Polyurethane triblock copolymers were synthesized by reacting 4,4'-methylenebis(phenyl isocyanate) (MDI)-endcapped poly(tetramethylene oxide) (PTMO) with mono-amine-amide (MMA) units. Four different MMA units were used, i.e. no-amide (6m), mono-amide (613), di-amide (6T6m) and tri-amide (MB), based on hexylamine (6m), 1,6-hexamethylenediamine (6), terephthalic acid M, and benzoic acid (B). The PTMO had a molecular weight of 2000 g/mol. Thermal and thermo-mechanical properties were studied by means of differential scanning calorimetry and dynamic mechanical analysis, respectively. The structure of the carbonyl bond was explored by infra-red analysis and the elastic behavior of the materials by compression set experiments. The triblock polyurethanes with mono-disperse, hard end-segments displayed low molecular weights (3200-3800 g/mol). The crystallinity of the MDI urethane-urea group was found to depend on the structure of the amide. Increasing the number of amide bonds in the mono-disperse hard segment increased the modulus and the hard segment melting temperature, and decreased the compression set values. The low temperature properties were hardly affected by the amide length.