A flash photolysis-resonance fluorescence technique was used to study the rate constant for the reaction of OH radicals with dimethyl carbonate over the temperature range 252-370 K, The rate constant exhibited a weak temperature dependence, increasing at both low and high temperature from a minimum value of approximately 3.1 x 10(-13) cm(3) molecule(-1) s(-1) near room temperature. Pulse radiolysis/transient UV absorption techniques were used to study the ultraviolet absorption spectra and kinetics of CH3OC(O)OCH2 and CH3OC(O)CH2O2 radicals at 296 K. Absorption cross sections of CH3OC(O)OCH2 and CH3OC(O)OCH2O2 at 250 nm were (3.16 +/- 0.34) x 10(-18) and (3.04 +/- 0.43) x 10(-18) cm(2) molecule(-1), respectively. Rate constants measured for the self-reactions of CH3OC(O)OCH2 and CH3OC(O)OCH2O2 radicals and reactions of CH3OC(O)OCH2O2 radicals with NO and NO2 were (5.6 +/- 1.1) x 10(-11), (1.27 +/- 0.21) x 10(-11), (1.2 +/- 0.2) x 10(-11), and (1.2 +/- 0.2) x 10(-11) cm(3) molecule(-1) s(-1), respectively. The rate constant for reaction of F atoms with dimethyl carbonate was determined by a pulse radiolysis absolute rate technique to be (6.1 +/- 0.9) x 10(-11) cm(3) molecule(-1) s(-1) A FTIR smog chamber system was used to show that, in 760 Torr of air at 296 K, CH3OC(O)OCH2O radicals are lost via three competing processes : 42 +/- 15% via reaction with O-2, 14 +/- 2% via H atom elimination, and 44 +/- 10% via decomposition and/or isomerization. Relative rate techniques were used to measure rate constants for the reactions of F atoms with CH3OC(O)OCH3, (6.4 +/- 1.4) x 10(-11) cm(3) molecule(-1) s(-1), and Cl atoms with CH3OC(O)OCH3, CH3OC(O)OCH2Cl, CH3OC(O)OCHO, and HC(O)OC(O)OCHO, (2.3 +/- 0.8) x 10(-12), (4.6 +/- 2.8) x 10(-13), (1.7 +/- 0.1) x 10(-13), and (1.7 +/- 0.1) x 10(-14) cm(3) molecule(-1) s(-1), respectively. Results are discussed in the context of the atmospheric chemistry of CH3OC(O)OCH3.