Literature DB >> 3244652

Thermodynamics in the prediction of the solubilities of binary mixtures of the diastereoisomers and enantiomers of ephedrine.

W F Schmidt1, W Porter, J T Carstensen.   

Abstract

Equations derived from the Clausius-Clapeyron and Prigogine-Defay equations were used to determine the free energy of mixing for diastereoisomers and enantiomers from heats of fusion and transition temperature data. These equations are applied to the thermodynamics of mixing of the six binary equimolar combinations of (1R,2S)-ephedrine, (1S,2R)-ephedrine; and (1R,2R)- and (1S,2S)-pseudoephedrine isomers. The relative equilibrium solubility of the binary mixtures in water is consistent with thermodynamic calculations.

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Year:  1988        PMID: 3244652     DOI: 10.1023/a:1015919913896

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  9 in total

1.  Cosolvency and cosolvent polarity.

Authors:  J T Rubino; S H Yalkowsky
Journal:  Pharm Res       Date:  1987-06       Impact factor: 4.200

2.  Theoretical derivation of solute-solvent interaction parameter in binary solution: case of the deviation from Raoult's law.

Authors:  Z Liron; S Srebrenik; A Martin; S Cohen
Journal:  J Pharm Sci       Date:  1986-05       Impact factor: 3.534

3.  Steric aspects of adrenergic drugs. II. Effects of DL isomers and desoxy derivatives on the reserpine-pretreated vas deferens.

Authors:  P N Patil; J B LaPidus; D Campbell; A Tye
Journal:  J Pharmacol Exp Ther       Date:  1967-01       Impact factor: 4.030

4.  Solubility properties in polymers and biological media 5: an analysis of the physicochemical properties which influence octanol-water partition coefficients of aliphatic and aromatic solutes.

Authors:  R W Taft; M H Abraham; G R Famini; R M Doherty; J L Abboud; M J Kamlet
Journal:  J Pharm Sci       Date:  1985-08       Impact factor: 3.534

Review 5.  Molecular geometry and adrenergic drug activity.

Authors:  P N Patil; D D Miller; U Trendelenburg
Journal:  Pharmacol Rev       Date:  1974-12       Impact factor: 25.468

6.  Extended solubility approach: solubility parameters for crystalline solid compounds.

Authors:  A Martin; J Carstensen
Journal:  J Pharm Sci       Date:  1981-02       Impact factor: 3.534

7.  Stereochemical studies on medicinal agents. IV. Conformational analysis of ephedrine isomers and related compounds.

Authors:  P S Portoghese
Journal:  J Med Chem       Date:  1967-11       Impact factor: 7.446

8.  Expanded solubility parameter approach. I: Naphthalene and benzoic acid in individual solvents.

Authors:  A Beerbower; P L Wu; A Martin
Journal:  J Pharm Sci       Date:  1984-02       Impact factor: 3.534

9.  Linear solvation energy relationships: 36. Molecular properties governing solubilities of organic nonelectrolytes in water.

Authors:  M J Kamlet; R M Doherty; J L Abboud; M H Abraham; R W Taft
Journal:  J Pharm Sci       Date:  1986-04       Impact factor: 3.534

  9 in total
  2 in total

1.  Formation of the racemic compound of ephedrine base from a physical mixture of its enantiomers in the solid, liquid, solution, or vapor state.

Authors:  S P Duddu; D J Grant
Journal:  Pharm Res       Date:  1992-08       Impact factor: 4.200

2.  Nuclear magnetic resonance (NMR) spectroscopic investigation of interaction energies of ephedrine stereoisomers in noncrystalline solids and its correlation with thermodynamic data.

Authors:  W F Schmidt; I L Honigberg
Journal:  Pharm Res       Date:  1991-09       Impact factor: 4.200

  2 in total

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