Solubility Measurements of Finerenone in Ten Monosolvents and Two Binary Solvent Mixtures

The solubility of finerenone, a third-generation nonsteroidal mineralocorticoid receptor antagonist drug, was measured in 10 monosolvents (methanol, ethanol, isopropanol, methyl acetate, ethyl acetate, isopropyl acetate, acetone, 2-butanone, acetonitrile, and dichloromethane) and two binary solvent mixtures (methanol + water and acetonitrile + water). Measurements were conducted at temperatures ranging from 273.15 to 313.15 K using PAT tools. In the methanol + water system, water acted solely as an antisolvent. However, in the acetonitrile + water system, finerenone’s solubility exceeded its solubility in pure acetonitrile, reaching a maximum at a water mass fraction of approximately 0.2. To expand the applicability of the results, the experimental solubility data was correlated with the modified Apelblat model, the λh model, and the CNIBS/R-K model. The relative average deviation and root-mean-square deviation values indicate that the correlation results align well with the experimental data, and the modified Apelblat model proved the most suitable.

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Publication Details

Journal
Journal of Chemical & Engineering Data
Published
2025-03-04
DOI
https://doi.org/10.1021/acs.jced.5c00011
Citations
2
Primary Topic
Crystallization and Solubility Studies
Type
article
Field-Weighted Citation Impact
1.04
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article

Solubility Measurements of Finerenone in Ten Monosolvents and Two Binary Solvent Mixtures

Yanfang Wu, Shu‐Wei Chang, Yan Liu, Lin Jia
2 citations
Journal of Chemical & Engineering Data
Crystallization and Solubility Studies
1.04
article

Solubility Measurements of Finerenone in Ten Monosolvents and Two Binary Solvent Mixtures

Yanfang Wu, Shu‐Wei Chang, Yan Liu, Lin Jia
article en
2 citations

Abstract

The solubility of finerenone, a third-generation nonsteroidal mineralocorticoid receptor antagonist drug, was measured in 10 monosolvents (methanol, ethanol, isopropanol, methyl acetate, ethyl acetate, isopropyl acetate, acetone, 2-butanone, acetonitrile, and dichloromethane) and two binary solvent mixtures (methanol + water and acetonitrile + water). Measurements were conducted at temperatures ranging from 273.15 to 313.15 K using PAT tools. In the methanol + water system, water acted solely as an antisolvent. However, in the acetonitrile + water system, finerenone’s solubility exceeded its solubility in pure acetonitrile, reaching a maximum at a water mass fraction of approximately 0.2. To expand the applicability of the results, the experimental solubility data was correlated with the modified Apelblat model, the λh model, and the CNIBS/R-K model. The relative average deviation and root-mean-square deviation values indicate that the correlation results align well with the experimental data, and the modified Apelblat model proved the most suitable.

Journal of Chemical & Engineering DataVol. 70(3)
East China University of Science and Technology (CN)
Openalex Percentile: Top 27%
Crystallization and Solubility Studies
1.04
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Solubility Measurements of Finerenone in Ten Monosolvents and Two Binary Solvent Mixtures — Yanfang Wu, Shu‐Wei Chang, et al. · Journal of Chemical & Engineering Data (2025) | TGRS Research Map | TGRS