teilen 5-Aminoacenaphthen-8-sulfonsäure er haltenen Diazoverbindung wird bei 0 all mählich in eine essigsauer gestellte wässrige Lösung von 126 Gewichtsteilen Phloroglucin und 300 Gewichtoteilen kristallisiertem Na- triumaeetat unter Rühren gegeben.
Nach be endeter Kupplung wird die erhaltene Lösung ,des Monoazofarbstoffes bei 0 C mit der Diazoverbindung aus 385 Gewichtsteilen 4- Amino - 3. 2'-,dimethyl-1 . 1'- azobenzol-5 . 4'- disulfonsäure in Gegenwart von 400 Ge wichtsteilen calciniertem Natriumkarbonat langsam und unter Rühren versetzt. Die Bil- dung des Trisazofarbstoffes ist rasch beendet. Der Farbstoff wird isoliert und .getrocknet.
Er bildet ein schwarzbraunes Pulver, das sich in Wasser mit rotbrauner Farbe löst und Leder in dunkelrotbraunen Tönen von guten Echtheitseigenschaften färbt.
Process for the preparation of a water-soluble azo dye. The subject of the present additional patent is a method for the preparation of a water-soluble azo dye, which is characterized in that one Hol.
Phloroglucinol with 1 mol. Of diazotized 5-aminoacenaphthene - $ - sulfonic acid and 1 mol. Of diazotized 4-amino-3-. 2 '-. Dimethyl-l. l'-azo-benzene-5. 4 '- @ disulfonic acid combined.
<I> Example: </I> The suspension of the diazo compound obtained from 249 parts by weight of 5-aminoacenaphthene-8-sulfonic acid is gradually transferred at 0 to an aqueous solution of 126 parts by weight of phloroglucinol and 300 parts by weight of crystallized sodium acetate with stirring given.
After coupling has ended, the solution obtained is the monoazo dye at 0 C with the diazo compound from 385 parts by weight of 4-amino - 3.2 '-, dimethyl-1. 1'-azobenzene-5. 4'-disulfonic acid in the presence of 400 parts by weight of calcined sodium carbonate is added slowly and with stirring. The formation of the trisazo dye ends quickly. The dye is isolated and dried.
It forms a black-brown powder which dissolves in water with a red-brown color and dyes leather in dark red-brown shades with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE195541X | 1935-06-29 | ||
CH192371T | 1936-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH195541A true CH195541A (en) | 1938-01-31 |
Family
ID=25722269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH195541D CH195541A (en) | 1935-06-29 | 1936-06-24 | Process for the preparation of a water-soluble azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH195541A (en) |
-
1936
- 1936-06-24 CH CH195541D patent/CH195541A/en unknown
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