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Imidazole, heptafluorobutyryl

Procedures based on GC/MS for the determination of the lewisite 1 decomposition product 2-chlorovinylarsonous acid (CVAA, CAS number 85090-33-1) in urine and blood have also been developed. In one procedure, CVAA is converted with BAL the resulting CVAA/BAL product isolated by SPE on a C18-cartridge and further derivatized with heptafluorobutyryl imidazole (51). A later developed procedure is based on the derivatization of CVAA with 1,3-propanedithiol followed by SPME isolation and GC/MS analysis. Using SIM at the molecular ion peaks, the limit of detection was determined at 7.4 pg per ml urine (52). [Pg.276]

Use. For glpc separation of catecholamines. Horning et at.1 converted these substances first into the trimethylsilyl ethers by reaction with trimethylsilyl-imidazole in acetonitrile acylation of primary and secondary groups was then effected by addition of N-heptafluorobutyrylimidazole. The resulting trimethylsilyl ether-heptafluorobutyryl (TMSi-HFB) derivatives were found to have excellent glpc properties.1... [Pg.77]


See other pages where Imidazole, heptafluorobutyryl is mentioned: [Pg.1030]    [Pg.413]    [Pg.173]    [Pg.1030]    [Pg.1030]    [Pg.272]    [Pg.454]    [Pg.1021]    [Pg.1030]    [Pg.413]    [Pg.173]    [Pg.1030]    [Pg.1030]    [Pg.272]    [Pg.454]    [Pg.1021]    [Pg.77]   
See also in sourсe #XX -- [ Pg.173 ]




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