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Ac 400 and 600 mhz nmr spectrometer

Manufactured by Bruker

The AC 400 and 600 MHz NMR spectrometers are high-performance nuclear magnetic resonance (NMR) instruments designed for analytical and research applications. They provide precise measurements of the magnetic properties of atomic nuclei within a sample, enabling identification and structural analysis of organic and inorganic compounds. The core function of these spectrometers is to generate and detect radio frequency signals that interact with the nuclear spins, producing a spectrum that can be analyzed to determine the chemical composition and structure of the sample.

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2 protocols using ac 400 and 600 mhz nmr spectrometer

1

Analytical Characterization of Alkaloids

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Chemicals and reagents were sourced from Sigma-Aldrich and were used without any further purification required. High pressure (or high performance) liquid chromatography (HPLC) grade chloroform, methanol and acetonitrile were used with no further purification. All other solvents were used as supplied. Morphine and oripavine were provided from Johnson Matthey MacFarlan Smith Ltd. Thin layer chromatography was performed on Fluka Silica gel (60 F254) coated on aluminium plates. The TLC plates were visualized using UV light. Davisil 60 Å silica gel was used for column chromatography. 1H and 13C NMR spectra were obtained on a Bruker AC 400 and 600 MHz NMR spectrometer. The pH was monitored by a Mettler Toledo InLab Expert Pro-ISM pH probe. Electrospray ionization mass spectra (ESI-MS) were recorded using a Thermo Fisher Exactive Orbitrap mass spectrometer coupled to an Advion TriVersa Nanomate injection system with samples being prepared in 100% HPLC-grade acetonitrile prior to ESI-MS analysis. CD spectrometry was conducted on an Applied Photophysics Chirascan plus qCD spectrometer with samples being prepared in acetonitrile.
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2

Characterization of Chemical Compounds

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Chemicals, reagents and high-performance liquid chromatography (HPLC) grade solvents including CHCl3, MeOH and CH3CN were sourced from Sigma-Aldrich (Ireland) or Tokyo Chemical Industry (TCI, UK Ltd) and used without further purification. 1 H and 13 C NMR spectra were obtained on a Bruker AC 400 and 600 MHz NMR spectrometer. pH was monitored by a Mettler Toledo InLab Expert Pro-ISM pH probe. Electrospray ionization mass spectrometry (ESI-MS) measurements were recorded using a ion trap Bruker HCT mass spectrometer with samples being prepared in 100% HPLC-grade CH3CN prior to ESI-MS analysis. UV/Vis absorption spectroscopy studies were carried out on a Shimadzu UV-2600 spectrophotometer. FTIR measurements were conducted on a PerkinElmer Spectrum Two spectrometer. Fluorescence DNA binding studies were carried out on a Perkin Elmer LS55 Fluorescence Spectrometer.
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