Role of Five Synthetic Reaction Conditions on the Stable Isotopic Composition of 3,4-Methylenedioxymethamphetamine

被引:20
作者
Buchanan, Hilary A. S. [1 ]
Daeid, Niamh Nic [1 ]
Kerr, William J. [1 ]
Carter, James F. [2 ]
Hill, Jenny C. [2 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, Ctr Forens Sci, Glasgow G1 1WX, Lanark, Scotland
[2] Mass Spec Analyt Ltd, Bristol BS99 7AR, Avon, England
基金
英国工程与自然科学研究理事会;
关键词
HEROIN; C-13; TOOL; ECSTASY; SAMPLES; ANALOGS; MDMA; 3,4-METHYLENEDIOXYAMPHETAMINE; AMPHETAMINES; TABLETS;
D O I
10.1021/ac1002432
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The identification of links between seizures of illicit 3,4methylenedioxymethamphetamine (MDMA or "ecstasy") has been a global target of law enforcement agencies in recent years. Previous work has shown that, when the reaction conditions are carefully repeated from batch to batch, stable isotope ratios allow the discrimination of MDMA.HCI batches according to synthetic route used for manufacture. In this study, the effects of altering five reaction conditions relating to the Pt/H-2 reductive amination synthesis were, for the first time, systematically investigated using a two level, five factor factorial design. Results indicate that the (delta H-2 values of MDMA. HCI are affected by the length of imine stir time, and the (delta N-15 values are affected by the degree of excess methylamine employed. Furthermore, the (delta C-13 and (5180 values have been shown to be affected by the efficiency of the reaction, despite the similarity in carbon and oxygen composition of the starting material and product molecules. In addition to being of theoretical importance in this field of analytical science overall, this work is essential in order to more fully contextualize the interpretation of IRMS data which may be used as potential forensic evidence.
引用
收藏
页码:5484 / 5489
页数:6
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