CH145320A - Process for the preparation of an azophthalein dye. - Google Patents
Process for the preparation of an azophthalein dye.Info
- Publication number
- CH145320A CH145320A CH145320DA CH145320A CH 145320 A CH145320 A CH 145320A CH 145320D A CH145320D A CH 145320DA CH 145320 A CH145320 A CH 145320A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- azophthalein
- acid
- green
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azophtaleinfarbstoffes. Gegenstand dieser Erfindung ist -ein Ver fahren zur Darstellung eines Azophtalein- farbstoffes von nachstehender Formel:
EMI0001.0004
welches dadurch gekennzeichnet ist, dass man den Monoazofarbstoff auf der nitrierten 1,2,4- Diazonaphtolsulfosäüre und Resorcin mit Dimethylamido-m-oxybenzoylbenzoesäure im Verhältnis gleicher Moleküle kondensiert.
<I>Beispiel:</I> 36 Teile des Farbstoffes aus der nitrier ten 1,2,4-Diazonaphtolsulfosäure und Resor- cin werden mit 28,5 Teilen Dimethylamido- m-oxybenzoylbenzoesäure vermischt und ein getragen in 300 Teile konz. Schwefelsäure. Man rührt acht Stunden bei<B>60'</B> und giesst darauf in Wasser; die Farbstoffsäure fällt vollständig aus.
Sie bildet getrocknet eia bronzierendes Pulver, das in Wasser auf Zu satz von Alkali blaugrün, in konz. Schwefel säure violett löslich ist. Die nachchromierteii oder nachgekupferten Färbungen auf Wolle und Seide des nach bekannten Verfahren in das Alkalisalz übergeführten Farbstoffe sind grün und besitzen gute Echtheitseigen schaften.
Process for the preparation of an azophthalein dye. The subject of this invention is a process for the preparation of an azophtalein dye of the following formula:
EMI0001.0004
which is characterized in that the monoazo dye is condensed on the nitrated 1,2,4-diazonaphthol sulfonic acid and resorcinol with dimethylamido-m-oxybenzoylbenzoic acid in proportions of the same molecules.
<I> Example: </I> 36 parts of the dye from the nitrated 1,2,4-diazonaphtholsulfonic acid and resorcin are mixed with 28.5 parts of dimethylamido-m-oxybenzoylbenzoic acid and added to 300 parts of conc. Sulfuric acid. The mixture is stirred for eight hours at <B> 60 '</B> and then poured into water; the dye acid precipitates out completely.
When dried, it forms a bronzing powder, which in water with the addition of alkali is blue-green, in conc. Sulfuric acid is soluble in violet. The afterchromized or coppered dyeings on wool and silk of the dyes converted into the alkali salt by known processes are green and have good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE145320X | 1928-05-24 | ||
CH142447T | 1929-05-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH145320A true CH145320A (en) | 1931-02-15 |
Family
ID=25714069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH145320D CH145320A (en) | 1928-05-24 | 1929-05-21 | Process for the preparation of an azophthalein dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH145320A (en) |
-
1929
- 1929-05-21 CH CH145320D patent/CH145320A/en unknown
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