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Rxi 5ht capillary column

Manufactured by Restek
Sourced in United States

The Rxi-5HT capillary column is designed for the separation and analysis of a wide range of compounds, including high-boiling and thermally-labile samples. It features a 5% diphenyl-95% dimethyl polysiloxane stationary phase that provides excellent thermal stability and peak shape.

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4 protocols using rxi 5ht capillary column

1

GC-MS Analysis of Chemical Compounds

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GC-MS analysis was performed using an Agilent 7890 B gas chromatograph equipped with a 5977B mass selective detector (GC/MSD) (Agilent Technologies, Santa Clara, CA, USA). Chromatographic separation was achieved using a Rxi-5HT capillary column (30 m × 0.25 mm I.D., 0.25 μm film thickness; RESTEK, Bellefonte, PA, USA). An autosampler (Agilent Technologies; 7683B) was used for all experiments. The temperature of the injector was 280 °C. Using split mode, 1 µL of each extract was injected at a ratio of 1/50. The carrier gas was helium C-60 at a constant flow rate of 1 mL/min. The GC oven temperature was initially 60 °C for 1 min, increased to 160 °C in 3 °C/min increments, and then increased to 320 °C in 10 °C/min increments, followed by a hold for 10 min. The mass spectrometer used the electron ionization mode at 70 eV with the ion source temperature set at 250 °C. The running time was 30 min. Scan mode was used in the range of 30–600 m/z with a scan rate of 2.6 scan/s. Agilent Mass Hunter Qualitative Analysis B.04.00 software was used for data analysis. Single compounds were identified by comparing mass spectra with NIST mass spectral libraries (National Institute of Standards, 2020 version) and the Wiley Registry 12th Edition.
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2

GC-MS Analysis of Chemical Compounds

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GC–MS analysis was performed using an Agilent 7890 B gas chromatograph equipped with a 5977B mass selective detector (GC/MSD) (Agilent Technologies, Santa Clara, CA, USA). Chromatographic separation was achieved using a Rxi-5HT capillary column (30 m × 0.25 mm I.D., 0.25 μm film thickness; RESTEK, Bellefonte, PA, USA). An automatic autosampler (Agilent 7683B) was used for all experiments. The temperature of the injector was 280 °C. One microliter of each extract was injected in split mode with a ratio of 1/50. The carrier gas was helium C-60 at a constant flow of 1 mL/min. The GC oven temperature was initially 60 °C for 1 min, increased to 160 °C in 3 °C/min increments, and then increased to 320 °C in 10 °C/min increments, followed by a hold for 10 min. The mass spectrometer was tuned on electron ionization mode at 70 eV with the ion source temperature set at 250 °C. The running time was 30 min. Scan mode was used in the range of 30–600 m/z with a scan rate of 2.6 scan/s. The Agilent Mass Hunter Qualitative Analysis B.04.00 software was used for data analysis. Single compounds were identified by comparing mass spectra with NIST mass spectral libraries (National Institute of Standards, 2005 version) and the Wiley Registry 8th Edition.
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3

GC-based Saponin Derivatization Protocol

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It was performed using gas chromatography (Medina-Meza et al., 2016) (link). It consists of taking an aliquot of the final dry extract. The extracted saponins were then derivatized, using 100 µL of anhydrous pyridine, 100 µL of bis (trimethylsilyl) trifluoroacetamide (BSTFA), and 10 µL of cholesterol decanoate (internal standard, IS). They are added to the dry extract and heated at 70°C for one hour. Derivatized extracts (2 µL) are injected into an Agilent 6890N gas chromatograph. A RESTEK Rxi-5HT capillary column (60 m × 0.25 mm × 0.25 mm) was used. The injector and detector temperatures were adjusted to 350°C, while the oven temperature was programmed from 160 to 220°C at 15°C/min, from 220 to 290°C at 10°C/min, for 7 min, from 290 to 330°C at 8°C/min maintained for 15 min.
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4

GC-based Saponin Derivatization Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
It was performed using gas chromatography (Medina-Meza et al., 2016) (link). It consists of taking an aliquot of the final dry extract. The extracted saponins were then derivatized, using 100 µL of anhydrous pyridine, 100 µL of bis (trimethylsilyl) trifluoroacetamide (BSTFA), and 10 µL of cholesterol decanoate (internal standard, IS). They are added to the dry extract and heated at 70°C for one hour. Derivatized extracts (2 µL) are injected into an Agilent 6890N gas chromatograph. A RESTEK Rxi-5HT capillary column (60 m × 0.25 mm × 0.25 mm) was used. The injector and detector temperatures were adjusted to 350°C, while the oven temperature was programmed from 160 to 220°C at 15°C/min, from 220 to 290°C at 10°C/min, for 7 min, from 290 to 330°C at 8°C/min maintained for 15 min.
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