The GC-MS analysis were performed using a Hewlett-Packard HP 7890A GC coupled to a 5975C MS (Agilent Technologies, SC, USA) with a SLB-5ms column (Supelco) (30 m × 0.25 mm × 0.5 µm). Operating conditions for GC/MS analysis were as follows: helium flow, 0.8 mL/min; initial oven temperature, 40 °C (2 min), raised to 240 °C at 8 °C/min rate, held for 6 min isothermally. For all peaks retention indices were calculated to compare results obtained by GC/MS with literature data and mass spectra of eluting compounds to those of the NIST 05 library match (NIST MS Search v2.0, Toronto, Canada 2005). Retention indices were calculated for each compound using homologous series of C7–C20 n-alkanes. Mass spectra were recorded in an electron impact mode (70 eV) in a scan range of m/z 33–350 [18 (link)]. The ion source temperature was set at 200 °C. The composition of EO has been expressed as the percentage composition calculated from the chromatogram obtained on the SLB-5 column. Normalized peak area % were calculated based on the total ion chromatogram (TIC) without obtaining response factor for particular compounds.
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