CH223538A - Process for the preparation of a new hydrazine derivative. - Google Patents
Process for the preparation of a new hydrazine derivative.Info
- Publication number
- CH223538A CH223538A CH223538DA CH223538A CH 223538 A CH223538 A CH 223538A CH 223538D A CH223538D A CH 223538DA CH 223538 A CH223538 A CH 223538A
- Authority
- CH
- Switzerland
- Prior art keywords
- hydrazine derivative
- preparation
- new
- new hydrazine
- acid
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Hydrazinderivates. Es wurde gefunden, dass man zu einem neuen Hydrazinderivat gelangt, wenn man 1 Mol techn. Stearinsäure mit etwa 1 Mol ss,ss-Di-( oxäthyl)-hydrazin umsetzt.
Die Umsetzung wird zweckmässig bei höherer Temperatur, z. B. bei 160 bis<B>180</B> , vorteilhaft in Gegenwart von Borsäure und -unter Ausschluss von Sauerstoff, vorgenom men.
Das neue Hydrazinderivat ist eine bräun lich gefärbte, halbfeste Masse, die schwach kationaktive Eigenschaften besitzt und die von Wasser zu einer schwach getrübten, gegen Säure beständigen Lösung aufgenom men wird. Es kann als Textilhilfsstoff, z. B. als Weichmachungsmittel, angewendet wer den.
<I>Beispiel:</I> 12 Gewichtsteile ss,ss-Di-(oxäthyl)-hydra- zin (hergestellt aus Äthylenoxyd und Hy- drazinhydrat) werden mit 27 Gewichtsteilen techn. Stearinsäure und 1,2 Gewichtsteilen Borsäure während 2 Stunden unter Aus schluss von Sauerstoff bei gleichzeitigem Rühren auf 160 bis 180 erhitzt, wobei die der Theorie entsprechende Menge Wasser ab- destilliert.
Es resultiert eine bräunlich ge färbte, halbfeste Masse, die sich in Wasser mit nur schwacher Trübung löst und deren wässerige Lösung auch auf Zusatz von Säu- ; ren nicht gefällt wird. Das Produkt besitzt schwach kationaktive Eigenschaften.
Process for the preparation of a new hydrazine derivative. It has been found that a new hydrazine derivative is obtained if 1 mole of techn. Reacts stearic acid with about 1 mol of ss, ss-di (oxethyl) hydrazine.
The reaction is conveniently carried out at a higher temperature, e.g. B. at 160 to <B> 180 </B>, advantageously in the presence of boric acid and in the absence of oxygen, vorgenom men.
The new hydrazine derivative is a brownish colored, semi-solid mass which has weakly cationic properties and which is taken up by water to form a slightly cloudy, acid-resistant solution. It can be used as a textile auxiliary, e.g. B. as a plasticizer, who applied the.
<I> Example: </I> 12 parts by weight of ss, ss-di (oxethyl) hydrazine (made from ethylene oxide and hydrazine hydrate) are combined with 27 parts by weight of techn. Stearic acid and 1.2 parts by weight of boric acid are heated to 160 to 180 for 2 hours with exclusion of oxygen while stirring, the amount of water corresponding to theory being distilled off.
The result is a brownish-colored, semi-solid mass which dissolves in water with only slight turbidity and whose aqueous solution also reacts to the addition of acid; ren is not liked. The product has weakly cationic properties.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH223538T | 1940-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH223538A true CH223538A (en) | 1942-09-30 |
Family
ID=4453067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH223538D CH223538A (en) | 1940-12-24 | 1940-12-24 | Process for the preparation of a new hydrazine derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH223538A (en) |
-
1940
- 1940-12-24 CH CH223538D patent/CH223538A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH223538A (en) | Process for the preparation of a new hydrazine derivative. | |
DE588650C (en) | Process for the preparation of oxydiphenyl ether carboxylic acids | |
CH223211A (en) | Process for the preparation of a new hydrazine derivative. | |
DE861608C (en) | Process for the production of condensation products | |
CH177456A (en) | Process for the preparation of an amine oxide. | |
DE679341C (en) | Process for the production of resinous condensation products from nitrogen-containing heterocyclic compounds and low molecular weight aldehydes of the fatty series | |
AT152741B (en) | Process for the preparation of formaldehyde sodium sulfoxylates from arsenobenzene compounds. | |
AT133505B (en) | Process for the preparation of ω-Oxyacylaminobenzolarsin- or -stibinoxden or ω-Oxyacylaminobenzolarsin- or -stibinsäuren. | |
CH162292A (en) | Process for the preparation of the salt of 2. 3-Dimethoxy-6-nitro-9- (γ-diethylamino-B-oxypropylamino) acridine with p-glycolylaminobenzenic acid. | |
CH210982A (en) | Process for the production of a new condensation product. | |
CH236163A (en) | Process for the production of a polyether. | |
CH223213A (en) | Process for the preparation of a new hydrazine derivative. | |
CH220404A (en) | Process for the preparation of a new derivative of a heterocyclic compound. | |
CH206357A (en) | Process for the production of a new textile auxiliary. | |
CH169578A (en) | Process for the preparation of the salt of 2,3-dimethoxy-6-nitro-9- (Y-diethylamino-B-oxy-propylamino) -acridine with p-glycolylaminobenzolaric acid. | |
CH239207A (en) | Process for the preparation of a new sulfamic acid derivative. | |
CH252071A (en) | Process for the preparation of a new amide derivative. | |
CH182592A (en) | Process for the preparation of an amine oxide. | |
CH191847A (en) | Process for the preparation of ethyleneimine. | |
CH213419A (en) | Process for the production of a new condensation product. | |
CH234719A (en) | Process for the production of a polyether. | |
CH231842A (en) | Process for the preparation of a basic compound. | |
CH223030A (en) | Process for the production of a condensation product. | |
CH189136A (en) | Process for the production of a new textile auxiliary. | |
CH205062A (en) | Process for the preparation of a quaternary nitrogen compound. |