This compound combines with hydrocyanic acid to form a nitrile which hydrolyses to dichlorhydroxy iso-butyric acid.
A boiling solution of caustic potash hydrolyses it to ammonia and succinic acid.
Japaconitine, obtained from the Japanese aconites, known locally as "kuza-uzu," hydrolyses to japbenzaconine, which further breaks down to benzoic acid and japaconine.
Above), also known as diethylene diamine, may be prepared by reducing pyrazine, or, better, by combining aniline and ethylene bromide to form diphenyl diethylene diamine, the dinitroso compound of which hydrolyses to para-dinitrosophenol and pipera zine.
Zinc and hydrochloric acid in the cold convert it into alloxantin, hydroxylamine gives nitroso-barbituric acid, C 4 H 2 N 2 0 3: NOH, baryta water gives alloxanic acid, C 4 H 4 N 2 0 5, hot dilute nitric acid oxidizes it to parabanic acid, hot potassium hydroxide solution hydrolyses it to urea and mesoxalic acid and zinc and hot hydrochloric acid convert it into dialuric acid, C4H4N204.
Baryta water hydrolyses it to carbon dioxide, ammonia and urea.
Baryta water hydrolyses it to urea.
Moringa-tannin or maclurin, C1,H1006 H20, found in Morus tinctoria, hydrolyses on fusion with caustic potash to phloroglucin and protocatechuic acid.