CH183882A - 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
- CH183882A CH183882A CH183882DA CH183882A CH 183882 A CH183882 A CH 183882A CH 183882D A CH183882D A CH 183882DA CH 183882 A CH183882 A CH 183882A
- Authority
- CH
- Switzerland
- Prior art keywords
- parts
- amino
- containing dye
- nitro
- phenol
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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-Nitro-2-amino-l-phenol, 1 Mol dianotierte 4-Niti-o-2-amino-l-plienol-6-sulfonsäui,e, 1 Mol 1-Methyl-2.4-diaminobenzol und ein Eisen, sowie ein Kupfer abgebendes Mittel aufein ander einwirken lässt.
Der erhaltene Farbstoff stellt ein schwarzes Pulver dar, das sich in Wasser mit schwärz lich brauner Farbe löst. Es färbt chromge gerbtes Leder aus neutralem Bade in echten dunkelbraunen Tönen.
<I>Beispiel:</I> 12,3 Teile 1-Methyl-2.4-diaininobenzol werden in 100 Teilen Wasser gelöst, mit Eis auf 3 0 abgekühlt und mit einer Metall hydroxydsuspension aus 12,1"o Teilen Ferri- chlorid, 6,25 Teilen Kupfersulfat kristallisiert, 60 Teilen Wasser und 43 Teilen 30 %igei, Natronlauge, versetzt.
Hierauf fügt man weitere 13,3 Teile 30 %ige Natronlauge zu und die in üblicher Weise erhaltene und mit Soda neutralisierte Diazomischung aus 15,4 Teilen 4-Nitro-2-amino-l-phenol und 23,4 Teilen 4-Nitro-2-amino-l-phenol-6-sulfonsäure. Man kuppelt während 24 Stunden bei 10-200, kocht hierauf auf, hält eine Stunde im Kochen und fällt die gebildete Metallverbindung mit 100 Teilen Kochsalz und 13,
8 Teilen 300/öiger Salzsäure, filtriert und trocknet bei mässiger Temperatur oder im Vakuum.
<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 if 1 mole of dianotated 4-nitro-2-amino-1-phenol, 1 mole of dianotated 4-nitri-o-2-amino-l-plienol- 6-sulfonsäui, e, 1 mole of 1-methyl-2,4-diaminobenzene and an iron and a copper-releasing agent can act on one another.
The dye obtained is a black powder which dissolves in water with a blackish brown color. It dyes chrome-tanned leather from neutral bath in real dark brown tones.
<I> Example: </I> 12.3 parts of 1-methyl-2,4-diaininobenzene are dissolved in 100 parts of water, cooled to 30 with ice and treated with a metal hydroxide suspension of 12.1 parts of ferric chloride, 6 , 25 parts of copper sulfate crystallized, 60 parts of water and 43 parts of 30% strength sodium hydroxide solution were added.
A further 13.3 parts of 30% strength sodium hydroxide solution are then added, and the diazo mixture of 15.4 parts of 4-nitro-2-amino-1-phenol and 23.4 parts of 4-nitro-2, obtained in the usual way and neutralized with soda, is added -amino-1-phenol-6-sulfonic acid. You couple for 24 hours at 10-200, then boil, keep boiling for an hour and precipitate the metal compound formed with 100 parts of table salt and 13,
8 parts of 300 / o hydrochloric acid, filtered and dried at moderate temperature or in vacuo.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH182047T | 1935-01-24 | ||
CH183882T | 1935-01-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH183882A true CH183882A (en) | 1936-04-30 |
Family
ID=25720651
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH183882D CH183882A (en) | 1935-01-24 | 1935-01-24 | Process for the preparation of a complexed metal-containing dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH183882A (en) |
-
1935
- 1935-01-24 CH CH183882D patent/CH183882A/en unknown
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