Essential oils were chemically analyzed [25 (link)] within two months of their production date. Ten microliter of each essential oil sample was added into a clear screw-top GC-vial (6.0 mm diameter, silicone septa, 2 mL volume), and then 1.5 mL of dichloromethane was added to each vial. A blank containing only dichloromethane was included to confirm its purity. Essential oils were analyzed using a gas chromatography apparatus equipped with a quadruple mass spectrometer (GC-MS) (Shimadzu, GC-MS-QP/5050A). A nonpolar capillary column (DB-5MS, thickness; 0.25 μm, length; 30 m, internal diameter; 0.25 mm) was used to separate the components of the essential oils using a splitless mode. The temperature was kept at 51 °C for 1 min and then raised to 211 °C at a rate of 3 °C min−1. The injector temperature was 275 °C, and the interface temperature was 300 °C. Helium was used as the carrier gas. Chemical compounds were identified by matching their fragmentation patterns in the resultant mass spectra with those stored in the computer’s mass spectral database.
Free full text: Click here