CH232050A - Process for the preparation of a new monoazo dye. - Google Patents
Process for the preparation of a new monoazo dye.Info
- Publication number
- CH232050A CH232050A CH232050DA CH232050A CH 232050 A CH232050 A CH 232050A CH 232050D A CH232050D A CH 232050DA CH 232050 A CH232050 A CH 232050A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- new monoazo
- dye
- new
- 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
Verfahren zur Herstellung eines neuen Monoazofarbstoffes. Die vorliegende Erfindung betrifft ein Verfahren zur Herstellung eines neuen Monoazofarbstoffes und ist .dadurch Bekenn zeichnet, dass man diazotierte 4-Amino-6- s sulfosalicylsäure mit 2-Naphthol-4-sulfon- säure vereinigt.
<I>Beispiel:</I> 23,3 Teile 4-Amino-6-sulfosalicylsäure werden in 80 Teilen Wasser und 17,5 Teilen i 30 % iger Salzsäure suspendiert und bei 0-2 auf bekannte Weise mit 6,9 Teilen Natrium nitrit diazotiert. Der erhaltenen Suspension der Diazoverhindung werden 24,6 Teile 2 naphthol-4-sulfonsaures Natrium zugefügt.
Die Kupplung erfolgt durch allmähliche Neutralisation der sauren Reaktion bei 0 bis 5 C und längeres Rühren bis zum Ver- schwinden der Diazoverbindung. Der Farb stoff wird in üblicher Weise isoliert und färbt Wolle nachchromiert in orangebrau- nen Tönen. Ergibt im gattundruck sehr gut seifen- und chlorechte, schnell fixierende Drucke von einem etwas rotstichigen Braun.
Process for the preparation of a new monoazo dye. The present invention relates to a process for the preparation of a new monoazo dye and is characterized by the fact that diazotized 4-amino-6-sulfosalicylic acid is combined with 2-naphthol-4-sulfonic acid.
<I> Example: </I> 23.3 parts of 4-amino-6-sulfosalicylic acid are suspended in 80 parts of water and 17.5 parts of 30% strength hydrochloric acid and, at 0-2, in a known manner with 6.9 parts of sodium nitrite diazotized. 24.6 parts of 2-naphthol-4-sulfonic acid sodium are added to the suspension of the diazo compound obtained.
The coupling takes place by gradual neutralization of the acidic reaction at 0 to 5 C and prolonged stirring until the diazo compound disappears. The dye is isolated in the usual way and re-chromed wool in orange-brown tones. In gattundruck it produces very good soap and chlorine-proof, quick-setting prints of a somewhat reddish brown.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH232050T | 1942-07-17 | ||
CH230264T | 1942-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH232050A true CH232050A (en) | 1944-04-30 |
Family
ID=25727452
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH232050D CH232050A (en) | 1942-07-17 | 1942-07-17 | Process for the preparation of a new monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH232050A (en) |
-
1942
- 1942-07-17 CH CH232050D patent/CH232050A/en unknown
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