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Vion im qtof mass spectrometer

Manufactured by Waters Corporation
Sourced in United States

The Vion IM-QTOF mass spectrometer is a high-resolution, tandem mass spectrometry instrument designed for accurate mass measurement and ion mobility separation. It features a quadrupole time-of-flight (QTOF) analyzer and an ion mobility separation module. The Vion IM-QTOF provides high mass accuracy, resolving power, and sensitivity for analytical applications requiring precise structural information.

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2 protocols using vion im qtof mass spectrometer

1

Spectroscopic Analysis of Natural Compounds

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Optical rotation was obtained using a JASCO P-1020 polarimeter. UV spectra were recorded on an Optizen 2120 UV spectrophotometer. NMR experiments were operated on a Bruker AVANCE HD 800 MHz NMR spectrometer (Bruker, Germany) at the Korea Basic Science Institute (KBSI) in Ochang, Korea. NMR spectra were recorded in DMSO-d6 as an internal standard (δH 2.50/δC 39.51). High resolution electrospray ionization mass spectra (HR-ESIMS) were recorded on a Waters Vion IM-QTOF mass spectrometer (Waters, USA) at the KRIBB in Ochang, Korea. Column chromatography was performed on reversed phase silica gel (0.075 mm; Cosmosil, Japan). Analytical C18 (Waters Sunfire, 5 μm, 4.6 × 150 mm) and semi-preparative C18 (Waters Atlantis T3, 5μm, 10 × 250 mm) columns were used for reverse phase HPLC on a 515 pump HPLC system (Waters) equipped with a 2996 PDA detector (Waters) using HPLC grade solvents (Honeywell). Liquid chromatography-mass spectrometry (LC-MS) was operated using an LTQ XL linear ion trap (Thermo Scientific, USA) equipped with an electrospray ionization (ESI) source that was coupled to a rapid separation LC (RSLC; ultimate 3000, Thermo Scientific) system (ESI-LC-MS).
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2

UPLC-MS Analysis of Unknown Compounds

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By employing ACQUITY™ UPLC system (Waters, Milford, USA), chromatographic separation was carried out on an ACQUITY™ UPLC BEH C18 column (2.1 × 100 mm, 1.7 μm) held at 40 °C. The mobile phase consisted of 0.2% formic acid aqueous solution (A) and acetonitrile (B) with a flow rate of 0.3 mL/min using a gradient elution of 3%–10% B between 0 and 2 min, 10%–20% B between 2 and 3 min, 20%–28% B between 3 and 7 min, 28%–45% B between 7 and 7.5 min, 45%–90% B between 7.5 and 20 min, and 90%–3% B between 20 and 21 min. The injection volume was 5 μL.
The MS analysis was performed on a Vion IM-Q TOF mass spectrometer (Waters Corporation, Milford, USA) using electrospray ionization (ESI) in both positive and negative ion modes. MS conditions were as follows: the capillary voltage at 3.0 and −2.5 kV in positive and negative ion modes, respectively; the source temperature at 120 °C; the temperature of the desolvation gas at 400 °C; the flow rate of the desolvation gas (N2) at 700 L/h; the flow rate of the cone gas (N2) and collision gas (Ar) at 50 L/h and 0.20 mL/min, respectively; mass range: m/z 150–1500; collision energy, 6 eV and 20–60 eV ramping. Data acquisition was controlled with UNIFI 1.8.0 informatics platform (Waters Corporation, Milford, USA).
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