CH228371A - Process for the preparation of a substantive copper-containing disazo dye. - Google Patents
Process for the preparation of a substantive copper-containing disazo dye.Info
- Publication number
- CH228371A CH228371A CH228371DA CH228371A CH 228371 A CH228371 A CH 228371A CH 228371D A CH228371D A CH 228371DA CH 228371 A CH228371 A CH 228371A
- Authority
- CH
- Switzerland
- Prior art keywords
- copper
- disazo dye
- preparation
- amino
- substantive
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 223777. Gegenstand des vorliegenden Zusatz patentes ist ein Verfahren zur Darstellung eines substantiven kupferhaltigen Disazofarb- stoffes, dadurch gekennzeichnet, dass man je 1 Mol .diazotierter 2-Aminobenzoesäure und 6 - Chlor- 2 -amino-1-o@xybenzol-4-tsulfonsäure mit einem Mo:l eines Kondensationsproduktes aus 2 Mol 2-Amino-5-oxynaphthalin-7-sulfo:
n- s:äure und 1 Mol Cyanurchlurid kuppelt und den erhaltenen Disazofarbstoff mit kupfer abgebenden Mitteln bichandelt.
Beispiel: 137 Teile 2- Aminobenzoesäure werden in üblicher Weise diazotiert und zu einer Lö sung von 589,5 Teilen des sekundären Kon densationsproduktes aus 2 Mol 2-Amino-5- oxynaphthaIin-7-sulfonsäure und 1 Mol Cyanurchlorid in 7000 Teilen Wasser und 200 Teilen Soda gegeben. Nach beendigter Kupplung wird der Farbstoff mit Kochsalz ausgefällt, filtriert und mit 10 000 Teilen Wasser und 200 Teilen Soda wieder ange:- schlämmt.
Es werden nun bei 5 223,5 Teile diazotierte 6-Chlor-2-amino-l-oxyben7,ol-4- sulfo:nsäure zufliessen gelassen und nach be endigter Kupplung :der Disazofarbstoff mit Kochsalz ausgefällt und filtriert.
Der feuchte Filterkuchen wird in 20 000 Teilen Wasser bei 80 .gelöst und mit einer Lösung von 500 Teilen krist. Kupfersulfat in 2000 Teilen Wasser und 1000 Teilen 25/"ö igem Ammoniak versetzt. Es wird 3-4 Stunden bei 80-90 gerührt, mit Kochsalz ausgefällt und filtriert.
Der Farbstoff stellt ein schwärzli@ch- violettes Pulver dar, das sich in Wasser mit roter Färbe löst und Zellulo:sefasern in :sehr lichtechten blaustichigen Rottönen färbt.
Die Kupferung kann auch nach dem im Hauptpatent erwähnten Verfahren vo:rg.e- nommen werden, ebenso ist eine Isolierung des Mono- und des Disazofarbstoffes nicht unbedingt erforderlich, hat aber :den Vorteil, dass dadurch etwas reinere Produkte erhalten werden.
<B> Additional patent </B> to the main patent no. 223777. The subject of the present additional patent is a process for the preparation of a substantive copper-containing disazo dye, characterized in that 1 mol of diazotized 2-aminobenzoic acid and 6-chloro-2 -amino-1-o @ xybenzene-4-tsulfonic acid with a Mo: l of a condensation product of 2 moles of 2-amino-5-oxynaphthalene-7-sulfo:
n-s: acid and 1 mole of cyanuric acid coupling and the disazo dye obtained with copper-releasing agents.
Example: 137 parts of 2-aminobenzoic acid are diazotized in the usual way and to a solution of 589.5 parts of the secondary condensation product of 2 moles of 2-amino-5-oxynaphthaIin-7-sulfonic acid and 1 mole of cyanuric chloride in 7000 parts of water and 200 Share soda given. After the coupling is complete, the dye is precipitated with sodium chloride, filtered and slurried again with 10,000 parts of water and 200 parts of soda.
There are now at 5223.5 parts of diazotized 6-chloro-2-amino-1-oxyben7, ol-4-sulfonic acid allowed to flow in and, after coupling is complete: the disazo dye is precipitated with sodium chloride and filtered.
The moist filter cake is dissolved in 20,000 parts of water at 80 and with a solution of 500 parts of crystalline. Copper sulfate in 2000 parts of water and 1000 parts of 25% ammonia are added. The mixture is stirred for 3-4 hours at 80-90, precipitated with sodium chloride and filtered.
The dye is a blackish-violet powder that dissolves in water with a red color and colors cellulose fibers in very lightfast blue-tinged red tones.
The copper plating can also be carried out according to the process mentioned in the main patent, and isolation of the mono and disazo dyes is not absolutely necessary, but has the advantage that somewhat purer products are obtained.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH223777T | 1941-09-19 | ||
CH228371T | 1941-09-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH228371A true CH228371A (en) | 1943-08-15 |
Family
ID=25726745
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH228371D CH228371A (en) | 1941-09-19 | 1941-09-19 | Process for the preparation of a substantive copper-containing disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH228371A (en) |
-
1941
- 1941-09-19 CH CH228371D patent/CH228371A/en unknown
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