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- W2086765622 abstract "A systematic investigation of the polymorph−hydrate system for Compound I was carried out with the objective of understanding the phase relationships between the different forms as it relates to crystallization conditions. The ternary phase diagram was determined from solubility and KF measurements of the supernatant liquor for Compound I−water−ethanol mixtures. Water concentrations were converted to water activities using the NRTL-RK model as implemented in ASPEN Properties. These water activities were then used in defining phase boundaries between anhydrous and the various hydrated forms of Compound I. Since the critical water activity at the phase boundaries between anhydrous and hydrated forms in water−cosolvent systems is independent of the nature of the cosolvent it can be used to extrapolate the water concentrations defining ternary phase boundaries in any other cosolvent−water system. This was demonstrated in the cases of acetonitrile−water and dimethyl acetamide−water. Triple points (anhydrate−hydrate−solvent) were estimated in these two cosolvent−water systems. Two representative crystallizations in these crystallization solvents produced a hemihydrate in 15% acetonitrile−water, and the tetrahydrate in 15% dimethyl acetamide−water, both of which were predicted by the phase diagrams in these systems. The importance of this work lies in obviating the need for phase equilibria measurements in every cosolvent−water system used in crystallization processes. Additionally the crystal structure of hemihydrate was solved by single-crystal X-ray diffraction, and the binding mode of water in the lattice elucidates the thermal and hygroscopicity behavior of this form. In addition the crystal structure unambiguously identified the hemihydrate and enabled the design on an appropriate crystallization process incorporating aw as a major variable." @default.
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- W2086765622 date "2007-03-01" @default.
- W2086765622 modified "2023-10-16" @default.
- W2086765622 title "Water Activity-Mediated Control of Crystalline Phases of an Active Pharmaceutical Ingredient" @default.
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- W2086765622 doi "https://doi.org/10.1021/op600277t" @default.
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