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Trace 1300 series gc

Manufactured by Thermo Fisher Scientific
Sourced in Germany

The TRACE 1300 series GC is a gas chromatograph designed for accurate and reliable chemical analysis. It features a modular design and advanced technology to provide high-performance separation and detection of a wide range of analytes.

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4 protocols using trace 1300 series gc

1

GC-MS Analysis of Rhizome and Leaf ACEOs

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The ACEOs from rhizome and leaf were analyzed by Thermo Scientific™ TRACE™ 1300 Series GC operated with a split mode injector, Thermo Scientific AI/AS 1310 Series autosampler, and Thermo Scientific™ ISQ™ Series GC-Single Quadrupole MS. The following were the specifications used for analysis: column: TG Wax MS (acid-deactivated polyethylene glycol) 30 m, 0.25 mm i.d., 0.25 μm film thickness (Thermo Scientific, USA); temperature program: from 60°C to 150°C at 3°C/min and from 150°C to 240°C at 7°C/min; injector temperature: 240°C; injection volume: 1.0 μL; inlet pressure: 86.3 kPa; carrier gas: He; flow rate: 1.000 mL/min; injection mode: split (50 : 1); mass interface temp.: 250°C; MS mode: EI; detector voltage: 70 eV; mass range: 40–450; and interval: 0.2 sec. Data handling was made through Xcalibur software. The relative amount of individual components of the total oil is expressed as percentage peak area relative to total peak area. Qualitative identification of the different constituents was performed by comparison of their relative retention times and mass spectra with those of authentic reference compounds, or by retention indices (RI) and mass spectra. Compound identification was done by comparing the National Institute of Standards and Technology (NIST 2014) library data of the mass spectra peaks with those reported in the literature.
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2

GC-MS Analysis of Organic Compounds

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GC/MS measurements were performed with a Q Exactive GC (Thermo Fisher, Bremen, Germany), consisting of a AI/AS 1310 autosampler equipped TRACE 1300 series GC coupled to a Q Exactive Orbitrap MS. The injection volume of an individual sample was 0.2 μL and dichloromethane was used as injector cleaning solvent. The sample injector was operated at 300°C and split mode was selected with a split flow of 80 mL min−1, and a purge flow of 5 mL min-1. High purity helium (N5.0) was used as a carrier gas at a constant flow rate of 1.2 mL min-1. The GC separation was carried out on a RTX@-1ms capillary column (30 m × 0.25 mm ID, 0.25 um). The temperature program was performed with a starting temperature of 35°C, which was increased to a final temperature of 320°C at a heating rate of 10°C min−1 and then held at 320°C for additional 5 min. Transfer line temperature was set to 320°C. The eluted compounds from GC were ionized by EI at an electron energy of 70 eV. The mass spectra were recorded in full scan mode with a mass range of 30–600 Da at a mass resolution of 120,000 (FWHM at m/z 200). Collected GC-MS data were imported and characterized against NIST and our own MPI libraries by using the MassLib software package (MSP Kofel, Zollikofen, Switzerland).
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3

GC-MS Analysis of Chemical Samples

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Gas chromatography-mass spectrometry (GC-MS) analyses of the samples were performed using a Thermo Scientific Trace 1300 Series GC coupled to a Thermo Scientific Quantum XLS Ultra MS. The GC capillary column used was a Phenomenex Zebron ZB–5MS (30 m, 0.1 µm film thickness, inner diameter 0.25 mm). Compounds were transferred splitless to the GC column at an injector temperature of 300 °C. Helium was used as the carrier gas at a flow rate of 1.5 mL/min. The GC temperature program was as follows: 80 °C (hold 1 min), 80 °C to 310 °C at 5 °C/min (hold 20 min). Electron ionization mass spectra were recorded at 70 eV electron energy in full scan mode (mass range m/z 50–600, scan time 0.42 s). Peak areas were integrated using Thermo Xcalibur software version 2.2 (Thermo Fisher Scientific Inc., Waltham, MA, USA).
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4

GC-Orbitrap-MS Analysis of Complex Samples

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All samples were analyzed using a TRACE 1300 series GC coupled to a ThermoScientific Q Exactive Orbitrap. The system is equipped with a TriPlus RSH autosampler. A Zebron Capillary GC column ZB-5MS (30 m length 0.25 mm internal diameter x 0.25 μm film thickness) was used. Helium was used as carrier gas at 1 mL min -1 flow. The injection volume was 2 μL in splitless mode.
The oven program started at 70 °C (hold time 1 min), then heated to 175 °C at 6 °C min -1 (hold time 4 min), to 235 °C at 3 °C min -1 (hold time 0 min), and to 305 °C at 7 °C min -1 (hold time 8 min). The transfer line and ion source temperatures were 280 °C and 260 °C, respectively. Data were acquired in full scan mode, using a mass range from 70 to 10 0 0 m/z and at a resolution of 60 0 0 0. Electron ionization (EI) operated at 70 eV. Every GC-Orbitrap-MS chromatographic run from the analysis of one sample resulted in a data file. The raw files were first converted into NETcdf files using the Thermo software package Xcalibur, and then imported to MAT-LAB (The Mathworks Ltd,) computer and visualization environment for data analysis.
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