Literature DB >> 16863194

Crystallization of a salt of a weak organic acid and base: solubility relations, supersaturation control and polymorphic behavior.

H P Jones1, R J Davey, B G Cox.   

Abstract

Control of crystallization processes for organic salts is of importance to the pharmaceutical industry as many active pharmaceutical materials are marketed as salts. In this study, a method for estimating the solubility product of a salt of a weak acid and weak base from measured pH-solubility data is described for the first time. This allows calculation of the supersaturation of solutions at known pH. Ethylenediammonium 3,5-dinitrobenzoate is a polymorphic organic salt. A detailed study of the effects of pH, supersaturation, and temperature of crystallization on the physical properties of this salt shows that the desired polymorph may be produced by appropriate selection of the pH and supersaturation of crystallization. Crystal morphology is also controlled by these crystallization conditions.

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Year:  2005        PMID: 16863194     DOI: 10.1021/jp045000q

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  3 in total

1.  Analysis of relationships between solid-state properties, counterion, and developability of pharmaceutical salts.

Authors:  Peter Guerrieri; Alfred C F Rumondor; Tonglei Li; Lynne S Taylor
Journal:  AAPS PharmSciTech       Date:  2010-08-03       Impact factor: 3.246

2.  Improving pharmacy students' understanding and long-term retention of acid-base chemistry.

Authors:  Victoria F Roche
Journal:  Am J Pharm Educ       Date:  2007-12-15       Impact factor: 2.047

3.  Incorporation of physiologically based pharmacokinetic modeling in the evaluation of solubility requirements for the salt selection process: a case study using phenytoin.

Authors:  Po-Chang Chiang; Harvey Wong
Journal:  AAPS J       Date:  2013-08-14       Impact factor: 4.009

  3 in total

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