The thermal decomposition of methylphenidate in the gas chromatograph mass spectrometer
β Scribed by B. L. Flamm; J. Gal
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 284 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
β¦ Synopsis
Methylphenidate undergoes partial thermal decomposition in the injection port of a gas chromatograph. This decomposition explaiqs inconsistencies in some of the previously published mass spectra of the drug. The decomposition products were identified by gas chromatography mass spectrometry as methyl phenylacetate and a tetrahydropyridine. The extent of decomposition was found to be a function of the injector temperature and was also influenced by other factors, resulting in considerable variability. The ethyl ester analog behaved similarly. Derivatization with trifluoroacetic anhydride eliminates the thermal decomposition.
π SIMILAR VOLUMES
## Abstract The cyclic sulfenic ester 1,2βoxathiolane (**1**) decomposes thermally (400 β 450 K) exclusively to give acrolein (**3**) __via__ 3βmercaptopropanal (**2**) by loss of hydrogen sulfide. Isotopic labelling experiments reveal the presence of a 1,2βoxathiolaneβthietane 1βoxide equilibrium
An on-line, solid-phase extraction gas chromatography/mass spectrometry method for the automated pretreatment of biological fluids is proposed. Several drugs of abuse were used as model compounds. The analytes are trapped on a home-made RP-C 18 column and subsequently eluted with chloroform. The fra
An increasing amount of evidence is accumulating to support the proposal that steroidogenesis can occur by a sesterterpene pathway as well as the cholesterol pathway. Key intermediates on the sesterterpene pathway are 23,24-dinor-5-cholen-3~ol (guneribol) and some of its metabolites, e.g. 23,24dinor