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Agilent 400 dd2 spectrometer

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 400 DD2 spectrometer is a laboratory instrument designed for the analysis of molecular structures. It utilizes nuclear magnetic resonance (NMR) technology to provide detailed information about the chemical composition and structure of samples. The spectrometer is capable of performing advanced NMR experiments and data processing to assist researchers in their investigations.

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3 protocols using agilent 400 dd2 spectrometer

1

Solvent Optimization and Characterization

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All the solvents used in
the reactions are commercially available superdry solvents (Energy
Chemical). The silica gel with a mesh of 200–300 was obtained
from Shanghai Titan Scientific General-Reagent (Shanghai, China).
The eluents were also produced by General-Reagent. The 1H NMR and 13C NMR spectra were recorded at room temperature
using an Agilent 400 DD2 spectrometer (California, USA). The HRMS
was measured using Thermo Scientific Q Exactive Orbitrap Mass Spectrometers
(Massachusetts, USA). All other chemicals were analytical grade.
Fetal bovine serum (FBS) was purchased from AusGeneX (Molendinar,
Australia), RPMI 1640 medium (with penicillin and streptomycin) was
obtained from KeyGEN BioTECH (NanJing, China), trypsin EDTA (0.25%)
was purchased from Gibco Invitrogen (Grand Island, USA), and cellular-grade
DMSO was from Beijing Solarbio Science & Technology Co., Ltd.
(Beijing, China).
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2

Silica Gel Column Chromatography Protocol

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All reagents were obtained from Energy Chemical Co. Ltd. (Weinan, China) and used as received. Solvents were of analytical grade. Flash column chromatography was performed with silica gel (200–300 mesh) and dichloromethane/methanol was used as eluent. All NMR experiments were measured by using an Agilent 400 DD2 spectrometer (Agilent, Santa Clara, CA, USA) at room temperature. The HRMS were obtained with Electrospray-quadrupole time-of-flight mass spectrometer (MicrOTOF-Q II 10410, Bruker, NASDAQ, Billerica, MA, USA).
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3

Spectroscopic Analysis of Chemical Compounds

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All chemicals reagents were of analytical grade and
applied without
treatment. Double-distilled water was applied for all tests. The NMR
tests were performed on an Agilent-400 DD2 spectrometer (Agilent,
Palo Alto, CA) in DMSO-d6 with tetramethylsilane
(TMS) as the internal standard. The chemical shifts (δ) were
expressed in units of parts per million (ppm) relative to TMS. High-resolution
mass spectrometry (HR-MS) experiments were conducted on a time-of-flight
Micromass LCT Premier XE spectrometer (McKinley Scientific, Sparta
Township, NJ). Fluorescence spectra were recorded on a Cary Eclipse
spectrophotometer (Agilent, Palo Alto, CA). UV–vis absorption
spectra were recorded on a TU-1901 UV–vis spectrophotometer
(PuXi Science and Technology Development Co. Ltd., Beijing, China).
IR spectra were recorded on a Vary 1000 FT-IR spectrophotometer (Varian,
Palo Alto, CA). Fluorescence images of the cells were obtained by
an Olympus IX73+DP73 inverted microscope. Small-animal living imaging
was performed on IVIS Lumina LT Series III instrument (Caliper Life
Sciences, Hopkinton, MA). Additional experiment procedures are found
in the Supporting Information.
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