Abstract
Differential scanning calorimetry has been used to investigate the heat of fusion (ΔHf=712 kcal per g mol) and true melting temperature (T0=4224°K) of pure cholesterol (995 mole%). In addition to analysis of the thermograph by an existing method a new and more rapid procedure has been used for evaluation of the purity of substances. Evidence is given that differential scanning calorimetry measurements at low scanning rates (05,1° min−1), followed by correction for premelting, are essential for estimation of ΔHf of substances not ultra-pure, at higher scanning rates large errors result. The entropy of fusion of cholesterol is similar to that of the simpler cholesteryl esters.

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