Fracture properties of model elastomeric networks of polyurethane have been investigated with a double-edge notch geometry. The networks were synthesized from monodisperse end-functionalized polypropylene glycol precursors and a trifunctional isocyanate. All reagents were carefully purified and nearly defect-free ideal networks were prepared at a stoichiometry very close to the theoretical one. Three networks were prepared: an unentangled network of short chains (M n ¼ 4 kg mol À1 ), an entangled network of longer chains (M n ¼ 8 kg mol À1 ) and a bimodal network with 8 kg mol À1 and 1 kg mol À1 chains. The presence of entanglements was found to increase significantly the toughness of the rubber, in particular at room temperature, relative to the bimodal networks and to the short chains network.Fracture experiments were carried out at different strain rates and temperatures and showed for all three networks a marked decrease in fracture toughness with increasing temperature and decreasing strain rate which mirrored reasonably well the rate and temperature dependence of tan d, the dissipative factor. However the proportionality factor between tan d, and G IC was very material dependent and the shift factors obtained for the master curves of the viscoelastic properties could not be used to build fracture energy master curves.