4-(Trifluoromethyl)-2,3, 5,6-Tetrafluorobenzyl Bromide as a New Electrophoric Derivatizing Reagent
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1993/07/09
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Description:4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide (TMB) was synthesized in a single step from a,a,a,2,3,5,6- heptafluoro-p-xylene. The purpose of TTBB is to function as an analogue of pentafluorobenzyl bromide (PFBB) in electrophoric derivatization reactions prior to detection by gas chromatography-electron-capture negative ion mass spectrometry (GC-ECNI-MS). In more detail, it was anticipated that TTBB could be used along with, or as a substitute for, PFBB to help control some interferences and confirm results. This is because a TTBB-product (of an analyte) would have different retention and sometimes m/z characteristics than a corresponding PFBB product in GC-ECNI-MS, while the two products should be similar in their ease of formation and yields. Results demonstrating these expectations were achieved by derivatizing and detecting two analytes with these reagents: N7-(2-hydroxyethyl)xanthine, and 2,3-pyrenedicarboxylic acid. [Description provided by NIOSH]
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ISSN:0021-9673
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Pages in Document:400-404
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Volume:641
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Issue:2
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NIOSHTIC Number:nn:20056725
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Citation:J Chromatogr 1993 Jul; 641(2):400-404
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Contact Point Address:Roger W. Giese, Department of Pharmaceutical Sciences in the Bouve Pharmacy and Health Sciences, and Barnett Institute, Northeastern University, 360 Huntington Avenue, Boston, MA 02115
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Federal Fiscal Year:1993
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Performing Organization:Northeastern University, Boston, Massachusetts
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Peer Reviewed:True
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Start Date:19910101
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Source Full Name:Journal of Chromatography
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End Date:19961130
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Main Document Checksum:urn:sha-512:5ff700e860da60943a6d5640344391a1cf86beb970584009740879e18ef1681443ce9d3026d048797a75b0a6b722f51a0093212aad0341d559dfb771e130b768
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