2000
DOI: 10.1016/s0926-2040(00)00071-0
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High-resolution solid state 13C nuclear magnetic resonance spectra of 3,4-methylenedioxyamphetamine hydrochloride and related compounds and their mixtures with lactose

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Cited by 13 publications
(4 citation statements)
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“…These are α,α′-dimethyldiphenethylamine and N ,α,α′-trimethyldiphenethylamine. These two impurities were originally associated with the Leuckart method in the 1970’s (by Barron et al, 18 and Kram and Kreugal 1 ), but it was not possible at that time to preclude them from being formed by other synthetic methods. In the present study, these two impurities were only identified in the samples synthesized by the Leuckart method.…”
Section: Resultsmentioning
confidence: 99%
“…These are α,α′-dimethyldiphenethylamine and N ,α,α′-trimethyldiphenethylamine. These two impurities were originally associated with the Leuckart method in the 1970’s (by Barron et al, 18 and Kram and Kreugal 1 ), but it was not possible at that time to preclude them from being formed by other synthetic methods. In the present study, these two impurities were only identified in the samples synthesized by the Leuckart method.…”
Section: Resultsmentioning
confidence: 99%
“…The solid‐state 13 C NMR analysis of several amphetamines and their mixtures with lactose monohydrate have been reported 144. The lactose monohydrate mixture of one amphetamine (3,4‐methylenedioxyamphetamine hydrochloride) produced distinct chemical shift differences for the amphetamine resonances, and the authors attribute the changes to relaxed crystal packing forces rather than hydrogen bonding.…”
Section: Pharmaceutical Applicationsmentioning
confidence: 99%
“…One of the most important advantages is that NMR can quickly and accurately provide a wealth of structural information about compounds without destroying the properties of the compound [ 14 , 15 ]. Recently, both liquid and solid NMR instruments have been used to study illicit drugs [ 16 19 ].…”
Section: Introductionmentioning
confidence: 99%