The H. petiolaris essential oil composition was analyzed in an HP 6890N Series Plus gas chromatograph (Agilent Technologies, Palo Alto, California, EE. UU.), equipped with a model 5973N mass selective detector (Agilent Technologies, Palo Alto, California, EE. UU.) and an HP 6890 Series autoinjector. The separation of the compounds was achieved using an HP-5 MS capillary column (30 m × 0.25 mm I.D., 0.25 m film thickness, and 5% phenylmethylsiloxane), supplied by J&W Scientific (Folsom, CA, USA). Based on a mass scan range of 50–550 atomic mass units (AMU) with SCAN mode, the retention times of the compounds were determined by comparing the MS fragmentation pattern of the standards and the National Institute of Standards and Technology (NIST) 2.0 GC–MS library.
Model 5973n mass selective detector
The Agilent Model 5973N mass selective detector is a laboratory instrument used for the identification and quantification of chemical compounds. It operates by ionizing and separating molecules based on their mass-to-charge ratio, providing detailed information about the chemical composition of a sample.
Lab products found in correlation
2 protocols using model 5973n mass selective detector
Extraction and Analysis of H. petiolaris Essential Oil
The H. petiolaris essential oil composition was analyzed in an HP 6890N Series Plus gas chromatograph (Agilent Technologies, Palo Alto, California, EE. UU.), equipped with a model 5973N mass selective detector (Agilent Technologies, Palo Alto, California, EE. UU.) and an HP 6890 Series autoinjector. The separation of the compounds was achieved using an HP-5 MS capillary column (30 m × 0.25 mm I.D., 0.25 m film thickness, and 5% phenylmethylsiloxane), supplied by J&W Scientific (Folsom, CA, USA). Based on a mass scan range of 50–550 atomic mass units (AMU) with SCAN mode, the retention times of the compounds were determined by comparing the MS fragmentation pattern of the standards and the National Institute of Standards and Technology (NIST) 2.0 GC–MS library.
GC-MS Fatty Acid Profiling
The mass spectra were compared with the NIST02.L and NIST5a.L databases and the information was generated with MSD ChemStation software. The relative abundance of the fatty acids was calculated with the area under the curve of each chromatographic peak of the methyl ester derivatives. Each analysis was performed in triplicate.
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