4-(4′-methyltetrafluorophenyl)-2,3,5,6-tetrafluorobenzyl bromide:: A new electrophoric derivatizing reagent

被引:3
作者
Murugaiah, Veeravagu
Naim, Abdul
Peng, Shiqi
Cui, Guohui
Giese, Roger W. [1 ]
机构
[1] Northeastern Univ, Barnett Inst Chem Anal, Bouve Coll Pharm & Hlth Profess, Dept Pharmaceut Sci, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Chem, Boston, MA 02115 USA
[3] Alnylam Pharmaceut, Cambridge, MA 02142 USA
[4] Vintage Pharmaceut, Huntsville, AL 35811 USA
[5] Capital Univ Med Sci, Coll Chem Biol & Pharmaceut Sci, Beijing 100069, Peoples R China
关键词
gas chromatography; electron-capture mass spectrometry; derivatization;
D O I
10.1016/j.chroma.2006.09.049
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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-O-6-(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. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:338 / 340
页数:3
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