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Quinoline and some of its derivatives were reported to be carcinogenic, toxic and mutagenic[1-3]. The widespread use of quinoline and its derivatives entails that these compounds are distributed in the environment, polluting soil and water together with many other environmental chemicals.Time-resolved laser flash photolysis and pulse radiolysis have been used to study the reaction of quinoline (Q), 2, 6-dimethyl-quinoline (DMQ) and isoquinoline (IQ) with hydrated electrons, hydroxyl radicals and hydrogen radicals. Transient absorption spectra were obtained and reaction rate constants to the reactions were determined, as showed in Table 1. Rossible mechanisms of the reactions were suggested.In addition, oxidization reactions of SO4·-, Br2·- and N3·- with isoquinoline, quinoline and its derivatives were studied. It showed that SO4- could oxidize quinoline, 2, 6-dimethylquinoline and isoquinoline; Br2·-could oxidize isoquinoline to its cation radicals, but it could not oxidize quinoline or 2, 6-diemethylquinoline; N3·- could oxidize none of them.With a better understandings on photolysis and radiolysis of isoquinoline, quinoline and its derivates, the study is of help for degradation of the chemicals and for environment protection.