CH203035A - Process for the preparation of an azo dye containing complexed chromium. - Google Patents
Process for the preparation of an azo dye containing complexed chromium.Info
- Publication number
- CH203035A CH203035A CH203035DA CH203035A CH 203035 A CH203035 A CH 203035A CH 203035D A CH203035D A CH 203035DA CH 203035 A CH203035 A CH 203035A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- red
- preparation
- dye containing
- 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
-
- 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
- C09B45/18—Monoazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines komplex gebundenes Chrom enthaltenden Azofar bstoffes. Es wurde gefunden, dass ein komplex ge bundenes Chrom enthaltender Azofarbstoff hergestellt werden kann, wenn der Azofarb- stoff der Formel
EMI0001.0009
mit chromabgebenden Mitteln behandelt wird. Die neue Chromverbindung stellt ein ,graues Pulver dar, das sich in Wasser mit roter, in 10%iger Sodalösung,
,sowie in 10 % iger Natronlauge mit Totoranger und in. konzentrierter Schwefelsäure mit oranger Farbe löst. Sie erzeugt auf Wolle und Leder braunrote Töne von guten Echtheitseigen schaften.
Der dem Verfahren als Ausgangsstoff dienende Azofarbstoff :der obigen Formel kann durch Kupplung in alkalisohem Me dium von diazotierter 2-Amino-4-nitro-l-oxy- b-en,zol-j6-sul:fonsäure und 5@Nitroperinaplith- indandion erhalten werden.
Die Behandlung mit chromab#gebenden Mitteln erfolgt nach den bekannten Metho den, beispielsweise durch Erhitzen in wässe riger Lösung mit Salzen des dreiwertigen Chroms.
<I>Beispiel:</I> Man löst 4,8 Teile :des Azofarbstoffm aus diazotierter 4 - Nitro - 2 - amino-l-oxybenzol-j6- sulfonsäure und 5-Nitroperinaphthindandion in 100 Teilen Wasser und setzt 2,1 Teile kri stallisiertes Natriumacetat hinzu. Dieser Lö sung setzt man eine Fluorchromlösung, ent haltend 0,91 Teile Cr203,, zu und kocht '24 Stunden rückfliessend.
Hierauf filtriert man von vorhandenen unlöslichen Bestandteilen ab, dampft das Filtrat im Vakuum auf ein kleines Volumen ein, scheidet -den Farbstoff durch Zugabe von Kochsalz ab, filtriert und trocknet.
Process for the production of an azo dye containing complexed chromium. It has been found that an azo dye containing complexly bound chromium can be produced if the azo dye of the formula
EMI0001.0009
is treated with chromium-releasing agents. The new chromium compound is a gray powder that dissolves in water with a red 10% soda solution,
, as well as in 10% sodium hydroxide solution with Totoranger and in concentrated sulfuric acid with orange color. It produces brown-red tones with good fastness properties on wool and leather.
The azo dye used as starting material for the process: of the above formula can be obtained from diazotized 2-amino-4-nitro-l-oxy-b-ene, zol-j6-sulfonic acid and 5 @ nitroperinaplith indanedione by coupling in alkali-hydrogen medium will.
Treatment with chromium-donating agents is carried out according to the known methods, for example by heating in an aqueous solution with salts of trivalent chromium.
<I> Example: </I> 4.8 parts of the azo dye from diazotized 4-nitro-2-amino-1-oxybenzene-6-sulfonic acid and 5-nitroperinaphthindanedione are dissolved in 100 parts of water and 2.1 parts are added to the kri Installed sodium acetate added. A fluorochrome solution containing 0.91 parts of Cr203 is added to this solution and refluxed for 24 hours.
The insoluble constituents present are then filtered off, the filtrate is evaporated to a small volume in vacuo, the dye is separated out by adding sodium chloride, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH203035T | 1937-05-22 | ||
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203035A true CH203035A (en) | 1939-02-15 |
Family
ID=25723299
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203035D CH203035A (en) | 1937-05-22 | 1937-05-22 | Process for the preparation of an azo dye containing complexed chromium. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH203035A (en) |
-
1937
- 1937-05-22 CH CH203035D patent/CH203035A/en unknown
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