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Both chiral analysis and compound-specific stable carbon isotope analysis have limitations when applied to environmental research. However, the combination of these two techniques might overcome their respective limitation and give more insight into the enantioselective fate and source apportionment of chiral organic contaminants.
After Soxhlet extraction and clean-up, sediment extracts were further pre-concentrated using normal-phase preparative high-performance liquid chromatography to isolate sufficient quantities of highly purified galaxolide (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran; HHCB). The enantiomeric fractions and stable carbon isotopes of the HHCB were determined using gas chromatography/mass spectrometry (GC/MS) and GC/isotope ratio mass spectrometry (IRMS).