Determination of 3,4-methylenedioxyamphetamine analogues (“ecstasy”) by proton nuclear magnetic resonance spectrometry

1997 ◽  
Vol 339 (3) ◽  
pp. 259-263 ◽  
Author(s):  
D.Thorburn Burns ◽  
Robert J. Lewis ◽  
P. Stevenson
1996 ◽  
Vol 79 (4) ◽  
pp. 823-828 ◽  
Author(s):  
Jon Beihoffer ◽  
Ed Bour ◽  
Joe H Lowry ◽  
John J Reschl ◽  
Jivbmy L Seidel ◽  
...  

Abstract Proton nuclear magnetic resonance spectrometry (1H NMR) was used to identify and quantitate the 4 isomeric bromo- and/or chloro-substituted 1,3-dihalo-5,5-dimethylhydantoins in technical-grade materials used to prepare commercial disinfectants and molluscicides. We found that the technical grades of bromo/chloro-substituted 1,3-dihalo-5,5-dimethylhydantoins are mixtures of the 4 possible isomers, that interconversion among isomers occurs in solution and can be detected by 1H NMR, and that isomer interconversion occurs over times greater than those of the NMR timescale.


Sign in / Sign up

Export Citation Format

Share Document