CH103143A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH103143A CH103143A CH103143DA CH103143A CH 103143 A CH103143 A CH 103143A CH 103143D A CH103143D A CH 103143DA CH 103143 A CH103143 A CH 103143A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- indigoid dye
- dye
- chloro
- 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
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Terfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff erhält, wenn das 1-Chlor- 2#3-thionaphthisatin, welches durch Konden sieren von 1-Chlor-2-thionaphthol mit Oxalyl- chlorid erhalten werden kann, mit 6-Chlor- oxythionaplitenkarbonsäure kondensiert.
Der neue Farbstoff bildet ein violettrotes Pulver, löst sich in konz. Schwefelsäure mit olivegrüner Farbe und gibt mit Hydrosulfit und Natronlauge eine bräunlich-gelbe Küpe, aus welcher Baumwolle in violetten Tönen gefärbt wird, die beim Seifen etwas röter und sehr echt werden.
getragen und hierauf längere Zeit am Beispiel In 10000 Teile Alkohol werden 248,5 Teile 1-Chlor-2#3-thionaphthisatin und<B>228,5</B> Teile 6-Chloroxy thionaphtenkarbonsiture ein- gekocht. Der gebildete Farbstoff wird filtriert, gewaschen und getrocknet.
Technique for the production of a new indigoid dye. It has been found that a new indigoid dye is obtained if 1-chloro-2 # 3-thionaphthisatin, which can be obtained by condensing 1-chloro-2-thionaphthol with oxalyl chloride, with 6-chlorooxythionaplitic acid condensed.
The new dye forms a purple-red powder, dissolves in conc. Sulfuric acid with an olive-green color and, with hydrosulfite and sodium hydroxide solution, gives a brownish-yellow vat, from which cotton is dyed in violet tones, which become a little redder and very real when soapy.
and then for a long time using the example. 248.5 parts of 1-chloro-2 # 3-thionaphthisatin and 228.5 parts of 6-chlorooxy thionaphthene carbonate are boiled down in 10,000 parts of alcohol. The dye formed is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH103143T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH103143A true CH103143A (en) | 1924-01-16 |
Family
ID=25705824
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH103143D CH103143A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH103143A (en) |
-
1922
- 1922-12-07 CH CH103143D patent/CH103143A/en unknown
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