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Journal ArticleDOI

The transfer of neutral molecules, ions and ionic species from water to wet octanol

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TLDR
It is shown that differences in partition coefficients between neutral species and the corresponding ionic species, as log P(oct), are not at all constant.
Abstract
Partition coefficients for transfer from water to wet octanol have been set out for permanent ions, and for ionic species derived from neutral molecules by loss or acceptance of a proton. A previous equation for the partition of neutral compounds from water to wet octanol has been extended to include the partition of permanent ions, and ionic species; the only additional descriptors required are J+ for cations and J− for anions. Fourteen cations and twelve anions are included in the equation. It is shown that differences in partition coefficients between neutral species and the corresponding ionic species, as log P(oct), are not at all constant. For carboxylic acids and the corresponding anion, differences are about 5.0 log units, for phenols and the corresponding anion differences range from 2.2 to 4.9 log units, and for amines and the corresponding protonated cations there is an enormous range of differences from 0.6 to 7.1 log units.

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Citations
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Estimation of the environmental properties of compounds from chromatographic measurements and the solvation parameter model.

TL;DR: The central role chromatographic methods, together with liquid-liquid partition coefficients, occupy in the determination of the six descriptors used in the solvation parameter model is detailed.
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Polyfunctional ionogenic compound sorption: challenges and new approaches to advance predictive models.

TL;DR: The unique mapping of sorbate structural moieties, sorbent receptor sites, and sorption mechanisms is used to advance mechanism-specific probe compounds for cation exchange and surface complexation/cation bridging for quantifying the relevant site abundance and baseline sorption free energy.
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Review of the toxic effects of ionic liquids

TL;DR: In this article, the authors discuss the key findings of toxicological information of ionic liquids, collect some toxicity data of ILs to different species, and explain the influence of IL structure on their toxic properties.
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Ionic liquids: predictions of physicochemical properties with experimental and/or DFT-calculated LFER parameters to understand molecular interactions in solution.

TL;DR: In this article, an evolutionary model was proposed to predict octanol-water partition coefficients, water solubilities, and critical micelle concentrations (CMCs) of ionic liquids (ILs), as well as the anionic activity coefficients and hydrophobicities in pure water and octanol water.
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Human Skin Permeation of Neutral Species and Ionic Species: Extended Linear Free Energy Relationship Analyses

TL;DR: It is shown that the poor permeability of ionic species is largely due to slow diffusion through the stratum corneum, especially marked for a number of protonated base cations.
References
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Journal ArticleDOI

Determination of sets of solute descriptors from chromatographic measurements

TL;DR: It is concluded that for processes that entail transfer of a solute from one phase to another, only a small number of solute descriptors is needed to provide a reasonably accurate analysis of the process.
Journal ArticleDOI

Prediction of solubility of drugs and other compounds in organic solvents

TL;DR: A procedure for the prediction of solubilities of drugs and other compounds in a wide range of solvents, based on the Abraham solvation equations, which is especially useful for very hydrophobic compounds such as cholesteryl acetate and cholesterol.
Journal ArticleDOI

Drug liposome partitioning as a tool for the prediction of human passive intestinal absorption

TL;DR: Liposome distribution coefficients of ionizable drugs derived by a pH-metric titration were successfully used to calculate a parameter that correlates with the percentage of passive intestinal absorption in humans.
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