CH261836A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH261836A CH261836A CH261836DA CH261836A CH 261836 A CH261836 A CH 261836A CH 261836D A CH261836D A CH 261836DA CH 261836 A CH261836 A CH 261836A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- dye
- preparation
- monoazo dye
- parts
- 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'- A mino-4'-sulfo-benzoyl) - amino-2 - oxy@-benzoe- säure mit 2-Amino-8-oxy-naphthalin-6-sulfon- säure kuppelt.
Der so erhaltene Farbstoff ist ein rotes Pulver, das in Wasser in der Wärme leicht löslich ist und Wolle aus saurem Bad in leuchtend roten Tönen färbt, welche beim Nachchromieren etwas blaustichiger werden. <I>Beispiel:</I> 70,4 Gewichtsteile 5-(3'-Amino-4'-sulfo- benzoyl)-arnino-2-oxy-benzoesäure werden in 700 Volumteilen Wasser mit.
Soda neutral ge löst, mit 200 Volumteilen n-Nitrit vermischt und innert einer halben Stunde zu 70 Volum- teilen konz. Salzsäure in 300 Volumteilen Wasser gegeben, wobei die Temperatur nicht über 5 bis 70 steigen soll. Die Diazoniumver- bindung fällt zum grössten Teil aus.
Nach beendeter Diazotierung gibt man bei höch stens 50 langsam eine schwach laekmussaure Lösung von 47,8 Gewichtsteilen 2-Amino-8- oxy-naphthalin-6-sulfonsäure in 500 Volum- teilen Wasser zu der entstandenen Suspen sion. Nach Beendigung der Farbstoffbildung wird neutralisiert, auf 800 aufgeheizt, mit <B>10%</B> Kochsalz versetzt und nach dem Abküh len auf 200 der ausgeschiedene Farbstoff ab filtriert.
Getrocknet stellt der Farbstof ein rotes, in Wasser in der Wärme leicht lösliches Pulver dar, das Wolle aus saurem Bade in leuchtend roten Tönen färbt, welche beim Nachchromieren noch etwas blaustichiger wer den.
Process for the preparation of a monoazo dye. The present patent relates to a process for the preparation of a monoazo dye. The procedure is. characterized in that diazotized 5- (3'-A mino-4'-sulfo-benzoyl) -amino-2-oxy @ -benzoic acid with 2-amino-8-oxy-naphthalene-6-sulfonic acid clutch.
The dye obtained in this way is a red powder, which is easily soluble in water when heated, and dyes wool from an acid bath in bright red shades, which become a little more bluish when they are chromed. <I> Example: </I> 70.4 parts by weight of 5- (3'-amino-4'-sulfobenzoyl) -arnino-2-oxy-benzoic acid are mixed with 700 parts by volume of water.
Soda dissolved neutrally, mixed with 200 parts by volume of nitrite and concentrated to 70 parts by volume within half an hour. Hydrochloric acid in 300 parts by volume of water, the temperature should not rise above 5 to 70 Most of the diazonium compound fails.
When the diazotization is complete, a weakly laekmus acidic solution of 47.8 parts by weight of 2-amino-8-oxynaphthalene-6-sulfonic acid in 500 parts by volume of water is slowly added to the resulting suspension at a maximum of 50. When the dye formation has ended, the mixture is neutralized, heated to 800, mixed with 10% sodium chloride and, after cooling to 200, the precipitated dye is filtered off.
When dried, the dye is a red powder that is easily soluble in water when heated, which dyes wool from an acid bath in bright red tones, which become even more bluish when they are re-chromed.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH261836T | 1943-11-23 | ||
CH255412T | 1948-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH261836A true CH261836A (en) | 1949-05-31 |
Family
ID=25729901
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH261836D CH261836A (en) | 1943-11-23 | 1943-11-23 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH261836A (en) |
-
1943
- 1943-11-23 CH CH261836D patent/CH261836A/en unknown
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