CH147692A - Process for the preparation of a product which can be used as an azo dye component. - Google Patents
Process for the preparation of a product which can be used as an azo dye component.Info
- Publication number
- CH147692A CH147692A CH147692DA CH147692A CH 147692 A CH147692 A CH 147692A CH 147692D A CH147692D A CH 147692DA CH 147692 A CH147692 A CH 147692A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- product
- azo dye
- dye component
- preparation
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
'Verfahren zur Herstellung eines als Azofarbstoffkomponente verwendbaren Produktes. (xegenstand dieses Patentes ist ein Ver fahren zur Herstellung eines als Azofarbstoff- komponente verwendbaren Produktes, welches dadurch gekennzeichnet ist, dass man 1 . 5- Aminonaphtol in der Wärme mit Dicyandi- amid umsetzt.
Beispiel: 195 Gewichtsteile (1 Mol) salzsaures 1.5- Aminona.phtol werden zusammen mit 125 Gewichtsteilen Dicyandiamid in 500 cms Wasser ungefähr<B>10-15</B> Stunden erhitzt. Aus der mit Tierkohle behandelten Lösung erhält man das 5 - Oxynaphtalin-l-biguanidin als Chlorhydrat. Es kristallisiert aus Wasser in breiten, langen Nadeln vom Schmelzpunkt 216-2170. Es ist schwer löslich in Alkohol, Aceton, leicht in Wasser.
Die freie Base kristallisiert aus Wasser in kleinen Blättchen; sie ist leicht löslich in verdünnten Alkalien und heissem Wasser, sehr wenig in Äther. Sie schmilzt unter Aufblähen bei 143-144 .
Process for the preparation of a product which can be used as an azo dye component. (The subject of this patent is a process for the production of a product that can be used as an azo dye component, which is characterized in that 1,5-aminonaphthol is reacted with dicyandiamide under heat.
Example: 195 parts by weight (1 mol) of hydrochloric acid 1.5-aminona.phtol are heated together with 125 parts by weight of dicyandiamide in 500 cms of water for about 10-15 hours. The 5-oxynaphthalene-1-biguanidine is obtained as chlorohydrate from the solution treated with animal charcoal. It crystallizes from water in broad, long needles with a melting point of 216-2170. It is sparingly soluble in alcohol, acetone, slightly soluble in water.
The free base crystallizes from water in small flakes; it is easily soluble in dilute alkalis and hot water, very little in ether. It melts with puffing at 143-144.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147692X | 1928-10-19 | ||
CH145994T | 1929-10-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147692A true CH147692A (en) | 1931-06-15 |
Family
ID=25714783
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147692D CH147692A (en) | 1928-10-19 | 1929-10-11 | Process for the preparation of a product which can be used as an azo dye component. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147692A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6419976B1 (en) | 1997-09-02 | 2002-07-16 | Inland Empire Foods, Inc. | Bean-nut popping beans |
-
1929
- 1929-10-11 CH CH147692D patent/CH147692A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6419976B1 (en) | 1997-09-02 | 2002-07-16 | Inland Empire Foods, Inc. | Bean-nut popping beans |
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