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Waters xevo g2s q tof mass spectrometer

Manufactured by Waters Corporation
Sourced in United States

The Waters Xevo G2S Q TOF mass spectrometer is a high-resolution, time-of-flight mass spectrometer designed for qualitative and quantitative analysis. It features a quadrupole time-of-flight (Q-TOF) mass analyzer configuration and is capable of generating accurate mass measurements with high resolution.

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4 protocols using waters xevo g2s q tof mass spectrometer

1

LC/MS Analysis of Carotenoids

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The LC/MS analysis of carotenoids was carried out using a Waters Xevo G2S Q TOF mass spectrometer (Waters Corporation, Milford, CT, USA) equipped with an Acquity UPLC system. The ESI-TOF/MS spectra were acquired by scanning from m/z 100 to 1500 with a capillary voltage of 3.2 kV, cone voltage of 20 eV, and source temperature of 120 °C. Nitrogen was used as a nebulizing gas at a flow rate of 30 L/h. The MS/MS spectra were measured with a quadrupole-TOF MS/MS instrument with argon as a collision gas at a collision energy of 20 V. The UV-Vis absorption spectra were recorded from 200 to 600 nm using a photodiode-array detector (PDA) (Acquity UPLC PDA eλ Detector, Waters, Milford, MA, USA). An Acquity 1.7 μm BEH UPLC C18 (2.1 id X 100 mm) column (Waters Corporation, Milford, CT, USA) was used as a stationary phase and MeCN/H2O (85:15)–MeCN/MeOH (65:35) (linear gradient 0 to 15 min) as a mobile phase, at a flow rate of 0.4 mL/min for the HPLC system.
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2

UPLC-QTOF Analysis of Compounds

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The following instruments and reagents were used: distilled water (Guangzhou Watsons Food & Beverage Co Ltd), chromatographic pure acetonitrile (Oceanpak Co), chromatographic pure formic acid (ROE Co), low-temperature high-speed centrifuge (Changsha Xiangyi Centrifuge Instrument Co Ltd), JKYMEN ultrasonic cleaner, small oscillation vortex (Haimen Qilin Bell Instrument Manufacturing Co Ltd), Waters Acquity UPLC Liquid Chromatograph (Waters Co), Waters Xevo G2S Q-TOF Mass Spectrometer (Waters Co), ACQUITY UPLC BEH C18 Chromatography Column (2.1 × 100 mm, 1.7 μm, Waters Corp).
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3

Spectroscopic Analysis of Organic Compounds

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The UV–visible (UV–VIS) spectra were recorded with a Hitachi U-2001 (Hitachi High-Technologies Corporation, Tokyo, Japan) in diethyl ether (Et2O). The positive ion fast atom bombardment mass spectrometry (FAB MS) spectra were recorded using a JEOL JMS-HX 110A mass spectrometer (JEOL, Tokyo, Japan) with m-nitrobenzyl alcohol as a matrix. The positive ion electro spray ionization time of flight mass (ESI-TOF MS) spectra were recorded using a Waters Xevo G2S Q TOF mass spectrometer (Waters Corporation, Milford, CT, USA). The 1H-NMR (500 MHz) and 13C-NMR (500 MHz) spectra were measured with a Varian UNITY INOVA 500 spectrometer (Agilent Technologies, Santa Clara, CA, USA) in CDCl3. The chemical sifts are expressed in ppm relative to tetramethyl silane (TMS) (δ = 0) as an internal standard for 1H-NMR and CDCl3 (δ = 77) as an internal standard for 13C-NMR. J values are given in Hz. The CD spectra were recorded in EPA [Et2O–isopentane–ethanol (5:5:2)] at room temperature with a Jasco J-500C spectropolarimeter (Jasco corporation, Tokyo, Japan). Preparative high-performance liquid chromatography (HPLC) was performed on a Shimadzu LC-6AD with a Shimadzu SPD-6AV spectrophotometer (Shimadzu Corporation, Kyoto, Japan) set at 450 nm. The column used was a 250mmX10mm i.d. 10 μm Cosmosil 5SL-II and 5C18 II (Nacalai tesque, Kyoto, Japan).
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4

Spectroscopic and Analytical Characterization

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The absorption spectra and emission spectra were recorded using a UV-Vis 2450 instrument (Shimadzu, Kyoto, Japan) and an RF5301PC fluorescence fluorometer (Shimadzu, Kyoto, Japan). The emission spectra were performed on a set 5.0 nm for excitation and emission slit widths. The fluorescence imaging in vivo was obtained by a Zeiss LSM710 microscope (Jena, Germany). The pH experiment was adjusted by a PHS-3C pH meter (Leici, Shanghai, China). A Waters ® Xevo G2-S QTof™ mass spectrometer was used for mass spectra (Waters®, Manchester, UK), and a BRUKER 600 spectrometer was used for NMR spectra (Rheinstetten, Germany). No further purification was operated for all reagents before work. The thin-layer chromatography (TLC) plates and silica gel (mesh 200–300) were purchased from Qingdao Chemical (Qingdao, China).
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