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Rxi 624sil ms

Manufactured by Restek
Sourced in Panama, Australia, United States

The Rxi-624Sil MS is a fused silica column designed for gas chromatography-mass spectrometry (GC-MS) applications. It features a 624-type stationary phase with a siloxane film for enhanced inertness and improved separation of a wide range of analytes.

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3 protocols using rxi 624sil ms

1

Comprehensive Metabolite Profiling with GC×GC-TOFMS

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The GC×GC-TOFMS (Pegasus 4D, LECO Corporation, St. Joseph, MI) was equipped with a rail autosampler (MPS, Gerstel, Linthicum Heights, MD) and fitted with a two-dimensional column set consisting of an Rxi-624Sil MS (60 m × 250 μm × 1.4 μm (length × internal diameter × film thickness); Restek Corporation, Bellefonte, PA) first column followed by a Stabilwax (Crossbond Carbowax polyethylene glycol; 1 m × 250 μm × 0.5 μm; Restek) second column. The primary oven ramped at 5.0 °C/min from 35 °C to 230 °C, with a 5 min hold at 230 °C. The secondary oven, and quad-jet modulator (2.0 s modulation period, 0.5 s alternating hot and cold pulses), were heated in step with the primary oven with +5 °C and +25 °C offsets, respectively. The helium carrier gas flow rate was 2 mL/min. A splitless injection was used, with a 180 s desorption time. The inlet and transfer line temperatures were set to 270 °C and 250 °C, respectively. Time-of-flight mass spectra were acquired over the range of 30 to 500 m/z, with an acquisition rate of 200 spectra/s, and a 70 eV electron ionization. Data acquisition and analysis were performed using ChromaTOF software, version 4.50 (LECO Corp.).
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2

GC×GC-TOF-MS Analysis of Complex Samples

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SPME fibres were desorbed directly into the GC×GC inlet at 250 • C for 5 min. The GC×GC analyses were performed with a LECO Pegasus 4D ® (LECO, Australia) consisting of an Agilent 7890A GC (Agilent Technologies, Australia) with a dual stage quad jet thermal modulator, secondary oven and Pegasus TOFMS. The column configurations consisted of a Rxi ® 624Sil MS (Restek Corporation, Australia) primary column (30.0 m × 0.25 mm i.d., with a 1.4 µm coating), connected to a Stabilwax ® secondary column (Restek Corporation, Australia) (2 m × 0.25 mm i.d., with a 0.5 µm coating). Helium was used as the carrier gas for all analyses and held at a flow rate of 1 mL/min. All injections were performed manually and were carried out in splitless mode. The GC oven temperature was initially set to 35 • C and held for 5 min, ramping to 240 • C at a rate of 5 • C/min and held for 5 min. The secondary oven temperature offset was 10 • C. Data were acquired at a rate of 100 spectra per second and processed using ChromaTOF ® (version 4.51.6.0; LECO).
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3

Headspace GC Analysis of IPA in Formulations

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IPA content in the formulations was determined by the HS-GC method. The headspace sampler was a pressure-loop HT3 model (Teledyne Tekmar, USA). The HS parameters used were: GC cycle time 19.25 min, valve oven temperature 105 o C, transfer line temperature 110 o C, platen temperature 80 o C, platen temperature equilibration time 0.5 min, sample equilibration time 25 min, vial pressure 204.7 kPa, pressurization time 1 min, pressure equilibration time 0.5 min, loop fill pressure 170.3 kPa, loop fill time 1 min and inject time 1 min.
The GC system used was a 7890 model (Agilent Technologies, USA), equipped with split/splitless injector (8:1 split ratio, 150 °C) and a flame ionization detector maintained at 300 o C, with gas flows of 450 mL min -1 air, 50 mL min -1 hydrogen and 25 mL min -1 helium makeup. The capillary column used was a 30 m × 0.32 mm × 1.8 µm Rxi ® -624Sil MS (Restek Corporation, USA). Column initial temperature was 50 o C maintained for 3.5 min, then ramped to 120 o C at 40 o C min -1 and kept for 6 min. Helium was used as a carrier gas flowing at a rate of 5.695 mL min -1 .
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