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1.
J Forensic Sci ; 37(2): 513-27, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1500896

ABSTRACT

Common analytical methods used for identifying samples obtained from clandestine laboratories were evaluated for their ability to differentiate between possible amphetamine isomers and homologs. A series of ring-substituted (4-methyl, 4-methoxy, and 3,4-methylenedioxy) amphetamine and N-methylphenethylamine isomers was analyzed using color tests, thin-layer chromatography, gas chromatography/mass spectrometry (GC/MS) and GC/infrared (GC/IR). The N-acetyl derivatives of the isomers were analyzed using GC/IR/MS. GC/IR/MS readily differentiated the 4-methylphenylalkylamine isomers. MS and IR spectra were also obtained for each pair of the 4-methoxyphenylalkylamine isomers and the 3,4-methylenedioxyphenylalkylamine isomers, but differentiation via GC/IR/MS was difficult. The N-acetyl derivatives of each pair of isomers could be readily differentiated using GC/IR/MS. Good library researchable spectra for N-acetylamphetamine could be obtained for IR identification with 10 ng (on-column) and MS identification with 2 ng. The spectrometrically independent IR and MS data obtained for the N-acetyl derivatives indicated that the combination of GC/IR/MS can add a significant level of confidence in the analysis of ring-substituted arylalkylamines.


Subject(s)
Amphetamines/chemistry , Chromatography, Gas , Chromatography, Thin Layer , Gas Chromatography-Mass Spectrometry , Isomerism , Molecular Structure , Spectrophotometry, Infrared
5.
J Protozool ; 19(4): 551-2, 1972 Nov.
Article in English | MEDLINE | ID: mdl-4565845
7.
J Protozool ; 16(1): 1-5, 1969 Feb.
Article in English | MEDLINE | ID: mdl-4979862
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