Challenges in the identification process of phenidate analogues in LC-ESI-MS/MS analysis: Information enhancement by derivatization with isobutyl chloroformate.
LC-ESI-MS/MS
derivatization
isobutyl chloroformate
phenidate analogues
structural elucidation
Journal
Journal of mass spectrometry : JMS
ISSN: 1096-9888
Titre abrégé: J Mass Spectrom
Pays: England
ID NLM: 9504818
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
received:
06
11
2018
revised:
19
12
2018
accepted:
19
12
2018
pubmed:
1
1
2019
medline:
1
1
2019
entrez:
1
1
2019
Statut:
ppublish
Résumé
A new analytical technique for the structural elucidation of four representative phenidate analogues possessing a secondary amine residue, which leads to a major/single amine-representative fragment/product ion at m/z 84 both in their GC-EI-MS and LC-ESI-MS/MS spectra, making their identification ambiguous, was developed. The method is based on "in vial" chemical derivatization with isobutyl chloroformate in both aqueous and organic solutions, followed by liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS/MS). The resulting carbamate derivatives promote rich fragmentation patterns with full coverage of all substructures of the molecule, enabling detailed structural elucidation and unambiguous identification of the original compounds at low ng/mL levels.
Types de publication
Journal Article
Langues
eng
Pagination
266-273Informations de copyright
© 2018 John Wiley & Sons, Ltd.