Chlorinated phenoxy acids are a widely used class of herbicides and have been found in remote regions far from sources. However, the atmospheric chemistry of these compounds is poorly understood. We use an oxidative flow reactor coupled to chemical ionization mass spectrometry to investigate OH oxidation of two chlorinated phenoxyacid herbicides (2-methyl-4-chlorophenoxyacetic acid (MCPA) and mecoprop-p) and one chlorinated pyridine herbicide (triclopyr). OH radicals add to the aromatic rings of the three herbicides, produce peroxides via hydrogen abstraction, or fragment at the ether bond. OH oxidation of MCPA produced two potentially toxic compounds: chlorosalicylaldehyde and chlorosalicylic acid. We use standards to validate the detection of these oxidation products by acetate CIMS and quantify the reaction rate. Oxidation of triclopyr produced a known endocrine disruptor, 3,5,6-trichloro-2-pyridinol. Thus, while some OH oxidation products are less toxic than the parent molecules (e.g., C1-5 carboxylic acids), others may be as or more toxic than the parent herbicide. We determine effective rate coefficients for OH addition to the aromatic ring ( kOH) for mecoprop-p of 1.5 (±0.7) × 10-12 cm3 molecules-1 s-1 and for MCPA of 2.6 (±0.3) × 10-12 cm3 molecules-1 s-1. The atmospheric lifetimes with respect to OH are thus long enough that photochemistry may be relevant to the environmental fate of these pesticides.