CH149622A - Process for the preparation of a thiazine dye. - Google Patents
Process for the preparation of a thiazine dye.Info
- Publication number
- CH149622A CH149622A CH149622DA CH149622A CH 149622 A CH149622 A CH 149622A CH 149622D A CH149622D A CH 149622DA CH 149622 A CH149622 A CH 149622A
- Authority
- CH
- Switzerland
- Prior art keywords
- violet
- red
- acid
- dye
- sulfonic acid
- Prior art date
Links
Landscapes
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Description
Verfahren zur Darstellung eines Thiazinfarbstoffes. Vorliegendes Patent bezieht sich auf ein Ver fahren zur Herstellung eines Thiazinfarbstoffes, dadurch gekennzeichnet, dass man das Kon densationsprodukt aus 1.3-Dimethyl-4-amirro- benzol-6-sulfosäure und f-Naphthochinorr-4- sulfosäure mit Schwefelungsmitteln behandelt.
Der Farbstoff ist als freie Säure ein rot violettes Pulver. In verdünnter Natronlauge löst er sich mit blauer Farbe, die beim An säuern irr ein lebhaftes Rotviolett umschlägt. Wolle wird aus saurein Bade rotviolett ge färbt. Bei Nachchromieren erhält man ein besonders gelbstichiges reines Grün.
<I>Beispiel:</I> 18 kg des Kondensationsproduktes aus 1. 3-Dirnethyl-4-aminobenzol-6-sulfosäure und f-Naphthochirron-4-sulfosäure werden in eine Lösung von 12 kg Schwefel in 250 kg 28 o/oigem Oleurn bei 20-30 o eingetragen; hierauf wird langsam auf 40 erhitzt und bei dieser Temperatur etwa 4 Stunden ge rührt. Man giesst die Schmelze auf Eis, fil triert den ausgeschiedenen Farbstoff und wäscht mit Salzwasser aus.
Process for the preparation of a thiazine dye. The present patent relates to a process for the preparation of a thiazine dye, characterized in that the condensation product of 1,3-dimethyl-4-amirrobenzene-6-sulfonic acid and f-naphthoquinor-4-sulfonic acid is treated with sulfurizing agents.
As a free acid, the dye is a red-violet powder. In dilute caustic soda it dissolves with a blue color, which turns a vivid red-violet when acidified. Wool is dyed red-violet from acidic bath. Chromium plating produces a particularly yellowish pure green.
<I> Example: </I> 18 kg of the condensation product of 1. 3-methyl-4-aminobenzene-6-sulfonic acid and f-naphthochirronic-4-sulfonic acid are dissolved in a solution of 12 kg of sulfur in 250 kg of 28% Oleur added at 20-30 o; it is then slowly heated to 40 and stirred at this temperature for about 4 hours. The melt is poured onto ice, the precipitated dye is filtered off and washed with salt water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE149622X | 1928-10-10 | ||
CH145455T | 1929-09-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH149622A true CH149622A (en) | 1931-09-15 |
Family
ID=25714709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH149622D CH149622A (en) | 1928-10-10 | 1929-09-30 | Process for the preparation of a thiazine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH149622A (en) |
-
1929
- 1929-09-30 CH CH149622D patent/CH149622A/en unknown
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