ß-Carotene absorbed 2 equimolar amounts of N0 2 accompanying the complete destruction of ß-carotene. Electron spin resonance study using 2-phenyl-4,4,5,5-tetramethylimidazoline-3-oxide-l-oxyl revealed that no significant amounts of NO were released by the interaction. Nitrogen atoms derived from N0 2 were tightly bound to the ß-carotene molecules. Destruction of ß-carotene was inhibited little by a-tocopherol and polyunsaturated fatty esters, and slightly by ascorbyl palmitate, indicating that ß-carotene was a more effective scavenger of N0 2 . ONOOH/ONOO -and 3-morpholinosydononimine similarly destroyed ß-carotene. The results suggest that ß-carotene contributes to the prevention of cytotoxicity and genotoxicity of N0 2 and ONOOH/ONOO" derived from NO.