Literature DB >> 7241352

Solubility and partitioning IV: Aqueous solubility and octanol-water partition coefficients of liquid nonelectrolytes.

S C Valvani, S H Yalkowsky, T J Roseman.   

Abstract

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.

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Year:  1981        PMID: 7241352     DOI: 10.1002/jps.2600700510

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

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Authors:  J T Rubino; S H Yalkowsky
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4.  Solubility Study of Acetylsalicylic Acid in Ethanol + Water Mixtures: Measurement, Mathematical Modeling, and Stability Discussion.

Authors:  Ali Nokhodchi; Taravat Ghafourian; Nour Nashed; Kofi Asare-Addo; Elmira Behboudi; Yasaman Sefid-Sefidehkhan; Aynaz Zarghampour; Elaheh Rahimpour; Abolghasem Jouyban
Journal:  AAPS PharmSciTech       Date:  2021-12-28       Impact factor: 3.246

  4 in total

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