Valvani S C, Yalkowsky S H, Roseman T J
J Pharm Sci. 1981 May;70(5):502-7. doi: 10.1002/jps.2600700510.
The aqueous solubility and octanol-water partition coefficient of over 100 nonelectrolyte organic liquid solutes are related by the simple equation log Sw = -1.016 log PC +0.515, where Sw is the molar solubility of liquid solutes in water and PC is the experimental partition coefficient of the solutes in the octanol-water system. The liquids studied represent a wide variety of organic compounds including aliphatic and aromatic hydrocarbons, alcohols, esters, ethers, aldehydes, and ketones. This finding is in agreement with that reported by Hansch and coworkers. However, these results are significant because only the experimental values for the aqueous solubilities and octanol-water partition coefficients are included, as opposed to the calculated partition coefficients used by Hansch. This relationship is extremely useful in understanding the overall solubility and partitioning phenomenon for organic liquids are provides a basis for studying crystalline solids and gases.
100多种非电解质有机液体溶质的水溶性和正辛醇-水分配系数可通过简单方程log Sw = -1.016 log PC +0.515建立联系,其中Sw是液体溶质在水中的摩尔溶解度,PC是溶质在正辛醇-水体系中的实验分配系数。所研究的液体代表了多种有机化合物,包括脂肪烃和芳香烃、醇类、酯类、醚类、醛类和酮类。这一发现与Hansch及其同事报道的结果一致。然而,这些结果具有重要意义,因为只纳入了水溶性和正辛醇-水分配系数的实验值,而非Hansch所使用的计算分配系数。这种关系对于理解有机液体的整体溶解度和分配现象极为有用,并为研究晶体固体和气体提供了基础。