Experimental NO flame profiles were measured for N 2 -diluted, CH 4 -, C 2 H 2 -, and C 3 H 8 -N 2 O premixed flames stabilized on a flat flame apparatus at stoichiometric proportions. The NO measurements were obtained using laserinduced fluorescence in the saturated region and calibrated by microprobe postflame sampling using Fourier transform infrared spectroscopy. These experimental data were compared to predictions using a burner-stabilized flame model using three different published chemical mechanisms. Compared to the Fourier transform infrared results, the NO model predictions using the chemical mechanisms varied depending on the mechanism and the fuel. For example, for the CH 4 flame, all three predictions fell within the Fourier transform infrared uncertainty, whereas only the Glarborg mechanism is within the Fourier transform infrared uncertainty for the C 2 H 2 flame. The normalized, spatial NO profile predictions for all three chemical mechanisms showed reasonable agreement with the normalized experimental NO profiles in the postflame region; however, there was appreciable disparity between the experimental and model predictions of the spatial location of the peak NO mole fraction above the burner surface. Sensitivity and rate-of-production analyses showed that NH x =NO chemical interactions are important to accurately model NO profiles in hydrocarbon-nitrous-oxide flames. The experimental data provided additional constraints for the rate constants of important NH x =N x H y chemical interactions, and some modifications were considered for improving comparisons between model predictions and experiments.