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Uplc ms instrument

Manufactured by Waters Corporation

The UPLC-MS instrument is a powerful analytical tool used for the separation, identification, and quantification of chemical compounds. It combines the high-resolution capabilities of Ultra-Performance Liquid Chromatography (UPLC) with the sensitivity and precision of Mass Spectrometry (MS) technology. This instrument is designed to provide efficient and accurate analysis of complex samples, making it a valuable asset in various analytical applications.

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3 protocols using uplc ms instrument

1

Synthesis and Characterization of Novel Compounds

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Melting points were determined by a Mettler Toledo FP 62 melting point apparatus and are uncorrected. 1H NMR spectra were recorded at 400 MHz on a Varian Unitynova 400 NMR spectrometer using tetramethylsilane as an internal standard, and then 13C NMR spectra were recorded at 100 MHz. Mass spectra were run on a Waters UPLC-MS instrument. UV spectra were determined by a Lambda 25 spectrometer. HPLC spectra were run through a Waters SunfireTM C18, 5 µm, 4.6 mm × 250 mm column on a Waters apparatus (pump: e 2695; detector: 2998). TLC plates (GF 254) were bought from Branch Qingdao Haiyang Chemical Plant. All the solvents and commercial materials are bought from Sinopharm.
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2

NMR and Mass Spectrometry Analysis

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1H NMR spectra were recorded at 400 MHz on a Varian Unity INOVA 400 MHz NMR spectrometer using tetramethylsilane as an internal standard, and 13C NMR spectra were recorded at 100 MHz. Mass spectra were run on a Waters UPLC-MS instrument. Melting points were determined by a Mettler Toledo FP62 melting point apparatus and are uncorrected. Thin-layer chromatography plates (GF 254) were bought from Branch Qingdao Haiyang Chemical Plant.
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3

UPLC-MS Analysis of Small Molecules

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Analytical ultra high-performance liquid chromatography–MS (UPLC-MS) was performed on a Waters UPLC-MS instrument equipped with a reverse-phase C18 column (1.7 μm particle size, 2.1 by 50 mm), dual atmospheric pressure chemical ionization (API)/electrospray (ESI) MS detector, and photodiode array detector. Samples were eluted with a linear gradient of 5% acetonitrile–water containing 0.1% formic acid→100% acetonitrile containing 0.1% formic acid over 0.75 min, followed by 100% acetonitrile containing 0.1% formic acid for 0.75 min, at a flow rate of 800 μL/min.
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