Raman spectroscopy with far-red excitation has been used to study seized, t
ableted samples of MDMA (N-methyl-3,4-methylenedioxyamphetamine) and relate
d compounds (MDA, MDEA, MBDB, 2C-B and amphetamine sulfate), as well as pur
e standards of these drugs. We have found that by using far-red (785 nm) ex
citation the level of fluorescence background even in untreated seized samp
les is sufficiently low that there is little difficulty in obtaining good q
uality data with moderate 2 min data accumulation times. The spectra can be
used to distinguish between even chemically-similar substances, such as th
e geometrical isomers MDEA and MBDB, and between different polymorphic/hydr
ated forms of the same drug. Moreover, these differences can be found even
in directly recorded spectra of seized samples which have been bulked with
other materials, giving a rapid and non-destructive method for drug identif
ication. The spectra can be processed to give unambiguous identification of
both drug and excipients (even when more than one compound has been used a
s the bulking agent) and the relative intensities of drug and excipient ban
ds can be used for quantitative or at least semi-quantitative analysis. Fin
ally, the simple nature of the measurements lends itself to automatic sampl
e handling so that sample throughputs of 20 samples per hour can be achieve
d with no real difficulty.