CH145847A - Process for the production of a metal-containing dye. - Google Patents
Process for the production of a metal-containing dye.Info
- Publication number
- CH145847A CH145847A CH145847DA CH145847A CH 145847 A CH145847 A CH 145847A CH 145847D A CH145847D A CH 145847DA CH 145847 A CH145847 A CH 145847A
- Authority
- CH
- Switzerland
- Prior art keywords
- violet
- metal
- dye
- iron
- production
- 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
- C09B45/22—Monoazo compounds containing other metals
-
- 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)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 141635. Verfahren zur Herstellung eines metallhaltigen Farbstoffes. Es wurde gefunden, dass man einen neuen metallhaltigen Farbstoff erhält, wenn man den Farbstoff aus diazotiertem 4-Chlor- 2-amino-l-phenol und ss-Naphthylamin mit einem eisen- und kobalthaltigen Produkt,
das durch Einwirkung einer hydroxylgruppen- haltigen organischen Verbindung auf Eisen- und Kobaltverbindungen in Gegenwart von Alkalien erhalten wird, behandelt.
Der metallhaltige Farbstoff ist in Was ser oder Na..ronlauge unlöslich. In konzen trierter Schwefelsäure löst er sich mit violet- l er, in organischen Lösungsmitteln mit braunvioletter Farbe. Aus einer Lösung in Zaponlack erhält man auf geeigneten Unter lagen je nach der Konzentration braunstichig violette bis schwarzviolette Überzüge.
<I>Beispiel:</I> ,l> 5,95 Teile des Farbstoffes aus diazotier- tem 4-Chlor-2-amino-l-phenol und ss-Naph- thylamin werden in 5,00 Teilen Wasser und 1.0 Teilen Natronlauge von 36 B6 aufge- kocht und mit einer aus 2,6 Teilen Eisen chlorid, 0,95 Teilen kristallisiertem Kobalt- chlorid, 50 Teilen Wasser, i Teilen Glycerin und 20 Teilen Natronlauge erhaltenen 11Ie- tallhydroxydlösung zwei Stunden am Rück fluss im Sieden gehalten.
Hierauf wird der ausgeschiedene Farbstoff abfiltriert, ausge waschen und getrocknet.
Ein gleiches Endprodukt wird erhalten, wenn statt Glycerin andere hydroxylgrup- penhaltige organische Verbindungen, wie Glykol, Tannin, Gallussäure, Zuckerarten, Kohlenhydrate, verwendet werden.
Additional patent to main patent no. 141635. Process for the production of a metal-containing dye. It has been found that a new metal-containing dye is obtained if the dye is obtained from diazotized 4-chloro-2-amino-1-phenol and ß-naphthylamine with an iron and cobalt-containing product,
which is obtained by the action of an organic compound containing hydroxyl groups on iron and cobalt compounds in the presence of alkalis.
The metal-containing dye is insoluble in water or sodium hydroxide solution. In concentrated sulfuric acid it dissolves with violet color, in organic solvents with brownish-violet color. From a solution in Zapon lacquer, brownish violet to black violet coatings are obtained on suitable substrates, depending on the concentration.
<I> Example: </I>, l> 5.95 parts of the dye from diazotized 4-chloro-2-amino-1-phenol and ß-naphthylamine are dissolved in 5.00 parts of water and 1.0 part of sodium hydroxide solution of 36 B6 are boiled up and boiled under reflux for two hours with a metal hydroxide solution obtained from 2.6 parts of iron chloride, 0.95 parts of crystallized cobalt chloride, 50 parts of water, 1 part of glycerol and 20 parts of sodium hydroxide solution.
The precipitated dye is then filtered off, washed out and dried.
The same end product is obtained if, instead of glycerine, other organic compounds containing hydroxyl groups, such as glycol, tannin, gallic acid, sugars, carbohydrates, are used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH145847T | 1928-10-05 | ||
CH141535T | 1929-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH145847A true CH145847A (en) | 1931-03-15 |
Family
ID=25713801
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH145847D CH145847A (en) | 1928-10-05 | 1928-10-05 | Process for the production of a metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH145847A (en) |
-
1928
- 1928-10-05 CH CH145847D patent/CH145847A/en unknown
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