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Advance dpx spectrometer

Manufactured by Bruker
Sourced in United States

The Advance DPX spectrometer is a Nuclear Magnetic Resonance (NMR) spectrometer manufactured by Bruker. It is designed to perform high-resolution NMR analysis of various samples. The core function of the Advance DPX is to generate and detect radio frequency signals to obtain NMR spectra, which provide information about the chemical structure and composition of the analyzed samples.

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3 protocols using advance dpx spectrometer

1

Organic Synthesis Characterization Protocols

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Unless otherwise specified, all the reagents were acquired from commercial sources and used directly. Acetonitrile, dichloromethane, dimethylformamide (DMF), and pyridine were all distilled from calcium hydride. NMR spectra (400 MHz/100 MHz) were recorded on an Advance DPX spectrometer (Bruker, Billerica, MA, USA) at room temperature with DMSO-d6 or CDCl3 as solvent. 1H NMR data are reported as the following format: chemical shift, multiplicity (s = singlet, d = doublet, t = triplet, br = broad, m = multiplet), coupling constant and integration. Specific rotations were acquired on an Autopol IV polarimeter (Rudolph, Hackettstown, NJ, USA). High resolution mass spectrometry (HRMS) data were measured with an AB Sciex TOF 4600 instrument (AB Sciex, Singapore). Melting points were measured on an X-4 digital melting point apparatus (Beijing Taike Corparation, Beijing, China). X-ray diffraction analysis was performed on a Bruker Smart Apex II system (Bruker, Billerica, MA, USA).
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2

RP-HPLC and NMR Characterization of Products

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Reversed phase high performance liquid chromatography (RP-HPLC) characterization was performed on an Agilent 1100 Infinity Quaternary HPLC System using an analytical column (ZORBAX SB-C18, 4.6 × 150 mm, 5 μm). An Agilent 7200B Quadruple Mass Spectrometer (MS) was used to obtain the mass spectrum of the final products in the range of 100 to 4200 m/z (Agilent, CA). 1H-NMR and 13C-NMR analysis were performed on a Bruker Advance DPX spectrometer at 500 MHz (Bruker, WI). The chemical shifts are based on the peaks of the deuterated solvent of CDCl3 or CH3OH-d4 using TMS as an internal standard.
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3

NMR and Characterization of Compounds

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Unless otherwise specified, all the reagents were acquired from commercial sources and used directly. NMR spectra (400 MHz/100 MHz) were recorded on an Advance DPX spectrometer (Bruker, Billerica, MA, USA) at room temperature with DMSO-d6 as solvent. Tetramethylsilane (TMS) was used as an internal reference. Specific rotations were acquired on an Autopol IV polarimeter (Rudolph, Hackettstown, NJ, USA). High resolution mass spectrometry (HRMS) data were measured with an AB Sciex TOF 4600 instrument (Billerica, MA, USA). Melting points were measured on an X-4 digital melting point apparatus (Beijing Taike Corparation, Beijing, China). X-ray diffraction analysis was performed on a Bruker Smart Apex II system (Bruker, Billerica, MA, USA).
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