The dynamics of the formation of OH radical upon 193 nm excitation of pyruvic acid has been nvestigated by the laser-photolysis laser-induced-fluorescence technique. OH radicals were generated in the ground electronic state, with no  vibrational excitation. The estimated rotational temperature is 720±90 K, and the translational energy is 18.7±6.5 kcal mol^–1. Ab initio calculations on excited electronic states were performed at the configuration interaction with single electronic excitation level with 6-31+G(d,p) basis function. All low-lying electronic excited states (S1–S3 and T1–T6) were characterized and the transitions were identified. A transition state for the C–OH dissociation channel has been obtained from the T1 state with a late exit barrier. A mechanism for the formation of OH radicals involving internal conversion and intersystem crossing from the initially populated S3 state to T1 state and the dissociation from the T1 potential energy surface with the calculated barrier is proposed, which reproduces the observed partitioning of available energy in the fragments according to the hybrid model.