The self-association of random copolymers of acrylic acid (AA) and N-dodecylmethacrylamide (DodMAm) with 5.1-28.4 mol % DodMAm contents (fDod) in water was investigated by fluorescence, quasielastic light scattering (QELS), and rheological methods as a function of fDod and pH. The copolymers exhibited a strong tendency for interpolymer association, forming micelle-like multipolymer aggregates. This is a striking contrast to the previous finding that random copolymers of 2-(acrylamido)-2-methylpropanesulfonate (AMPS) and DodMAm exhibited a strong tendency for intrapolymer association, forming unimolecular micelles. At pH 10, the AA/DodMAm copolymers with a smaller fDod formed multipolymer aggregates with a larger size, the size decreasing with increasing fDod. At pH 4, this trend was opposite; the size of the multipolymer aggregate increased with increasing fDod. Independent of fDod and pH, the size of the multipolymer aggregates increased with increasing polymer concentration (Cp). The association behavior and the nature of multipolymer aggregates of the AA/DodMAm copolymers with small fDod values (e9.1 mol %) were markedly different from those with larger fDod (g12.8 mol %). As the pH was decreased, the size of the multipolymer aggregate decreased when fDod e 9.1 mol % whereas it increased when fDod g 12.8 mol %. Independent of fDod, the mean aggregation number (Nagg) of dodecyl groups in one hydrophobic microdomain decreased with decreasing pH. Multipolymer aggregates formed from the AA/DodMAm copolymer of a small fDod (9.1 mol %) at high Cp were more dynamic in nature than those from the copolymer of larger fDod (22.4 mol %), the former showing shear rate dependent viscosity behavior while the latter did not. On the basis of the characterization data, multipolymer association models for the AA/DodMAm copolymers were proposed.