Related Experiment Video
Updated: Jul 2, 2026

Methods to Identify the NMR Resonances of the 13C-Dimethyl N-terminal Amine on Reductively Methylated Proteins
Published on: December 12, 2013
Three New Calcium Formate Reference Materials for δ13C Measurements and a Redetermination of the R(13C/12C) Ratio for
David W Hoffman1, Cornelia Rasmussen2, Arndt Schimmelmann3
1Department of Molecular Biosciences, College of Natural Science, University of Texas at Austin, Austin, Texas, USA.
Rationale:
Isotope ratio mass spectrometry (IRMS) and proton nuclear magnetic resonance (1H NMR) spectroscopy are independent techniques for determining the isotope ratio R(13C/12C) in organic compounds. However, the lack of suitable reference materials has limited intercalibration of results from these methods.
Methods:
Three high-purity calcium formate isotopic reference materials were developed, each ideal for accurate isotope ratio measurements by both 1H NMR and isotope-ratio mass spectrometry (IRMS). For each material, R(13C/12C) was determined by 1H NMR, and the relative isotope abundance (δ13CVPDB-LSVEC) by IRMS. The combined IRMS and NMR results were used to determine the R(13C/12C) value of Vienna Peedee belemnite (VPDB).
Results:
The combined datasets yield a value for R(13C/12C) of 0.0111050 ± 0.0000047 (k = 2) for VPDB, which is 6.7‰ lower than the commonly cited value of 0.011180, but similar to other recent determinations. These three calcium formate reference materials exhibit high accuracy across both analytical methods and provide robust tools for instrument calibration, method validation, and inter-laboratory comparison in carbon stable isotope ratio analysis.
Conclusions:
An accurate R(13C/12C) value for VPDB strengthens the link between relative (δ13CVPDB-LSVEC) values from IRMS and R(13C/12C) isotope ratios from NMR and other techniques. These three calcium formate isotopic reference materials (USGS106, USGS107, and USGS108) are available from the US Geological Survey and provide reference materials for calibration, method validation, and inter-laboratory comparison in carbon isotope ratio analysis.
Related Concept Videos
Chemical Shift: Internal References and Solvent Effects
The internal reference compound generally used in NMR spectroscopy is tetramethylsilane (TMS). TMS is preferred because it is chemically inert, soluble in NMR solvents, and easily removable. Also, the highly shielded methyl protons in TMS yield an intense...
Carbon-13 (¹³C) NMR: Overview
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
¹³C NMR: ¹H–¹³C Decoupling
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
Proton (¹H) NMR: Chemical Shift
Absorption signals of all the protium nuclei in a...
Mass Spectrum: Interpretation
