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Solid and Solution State Thermodynamics of Polymorphs of Butamben (Butyl 4-Aminobenzoate) in Pure Organic Solvents
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Transport Phenomena.ORCID iD: 0000-0002-6647-3308
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Transport Phenomena.
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2019 (English)In: Journal of Pharmaceutical Sciences, ISSN 0022-3549, E-ISSN 1520-6017, Vol. 108, no 7, p. 2377-2382Article in journal (Refereed) Published
Abstract [en]

The solubility of butamben has been measured gravimetrically in pure methanol, 1-propanol, 2-propanol, 1-butanol, and toluene over the temperature range 268-298 K. Polymorph transition and melting temperatures, associated enthalpy changes, and the heat capacity of the solid forms and the supercooled melt have been measured by differential scanning calorimetry. Based on extrapolated calorimetric data, the Gibbs energy, enthalpy and entropy of fusion, and the activity of solid butamben (the ideal solubility) have been calculated from below ambient temperature up to the melting point. Activity coefficients of butamben at equilibrium in the different solvents have been estimated from solubility data and the activity of the solid, revealing that all investigated systems exhibit positive deviation from Raoult's law. Solubility data are well correlated by a semiempirical regression model. On a mass basis, the solubility is clearly higher in methanol than in the other solvents, but mole fraction solubilities are very similar across all 5 solvents. The 2 known polymorphs are enantiotropically related, and the transition point is located at 283 K. Polymorph interconversions occur within 0.3 K of the transition point even in the solid state, and the 2 forms exhibit strong similarities in investigated properties.

Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 108, no 7, p. 2377-2382
National Category
Chemical Engineering
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URN: urn:nbn:se:kth:diva-260000DOI: 10.1016/j.xphs.2019.02.013ISI: 000477753400018PubMedID: 30807760Scopus ID: 2-s2.0-85063011446OAI: oai:DiVA.org:kth-260000DiVA, id: diva2:1355932
Note

QC 29181004

Available from: 2019-09-30 Created: 2019-09-30 Last updated: 2019-10-07Bibliographically approved

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Svärd, MichaelRasmuson, Åke C.

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