crystalline base
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2017 ◽  
Vol 476 (1) ◽  
pp. 973-977
Author(s):  
Z. G. Badredinov ◽  
B. A. Markovskii ◽  
E. A. Nozdrachev ◽  
I. V. Matyushkin ◽  
I. V. Grinkevich

1971 ◽  
Vol 13 (4) ◽  
pp. 491-499
Author(s):  
V.I. Kazanskiy ◽  
V.A. Krupennikov ◽  
Yu.A. Rozanov
Keyword(s):  

1938 ◽  
Vol 16b (2) ◽  
pp. 57-60 ◽  
Author(s):  
Richard H. F. Manske

Delphinium brownii contains a total of 0.5% of alkaloids, hydrolysis of which yields a crystalline base, probably C22H37O7N or C23H39O7N, together with anthranilic and methylsuccinic acids. Mannitol is present in considerable amounts.


1859 ◽  
Vol 9 ◽  
pp. 229-231

In a former Note addressed to the Royal Society (Proceedings, vol. ix. p. 150), I have alluded to some [new alkaloids which are pro­duced by the action of the bromides of triatomic alcohols upon the primary amidogen bases. I have since examined more minutely one of these bodies. At the common temperature, chloroform and aniline may be left in contact for a considerable time without any change becoming perceptible. Even at the temperature of boiling water scarcely any reaction takes place. But on exposing for ten or twelve hours a mixture of about equal volumes of chloroform and aniline in sealed tubes to a tem­perature of 180° or 190° C., a hard brown crystalline mass is ob­tained, which consists chiefly of the hydrochlorates of aniline and of a new crystalline base.


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