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.
Category
NMR Topics
- 100 MHz NMR
- 13C NMR
- 19F NMR
- 19F NMR Spectroscopy
- 31P NMR
- 3H NMR
- Agrochemicals
- Applications
- Biopolymers
- Botanicals
- COSY
- CPMG
- Cannabis
- Chemical Analysis
- Cosmetics
- DEPT
- Drug Analysis
- Edible Oils
- Educational NMR
- Energy
- Exchangeable Protons
- Exchangeable protons
- Flavor and Fragrances
- Flow NMR
- Fluorine-19 NMR
- Food Science
- Food and Beverage
- Forensics
- Forestry
- HMBC
- HSQC
- Hands-on Learning
- Hydroxyl value
- Hyphenated NMR
- Illicit Drugs
- Industrial Applications
- Interpretation of NMR
- Interpretation of NMR Spectra
- Inversion-Recovery
- Keto-Enol Tautomerism
- LF vs. HF NMR
- Lignin Analysis
- Literature
- Literature using Nanalysis benchtop NMR
- Mining
- NMR Applications
- NMR Instrumentation
- NMR Labelling
- NMR Pulse Programs
- NMR Signal Processing
What to expect: Chemical Shifts & Coupling Constants in Low-field NMR Spectroscopy
One of the questions that we always get at tradeshows and conferences is how our instrument compares to high-field data. There are significant inherent differences between low-field and high-field instruments, but the most important from a chemistry point of view are sensitivity (S/N) and resonance dispersion (signal separation). Read More.
Two solvents, two different spectra - Aromatic Solvent Induced Shifts
In my opinion, one of the most helpful papers[1] in the field of NMR spectroscopy in Organic Chemistry consists of ‘just’ two tables. In these, the chemical shifts (1H and 13C) of as many as forty-two common impurities in twelve different deuterated solvents are listed. This is gold! Why?
Your Nanalysis 60 Order!
‘The spectra were analyzed according to first order’. Does this sound familiar to you? Most of the supporting information documents out there contain this sentence. You find yourself asking ‘why does nobody care about second order effects?’, then check out this high-order blog entry on the topic.
Why 100 MHz Benchtop NMR?
While low-field NMR has extremely favourable accessibility and affordable characteristics, the most common question that we get asked about our family of benchtop NMR spectrometers is with respect to any trade-offs that come from moving to lower-field.
Two solvents, two different spectra - Aromatic Solvent Induced Shifts
In my opinion, one of the most helpful papers[1] in the field of NMR spectroscopy in Organic Chemistry consists of ‘just’ two tables. In these, the chemical shifts (1H and 13C) of as many as forty-two common impurities in twelve different deuterated solvents are listed. This is gold! Why?
Your NMReady-60 Order!
‘The spectra were analyzed according to first order’. Does this sound familiar to you? Most of the supporting information documents out there contain this sentence. You find yourself asking ‘why does nobody care about second order effects?’, then check out this high-order blog entry on the topic.
What to expect: Chemical Shifts & Coupling Constants in Low-field NMR Spectroscopy
One of the questions that we always get at tradeshows and conferences is how our instrument compares to high-field data. There are significant inherent differences between low-field and high-field instruments, but the most important from a chemistry point of view are sensitivity (S/N) and resonance dispersion (signal separation). Read More.
External Field Strength, Resolution and Sensitivity
As we’ve previously discussed, the development of NMR technology has largely been geared towards improving magnetic field strength. The original electromagnet spectrometers