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J Pharm Biomed Anal ; 31(4): 693-9, 2003 Mar 26.
Article in English | MEDLINE | ID: mdl-12644196

ABSTRACT

Protolytic equilibria in homogeneous and heterogeneous systems of lorazepam and oxazepam, which are sparingly soluble ampholytes from the class of 1,4-benzodiazepines, were studied at 25 degrees C and ionic strength of 0.1 M. Acidity constants and equilibrium constants in a heterogeneous system were determined. On the basis of the analysis of the corresponding 13C- and 1H-NMR spectra, deprotonation site in the molecules of the investigated compounds was predicted. Finally, the correlation between chemical shifts in the 1H-NMR spectra and the acidity of the amide proton of 1,4-benzodiazepines was established.


Subject(s)
Lorazepam/analysis , Lorazepam/chemistry , Oxazepam/analysis , Oxazepam/chemistry , Magnetic Resonance Spectroscopy/methods , Spectrophotometry, Ultraviolet/methods
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