Stress corrosion cracking is a potential failure mechanism of the copper canister proposed to be the main corrosion barrier in the Scandinavian design of the final nuclear waste disposal vault. The main target in SCC-oriented research is to determine the limiting values for the critical concentration of harmful species, the potential range in which these species cause SCC and the threshold stress level required for SCC. The present paper attempts to redefine the criteria for SCC susceptibility of copper in acetate solutions through analysis of potentiodynamic curves using both rotating disc and thin plate electrodes insulated on one side. A potential range in which the current densities at a slow sweep rate are lower than those at a fast sweep rate exists for Cu in 0.001 M - 0.1 M acetate. However, the values of the current densities within this range are significantly smaller than those postulated for active anodic dissolution, implying dissolution mediated by a surface film. New criteria for the SCC susceptibility of pure copper in acetate solutions have been formulated through Stern-Geary analysis of the polarisation curves. Several electrochemical characteristics, such as the current density at the positive crossover potential, the ratio between the corrosion current densities determined from the slow and fast sweeps, as well as the anodic current density in a fast sweep show a clear jump for concentrations between 0.01 M and 0.05 M. This, however, cannot yet be considered as an indication of SCC susceptibility at higher acetate concentrations, as evidenced by complementary SSRT tests.