The concentration of nitroxide has been measured in an acrylic melamine coating containing different hindered amine light stabilizers as a function of exposure harshness, time and stabilizer concentration using electron spin resonance spectroscopy. The four hindered amines are based on 2,2,6,6-tetramethylpiperidine and have the following substituents on the piperidine nitrogen: H, CH3, CH2CH2-polymer, and COCH5. Comparisons of nitroxide formation and decay kinetics with infrared spectroscopic measurements of hindered amine effectiveness reveal that a major factor in the ability of hindered amine to inhibit photo-oxidation in acrylic melamine coatings is the rate of conversion of the amine functionality to nitroxide. Conversion is fastest for the z.lbond2; group. The conversion of z.lbond2; to nitroxide is also fast and proceeds through the formation of z.lbond2; groups by at least two mechanisms. By contrast, the conversion of z.lbond2;-polymer and z.lbond2; to nitroxide is roughly an order of magnitude slower than that for z.lbond2; accounting for the decreased effectiveness of these stabilizers. © 1990.