Welcome to Nanalysis’ benchtop NMR Blog

We love benchtop NMR! In this blog section, you will find all things benchtop NMR. Please contact us if you would like to discuss about your project.

industry Paul Hui industry Paul Hui

How much medicine is in my medicine?

In this blog post we show a simple experiment that teaches student how common over the counter (OTC) medications can be qualified and quantified for their different active pharmaceutical ingredients (API) using qNMR spectroscopy.

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Educational Thais Barbosa Educational Thais Barbosa

Part 1 - T1 relaxation: definition, measurement and practical implications!

Nuclear Magnetic Resonance spectroscopy is based on the idea that some nuclei can behave as little magnetic bars (I spin number ≠ 0). In the presence of a magnetic field (B0) the nuclear spins feel a small torque for or against the B0 axis, which results in a net magnetization along the B0 direction. Benchtop NMR 1-855-NMREADY (667-3239) toll-free in the US and Canada.

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Educational Eva Lam Educational Eva Lam

DEPT: A tool for 13C peak assignments

Distortionless Enhancement by Polarization Transfer (DEPT) is a double resonance pulse program that transfers polarization from an excited nucleus to another – most commonly 1H → 13C. This results in a sensitivity enhancement relative to the standard decoupled 1D carbon spectra (13C), which benefits only from the small Nuclear Overhauser Effect (NOE) enhancements.

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Alexander Maier Alexander Maier

Synthetic Cannabinoids and Signal Patterns

Synthetic cannabinoids (SC) are designer drugs that aim to mimic the pharmacological effect of the natural cannabinoid (−)-trans-Δ9-tetrahydrocannabinol (THC). Many SCs have an even higher binding affinity to the CB1 receptor, which is responsible for the psychoactive effects…

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Educational Alexander Maier Educational Alexander Maier

β-Diketone (Beta-diketone) tautomerization ratio determined via 60 MHz benchtop NMR

Tautomers are constitutional isomers that interconvert into each other by an exchange reaction, most commonly a proton transfer. Such two isomers can for example be a ketone and an enol. Keto-enol tautomerism (KET) becomes possible when there are hydrogen atoms adjacent to a carbonyl group (these hydrogen atoms are called α hydrogens). This tautomerism is depicted in Scheme 1 and is also discussed…

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