CH128918A - Process for the preparation of the copper compound of a substantive azo dye. - Google Patents
Process for the preparation of the copper compound of a substantive azo dye.Info
- Publication number
- CH128918A CH128918A CH128918DA CH128918A CH 128918 A CH128918 A CH 128918A CH 128918D A CH128918D A CH 128918DA CH 128918 A CH128918 A CH 128918A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- copper
- copper compound
- substantive
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung der Kupferverbindung eines substantiven Azofarbstoffes. Es wurde gefunden, dass der substantive Azofarbstoff, wie er aus zwei Molekülen der Diazoverbindung aus 2-Amino-l-oxybenzol- glycerinäther und einem Molekül 5. 5'-Di- oxy - 2 . 2'- dinaphtylamin - 7.
7'- disulfosäure erhalten werden kann, in eine Kupferverbin- dung übergeführt wird, wenn man auf den selben ein kupferabgebendes Mittel einwirken lässt.
Der erhaltene kupferhaltige Farbstoff zieht auf die pflanzliche Faser in licht-, al- kali- und bügelechten violetten Tönen von bemerkenswerter Klarheit. Beispiel:
893 Gewichtsteile des Azofarbstoffes aus 2 Molekülen 2-Amino-l-oxybenzol-glycerin- äther
EMI0001.0023
und 1 Molekül 5.5'-Dioxy-2.2'-dinaphtyl- amin-7 . 7'-disulfosäure werden in 26 000 Volumteilen Wasser gelöst, mit Essigsäure deutlich sauer gemacht und bei<B>80'</B> mit 2,50 Gewichtsteilen kristallisiertem Kupfersulfat versetzt.
Unter Rühren wird 2 Stunden auf 80 erwärmt, die Ausscheidung der Farb- stoffsäure eventuell durch Kochsalz vervoll ständigt, abgepresst und getrocknet. Der Farbstoff zieht aus dem Glaubersalz-Soda- bad in licht-, alkali-, bügelechten violetten Tönen von bemerkenswerter Klarheit.
Process for the preparation of the copper compound of a substantive azo dye. It has been found that the substantive azo dye, as it is composed of two molecules of the diazo compound from 2-amino-1-oxybenzene-glycerol ether and one molecule of 5. 5'-dioxy-2. 2'-dinaphthylamine - 7.
7′-disulfonic acid can be obtained, is converted into a copper compound if a copper-releasing agent is allowed to act on the same.
The copper-containing dye obtained is absorbed by the vegetable fibers in light, alkali and iron-fast violet tones of remarkable clarity. Example:
893 parts by weight of the azo dye from 2 molecules of 2-amino-1-oxybenzene-glycerol ether
EMI0001.0023
and 1 molecule of 5.5'-dioxy-2.2'-dinaphthylamine-7. 7'-disulfonic acid is dissolved in 26,000 parts by volume of water, made significantly acidic with acetic acid and mixed with 2.50 parts by weight of crystallized copper sulfate at <B> 80 '</B>.
The mixture is heated to 80 for 2 hours with stirring, the precipitation of the dyestuff acid is possibly completed with sodium chloride, pressed off and dried. The dye draws from the Glauber's salt soda bath in light-, alkali- and iron-fast violet tones of remarkable clarity.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128918X | 1926-04-19 | ||
CH128005T | 1927-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128918A true CH128918A (en) | 1928-11-16 |
Family
ID=25711007
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128918D CH128918A (en) | 1926-04-19 | 1927-03-29 | Process for the preparation of the copper compound of a substantive azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH128918A (en) |
-
1927
- 1927-03-29 CH CH128918D patent/CH128918A/en unknown
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