By using 193 nm laser photolysis and cavity ring-down spectroscopy to produce and monitor the propargyl radical (CH2CCH), the self-reaction and oxygen termolecular association rate coefficients for the propargyl radical were measured at 295 K between total pressures of 300 Pa and 13300 Pa (2.25 and 100 Torr) in Ar, He, and N-2 buffer gases. The rate coefficients obtained by simple second-order fits to the decay data were observed to vary with the photolytic precursors: allene, propargyl chloride, and propargyl bromide. By using a numerical fitting routine and more comprehensive mechanisms, a distinct rate coefficient for the self-reaction was determined, k(infinity)(C3H3+C3H3) = (4.3 +/- 0.6) x 10(-11) cm(3) molecule(-1) s(-1) at 295 K. This rate coefficient which is a factor of 2.8 times slower than reported previously, was independent of total pressure and buffer choice over the entire pressure range. Other rate coefficients derived during the modeling included k(C3H3+H 665 Pa He) = (2.5 +/- 1.1) x 10(-10) cm(3) molecule(-1) s(-1), k(C3H3+C3H3Cl2) = (7 +/- 4) x 10(-11) cm(3) molecule(-1) s(-1), and k(C3H3+C3H3Br2) = (2.4 +/- 2) x 10(-11) cm(3) molecule(-1) s(-1). The association reaction C3H3+O-2 was found to lie in the falloff region between linear and saturated pressure dependence for each buffer gas (Ar, He, and N-2) between 300 Pa and 13300 Pa. A fit of these data derived the high-pressure limiting rate coefficient k(infinity)(C3H3+O-2) = (2.3 +/- 0.5) x 10(-13) cm(3) molecule(-1) s(-1). Three measurements of the propargyl radical-absorption cross-section obtained sigma(332.5) = (413 +/- 60) x 10(-20) cm(2) molecule(-1) at 332.5 nm. Stated uncertainties are two standard deviations and include the uncertainty of the absorption cross section, where appropriate.