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6890 series 2 a

Manufactured by Hewlett-Packard

The 6890 series II A is a high-performance gas chromatograph designed for laboratory use. It features a precise temperature control system and advanced data analysis software. The core function of this product is to separate, identify, and quantify chemical compounds in a complex mixture.

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2 protocols using 6890 series 2 a

1

GC-FID and GC-MS Analysis of Compounds

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GC-FID analysis was performed on a Hewlett Packard 6890 series II A gas chromatograph equipped with HP-5MS capillary column (30 m × 0.25 mm × 0.25 μm film thickness). Helium was used as a carrier gas at a flow rate of 0.7 mL/min. Injector and detector temperatures were set at 250 and 280 °C, respectively. The oven temperature was kept at 50 °C, then gradually raised to 280 °C at 5
°C/min and finally held isothermally for 15 min. Diluted samples (1/ 100 in diethyl ether, v/v) of 1.0 μL were injected manually (split ratio 50:1).
Gas chromatography-mass spectrometry (GC-MS) chromatograms were recorded using a Hewlett Packard Model 5890A gas chromatography and a Hewlett Packard Model 5989A mass spectrometer. The GC was equipped with HP-5 column. Helium was used as carrier gas at a flow rate of 1 mL/min. The injector temperature was 250 °C. The oven temperature was programmed from 50 °C (5 min hold) to 250 °C at 10 °C/min and finally held isothermally for 15 min. For GC-MS detection, an electron ionization system, with ionization energy of 70 eV was used. A scan rate of 0.5 s (cycle time: 0.2 s) was applied, covering a mass range from 50-400 amu.
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2

Hydrodistillation and GC Analysis of Essential Oils

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Extraction of essential oils was done by the hydrodistillation method. The fresh leaf and bark of each plant (300 g) were chopped and hydrodistilled using a Dean-stark apparatus for 8 h. The essential oils obtained were dried over anhydrous magnesium sulfate and stored at 4-6°C. Gas chromatography (GC) analysis was performed on a Hewlett Packard 6890 series II A gas chromatograph equipped with an Ultra-1 column (100% polymethylsiloxanes). Helium was used as a carrier gas at a flow rate of 0.7 mL min -1 . Injector and detector temperature were set at 250 and 280°C respectively. The oven temperature was kept at 50°C, then gradually raised to 280°C at 5°C min -1 and finally held isothermally for 15 min. Diluted samples (1/100 in diethyl ether, v/v) of 1.0 μL were injected manually (split ratio 50:1). The injection was repeated three times and the peak area percents were reported as means ±SD of triplicates. The calculation of peak area percentage was carried out by using the GC HP Chemstation software (Agilent Technologies, USA).
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