Site-specific C content by quantitative isotopic C Nuclear Magnetic Resonance spectrometry: A pilot inter-laboratory study |
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Authors: | Alain Chaintreau,Wolfgang Fieber,Horst Sommer,Alexis Gilbert,Keita Yamada,Naohiro Yoshida,Alain Pagelot,Detlef Moskau,Aitor Moreno,Jü rgen Schleucher,Fabiano Reniero,Margaret Holland,Claude Guillou,Virginie Silvestre,Serge Akoka,Gé rald S. Remaud |
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Affiliation: | 1. Firmenich SA, Corporate R&D Division, P.O. Box 239, 1211 Geneva 8, Switzerland;2. Department of Environmental Chemistry and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama, Kanagawa 226-8503, Japan;3. Earth-Life Science Institute, Tokyo Institute of Technology, Meguro, Tokyo 152-8551, Japan;4. Bruker Biospin SAS, 34 rue de l‘Industrie, 67166 Wissembourg Cedex, France;5. Bruker Biospin AG, Industriestrasse 26, 8117 Fällanden, Switzerland;6. Department of Medical Biochemistry & Biophysics, Umeå University, S-90187 Umeå, Sweden;g European Commission, Joint Research Centre – Institute for Health and Consumer Protection, via E. Fermi 2749, I-21027 Ispra (VA), Italy;h EBSI team, Interdisciplinary Chemistry: Synthesis, Analysis, Modelling (CEISAM), University of Nantes-CNRS UMR 6230, 2 rue de la Houssinière, BP 92208, F-44322 Nantes cedex 3, France |
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Abstract: | Isotopic 13C NMR spectrometry, which is able to measure intra-molecular 13C composition, is of emerging demand because of the new information provided by the 13C site-specific content of a given molecule. A systematic evaluation of instrumental behaviour is of importance to envisage isotopic 13C NMR as a routine tool. This paper describes the first collaborative study of intra-molecular 13C composition by NMR. The main goals of the ring test were to establish intra- and inter-variability of the spectrometer response. Eight instruments with different configuration were retained for the exercise on the basis of a qualification test. Reproducibility at the natural abundance of isotopic 13C NMR was then assessed on vanillin from three different origins associated with specific δ13Ci profiles. The standard deviation was, on average, between 0.9 and 1.2‰ for intra-variability. The highest standard deviation for inter-variability was 2.1‰. This is significantly higher than the internal precision but could be considered good in respect of a first ring test on a new analytical method. The standard deviation of δ13Ci in vanillin was not homogeneous over the eight carbons, with no trend either for the carbon position or for the configuration of the spectrometer. However, since the repeatability for each instrument was satisfactory, correction factors for each carbon in vanillin could be calculated to harmonize the results. |
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Keywords: | Collaborative study Quantitative Nuclear Magnetic Resonance spectrometry Intra molecular 13C isotope distribution Vanillin |
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