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Q tof lc ms 6510 series classic g6510a

Manufactured by Agilent Technologies
Sourced in United States

The Q-TOF LC/MS 6510 series classic G6510A is a high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (LC-QTOF MS) system. It is designed to provide accurate mass measurements and high-resolution mass analysis of a wide range of analytes.

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2 protocols using q tof lc ms 6510 series classic g6510a

1

Quantitative Analysis of Compounds by LC-Q-TOF-MS

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The chromatographic system consisting of an Agilent 1200 series LC instrument (Agilent Technologies, USA) coupled with quadrupole time–of–flight (Q–TOF) mass spectrometer (Q–TOF LC/MS 6510 series classic G6510A, Agilent Technologies, USA) equipped with an ESI source was used. Chromatography was performed on Waters Atlantis dC18 (150 mm×4.6 mm, 5 μm) column at 25 °C using acetonitrile and water (containing 0.1% formic acid) (85:15, v/v) as mobile phase in an isocratic elution mode at a flow rate of 0.75 mL/min, and the injection volume was 10 µL. The data acquisition was under the control of Mass Hunter workstation software. The typical operating source conditions for MS scan in positive ESI mode were optimized: the ionization voltage 80 V, the capillary voltage 3000–3500 V, the skimmer 60 V, nitrogen used as the drying (300 °C; 9 L/min) and nebulizer (45 psi) gas. External calibration of the TOF–MS was performed daily before the analysis.
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2

Garlic Compound Analysis by LC-MS

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The supernatant of garlic homogenate were filtered through 0.45 µm glass filter and diluted further to make appropriate solution. 20 µL was injected in LC-MS. The analysis was carried out on an Agilent 1200 series HPLC instrument (Agilent Technologies, USA) equipped with a quaternary pump (G13311A, USA), a de-gasser (G1322A, USA), a diode-array detector (G1315D, USA), an auto sampler (G1329A, USA) and a column compartment (G1316A, USA). Mass spectrometric detection was carried out on a quadrupole time-of-flight (Q-TOF) mass spectrometer (Q-TOF LC/MS 6510 series classic G6510A, Agilent Technologies, USA) equipped with an ESI source. The data acquisition was under the control of Mass Hunter workstation software. The typical operating source conditions for MS scan in positive ion ESI mode were optimized as follows; the fragmentor voltage was set at, 80 V; the capillary at, 3000–3500 V; the skimmer at, 60 V; nitrogen was used as the drying (300°C; 9 L/min) and nebulizing (45 psi) gas. For full scan MS mode, the mass range was set at m/z 100–2000. All the spectra were recorded under identical experimental conditions and are average of 20–25 scans.
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