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Lct premier xe micromass spectrometer

Manufactured by Waters Corporation
Sourced in United States

The LCT Premier XE Micromass spectrometer is a high-performance liquid chromatography-mass spectrometry (LC-MS) instrument designed for precise and accurate analysis of a wide range of molecular compounds. It features a dual-source electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) interface, enabling flexible ionization techniques to suit various sample types. The LCT Premier XE Micromass spectrometer provides accurate mass measurements and high-resolution capabilities to support advanced applications in fields such as pharmaceutical research, environmental analysis, and metabolomics.

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2 protocols using lct premier xe micromass spectrometer

1

Characterization and Evaluation of Cytotoxicity

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Optical rotations were measured in CH2Cl2 on a PerkinElmer 241 polarimeter (Waltham, MA, USA) using an Na lamp. NMR spectra were recorded on a Bruker AVANCE 500 MHz (Bruker Biospin, Fällanden, Switzerland). NMR spectra were obtained dissolving samples in CDCl3 (99.9%) and chemical shifts are reported relative to solvent (δH 7.26 and δC 77.0 ppm) and TMS as an internal pattern. HR-ESI-MS data were obtained on an LCT Premier XE Micromass spectrometer (Waters, Milford, CT, USA). Thin-layer chromatography (TLC; Merck, Darmstadt, Germany) was visualized by spraying with cobalt chloride reagent 2% (10% sulfuric acid) and heating.
Paclitaxel, cisplatin, DMEM/F12 medium, fetal bovine serum, gentamicin, penicillin–streptomycin, and Alamar Blue™ were obtained from Invitrogen (Gran Island, NY, USA). The reagents for general use were purchased from Sigma-Aldrich (St. Louis, MO, USA).
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2

Detailed NMR Spectroscopic Analysis Protocol

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General remarks: Nuclear magnetic resonance (NMR) spectra, 1 H-NMR (400 or 500 MHz) and experiments and was expressed by the abbreviations s (C), d (CH), t (CH 2 ) and q (CH 3 ).
Estimated error of reported values: 0.01 ppm (δ, 1 H-NMR), 0.1 ppm (δ, 13 C-NMR), 0.1 Hz (J, coupling constant). All NMR spectra are provided in the Supporting Information. Melting points were determined on a Büchi B-540 model. Mass spectra were recorded with a Waters LCT Premier XE Micromass spectrometer by using electrospray ionization (ESI + -TOF). Flash chromatography was performed with silica gel (230-400 mesh) as the stationary phase. The solvent system used as mobile phase is indicated in each case. Thin-layer chromatography (TLC) analysis were carried out on silica gel 60 F 254 aluminum sheets and visualized using UV light (365 nm), a phosphomolybdic acid solution 10 wt.% in MeOH or a vanillin solution (6 g of vanillin, 450 mL of ethanol, 40 mL of AcOH and 30 mL of H 2 SO 4 ). Chemical nomenclature was generated using ChemBioDraw Ultra 13.0.0.3015, and atoms of all the compounds were numbered according to the IUPAC name. Sonication treatments were done using a sonication bath USC200th VWR, 45 kHz, 60 W.
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