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https://doi.org/10.1002/chir.20075
DC Field | Value | |
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dc.title | Physicochemical properties, binary and ternary phase diagrams of ketoprofen | |
dc.contributor.author | Lu, Y.H. | |
dc.contributor.author | Ching, C.B. | |
dc.date.accessioned | 2014-06-17T07:46:53Z | |
dc.date.available | 2014-06-17T07:46:53Z | |
dc.date.issued | 2004 | |
dc.identifier.citation | Lu, Y.H., Ching, C.B. (2004). Physicochemical properties, binary and ternary phase diagrams of ketoprofen. Chirality 16 (8) : 541-548. ScholarBank@NUS Repository. https://doi.org/10.1002/chir.20075 | |
dc.identifier.issn | 08990042 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/64407 | |
dc.description.abstract | Compared to simulated moving bed (SMB) chromatography, fractional crystallization is a simple and economical method for enantioseparation. Therefore, the coupling of SMB chromatography and fractional crystallization is suggested for enantioseparation of racemic compounds. In this work, a nonsteroidal antiinflammatory drug, ketoprofen (Kp), was chosen to be studied. Kp was verified as a racemic compound by FTIR, PXRD, and thermodynamic calculations. To derive the condition where pure (S)-Kp could be crystallized from a solution, which was previously enantiomerically enriched, the binary melting phase diagram and the ternary solubility phase diagram in the mixed solvent of ethanol and water over a temperature range of 15-30°C were obtained. From these phase diagrams the eutectic point was determined as 91.6% mole percent (S)-Kp from the binary phase diagram and 91% from the ternary phase diagram. The results may provide valuable experiment data for the possibility of coupling fractional crystallization with SMB for Kp separation. © 2004 Wiley-Liss, Inc. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/chir.20075 | |
dc.source | Scopus | |
dc.subject | Antiinflammatory | |
dc.subject | Crystallization | |
dc.subject | Phase diagram | |
dc.subject | Racemic compound | |
dc.subject | Solubility | |
dc.type | Article | |
dc.contributor.department | CHEMICAL & BIOMOLECULAR ENGINEERING | |
dc.description.doi | 10.1002/chir.20075 | |
dc.description.sourcetitle | Chirality | |
dc.description.volume | 16 | |
dc.description.issue | 8 | |
dc.description.page | 541-548 | |
dc.description.coden | CHRLE | |
dc.identifier.isiut | 000223841100010 | |
Appears in Collections: | Staff Publications |
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