CH147698A - Process for the production of a new metal-containing dye. - Google Patents
Process for the production of a new metal-containing dye.Info
- Publication number
- CH147698A CH147698A CH147698DA CH147698A CH 147698 A CH147698 A CH 147698A CH 147698D A CH147698D A CH 147698DA CH 147698 A CH147698 A CH 147698A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- containing dye
- violet
- amino
- new metal
- 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
- C09B45/24—Disazo or polyazo compounds
- C09B45/26—Disazo or polyazo 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
- C09B45/24—Disazo or polyazo compounds
- C09B45/28—Disazo or polyazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 145448. Verfahren zur Herstellung eines neuen metallhaltigen Farbstoffes. Es wurde gefunden, dass man einen neuen metallhaltigen Farbstoff erhält, wenn man den Disazofarbstoff der Formel:
EMI0001.0005
der durch Kuppeln von diazotierter Anthra- nilsäure in saurem Medium mit 2-Amino-5- oxynaphthalin-7-sulfosäure und Einwirkung von diazotierter 6-Nitro-2-amino-l-phenol-4- sulfosäure auf den entstandenen Monoazofarb- stoff in alkalischem Medium erhalten werden kann, mit einem kupfer- und einem chrom abgebenden Mittel behandelt.
Der erhaltene metallhaltige Farbstoff stellt ein dunkel gefärbtes Pulver dar, das sich in Wasser mit violetter, in konzentrierter Schwe felsäure mit rotvioletter Farbe löst und Vis kose in egalen, grauvioletten Tönen färbt. <I>Beispiel:</I> 6,8 Teile des Farbstoffes aus diazotierter 6-Nitro-2-amino-l-phenol-4-sulfosäure und dem Monoazofarbstoff, erhalten durch saure Kupp lung von diazotierter Anthranilsäure mit 2 Amino-5-oxynaphthalin-7-sulfosäure, werden in 200 Teilen Wasser gelöst . und nach Zu gabe von etwas Ammoniak mit 1,25 Teilen CuS04 als Kupferoxydammoniaklösung wäh rend kurzer Zeit behandelt.
Der Farbstoff wird durch Essigsäure abgeschieden. Er wird neuerdings in 600 Teilen Wasser gelöst und mit 2,2 Teilen Cr20s als Fluorchromlösung rückfliessend gekocht, bis Chromierung erfolgt ist. Der Farbstoff wird, eventuell nach vor herigem Eindampfen, durch Salz abgeschieden.
Additional patent to main patent no. 145448. Process for the production of a new metal-containing dye. It has been found that a new metal-containing dye is obtained by using the disazo dye of the formula:
EMI0001.0005
by coupling diazotized anthranilic acid in an acidic medium with 2-amino-5-oxynaphthalene-7-sulfonic acid and the action of diazotized 6-nitro-2-amino-1-phenol-4-sulfonic acid on the resulting monoazo dye in alkaline Medium can be obtained treated with a copper and a chromium donating agent.
The metal-containing dye obtained is a dark-colored powder which dissolves in water with violet, in concentrated sulfuric acid with red-violet color and stains viscose in level, gray-violet tones. <I> Example: </I> 6.8 parts of the dye from diazotized 6-nitro-2-amino-1-phenol-4-sulfonic acid and the monoazo dye, obtained by acid coupling of diazotized anthranilic acid with 2 amino-5- oxynaphthalene-7-sulfonic acid are dissolved in 200 parts of water. and after adding a little ammonia, treated with 1.25 parts of CuS04 as a copper oxide ammonia solution for a short time.
The dye is deposited by acetic acid. It has recently been dissolved in 600 parts of water and refluxed with 2.2 parts of Cr20s as a fluorochrome solution until chromation has taken place. The dye is deposited by salt, possibly after prior evaporation.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH147698T | 1929-06-20 | ||
CH145448T | 1930-03-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147698A true CH147698A (en) | 1931-06-15 |
Family
ID=25714704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147698D CH147698A (en) | 1929-06-20 | 1929-06-20 | Process for the production of a new metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147698A (en) |
-
1929
- 1929-06-20 CH CH147698D patent/CH147698A/en unknown
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