Di-(<i>β</i>-Phenylisopropyl)amine in Illicit Amphetamine
Journal of Forensic SciencesPublished 1 April 1985
H. Huizer, Helmut Brussee, AJ Poortman-van der Meer
Citations23
SJR quartileQ2
SJR score0.62
SNIP1.10
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TL;DR
Di-(β-phenylisopropyl)amine formation during the Leuckart synthesis is discussed; the role of the compound in the comparison of illicit amphetamine samples is discussed.
Abstract
Abstract Illicit amphetamine samples frequently contain di-(β-phenylisopropyl)amine as a main impurity. Its formation during the Leuckart synthesis is discussed. A method for synthesis is given. Special attention is given to its stereoisomerism. Analytical data are presented; the role of the compound in the comparison of illicit amphetamine samples is discussed.
Keywords
NeurosciencePharmacology, Toxicology and Pharmaceutics
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