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Ltq ft instrument

Manufactured by Thermo Fisher Scientific

The LTQ-FT is a hybrid mass spectrometer that combines a linear ion trap (LTQ) and a Fourier transform ion cyclotron resonance (FT-ICR) mass analyzer. It provides high-resolution, high-mass accuracy mass spectrometry capabilities for a wide range of applications.

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2 protocols using ltq ft instrument

1

Analytical Techniques for Phytochemical Characterization

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Melting points were uncorrected and were measured on a Mettler Toledo instrument. IR spectra were recorded on an Alpha II FT-IR spectrometer from Bruker in the region of 4000–600 cm–1, using KBr pellet technique with 1.0 cm–1 resolution at room temperature. 1D and 2D NMR spectra were obtained on a Bruker DRX 500 (500 MHz for 1H and 125 MHz for 13C spectra) spectrometer (Bruker, Rheinstetten, Germany) with chemical shifts reported as δ (ppm), using TMS as an internal standard. The ESI-MS were obtained on LTQ-FT instrument (Thermo Scientific). LC–MS were measured with Shimadzu LC–MS system using a L-column 2 ODS (I.D. 2.1 × 100 mm, Chemical Evaluation and Research Institute, Japan), at a flow rate of 0.2 mL min−1 with a detection wavelength of 300 nm and FMW (HCOOH/MeCN/H2O = 1:12:87) as eluent, ESI+ 4.5 kV, ESI− 3.5 kV, 250 °C. Optical rotations were measured on a Perkin-Elmer 341 polarimeter. Silica gel 60 (230–400 mesh E. Merck, Darmstadt, Germany) and Sephadex® LH-20 were employed for CC, the solvent mixing systems for elution were mainly CH2Cl2/MeOH for the phytochemical study with increasing polarity and pure MeOH, while precoated aluminum sheets Silica gel 60 F254 were used for TLC [53 (link)].
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2

Spectroscopic Characterization of Compounds

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Melting points were uncorrected and were measured on a Mettler Toledo instrument. IR spectra were recorded on an Alpha FT-IR Spectrometer from Bruker, while 1D and 2D NMR spectra were obtained on a Bruker DRX 500 (500 MHz for 1 H and 125 MHz for 13 C spectra) spectrometer (Bruker, Rheinstetten, Germany) with chemical shifts reported in δ (ppm) using TMS (δ H ) as an internal standard. The ESI-MS were obtained on LTQ-FT instrument (Thermo Scientific). UPLC-MS were measured by a Shimadzu UPLC-MS system. Optical rotations were measured on a Perkin-Elmer 341 polarimeter. Silica gel 60 (230-400 mesh E.
Merck, Darmstadt, Germany) was employed for column chromatography, the solvent mixing systems for elution were mainly CH 2 Cl 2 /MeOH with increasing polarity. For non-polar constituents (2, 3 and 4), a Shimadzu GCMS-QP505A gas chromatograph equipped with a ZB-5 ms fused silica capillary column BPX5 (non-polar, 5% phenylarylene-95% dimethylpolysiloxane) (30 m x 0.25 mm internal diameter x 0.25 µm film thickness) was coupled to an ion-trap mass detector. Mass spectra were acquired in the electron-impact (EI) mode with an ionization voltage of 70 eV.
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