CH123455A - Process for the preparation of a new dye. - Google Patents
Process for the preparation of a new dye.Info
- Publication number
- CH123455A CH123455A CH123455DA CH123455A CH 123455 A CH123455 A CH 123455A CH 123455D A CH123455D A CH 123455DA CH 123455 A CH123455 A CH 123455A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- yellow
- new dye
- cold
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines neuen Farbstoffes. Es ist gefunden worden, dass man einen in Wasser löslichen Farbstoff erhält, der vorzugsweise die tierische Faser in gelben licht- und walkechten Tönen anfärbt, wenn man 1 Molekül 1. 3-Dihalogen-4. 6-dinitro- benzol mit 2 Molekülen 4'-Nitro-4-amino-di- phenylamin-2'-sulfosäure kondensiert.
Beispiel: 23,1 Gewichtsteile 1.3-Dichlor-4.6-di- nitrobenzol werden in der 15fachen Menge Wasser, .dem etwas Alkohol hinzugefügt ist, suspendiert. Dann lässt man innerhalb 15 Stunden in diese Suspension eine soloalka lische Lösung, hergestellt aus 61,8 Gewichts teilen 4'-Nitro-4-aminodiphenylamin-2'-sulfo- säure in 400 Teilen Wasser und 24 Ge wichtsteilen calcinierter Soda einlaufen. Es tritt unter Braunfärbung Lösung ein.
Nach dem einige Stunden nachgekocht worden ist, wird die tief braun gefärbte Lösung heiss filtriert und aus dem Filtrat das, Natronsalz des Farbstoffes ausgesalzen. Dem Farbstoff kommt folgendes Formelbild zu:
EMI0001.0019
Das Natronsalz des neuen Farbstoffes stellt ein rostbraunes Pulver dar, das sich in kalter konzentrierter Schwefelsäure gelb löst; beim Erwärmen wird die Lösung grün und schliesslich blaugrün. In kaltem Alko- hol ist der Farbstoff schwer löslich, in Was ser dagegen mit tiefgelber Farbe leicht lös lich. Auf der Wollfaser erzeugt er gelbe Pchte Töne.
Process for the preparation of a new dye. It has been found that a water-soluble dye is obtained which preferably dyes the animal fibers in yellow lightfast and whackfast shades if 1 molecule of 1,3-dihalo-4. 6-dinitrobenzene condensed with 2 molecules of 4'-nitro-4-amino-diphenylamine-2'-sulfonic acid.
Example: 23.1 parts by weight of 1,3-dichloro-4,6-dinitrobenzene are suspended in 15 times the amount of water to which a little alcohol has been added. Then, within 15 hours, a solo alkali solution, prepared from 61.8 parts by weight of 4'-nitro-4-aminodiphenylamine-2'-sulfonic acid in 400 parts of water and 24 parts by weight of calcined soda, is allowed to run into this suspension. Solution occurs with a brown color.
After boiling for a few hours, the deep brown colored solution is filtered hot and the sodium salt of the dye is salted out of the filtrate. The dye has the following formula:
EMI0001.0019
The sodium salt of the new dye is a rust-brown powder that dissolves yellow in cold concentrated sulfuric acid; when heated, the solution turns green and finally blue-green. The dye is sparingly soluble in cold alcohol, but easily soluble in water with a deep yellow color. He creates yellow pitch tones on the wool fiber.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE123455X | 1925-05-22 | ||
CH120527T | 1926-05-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH123455A true CH123455A (en) | 1927-11-16 |
Family
ID=25709494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH123455D CH123455A (en) | 1925-05-22 | 1926-05-19 | Process for the preparation of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH123455A (en) |
-
1926
- 1926-05-19 CH CH123455D patent/CH123455A/en unknown
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