CH182606A - 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
- CH182606A CH182606A CH182606DA CH182606A CH 182606 A CH182606 A CH 182606A CH 182606D A CH182606D A CH 182606DA CH 182606 A CH182606 A CH 182606A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitro
- amino
- diazotized
- phenol
- mol
- 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
- C09B45/32—Disazo or polyazo compounds containing other metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 178542. Verfahren zur Herstellung eines komplex. gebundenes Metall enthaltenden Farbstoffes. Es wurde gefunden, .dass man einen kom plex gebundenes Metall enthaltenden r'arb- stoff herstellen kann, wenn man 1 Mol diazo- tiertes 4-Nitro-2-amino-l-phenol, 1 Mol diazo- tierte 4-Nitro-2-amino-l-phenol-6-sulfonsäure, 1 Mol 1 .
3-Dioxybenzol und ein Eisen, sowie ein Nickel abgebendes Mittel aufeinander einwirken lässt.
Der erhaltene Farbstoff stellt ein in Wasser mit olivstichig brauner Farbe leicht lösliches, braunschwarzes Pulver dar. Er färbt aus ameisensaurem Bade vegetabilisch gegerbtes Leder oder aus neutralem Bade Chromleder in gelbstrohig olivbraunen, licht echten Tönen.
Das Verfahren kann beispielsweise derart ausgeführt werden, dass man auf das Ein wirkungsprodukt aus 1 Mol diazotiertem 4-Nitro-2-amino-l-phenol und 1 Mol 1. 3-Di- oxybenzol ein Eisen abgebendes Mittel, dann 1 Mol diazotierte 4-Nitro-2-amino-l-plienol- 6-sulfonsäure und hierauf ein Nickel ab- geberides Mittel einwirken lässt. Beispiel:
31,6 Teile der Eisenverbindung des Farb stoffes aus diazotiertem 4-Nitro-2-amino-l- pUenol und 1. 3-Dioxybenzol werden in 200 Teilen Wasser und 27 Teilen 30 % iger Natron lauge in der Kälte gelöst. und bei 10 bis<B>15'</B> mit der in üblicher Weise hergestellten und mit verdünnter Sodalösung neutralisierten Diazolösung aus 23,4 Teilen 4-Nitro-2-amino- 1-phenol-6-sulfonsäure vereinigt. Nach zehn bis zwölfstündigem Rühren ist die Kupplung beendet.
Man erwärmt auf<B>50',</B> versetzt mit 11,5 Teilen 30%iger Salzsäure, kocht auf und setzt eine Lösung von 15,4 Teilen Nickel sulfat in 60 Teilen Wasser hinzu. Nach zwei stündigem Kochen am Rückflusskühler schei det man den Farbstoff mit 100 Teilen ab, filtriert und trocknet bei mässiger Tempe ratur.
Additional patent to the main patent No. 178542. Process for the production of a complex. bonded metal containing dye. It has been found that a r'arbstoff containing complex bonded metal can be produced if 1 mol of diazotized 4-nitro-2-amino-1-phenol, 1 mol of diazotized 4-nitro-2 -amino-1-phenol-6-sulfonic acid, 1 mol 1.
3-Dioxybenzene and an iron, as well as a nickel-releasing agent, can act on one another.
The dye obtained is a brownish-black powder which is easily soluble in water with an olive-tinged brown color. It dyes vegetable-tanned leather from an acidic bath or chrome leather from a neutral bath in yellow-straw-like, olive-brown, light shades.
The process can, for example, be carried out in such a way that one mole of diazotized 4-nitro-2-amino-1-phenol and 1 mole of 1,3-dioxybenzene is an iron-releasing agent, then 1 mole of diazotized 4- Nitro-2-amino-1-plienol-6-sulfonic acid and then a nickel-releasing agent can act. Example:
31.6 parts of the iron compound of the dye from diazotized 4-nitro-2-amino-1-pUenol and 1,3-dioxybenzene are dissolved in 200 parts of water and 27 parts of 30% sodium hydroxide solution in the cold. and at 10 to 15 'with the diazo solution of 23.4 parts of 4-nitro-2-amino-1-phenol-6-sulfonic acid prepared in the usual way and neutralized with dilute soda solution. The coupling is complete after ten to twelve hours of stirring.
The mixture is heated to 50 ', 11.5 parts of 30% hydrochloric acid are added, the mixture is boiled and a solution of 15.4 parts of nickel sulfate in 60 parts of water is added. After boiling for two hours on the reflux condenser, 100 parts of the dye are separated off, filtered and dried at a moderate temperature.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH182606T | 1934-08-11 | ||
CH178542T | 1934-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH182606A true CH182606A (en) | 1936-02-15 |
Family
ID=25720165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH182606D CH182606A (en) | 1934-08-11 | 1934-08-11 | Process for the preparation of a complexed metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH182606A (en) |
-
1934
- 1934-08-11 CH CH182606D patent/CH182606A/en unknown
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