CH261837A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH261837A CH261837A CH261837DA CH261837A CH 261837 A CH261837 A CH 261837A CH 261837D A CH261837D A CH 261837DA CH 261837 A CH261837 A CH 261837A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- preparation
- dye
- monoazo dye
- red
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
-
- 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 Monoazofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines Monoazo- farbstoffes. Das Verfahren ist dadurch ge kennzeichnet, dass man diazotierte 5-[3'- Amino-@4'-(p-tolylsulfon) -benzoyl]-amino-2- o--xy-benzoesäure mit 2-Amino-8-oxy-naphtha- lin-6-sulfonsäure kuppelt.
Der so erhaltene Farbstoff ist ein rotvio lettes Pulver, das in Wasser in der Wärme leicht löslich ist und Wolle aus saurem Bad in lebhaft blauroten Tönen färbt, welche beim Nachchromieren etwas blaustichiger werden.
<I>Beispiel:</I> 85,2 Gewichtsteile 5-[3'-Amino-4'-(p-tolyl- sulfan) -benzoyl] -amino-2-oxy-benzoesäure wer den in 700 Volumteilen Wasser mit Soda neu tral gelöst, mit 200 Volumteilen n-Nitrit ver mischt und innert einer halben Stunde zu 70 Volumteilen konz. Salzsäure in 300 Volum- teilen Wasser gegeben, wobei die Temperatur nicht über 5 bis 7 steigen soll. Die Diazo- niumverbindung fällt zum grössten Teil aus.
Nach beendeter Diazotierung gibt. man bei höchstens 50 langsam eine schwach lackmus- saure Lösung von 47,8 Gewichtsteilen 2- Amino-8-oxy-naphthalin-6-sulfonsäure in 500 Volumteilen Wasser zu der entstandenen Sus pension.
Nach Beendigung der Farbstoffbil- dung wird neutralisiert, auf 800 aufgeheizt, mit 10 J0 Kochsalz versetzt und nach dem Ab kühlen auf 200 der ausgeschiedene Farbstoff abfiltriert. Getrocknet stellt der Farbstoff ein rotviolettes, in Wasser in der Wärme leicht lösliches Pulver dar, das Wolle aus saurem Bad in lebhaft blauroten Tönen färbt, wel che beim Nachchromieren noch etwas blausti chiger werden.
Process for the preparation of a monoazo dye. The present patent relates to a process for the preparation of a monoazo dye. The process is characterized in that diazotized 5- [3'-amino @ 4 '- (p-tolylsulfone) benzoyl] -amino-2- o - xy-benzoic acid with 2-amino-8-oxy- naphthalin-6-sulfonic acid couples.
The dye obtained in this way is a red-violet powder which is easily soluble in water when heated and dyes wool from an acid bath in vivid blue-red tones, which become a little more bluish when chromium-plating.
<I> Example: </I> 85.2 parts by weight of 5- [3'-amino-4 '- (p-tolylsulfane) -benzoyl] -amino-2-oxy-benzoic acid in 700 parts by volume of water with soda neutral dissolved, mixed with 200 parts by volume of n-nitrite and concentrated to 70 parts by volume within half an hour. Hydrochloric acid is added to 300 parts by volume of water, the temperature should not rise above 5 to 7. Most of the diazonium compound precipitates.
When the diazotization is complete. slowly add a weakly litmus acidic solution of 47.8 parts by weight of 2-amino-8-oxynaphthalene-6-sulfonic acid in 500 parts by volume of water to the resulting suspension at a maximum of 50.
When the formation of the dye has ended, the mixture is neutralized, heated to 800, mixed with 10 J0 sodium chloride and, after cooling to 200, the dye which has separated out is filtered off. When dried, the dye is a red-violet powder that is easily soluble in water when heated, which dyes wool from an acid bath in vivid blue-red tones, which become a little more bluish when they are chromed.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH261837T | 1943-11-23 | ||
CH255412T | 1948-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH261837A true CH261837A (en) | 1949-05-31 |
Family
ID=25729902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH261837D CH261837A (en) | 1943-11-23 | 1943-11-23 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH261837A (en) |
-
1943
- 1943-11-23 CH CH261837D patent/CH261837A/en unknown
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