Aldehyde contents and degree of polymerization values of polysaccharides were calculated from chlorite results obtained under various conditions and using the corresponding stoichiometric ratios determined for substances of low molecular weight. The polysaccharides were three native dextrans, a series of hydrolyzed dextrans including clinical dextran, a periodate dextran, a series of araban fractions, and starches including pea, wheat, and rice amylopectin, and a series of periodate cornstarch products. The results with various chlorite procedures were self-consistent and agreed well with those of other chemical methods, and fairly well with those of light-scattering for fractionated polymers. For native dextrans, where no agreement was to b e expected, the large divergence demonstrated inhomogeneity of substance. Agreement with osmotic pressure results was fair to poor. HE oxidation by sodium chlorite in T phosphate buffer of a variety of mono-and disaccharides and benzaldehyde was recently studied (12) with respect to the chlorite-aldehyde stoichiometry as affected by buffer strength, reaction rate, and concentration of reactants. Various experimental conditions employing sodium chlorite were dweloped for application t o the determination of aldehyde groups in polysaccharides.This communication describes the study of the rates of oxidation under those conditions and others of a series of periodate cornstarches; of a series of dextrans, including native, periodate, clinical, and more extensively acidhydrolyzed; and of a series of arabans.