CH183880A - Process for the preparation of a complexed metal-containing dye. - Google Patents
Process for the preparation of a complexed metal-containing dye.Info
- Publication number
- CH183880A CH183880A CH183880DA CH183880A CH 183880 A CH183880 A CH 183880A CH 183880D A CH183880D A CH 183880DA CH 183880 A CH183880 A CH 183880A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- parts
- phenol
- containing dye
- complexed 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/06—Disazo dyes in which the coupling component is a diamine or polyamine
-
- 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
- C09B45/32—Disazo or polyazo compounds containing other metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 182047. Verfahren zur Herstellung eines komplex gebundenes Metall enthaltenden Farbstoffes. Es wurde gefunden, dass man einen komplex gebundenes Metall enthaltenden Farbstoff her stellen kann, wenn man 1 Mol dianotiertes 4-Chlor-2-amirio-l-phenol, 1 Moi dianotierte 4-Nitro-2-amino-l-phenol-6-sulfonsäure, 1 Mol 1.3-Diaminobenzol und ein Eisen, sowie ein Nickel abgebendes Mittel aufeinander einwir ken lässt.
Der erhaltene Farbstoff stellt ein braun schwarzes Pulver dar, das sich in Wasser leicht mit violettstichig brauner Farbe löst und vegetabilisch- sowie chromgegerbtes Leder in echten dunkelbraunen Tönen färbt. <I>Beispiel:</I> 10,9 Teile 1.3-Diaminobenzol werden in 100 Teilen Wasser gelöst und mit Eis auf 0 0 gekühlt.
Dazu gibt man die aus 12,15 Teilen Fsrrichlorid, 7,0 Teilen Nickelsulfat kristalli- siert, 80 Teilen Wasser und 43 Teilen 80 %iger Natronlauge erhaltene Metallhydi-oxydsuspen- sion und hierauf weitere 13,
3 Teile 30 %ige Natronlauge. Zu der so erhaltenen und auf 3 0 abgekühlten Mischung lässt man die in üblicher Weise hergestellte und mit Soda neutralisierte Mischung der Diazolösungen aus 14,35 Teilen 4-Chlor-2-amino-l-phenol und 23,4 Teilen 4-Nitro-2-amino-l-phenol-6- sulfonsäure zulaufen. Man rührt 18-20 Stun den bei 10-18 0, nach welcher Zeit die Kupp lung beendigt ist. Hierauf wird das Reak tionsgemisch aufgekocht, wobei die sich bil dende Metallverbindung des Farbstoffes völlig in Lösung geht, und eine Stunde am Rück fluss im Sieden gehalten.
Der Farbstoff wird hierauf durch Zugabe von 150 Teilen Koch salz und 15 Teilen 30 0%iger Salzsäure ab geschieden, filtriert, abgepresst und bei mässiger Temperatur getrocknet.
<B> Additional patent </B> to main patent no. 182047. Process for the production of a complexed metal-containing dye. It has been found that a complex-bonded metal-containing dye can be produced by adding 1 mol of dianotated 4-chloro-2-amirio-l-phenol, 1 mol of dianotated 4-nitro-2-amino-l-phenol-6- sulfonic acid, 1 mole of 1,3-diaminobenzene and an iron, and a nickel-releasing agent can act on one another.
The dye obtained is a brown-black powder which dissolves easily in water with a purple-tinged brown color and dyes vegetable and chrome-tanned leather in real dark brown shades. <I> Example: </I> 10.9 parts of 1,3-diaminobenzene are dissolved in 100 parts of water and cooled to 0 ° with ice.
The metal hydroxide suspension obtained from 12.15 parts of ferric chloride, 7.0 parts of crystallized nickel sulfate, 80 parts of water and 43 parts of 80% strength sodium hydroxide solution are added, followed by a further 13,
3 parts of 30% sodium hydroxide solution. The mixture of 14.35 parts of 4-chloro-2-amino-1-phenol and 23.4 parts of 4-nitro-2, prepared in a conventional manner and neutralized with soda, is added to the mixture thus obtained and cooled to 30 -amino-l-phenol-6-sulfonic acid run in. The mixture is stirred for 18-20 hours at 10-18 0, after which time the coupling is completed. The reaction mixture is then boiled, the metal compound of the dye which forms being completely dissolved, and the mixture is kept boiling for one hour at reflux.
The dye is then separated out by adding 150 parts of sodium chloride and 15 parts of 30% strength hydrochloric acid, filtered, pressed off and dried at a moderate temperature.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH182047T | 1935-01-24 | ||
CH183880T | 1935-01-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH183880A true CH183880A (en) | 1936-04-30 |
Family
ID=25720649
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH183880D CH183880A (en) | 1935-01-24 | 1935-01-24 | Process for the preparation of a complexed metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH183880A (en) |
-
1935
- 1935-01-24 CH CH183880D patent/CH183880A/en unknown
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