Related Experiment Video
Updated: Jul 8, 2025

Elucidating the Metabolism of 2,4-Dibromophenol in Plants
Published on: February 10, 2023
Monthly variations of unregulated brominated disinfection by-products in chlorinated water are correlated with total
Christena Watts1, Jianxian Sun1, Paul D Jones1,2
1Toxicology Centre, University of Saskatchewan, Saskatoon, SK S7N 5B3, Canada.
Abstract:
Brominated disinfection by-products (Br-DBPs) can form during the chlorination of drinking water in treatment plants (DWTP). Regulations exist for a small subset of Br-DBPs; however, hundreds of unregulated Br-DBPs have been detected, and limited information exists on their occurrence, concentrations, and seasonal trends. Here, a data-independent precursor isolation and characteristic fragment (DIPIC-Frag) method were optimized to screen chlorinated waters for Br-DBPs. There were 553 Br-DBPs detected with m/z values ranging from 170.884 to 497.0278 and chromatographic retention times from 2.4 to 26.2 min. With MS2 information, structures for 40 of the 54 most abundant Br-DBPs were predicted. The method was then applied to a year-long study in which raw, clear well, and finished water were analyzed monthly. The 54 most abundant unregulated Br-DBPs were subjected to trend analysis. Br-DBPs with higher oxygen-to-carbon (O/C) and bromine-to-carbon (Br/C) ratios increased as water moved from the clear well to the finished stage, which indicated the dynamic formation of Br-DBPs. Monthly trends of unregulated Br-DBPs were compared to raw water parameters, such as natural organic matter, temperature, and total bromine, but no correlations were observed. It was found that total concentrations of bromine (TBr) in finished water (0.04-0.12 mg/L) were consistently and significantly greater than in raw water (0.013-0.038 mg/L, P < 0.001), suggesting the introduction of bromine during the disinfection process. Concentrations of TBr in treatment units, rather than raw water, were significantly correlated to 34 of the Br-DBPs at α = 0.05. This study provides the first evidence that monthly trends of unregulated Br-DBPs can be associated with the concentration of TBr in treated waters.
Related Concept Videos
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Reactions at the Benzylic Position: Halogenation
Formation of Halohydrin from Alkenes
Radical Substitution: Allylic Bromination
Mass Spectrometry: Alkyl Halide Fragmentation

