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Av 3 500 hd spectrometer

Manufactured by Bruker
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The AV-III-500-HD spectrometer is a high-performance nuclear magnetic resonance (NMR) spectrometer designed for advanced research applications. It features a 500 MHz superconducting magnet and provides high-resolution, high-sensitivity data acquisition capabilities.

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Lab products found in correlation

V 630 spectrometer, by Jasco (1 mentions) F 2500 spectrophotometer, by Hitachi (1 mentions)

Spelling variants of this product

AV-500 (112 citations) AV-500 spectrometer (100 citations) Bruker spectrometers (71 citations) AV-3-HD-500 (9 citations) AV III HD (9 citations) AV spectrometers (3 citations) AV-III HD Bruker spectrometer (2 citations) Bruker AV III (2 citations) 500 Spectrometers (2 citations) AV Ⅲ HD-500 NMR spectrometer (2 citations)

3 protocols using av 3 500 hd spectrometer

1

NMR Analysis of Pharmaceutical Compounds

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1H NMR spectra were collected using a Bruker AV-III-500-HD spectrometer equipped with a CryoProbe. Spectra were recorded at 25 °C in DMSO-d6 unless otherwise indicated using approximately 15 mg of each PR dissolved in 1 mL of solvent.
Mondjinou Y.A., Loren B.P., Collins C.J., Hyun S.H., Demoret A., Skulsky J., Chaplain C., Badwaik V, & Thompson D.H. (2018). Gd3+:DOTA-modified 2-Hydroxypropyl-β-Cyclodextrin/4-Sulfobutyl Ether-β-Cyclodextrin-based Polyrotaxanes as Long Circulating High Relaxivity MRI Contrast Agents. Bioconjugate chemistry, 29(11), 3550-3560.
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2

NMR Spectroscopy of Protein Samples

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1H NMR spectra were collected using a Bruker AV-III-500-HD spectrometer fitted with a cryoprobe. Spectra were recorded at 25°C at a concentration of approximately 10 mg PR/1 mL in DMSO-d6.
Samaddar S., Bose D., Loren B.P., Skulsky J.L., Ilnytska O., Struzik Z.J., Storch J, & Thompson D.H. (2022). Structure-function relationships of cholesterol mobilization from the endo-lysosome compartment of NPC1-deficient human cells by β-CD polyrotaxanes. PLOS ONE, 17(12), e0268613.
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3

Analytical and Preparative Characterization of Carbazole Derivatives

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Analytical GPC measurements were performed using an Agilent 1100 HPLC system with a JAIGEL 3HA column. Preparative GPC separations were made using a JAI LC-908 recycling HPLC system with two JAIGEL 3H columns in series. 1H NMR spectra were recorded on Bruker AV III 500 HD spectrometer. UV-vis spectra were measured using a JASCO V-630 spectrometer. Fluorescence measurements were performed on a Hitachi F-2500 spectrophotometer. MALDI-TOF mass spectra were obtained with a Bruker Autoflex with dithranol as a matrix. 3,6-Diiodo-9-(3,5,5-trimethyl)hexylcarbazole was prepared according to the literature.15 (link)
Ogawa K., Tanaka S, & Shimura K. (2020). Synthesis and fluorescence properties of butadiyne-linked linear and cyclic carbazole oligomers. RSC Advances, 10(16), 9657-9662.
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