CH128919A - 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
- CH128919A CH128919A CH128919DA CH128919A CH 128919 A CH128919 A CH 128919A CH 128919D A CH128919D A CH 128919DA CH 128919 A CH128919 A CH 128919A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- copper
- copper compound
- substantive azo
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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 4-Nitro-2-aminophenol- glykoläther und einem Molekül 5. 5'-Dioxy- 2.2'-dinaphtylamin-7.7'-disulfosäure erhal ten werden kann, in eine Kupferverbindung übergeführt wird, wenn man auf denselben ein kupferabgebendes Mittel einwirken lässt.
Der erhaltene kupferhaltige Azofarbstoff zieht auf die pflanzliche Faser in licht-, alkali- und bügelechten violetten Tönen.
Beispiel: 925 Gewichtsteile des Azofarbstoffes aus 2 Molekülen 4-Nitro-2-aminophenolglykol- äther und 1 Molekül 5.5'-Dioxy-2.2'-di- naphtylamin-7.7'-disulfosäure werden in 26 000 Volumteilen Wasser gelöst, mit Essig säure deutlich sauer gemacht und bei<B>80'</B> mit 250 Gewiehtsteilen kristallisiertem Kup fersulfat versetzt. Unter Rühren wird 2 Stunden auf<B>80'</B> erwärmt, die Ausscheidung der Farbstoffsäure eventuell durch Kochsalz vervollständigt, abgepresst und getrocknet.
Der Farbstoff zieht aus dem Glaubersalz Sodabad in licht-, alkali- und bügelechten violetten Tönen.
Process for the preparation of the copper compound of a substantive azo dye. It has been found that the substantive azo dye, as it can be obtained from two molecules of the diazo compound from 4-nitro-2-aminophenol glycol ether and one molecule of 5.5'-dioxy-2.2'-dinaphthylamine-7.7'-disulfonic acid, is converted into a copper compound when a copper-releasing agent is allowed to act on it.
The copper-containing azo dye obtained is absorbed by the vegetable fibers in light-, alkali- and iron-fast purple tones.
Example: 925 parts by weight of the azo dye from 2 molecules of 4-nitro-2-aminophenolglycol ether and 1 molecule of 5.5'-dioxy-2.2'-di-naphthylamine-7.7'-disulfonic acid are dissolved in 26,000 parts by volume of water, and acetic acid is clearly acidic made and at <B> 80 '</B> with 250 parts by weight of crystallized copper sulfate. The mixture is heated to <B> 80 '</B> for 2 hours while stirring, the precipitation of the dye 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 purple tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE128919X | 1926-04-19 | ||
CH128005T | 1927-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH128919A true CH128919A (en) | 1928-11-16 |
Family
ID=25711008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH128919D CH128919A (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) | CH128919A (en) |
-
1927
- 1927-03-29 CH CH128919D patent/CH128919A/en unknown
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