CH116503A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH116503A CH116503A CH116503DA CH116503A CH 116503 A CH116503 A CH 116503A CH 116503D A CH116503D A CH 116503DA CH 116503 A CH116503 A CH 116503A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new dye
- dye
- new
- nitro
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Znsatzpate'it zum Hauptpatent Nr. 111564. Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man den Azofarbstoff, welcher durch Kuppeln von dianotierter 4- Nitro-2-amino-l-phenol-6-sulfosäure mit Acet- essigester erhalten wird, mit Chromformiat behandelt.
Der neue Farbstoff bildet ein olives Pulver, löst sich in Wasser mit gelber, in verdünnter Natronlauge mit oranger Farbe und färbt Wolle aus saurem Bade in sehr gleichmässigen, echten, rotstichig gelben Tönen an.
<I>Beispiel:</I> 39,7 Teile des Farbstoffes, erhalten durch Kuppeln von 4-Nitro-2-diazo-l-phenol-6-sulfo- säure mit Acetessigester, werden einige Zeit in wässeriger Lösung mit einer Ohrornformiat- lösung entsprechend 22,5 Teilen Cr20s er- wärmt. Die Lösung wird sodann eingedampft und der Farbstoff mit Kochsalz- ausgefällt.
Addition to main patent no. 111564. Process for the production of a new dye. It has been found that a new dye is obtained if the azo dye, which is obtained by coupling dianotated 4-nitro-2-amino-1-phenol-6-sulfonic acid with acetic acetate, is treated with chromium formate.
The new dye forms an olive powder, dissolves in water with yellow, in dilute caustic soda with orange color and colors wool from acid baths in very even, genuine, reddish yellow tones.
<I> Example: </I> 39.7 parts of the dye, obtained by coupling 4-nitro-2-diazo-1-phenol-6-sulfonic acid with acetoacetic ester, are for some time in aqueous solution with an auron formate solution heated to the equivalent of 22.5 parts Cr20s. The solution is then evaporated and the dye is precipitated with sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH111564T | 1924-06-17 | ||
CH116503T | 1924-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116503A true CH116503A (en) | 1926-09-01 |
Family
ID=25707869
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116503D CH116503A (en) | 1924-06-17 | 1924-06-17 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH116503A (en) |
-
1924
- 1924-06-17 CH CH116503D patent/CH116503A/en unknown
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