CH104475A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH104475A CH104475A CH104475DA CH104475A CH 104475 A CH104475 A CH 104475A CH 104475D A CH104475D A CH 104475DA CH 104475 A CH104475 A CH 104475A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- production
- 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
Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff erhält, wenn man das 1.-Chlro-2.3-tliionaphthisatin, welches erhal ten werden kann durch Kondensieren von 1-Chlor-2-thionaphthol mit Oxalylchlorid, mit Oxythionaphthenkarbonsäüre konden siert.
Der neue Farbstoff bildet ein violett rotes Pulver, löst sich in konzentrierter Schwefelsäure mit olivegrüner Farbe und gibt mit Hydrosulfit und Natronlauge eine gelbe Küpe, aus welcher Baumwolle in blau violetten Farbtönen gefärbt wird, die beim Seifen röter und reiner werden. Diese Fär bungen sind sehr licht-, wasch-, bäuch- und chlorecht.
<I>Beispiel:</I> In 10000 Teile Alkohol werden 248,5 Teile 1-Chlor-2 . 3-thionaphthisatin und 194 Teile Oxyfhionaphtenkarbonsäure eingetragen und hierauf längere Zeit am Rückflusskühler ge- kocht. Der gebildete Farbstoff wird filtriert; gewaschen und getrocknet.
Process for the production of a new indigoid dye. It has been found that a new indigoid dye is obtained if the 1.-chloro-2,3-tliionaphthisatin, which can be obtained by condensing 1-chloro-2-thionaphthol with oxalyl chloride, is condensed with oxythionaphthene carboxylic acid.
The new dye forms a violet-red powder, dissolves in concentrated sulfuric acid with an olive-green color and, with hydrosulfite and sodium hydroxide solution, gives a yellow vat from which cotton is dyed in blue-violet hues, which become redder and purer when soapy. These colors are very light, wash, tummy and chlorine-proof.
<I> Example: </I> In 10,000 parts of alcohol there are 248.5 parts of 1-chloro-2. 3-thionaphthisatin and 194 parts of Oxyfhionaphtenkarbonsäure entered and then boiled for a long time on the reflux condenser. 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 | ||
CH104475T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH104475A true CH104475A (en) | 1924-04-16 |
Family
ID=25705825
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH104475D CH104475A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH104475A (en) |
-
1922
- 1922-12-07 CH CH104475D patent/CH104475A/en unknown
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