Molecular weight (M) dependence of the lateral growth rate (V) of a form crystal of isotactic polypropylene (iPP) was studied. Reliable equilibrium melting temperature determined in our previous study was used for the analysis of supercooling dependence of V. A power law of M of V proportional to M-n(-H), was obtained, where H is a small constant (H = 0.7). The small H, which is similar to that of the hexagonal phase of polyethylene (H = 0.7) in comparison with the value of H = 1.7 for the orthorhombic phase of polyethylene, confirmed our prediction of smaller H for "rod like" chain polymers because of easier chain sliding within the interface between the crystalline phase and the melt. Thus, the universality of the important role of topological nature in polymer crystallization was confirmed. Lateral surface free energy (sigma) of the alpha form of iPP was obtained as sigma congruent to 1.59 x 10(-6) J/cm(2). (c) 2006 Elsevier Ltd. All rights reserved.