CH182604A - 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
- CH182604A CH182604A CH182604DA CH182604A CH 182604 A CH182604 A CH 182604A CH 182604D A CH182604D A CH 182604DA CH 182604 A CH182604 A CH 182604A
- Authority
- CH
- Switzerland
- Prior art keywords
- phenol
- amino
- diazotized
- mole
- releasing agent
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 178542. Verfahren zur Herstellung eines komplex gebundenes Metall enthaltenden Farbstoffs. Es wurde gefunden, dass man einen kom plex gebundenes Metall enthaltenden Farb stoff herstellen kann, wenn man 1 Mol @diazo- tiertes 4-Nitro-2-amino-l-phenol, 1 Mol diazo- tierte 4-Chlor-2-amino-l-phenol-6-sulfonsäure, 1 Mol 1.
3-Dioxybenzol und ein Eisen, sowie ein Chrom abgebendes Mittel aufeinander einwirken lässt.
Der erhaltene Farbstoff stellt ein dunkel braunes Pulver dar, das sich in Wasser leicht mit bordeauroter und in konzentrierter Schwefelsäure mit schmutzig gelbroter Farbe löst. Er färbt vegetabilisch gegerbtes Leder in -,weinroten und chromgegerbtes Leder in violett- bis schokoladebraunen 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- Dioxybenzol ein Eisen abgebendes Mittel, dann 1 Mal diazotierte 4-Chlor-2-amino-l- phenol-6-sulfonsäure und hierauf ein Chrom abgebendes Mittel einwirken lässt. <I>Beispiel:
</I> 31,6 Teile der Eisenverbindung aus diazo- tiertem 4-Nitro-2-amino-l-phenol und 1.3- Dioxybenzol werden in 200 Teilen Wasser und 27 Teilen 30%iger Natronlauge kalt ge löst, hierauf mit .der neutralisierten Diazo- verbindung aus 22,3 Teilen 4-Chlor-2-amino- 1-phenol-6-sulfonsäure versetzt und bei 10 bis <B>18'</B> während 10 bis<B>12'</B> Stunden gerührt.
Nachdem die Kupplung beendet ist, wird aufgewärmt, bei<B>70'</B> mit 11,5 Teilen 30 % iger Salzsäure, .sowie kochend mit 60 Vol.-Teilen einer 15,2 Vol. % Cr_03 enthaltenden Chrom sulfatlösung versetzt und 24 Stunden am Rückfluss erhitzt. Hierauf lässt man ab kühlen, fällt .den Farbstoff durch Zugabe von 120 Teilen Kochsalz aus, filtriert und trocknet.
Additional patent to main patent no. 178542. Process for the preparation of a dye containing complexed metal. It has been found that you can produce a complexly bonded metal-containing dye if you 1 mol of @ diazo- tated 4-nitro-2-amino-1-phenol, 1 mol of diazo- tated 4-chloro-2-amino- l-phenol-6-sulfonic acid, 1 mole 1.
3-Dioxybenzene and an iron, as well as a chromium-releasing agent, can act on one another.
The dye obtained is a dark brown powder which dissolves easily in water with a reddish red color and in concentrated sulfuric acid with a dirty yellowish red color. It dyes vegetable-tanned leather in -, wine-red and chrome-tanned leather in real shades of purple to chocolate brown.
The process can, for example, be carried out in such a way that an iron-releasing agent is applied to the product of 1 mol of diazotized 4-nitro-2-amino-1-phenol and 1 mol of 1,3-dioxybenzene, then 4-chloro-2- amino-1-phenol-6-sulfonic acid and then a chromium-releasing agent can act. <I> example:
</I> 31.6 parts of the iron compound from diazotized 4-nitro-2-amino-1-phenol and 1,3-dioxybenzene are dissolved cold in 200 parts of water and 27 parts of 30% sodium hydroxide solution, then neutralized with .der Diazo compound of 22.3 parts of 4-chloro-2-amino-1-phenol-6-sulfonic acid was added and at 10 to 18 'for 10 to 12' hours touched.
After the coupling has ended, the mixture is warmed up, mixed with 11.5 parts of 30% hydrochloric acid at <B> 70 '</B> and, while boiling, with 60 parts by volume of a chromium sulfate solution containing 15.2% by volume of Cr_03 and refluxed for 24 hours. It is then allowed to cool, the dye is precipitated by adding 120 parts of sodium chloride, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH178542T | 1934-08-11 | ||
CH182604T | 1934-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH182604A true CH182604A (en) | 1936-02-15 |
Family
ID=25720163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH182604D CH182604A (en) | 1934-08-11 | 1934-08-11 | Process for the preparation of a complexed metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH182604A (en) |
-
1934
- 1934-08-11 CH CH182604D patent/CH182604A/en unknown
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