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Model 5973n mass selective detector

Manufactured by Agilent Technologies
Sourced in United States

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.

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2 protocols using model 5973n mass selective detector

1

Extraction and Analysis of H. petiolaris Essential Oil

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The aerial parts of H. petiolaris plants were collected after a cultivation period of 6 months. The essential oil was extracted by steam distillation from the dried plant biomass using a benchtop scale extractor (Figmay SRL, Argentina). From each site, five samples of floral water (a by-product from distillation) and essential oil were filtered (0.22 µm), and five samples of the plant waste were digested, as mentioned above, to determine Pb concentrations by inductively coupled plasma-atomic emission spectrometry (ICP-OES, Agilent Technologies, 700 series, Belgium).
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.
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2

GC-MS Fatty Acid Profiling

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GC-MS analysis of the methyl ester and pyrrolidine derivatives allowed identifiying the fatty acids present in each fraction. The analyses were performed on a model 6890N gas chromatograph (Agilent, USA) coupled to a model 5973N mass selective detector (Agilent, USA), on a DB-5MS column, using helium as carrier gas. The injection volume was 0.2 μL and temperatures of 175 °C and 250 °C were used for the injector and detector, respectively. The oven was programmed in three steps: it was started at a temperature of 50 °C for 1 min, then increased at a rate of 5 °C/min to 150 °C, where it remained for 3 min, and then increased at 10 °C/min to 300 °C and held for 16 min.
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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