CH145316A - Process for the preparation of an azophthalein dye. - Google Patents
Process for the preparation of an azophthalein dye.Info
- Publication number
- CH145316A CH145316A CH145316DA CH145316A CH 145316 A CH145316 A CH 145316A CH 145316D A CH145316D A CH 145316DA CH 145316 A CH145316 A CH 145316A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- dyestuff
- azophthalein
- acid
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azoplitaleinfarbstoffes. Gegenstand dieser Erfindung ist ein Ver fahren zur Darstellung eines Azophtaleinfarb- stoffes von nachstehender Formel:
EMI0001.0004
welches dadurch gekennzeichnet ist, dass man den Monoazofarbstoff aus o-Amido-o-kr-esol- p-sulfosäure und Resorcin mit Diäthylamido- m-oxyberrzoylberrzoesäui,e im Verhältnis glei cher Moleküle kondensiert.
<I>Beispiel:</I> 32,4 Teile des Farbstoffes aus o-Amido- o-kresol-p-sulfosäure und Resorcin werden mit 31,4 Teilen Diäthylarnido-m-oxybenzoylbenzoe- säure vermischt und eingetragen in 300 Teile konzentrierter Schwefelsäure. Nach 24-stün- digem Rühren bei 80<B>0</B> giesst man in Wasser; die Farbstoffsäure fällt vollständig aus.
Sie bildet getrocknet ein bronzierendes Pulver, das in Wasser auf Zusatz von Alkalien klar rotstichig blau, in konzentrierter Schwefel säure rotorange löslich ist. Die nachehro- mierten oder nachgekupferten Färbungen auf Wolle und Seide des nach bekannten Ver fahren in das Alkalisalz übergeführten Farb stoffes sind schön blau und zeigen hervorra gende Echtheitseigenschaften.
Process for the preparation of an azoplitalein dye. The subject of this invention is a process for the preparation of an azophtalein dyestuff of the following formula:
EMI0001.0004
which is characterized in that the monoazo dye from o-amido-o-kr-esol-p-sulfonic acid and resorcinol is condensed with diethylamido-m-oxyberrzoylberrzoesäui, e in a ratio of the same molecules.
<I> Example: </I> 32.4 parts of the dye from o-amido-o-cresol-p-sulfonic acid and resorcinol are mixed with 31.4 parts diethylarnido-m-oxybenzoylbenzoic acid and introduced into 300 parts of concentrated sulfuric acid . After stirring for 24 hours at 80 <B> 0 </B>, the mixture is poured into water; the dye acid precipitates out completely.
When dried, it forms a bronzing powder which, when alkalis are added, is clear, reddish-tinged blue and soluble in concentrated sulfuric acid red-orange. The re-chromed or re-coppered dyeings on wool and silk of the dye converted into the alkali salt by known processes are beautiful blue and show excellent fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE145316X | 1928-05-24 | ||
CH142447T | 1929-05-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH145316A true CH145316A (en) | 1931-02-15 |
Family
ID=25714065
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH145316D CH145316A (en) | 1928-05-24 | 1929-05-21 | Process for the preparation of an azophthalein dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH145316A (en) |
-
1929
- 1929-05-21 CH CH145316D patent/CH145316A/en unknown
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