Degenerate four-wave mixing spectroscopy has been used to study the photodissociation dynamics of tert-butyl hydroperoxide (t-BuOOH) at 266 nm, long-wavelength tail of the ultraviolet (UV) absorption continuum. The nascent rotational distributions, spin-orbit state ratio, and h-doublet population ratio of the OH (X (2 Pi)) fragments have been extracted. No vibrationally excited OH was observed. The rotational distribution peaked at N " = 5. The average rotational energy was estimated to be 4.2% of the available energy. A slight preference for the Pi(-) Lambda-doublet component and a statistical distribution of the spin-orbit states were observed. The experimental observations are similar to those found for OH from H2O2 photodissociation and are consistent with dissociation via a repulsive excited state.