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¹H NMR Signal Integration: Overview00:58

¹H NMR Signal Integration: Overview

2.9K
The intensity of a signal, which can be represented by the area under the peak, depends on the number of protons contributing to that signal. The area under each peak is shown as a vertical line called an integral, with the integral value listed under it, as seen in the proton NMR spectrum of benzyl acetate. Each integral value is divided by the smallest integral value to obtain the ratio of the number of protons producing each signal. The ratio reveals the relative number of protons and not...
2.9K
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR01:15

¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

1.4K
The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
1.4K
NMR Spectroscopy of Aromatic Compounds01:14

NMR Spectroscopy of Aromatic Compounds

5.8K
Aromatic compounds can be identified or analyzed using proton NMR and carbon‐13 NMR. Typically, aromatic hydrogens or hydrogens directly bonded to the aromatic rings are strongly deshielded by the aromatic ring current. Therefore, they absorb in the range of 6.5–8.0 ppm in proton NMR spectra. For instance, aromatic hydrogens directly bonded to the benzene ring absorb at 7.3 ppm. However, aromatic hydrogens of larger rings absorb farther upfield or downfield than the ideal range.
5.8K
NMR Spectrometers: Overview01:20

NMR Spectrometers: Overview

1.8K
NMR spectrometers consist of a strong magnet, a radiofrequency transmitter, and a detector attached to a computer console for recording spectra of samples containing NMR-active nuclei. In first-generation NMR instruments called continuous-wave spectrometers, the resonance frequencies of the nuclei are determined by frequency-sweep or field-sweep methods. The magnetic field strength is fixed and the rf signal is swept in the former, while the radiofrequency signal is fixed and the magnetic field...
1.8K
Qualitative Analysis01:10

Qualitative Analysis

1.1K
Qualitative analysis is the process of identifying elements, ions, or compounds in an unknown sample. It is the first and most fundamental type of analysis based on the hierarchy of analytical goals. This hierarchy is significant as it provides a structured approach to scientific research, with qualitative analysis serving as the initial step, providing essential information before moving on to quantitative or other forms of analysis.
There are two main approaches to qualitative analysis:...
1.1K
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution00:52

¹H NMR of Conformationally Flexible Molecules: Temporal Resolution

1.1K
At room temperature, the chair conformer of cyclohexane undergoes rapid ring flipping between two equivalent chair conformers at a rate of approximately 105 times per second. These two chair conformers are in equilibrium. The rapid ring flipping results in the interconversion of the axial proton to an equatorial proton and an equatorial to the axial proton. Such interconversions are too rapid and cannot be detected on the NMR timescale. Hence, the NMR spectrometer cannot distinguish between the...
1.1K

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Related Experiment Video

Updated: Dec 6, 2025

Ultrasonic-Assisted Extraction of Cannabidiolic Acid from Cannabis Biomass
05:46

Ultrasonic-Assisted Extraction of Cannabidiolic Acid from Cannabis Biomass

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Quantitative analysis of cannabinoids using benchtop NMR instruments.

Juan F Araneda1, Terry Chu, Matthew C Leclerc

  • 1Nanalysis Corp., 1-4600 5 St NE, Calgary, AB T2E 7C3, Canada. juan.araneda@nanalysis.com.

Analytical Methods : Advancing Methods and Applications
|October 12, 2020
PubMed
Summary

Benchtop NMR offers a new way to quantify major cannabinoids like THC and CBD in cannabis products. This method provides an orthogonal approach to HPLC, addressing discrepancies in current testing methods.

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Area of Science:

  • Analytical Chemistry
  • Cannabis Science

Background:

  • Cannabinoid quantification is vital for cannabis product testing and regulation.
  • High-Performance Liquid Chromatography (HPLC) is the standard method, but inter-laboratory discrepancies exist.
  • There is a growing need for alternative, reliable analytical techniques.

Purpose of the Study:

  • To evaluate benchtop Nuclear Magnetic Resonance (NMR) spectroscopy for quantifying Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD).
  • To compare NMR quantification results with those obtained by HPLC.
  • To highlight the importance of orthogonal methods in cannabis analysis.

Main Methods:

  • Utilized benchtop NMR instruments for cannabinoid quantification.
  • Analyzed various cannabis concentrates.
  • Compared NMR data against HPLC results.

Main Results:

  • Benchtop NMR successfully quantified THC and CBD in cannabis concentrates.
  • Observed discrepancies between NMR and HPLC values underscore the need for method validation.
  • NMR provides a valuable orthogonal data set for cannabinoid profiling.

Conclusions:

  • Benchtop NMR is a viable alternative method for cannabinoid quantification.
  • Orthogonal testing methods, like NMR, are essential for ensuring accuracy and reliability in cannabis testing.
  • NMR can help address inconsistencies arising from HPLC-based testing alone.