The epoxidation of styrene was studied using a titanium silicate molecular sieve TS-1 as catalyst and dilute (25%) H2O2 as oxidizing agent. Mainly two types of reactions were observed : The major reaction (similar to 75-85 mole%) was epoxidation and its further isomerization into phenylacetaldehyde. The other reaction was oxidative cleavage into benzaldehyde (similar to 10-20 mole%). While generally the products were analyzed by capillary GC and GCMS, in certain cases, the products were separated and isolated by column chromatography and analyzed by H-1 and C-13 NMR spectroscopy. Polar and nonpolar solvents have marked influence on product distribution in styrene epoxidation. In methanol, a significant part of styrene epoxide undergoes alcoholysis through the addition of methanol forming 2-methoxy-2-phenyl-ethanol. The influence of reaction time, temperature, and styrene/H2O2 molar ratio on the conversion and product distribution was also studied.