Abstract The rubber hydrocarbon in latex as it leaves the tree is already a high polymer, with a broad distribution of molecular weight ranging from several millions to below 100,000, with the major part of the hydrocarbon in the higher molecular weight ranges. Changes in the hydrocarbon subsequent to its leaving the tree tend to be degradative, but may also involve cross-linking reactions leading to changes in plasticity. Structural changes in rubber attributed to restricted cross-linking have a greater influence on plasticity than on solution viscosity. A gel component (probably microgel) present in the freshly tapped hydrocarbon is of considerable importance in determining the hardness of raw rubber, but greatly complicates the interpretation of viscometric data, of which evaluation by the equation: [η]=5.02×10−4 M0.67 only appears to be valid for gel-free rubber fractions. Plasticity and intrinsic viscosity cannot, therefore, be generally correlated, although the plasticity is influenced by the spread...