| Literature DB >> 17027999 |
Veeravagu Murugaiah1, Abdul Naim, Shiqi Peng, Guohui Cui, Roger W Giese.
Abstract
Commercially-available 4,4'-dimethyloctafluorobiphenyl was converted in a single step to 4-(4'-methyltetrafluorophenyl)-2,3,5,6-tetrafluorobenzyl bromide (MTFP-TFBBr) for the purpose of providing a new electrophoric derivatizing reagent. When reacted with this reagent, 2-fluoro-O6-(2'-hydroxyethyl)hypoxanthine, a model analyte, gave a mixture of isomeric products (apparently substituted at N7 and N9, analogous to its known reaction with pentafluorobenzyl bromide), and 53 femtograms of the mixture was detected at S/N = 10 by gas chromatography electron capture mass spectrometry (GC-EC-MS). As intended, the volatility of the MTFB-TFBBr derivative was much less (two-fold) than that of the corresponding pentafluorobenzyl derivative. It is anticipated that MTFB-TFBBr sometimes will be useful in providing an electrophoric derivative that encounters less background noise in analysis by electrophore derivatization/GC-EC-MS.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17027999 PMCID: PMC2062568 DOI: 10.1016/j.chroma.2006.09.049
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759