CH167047A - Process for the production of a metal-containing dye. - Google Patents
Process for the production of a metal-containing dye.Info
- Publication number
- CH167047A CH167047A CH167047DA CH167047A CH 167047 A CH167047 A CH 167047A CH 167047D A CH167047D A CH 167047DA CH 167047 A CH167047 A CH 167047A
- Authority
- CH
- Switzerland
- Prior art keywords
- bluish
- containing dye
- metal
- production
- nitro
- 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
- C09B45/22—Monoazo compounds containing other metals
Description
Zusatzpatent zum Hauptpatent Nr. <B>165155.</B> Verfahren zur Herstellung eines metallhaltigen Farbstoffes. Es wurde gefunden, dass man einen me tallhaltigen Farbstoff durch Behandeln des Azofarbstoffes aus diazotiertern <B>5 -</B> Nitro <B>-</B> 2- amiiio-l-phenol und 1-Phenyl-3-methyl-5-pyra- zolon mit ehrom- und aluminiumabgebenden Mitteln in alkalischem Medium erhalten kann, wenn diese Behandlung in Gegenwart von Salzen der Weinsäure erfolgt.
Der erhaltene ehrom- und aluminiumhal tige Farbstoff stellt ein blaurotes Pulver dar, das sich in Alkohol mit blaustichigroter Farbe löst und aus einer Lösung in Nitro- oder Ace- tylzelluloselack auf geeigneten Unterlagen lichtechte blaustichig rote Überzüge gibt.
<I>Beispiel:</I> 34 Teile des Farbstoffes aus diazotiertem 5-Nitro-2-amino-l-pheriol und 1-Phenyl-3- methyl-5-pyrazolon werden in<B>500</B> Teilen Wasser und 16 Teilen Natronlauge von 80 % aufgesehlämmt undbei650 miteinerLösung von<B>16</B> Teilen kristallisiertem Chromisulfat, <B>6,
8</B> Teilen kristallisiertem Aluminiumsulfat, <B>30</B> Teilen Weinsäure,<B>70</B> Teilen Wasser und <B>100</B> Teilen Natronlauge versetzt. Man erwärmt zum Kochen und hält während<B>18</B> Stunden unter Rückfluss im Sieden. Hierauf wird mit verdünnter Ameisensäure lakintissatter gestellt, filtriert, ausgewaschen und bei mässiger Tem- 0 peratur getrocknet.
Additional patent to main patent no. <B> 165155. </B> Process for the production of a metal-containing dye. It has been found that a metal-containing dye can be obtained by treating the azo dye from diazotized <B> 5 - </B> nitro <B> - </B> 2- amiiio-1-phenol and 1-phenyl-3-methyl- 5-pyrazolone can be obtained with ethyl and aluminum releasing agents in an alkaline medium if this treatment is carried out in the presence of salts of tartaric acid.
The chromium- and aluminum-containing dye obtained is a bluish-red powder which dissolves in alcohol with a bluish-tinged red color and, from a solution in nitro or acetyl cellulose lacquer, gives light-fast bluish-tinged red coatings on suitable substrates.
<I> Example: </I> 34 parts of the dye from diazotized 5-nitro-2-amino-1-pheriol and 1-phenyl-3-methyl-5-pyrazolone are in <B> 500 </B> parts of water and 16 parts of 80% sodium hydroxide solution and at650 with a solution of <B> 16 </B> parts of crystallized chromium sulfate, <B> 6,
8 parts of crystallized aluminum sulfate, 30 parts of tartaric acid, 70 parts of water and 100 parts of sodium hydroxide solution are added. The mixture is heated to the boil and refluxed for <B> 18 </B> hours. Then lacintissatter is made with dilute formic acid, filtered, washed out and dried at moderate temperature.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH167047T | 1932-07-22 | ||
CH165155T | 1933-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167047A true CH167047A (en) | 1934-01-31 |
Family
ID=25718080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167047D CH167047A (en) | 1932-07-22 | 1932-07-22 | Process for the production of a metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167047A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2698096A1 (en) * | 1992-11-19 | 1994-05-20 | Solvay | Complexes of a heavy metal and aluminum, their preparation and their use as colorants. |
US5731422A (en) * | 1991-09-05 | 1998-03-24 | Clariant Finance (Bvi) Limited | 2:1 Aluminum complexes of monoazo compounds |
DE4228572B4 (en) * | 1991-09-05 | 2006-03-30 | Clariant Finance (Bvi) Ltd. | 2: 1 aluminum complex dyes |
-
1932
- 1932-07-22 CH CH167047D patent/CH167047A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5731422A (en) * | 1991-09-05 | 1998-03-24 | Clariant Finance (Bvi) Limited | 2:1 Aluminum complexes of monoazo compounds |
DE4228572B4 (en) * | 1991-09-05 | 2006-03-30 | Clariant Finance (Bvi) Ltd. | 2: 1 aluminum complex dyes |
FR2698096A1 (en) * | 1992-11-19 | 1994-05-20 | Solvay | Complexes of a heavy metal and aluminum, their preparation and their use as colorants. |
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