In a sphingomyelin-enriched sample of polar lipids from bovine milk, molecular species of intact sphingomyelin were separated by normal-phase high-performance liquid chromatography and detected by mass spectrometry (MS) for structural information. First, by using electrospray with positive ionizatio
Identification of Fenton's reagent-generated atrazine degradation products by high-performance liquid chromatography and megaflow electrospray ionization tandem mass spectrometry
✍ Scribed by Scott M. Arnold; Rasmy E. Talaat; William J. Hickey; Robin F. Harris
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 663 KB
- Volume
- 30
- Category
- Article
- ISSN
- 1076-5174
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
High‐performance liquid chromatography megaflow electrospray tandem mass spectrometry (HPLC/ES‐MS/MS) with an on‐line radioisotope detector was used to identify [2,4,6‐^14^C] atrazine degradation products generated by treatment with Fenton's reagent (Fe^2+^ and H~2~O~2~). Fenton's reagent produced dealkylated and/or partially oxidized [2,4,6‐^14^C] atrazine products in preference to dechlorinated products. Seven major products were identified by collision‐induced dissociation spectra: 4‐acetamido‐2‐chloro‐6‐(isopropylamino)‐s‐triazine, 4‐amino‐2‐chloro‐6‐(isopropylamino)‐s‐triazine, 4‐acetamido‐2‐chloro‐6‐(ethylamino)‐s‐triazine, 6‐amino‐2‐chloro‐4‐(ethylamino)‐s‐triazine, 4‐acetamido‐6‐amino‐2‐chloro‐s‐triazine, 2‐chloro‐4,6‐diamino‐s‐triazine and the first report of 4‐acetamido‐2‐hydroxy‐6‐(isopropylamino)‐s‐triazine. HPLC/ES‐MS/MS provided a rapid method for identifying a wide range of atrazine transformation products in aqueous samples and obviated the need for fraction collection, extraction, and chemical derivatization of the more polar atrazine products. Furthermore, because analyte retention times in HPLC/UV and HPLC/ES‐MS/MS were similar, compound identities determined using the latter could be directly assigned to peaks in UV chromatograms.
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