Determination of the enantiomers of 3-tert.-butylamino-1,2-propanediol by high-performance liquid chromatography using mass spectrometric detection

J Chromatogr A. 2000 Oct 27;896(1-2):201-7. doi: 10.1016/s0021-9673(00)00558-6.

Abstract

The chiral synthesis of beta-blockers such as (S)-timolol requires a sensitive analytical method for the enantioseparation of its intermediate, 3-tert.-butylamino-1,2-propanediol, in the ng/ml range. The method developed is based on on-line normal-phase LC-MS-MS using a chiral stationary phase and an atmospheric pressure chemical ionization (APCI) interface. The MS detection of 3-tert.-butylamino-1,2-propanediol was first optimized with a pneumatically-assisted electrospray interface (ionspray). The APCI interface was then selected for LC-MS-MS because of the incompatibility of electrospray with n-hexane. The method was validated for both enantiomers in the 25-500 ng/ml concentration range.

MeSH terms

  • Atmospheric Pressure
  • Chromatography, High Pressure Liquid / methods*
  • Mass Spectrometry
  • Propylene Glycols / analysis*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Stereoisomerism

Substances

  • 3-tert-butylamino-1,2-propanediol
  • Propylene Glycols