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Solubility correlation by model with partial molar volume

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/jps.22589openalex-snapshot

Solubility Prediction of Drugs in Mixed Solvents Using Partial Solubility Parameters

inferredcites →https://doi.org/10.1002/jps.2600730106openalex-snapshot

Excess Free Energy Approach to the Estimation of Solubility in Mixed Solvent Systems III: Ethanol–Propylene Glycol–Water Mixtures

inferredcites →https://doi.org/10.1002/jps.2600740206openalex-snapshot

Prediction of Xanthine Solubilities Using Statistical Techniques

inferredcites →https://doi.org/10.1002/jps.2600810418openalex-snapshot

Solvent Effects on Chemical Processes, I: Solubility of Aromatic and Heterocyclic Compounds in Binary Aqueous—Organic Solvents

inferredcites →https://doi.org/10.1007/s10765-017-2323-6openalex-snapshot

Solubility Determination and Modeling and Dissolution Thermodynamic Properties of Raspberry Ketone in Binary Solvent Mixtures of Ethanol and Water

inferredcites →https://doi.org/10.1007/s10953-011-9719-xopenalex-snapshot

Partition Coefficients and Solubilities of Compounds in the Water–Ethanol Solvent System

inferredcites →https://doi.org/10.1007/s10953-012-9872-xopenalex-snapshot

Solubility of β-HMX in Acetone + Water Mixed Solvent Systems at Temperatures from 293.15 K to 313.15 K

inferredcites →https://doi.org/10.1007/s10953-012-9894-4openalex-snapshot

Solubility of Itaconic Acid in Aqueous Ethanol Mixtures from 278.15 K to 333.15 K

inferredcites →https://doi.org/10.1007/s10953-021-01121-3openalex-snapshot

Employing Abraham and Hansen Parameters for Solubility Prediction of Ketoconazole in Binary Solvents at Various Temperatures

inferredcites →https://doi.org/10.1007/s11814-011-0239-6openalex-snapshot

Density, viscosity, and surface tension of water+ethanol mixtures from 293 to 323K

inferredcites →https://doi.org/10.1016/0040-6031(92)85059-5openalex-snapshot

Mathematical representation of thermodynamic properties

inferredcites →https://doi.org/10.1016/j.cjche.2018.11.005openalex-snapshot

Determination and correlation solubility of m-phenylenediamine in (methanol, ethanol, acetonitrile and water) and their binary solvents from 278.15 K to 313.15 K

inferredcites →https://doi.org/10.1016/j.cjche.2020.09.054openalex-snapshot

Solubility measurement and thermodynamic modeling of carbamazepine (form III) in five pure solvents at various temperatures

inferredcites →https://doi.org/10.1016/j.fluid.2012.09.027openalex-snapshot

Thermodynamic analysis and correlation of solubility of candesartan cilexetil in aqueous solvent mixtures

inferredcites →https://doi.org/10.1016/j.fluid.2013.11.001openalex-snapshot

The solubility of mercaptosuccinic acid in water + (methanol, ethanol, acetone) mixtures from (278.15 to 333.15 K)

inferredcites →https://doi.org/10.1016/j.jct.2010.10.018openalex-snapshot

Densities and volume properties of (water + tert-butanol) over the temperature range of (274.15 to 348.15) K at pressure of 0.1 MPa

inferredcites →https://doi.org/10.1016/j.jct.2014.05.018openalex-snapshot

Determination and correlation of cefuroxime acid solubility in (acetonitrile + water) mixtures

inferredcites →https://doi.org/10.1016/j.jct.2015.12.022openalex-snapshot

Determination and correlation of solubility and thermodynamic properties of l-methionine in binary solvents of water + (methanol, ethanol, acetone)

inferredcites →https://doi.org/10.1016/j.jct.2016.08.023openalex-snapshot

Determination and thermodynamic modelling for 4-nitropyrazole solubility in (methanol + water), (ethanol + water) and (acetonitrile + water) binary solvent mixtures from T= (278.15 to 318.15) K

inferredcites →https://doi.org/10.1016/j.jct.2016.08.035openalex-snapshot

Solubility determination and thermodynamic modelling of allisartan isoproxil in different binary solvent mixtures from T= (278.15 to 313.15) K and mixing properties of solutions

inferredcites →https://doi.org/10.1016/j.jct.2016.09.039openalex-snapshot

Solubility of L-histidine in different aqueous binary solvent mixtures from 283.15 K to 318.15 K with experimental measurement and thermodynamic modelling

inferredcites →https://doi.org/10.1016/j.jct.2016.10.018openalex-snapshot

Solubility determination and correlation for o-phenylenediamine in (methanol, ethanol, acetonitrile and water) and their binary solvents from T= (283.15–318.15) K

inferredcites →https://doi.org/10.1016/j.jct.2016.10.022openalex-snapshot

Determination and correlation of Avermectin B1a solubility in different binary solvent mixtures at temperatures from (283.15 to 313.15) K

inferredcites →https://doi.org/10.1016/j.jct.2017.03.005openalex-snapshot

Preferential solvation of pioglitazone hydrochloride in some binary co-solvent mixtures according to the inverse Kirkwood–Buff integrals method

inferredcites →https://doi.org/10.1016/j.jct.2017.05.005openalex-snapshot

Solubility, solution thermodynamics and preferential solvation for 4-bromopyrazole in mixed solvents of (methanol/ethanol + water) from T= (283.15 to 318.15) K

inferredcites →https://doi.org/10.1016/j.jct.2017.07.027openalex-snapshot

Thermodynamic modelling of solubility and preferential solvation for ribavirin (II) in co-solvent mixtures of (methanol, n-propanol, acetonitrile or 1,4-dioxane) + water

inferredcites →https://doi.org/10.1016/j.molliq.2009.02.003openalex-snapshot

Prediction of drug solubility in mixed solvents using computed Abraham parameters

inferredcites →https://doi.org/10.1016/j.molliq.2016.07.063openalex-snapshot

Correlation and semi-empirical modeling of solubility of gallic acid in different pure solvents and in binary solvent mixtures of propan-1-ol + water, propan-2-ol + water and acetonitrile + water from (293.2 to 318.2) K

inferredcites →https://doi.org/10.1016/j.molliq.2016.10.127openalex-snapshot

Solubility and solution thermodynamics of cetilistat in water and (acetone, isopropyl alcohol, acetonitrile) binary solvent mixtures

inferredcites →https://doi.org/10.1016/j.molliq.2018.01.171openalex-snapshot

Mathematical derivation of the Jouyban-Acree model to represent solute solubility data in mixed solvents at various temperatures

inferredcites →https://doi.org/10.1016/j.molliq.2018.02.068openalex-snapshot

Measurement and correlation of clotrimazole solubility in ethanol + water mixtures at T = (293.2 to 313.2) K

inferredcites →https://doi.org/10.1016/j.molliq.2018.10.031openalex-snapshot

Prediction of paracetamol solubility in cosolvency systems at different temperatures

inferredcites →https://doi.org/10.1016/s0378-5173(03)00273-4openalex-snapshot

Solubility of drugs in aqueous solutions Part 2: Binary nonideal mixed solvent

inferredcites →https://doi.org/10.1021/acs.jced.0c00770openalex-snapshot

Solid–Liquid Phase Equilibrium and Ternary Phase Diagrams of Telmisartan-Saccharin Cocrystal in Methanol, Ethanol, and Methanol/Chloroform Mixtures at 298.15 and 313.15 K

inferredcites →https://doi.org/10.1021/acs.jced.5b00565openalex-snapshot

Measurement and Correlation of the Solubility of Maltitol in Different Pure Solvents, Methanol–Water Mixtures, and Ethanol–Water Mixtures

inferredcites →https://doi.org/10.1021/acs.jced.5b00617openalex-snapshot

Measurement and Correlation of Solubility of Cefathiamidine in Water + (Acetone, Ethanol, or 2-Propanol) from (278.15 to 308.15) K

inferredcites →https://doi.org/10.1021/acs.jced.6b00361openalex-snapshot

Measurement and Correlation of the Solubility of p-Coumaric Acid in Nine Pure and Water + Ethanol Mixed Solvents at Temperatures from 293.15 to 333.15 K

inferredcites →https://doi.org/10.1021/acs.jced.7b00245openalex-snapshot

Solubility Determination and Thermodynamic Modeling of Sodium Thioglycolate in Pure and Binary Solvent Mixtures from T = (293.15 to 333.15) K

inferredcites →https://doi.org/10.1021/acs.jced.8b00025openalex-snapshot

Solubility Measurement and Thermodynamic Modeling of Benzoic Acid in Monosolvents and Binary Mixtures

inferredcites →https://doi.org/10.1021/acs.jced.8b00309openalex-snapshot

Solubility Determination and Correlation for Pyridoxal 5-Phosphate Monohydrate in Different Binary Solvents from 278.15 K to 318.15 K

inferredcites →https://doi.org/10.1021/acs.jced.8b00361openalex-snapshot

Determination and Correlation of the Solubility of l -Fucose in Four Binary Solvent Systems at the Temperature Range from 288.15 to 308.15 K

inferredcites →https://doi.org/10.1021/acs.jced.9b00009openalex-snapshot

Measurement and Correlation of Solubility of Calcium Formate (Form α) in Different Binary Solvent Mixtures at Temperatures from 283.15 to 323.15 K

inferredcites →https://doi.org/10.1021/acssuschemeng.2c02270openalex-snapshot

Freeze-Dissolving Method: A Fast Green Technology for Producing Nanoparticles and Ultrafine Powder

inferredcites →https://doi.org/10.1021/ie402588topenalex-snapshot

Solubility of Nifedipine in Ethanol + Water and Propylene Glycol + Water Mixtures at 293.2 to 313.2 K

inferredcites →https://doi.org/10.1021/ie501000kopenalex-snapshot

Determination of Solubility of cAMPNa in Water + (Ethanol, Methanol, and Acetone) within 293.15–313.15 K

inferredcites →https://doi.org/10.1021/je00007a023openalex-snapshot

Partial molar volumes for acetonitrile + water

inferredcites →https://doi.org/10.1021/je020226copenalex-snapshot

Solubility in Binary Solvent Mixtures: Pyrene Dissolved in Alcohol + Acetonitrile Mixtures at 299.2 K

inferredcites →https://doi.org/10.1021/je030102fopenalex-snapshot

Experimental Densities and Excess Volumes for Binary Mixtures Containing Propionic Acid, Acetone, and Water from 283.15 K to 323.15 K at Atmospheric Pressure

inferredcites →https://doi.org/10.1021/je5000428openalex-snapshot

Solubility of Trehalose in Water + Ethanol Solvent System from (288.15 to 318.15) K

inferredcites →https://doi.org/10.1021/je500416kopenalex-snapshot

Measurement and Correlation of Solubility of Calcium- l -lactate Pentahydrate in Ethanol + Water and Acetone + Water Systems

inferredcites →https://doi.org/10.1021/je800063dopenalex-snapshot

Solubility of Lovastatin in Acetone + Water Solvent Mixtures

inferredcites →https://doi.org/10.1021/je900045zopenalex-snapshot

Solubilities of Triadimefon in Acetone + Water from (278.15 to 333.15) K

inferredcites →https://doi.org/10.1021/je9000729openalex-snapshot

Solubility of Ethyl Maltol in Aqueous Ethanol Mixtures

inferredcites →https://doi.org/10.1023/b:pham.0000016237.06815.7aopenalex-snapshot

A Quantitative Structure-Property Relationship for Predicting Drug Solubility in PEG 400/Water Cosolvent Systems

inferredcites →https://doi.org/10.1039/c6gc02440hopenalex-snapshot

Q-SA√ESS: a methodology to help solvent selection for pharmaceutical manufacture at the early process development stage

inferredcites →https://doi.org/10.1080/00319104.2016.1198481openalex-snapshot

Preferential solvation of etoricoxib in some aqueous binary cosolvent mixtures at 298.15 K

inferredcites →https://doi.org/10.1080/00319104.2019.1594227openalex-snapshot

Solubility of sulphadiazine in (acetonitrile + water) mixtures: measurement, correlation, thermodynamics and preferential solvation

inferredcites →https://doi.org/10.1248/cpb.46.1058openalex-snapshot

The Modified Wilson Model and Predicting Drug Solubility in Water-Cosolvent Mixtures.

inferredcites →https://doi.org/10.18433/j3pp4kopenalex-snapshot

Review of the cosolvency models for predicting solubility of drugs in water-cosolvent mixtures

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4864994openalex-extracted

A Volumetric Method for Fast Solubility Measurement - Isomaltitol as an Example

inferred← citeshttps://doi.org/10.1021/acs.iecr.4c02110openalex-snapshot

Data-Driven Point Adjusted Jouyban-Acree-Artificial Neural Network Hybrid Model for Predicting Solubility of Active Pharmaceutical Ingredients in Binary Solvent Mixtures

inferred← citeshttps://doi.org/10.1021/acs.jced.3c00462openalex-snapshot

Exploring the Dissolution Behavior of m -Hydroxybenzoic Acid in 14 Pure Solvents Using Thermodynamic, Molecular Simulation and Hansen Solubility Parameters

inferred← citeshttps://doi.org/10.1021/acs.jced.5c00667openalex-snapshot

Liquid–Liquid Phase Separation and Solubility of Isomalt in Five Binary Solvents: Hansen Solubility Parameters, Molecular Dynamics Simulations and Thermodynamic Properties at 283.15–323.15 K

inferred← citeshttps://doi.org/10.3390/ph17121594openalex-snapshot

Dissolution Thermodynamics of the Solubility of Sulfamethazine in (Acetonitrile + 1-Propanol) Mixtures

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