The interactions between 4-phenylazo-l-naphthylamine and 6 sodium alkyl sulfates have been studied by a spectrophotometer. At lower concentrations than each CMC, 3 surfactants (octyl, decyl and dodecyl sulfate) and the dye formed hydrophobic complexes with a binding molar ratio of 1 : 1, while the others (tetradecyl, hexadecyi, and octadecyl sulfate) and the dye made 2 : 1 complexes. The wavelength of the maximal absorption is 440 nm in th~ former, and 520 nm in the latter. In the neighborhood of each CMC region, thermochromism occurred in every surfactant solution. The temperature at which the maximal absomtion moved from 520 mn to 440 nm increased with an increase m the number of carbo~n atoms m the surfactant molecules. At higher concentrations than each CMC, in the case of the octyl and decyl sulfate, the maximal absorption occurred at the 440 nm band above room temperature; in the case of the dodecyl, tetradecyl, and hexadecyl sulfates, the maximal absorption occurred at the 520 nm band, regardless of temperature. In the case of octadecyl sulfate, the maximal absorption moved from 610 nm to 520 nm with increase in temperature. It is found that the protonation equilibrium of the dye is dependent on the micellar structure through the differences in the alkyl chain lengths of the surfactants, and the differences in interaction with surfactant crystals.