Please use this identifier to cite or link to this item: https://doi.org/10.1002/chir.20075
DC FieldValue
dc.titlePhysicochemical properties, binary and ternary phase diagrams of ketoprofen
dc.contributor.authorLu, Y.H.
dc.contributor.authorChing, C.B.
dc.date.accessioned2014-06-17T07:46:53Z
dc.date.available2014-06-17T07:46:53Z
dc.date.issued2004
dc.identifier.citationLu, 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.issn08990042
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64407
dc.description.abstractCompared 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.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/chir.20075
dc.sourceScopus
dc.subjectAntiinflammatory
dc.subjectCrystallization
dc.subjectPhase diagram
dc.subjectRacemic compound
dc.subjectSolubility
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/chir.20075
dc.description.sourcetitleChirality
dc.description.volume16
dc.description.issue8
dc.description.page541-548
dc.description.codenCHRLE
dc.identifier.isiut000223841100010
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