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Synthesis of 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-methylhydrazino-2,1,3-benzoxadiazole (DAABD-MHz) as a derivatization reagent for aldehydes in liquid chromatography/electrospray ionization–tandem mass spectrometry

✍ Scribed by Tomofumi Santa; Osama Y Al-Dirbashi; Tomoko Ichibangase; Mohamed S Rashed; Takeshi Fukushima; Kazuhiro Imai


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
159 KB
Volume
22
Category
Article
ISSN
0269-3879

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✦ Synopsis


Abstract

Benzofurazan derivatization reagent, 4‐[2‐(N,N‐dimethylamino)ethylaminosulfonyl]‐7‐N‐methylhydrazino‐2,1,3‐benzoxadiazole (DAABD‐MHz), for aldehydes in liquid chromatography/electrospray ionization–tandem mass spectrometry (LC/ESI‐MS/MS), was synthesized. DAABD‐MHz reacted with aliphatic aldehydes under mild conditions. The generated derivatives were separated on a reversed‐phase column and detected by ESI‐MS/MS with detection limits of 30–60 fmol on‐column. Upon collision‐induced dissociation, a single and intense fragment ion at m/z 151 was observed. These results suggested that DAABD‐MHz was suitable as a derivatization reagent in LC/ESI‐MS/MS. Copyright © 2007 John Wiley & Sons, Ltd.


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