In this blog, we describe the T2-filter experiment, including its description and application.

In this blog, we discuss why gradient-based 2D NMR experiments enhance both efficiency and data quality and become the preferred choice for many applications. 

In this blog, we introduce our value-added software module, Experiment Designer. A powerful tool which allows advanced NMR users to code NMR pulse sequences through an intuitive graphical interface.

As we kick off the new year, educators gear up for an exciting semester, and what better time to explore Nanalysis benchtop NMR? This powerful hands-on learning tool seamlessly integrates real-world analytical techniques into your chemistry classroom or undergrad lab. Read More.

In this blog, we showcase how benchtop NMR is an accessible and versatile tool for chemists and non-chemists to evaluate greener methods.

Acidity is something that you encounter on a daily basis, probably without even realizing it. The tangy taste of an orange (citric acid), that Vitamin C tablet you took this morning (ascorbic acid), those terrible jeans from the 80’s that you still wear (acid wash). My favourite acid is acetic acid.

Sugar substitutes are gaining more and more relevance due to the health problems associated with the consumption of high amounts of sugar...I thought it would be interesting to take a few of those substitutes and acquire their proton NMR spectrum in our benchtop NMR.

In this blog post, we show an example for on-line flow reaction monitoring via 19F NMR spectroscopy using the compact benchtop NMR. 1-855-NMREADY (667-3239) toll-free in the US and Canada

Electronegativity is a concept that we have to study and understand early in our science or engineering degrees. In chemistry this concept stays with us and we commonly invoke it in order to explain multiple phenomena what we observe or study…and of course, NMR is not the exception! Benchtop NMR 1-855-NMREADY (667-3239) toll-free in the US and Canada

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 more here.