Recent studies suggested that long-lived photooxidants (LLPO), which are reactive intermediates formed during irradiation of dissolved organic matter (DOM), may consist of phenoxyl radicals derived from phenolic moieties of the DOM. Besides the well-studied excited triplet states of chromophoric DOM (3CDOM*), LLPO presumably are important photooxidants for the transformation of electron-rich contaminants in surface waters. The main objective of this study was to further test the potential role of phenoxyl radical as LLPO. Suwannee River fulvic acid (SRFA) as a model DOM was pre-oxidised using the phenol-reactive oxidants chlorine and ozone, followed by its characterization by the specific UV absorption at 254 nm (SUVA254), the ratio of absorbance at lambda = 254 nm and lambda = 365 nm (E2:E3), and the electron donating capacity (EDC). Subsequently, the photoreactivity of pre -oxidized SRFA was tested using 3,4-dimethoxyphenol (DMOP) as a LLPO probe compound at two initial con-centrations ([DMOP]0 = 0.1 and 5.0 mu M). Linear inter-correlations were observed for the relative changes in SUVA254, E2:E3, and EDC for increasing oxidant doses. Pseudo-first-order transformation rate constants normalized to the changing SRFA absorption rate (i.e., kobs0.1/rabsCDOM and kobs 5.0 /rabs CDOM, for 0.1 and 5.0 mu M, respec-tively) exhibited the following distinct trends: The LLPO-dominated kobs 0.1/rabs CDOM ratio decreased with increasing oxidant dose and with decreasing SUVA254 and EDC, while the 3CDOM*-dominated kobs 5.0 /rabs CDOM ratio positively correlated with E2:E3. Finally, it was concluded that precursors of 3CDOM* and LLPO are chemically modified differently by pre-oxidation of DOM, and LLPO precursors likely consist of phenolic moieties of DOM, suggesting phenoxyl radicals as LLPO.