Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/67551
DC FieldValue
dc.titleSolubility phase diagram of praziquantel enantiomeric system
dc.contributor.authorLim, B.-G.
dc.contributor.authorTan, R.B.H.
dc.contributor.authorNg, S.-C.
dc.contributor.authorChing, C.-B.
dc.date.accessioned2014-06-17T10:02:31Z
dc.date.available2014-06-17T10:02:31Z
dc.date.issued1995
dc.identifier.citationLim, B.-G.,Tan, R.B.H.,Ng, S.-C.,Ching, C.-B. (1995). Solubility phase diagram of praziquantel enantiomeric system. Chirality 7 (2) : 74-81. ScholarBank@NUS Repository.
dc.identifier.issn08990042
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67551
dc.description.abstractThe solubility behaviour of praziquantel enantiomeric system at -15°C, 4°C, and 15°C is presented. This system exhibits both a pseudoracemate behaviour and one which leads to the formation of enantiomerically pure crystals. For solutions with lower enantiomeric purity, the pseudoracemate behaviour is more prominent. Solid solutions are formed when the mixtures of the enantiomers are crystallised. The phase diagram shows a complete absence of a eutectic. For mixtures with higher enantiomeric purity, pure crystals of the excess enantiomer are obtained when the solution is crystallised. Temperature dependency of this polymorphism is not significant. With these phase diagrams, a method is suggested to obtain enantiomerically pure isomers of praziquantel from a partially resolved mixture.
dc.sourceScopus
dc.subjectcrystallisation
dc.subjectoptical resolution
dc.subjectpolymorphism
dc.subjectpseudoracemate
dc.subjectsolid solution
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleChirality
dc.description.volume7
dc.description.issue2
dc.description.page74-81
dc.description.codenCHRLE
dc.identifier.isiutNOT_IN_WOS
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