A novel derivatization procedure and chiral gas chromatographic method for enantiomeric purity screening of L-carnitine

Acta Chim Slov. 2014;61(4):889-93.

Abstract

L-Carnitine is used extensively in functional foods and food supplements; consequently, the control of its enantiomeric purity is of paramount importance. A new derivatization procedure and chiral gas chromatographic method with flame ionization detection, using a cyclodextrin based stationary phase, enables prompt, simple, and inexpensive screening of the enantiomeric ratio of L- and D-carnitine in samples with different matrices. Conversion of carnitine to beta-acetoxy-gama-butyrolactone was optimized for maximum conversion (98% of the desired product lactone was formed and 2% of the side product gama-crotonolactone) and minimum racemization (no changes at the chiral center were detected) and time consumption. As it is shown in this study, a fast gas chromatographic method, with total run time of 7 min, together with the new derivatization procedure enables an effective enantiomeric purity screening of L-carnitine in real samples such as food supplements and L-carnitine raw ingredient.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives
  • 4-Butyrolactone / chemistry
  • Carnitine / analysis
  • Carnitine / chemistry*
  • Chemistry Techniques, Analytical
  • Chromatography, Gas / methods*
  • Chromatography, High Pressure Liquid
  • Cyclodextrins / chemistry
  • Dietary Supplements
  • Lactones / chemistry
  • Models, Chemical
  • Stereoisomerism
  • Time Factors

Substances

  • Cyclodextrins
  • Lactones
  • butenolide
  • 4-Butyrolactone
  • Carnitine