CH106466A - Process for the production of an indigoid dye of the anthracene series. - Google Patents
Process for the production of an indigoid dye of the anthracene series.Info
- Publication number
- CH106466A CH106466A CH106466DA CH106466A CH 106466 A CH106466 A CH 106466A CH 106466D A CH106466D A CH 106466DA CH 106466 A CH106466 A CH 106466A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- anthracene series
- green
- indigoid dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B7/00—Indigoid dyes
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthr acenr eihe. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff der Anthracenreihe er hält, wenn man das 2,3 - Anthra,cenoxythio- naphthen mit a-Isatinanilicl kondensiert.
Der neue Farbstoff bildet ein schwarz grünes Pulver, das in Schwefelsäure mit brauner Farbe löslich ist, und daraus durch Wasser in grünen Flocken gefällt wird; mit Hydrosulfit und Natronlauge gibt er eine violettbraune Küpe, aus welcher Baiunwolle in rein grünen, hervorragend echten Tönen gefärbt wird.
<I>Beispiel:</I> 26. Teile 2,3-Anthracenoxythionaphthen werden mit 25 Teilen a-Isatinanilid in 30(i Teilen Pyridin erwärmt. Die Farbstoffbil- dung ist in kurzer Zeit beendet. Der gebil- dete Farbstoff wird .abgesaust, mit Alkohol nachgewasehen und getrocknet.
Process for the production of an indigoid dye of the anthracene series. It has been found that a new indigoid dye of the anthracene series is obtained if the 2,3-anthra, cenoxythionnaphthene is condensed with a-isatinanilicl.
The new dye forms a black-green powder, which is soluble in sulfuric acid with a brown color, and is precipitated from it in green flakes by water; with hydrosulphite and caustic soda, he gives a violet-brown vat, from which cotton wool is dyed in pure green, outstandingly genuine shades.
<I> Example: </I> 26. parts of 2,3-anthracene oxythionaphthene are heated with 25 parts of α-isatin anilide in 30 (1 parts of pyridine. The formation of the dye is complete in a short time. The dye formed is acidified , washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103649T | 1923-01-24 | ||
CH106466T | 1923-01-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106466A true CH106466A (en) | 1924-09-01 |
Family
ID=25706530
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106466D CH106466A (en) | 1923-01-24 | 1923-01-24 | Process for the production of an indigoid dye of the anthracene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106466A (en) |
-
1923
- 1923-01-24 CH CH106466D patent/CH106466A/en unknown
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