The oxidative pyrolysis of methylene chloride, chloroform, and carbon tetrachloride has been investigated using a micro-bore, fused silica, tubular flow reactor operating under laminar flow conditions coupled to in-line GC-MS detection. Data were obtained over the temperature range 573-1273 K for the following conditions: chlorocarbon/oxygen equivalence ratios of 3.0, chlorocarbon concentrations of 2.7 ? 0.1 x mols/L, gas-phase residence times of 2.0 s, and reactor pressures of 1.15 2 0.05 atm. The parent stability (defined by the temperature required for 99% destruction) was evaluated as:CHpC12: 1028 K, CHC13: 873 K, CCl,: 1153 K Chemically activated recombination of chlorinated C1 radicals are proposed as important pathways to chlorinated ethane and olefin products. The most significant finding from analysis of product distributions containing 2 2 carbon atoms was the observation of ca. 1 mol% yields of higher-molecular-weight perchlorinated aromatic species from the decomposition of chloroform and carbon tetrachloride. Implications with respect to the controlled high-temperature incineration of these chlorinated methanes are briefly discussed.