Literature DB >> 10518283

Artefactual pyruvate and 2-oxobutyrate produced by trimethylsilylation of methylmalonic and ethylmalonic acids in the presence of oxygen.

O A Mamer1, L Choiniere, D Boismenu, F Lepine.   

Abstract

Trimethylsilylation of methylmalonic and ethylmalonic acids in the presence of headspace atmospheric oxygen is shown to produce the trimethylsilyl derivatives of pyruvic and 2-oxobutyric acids, along with 2-hydroxy-2-methylmalonic and 2-hydroxy-2-ethylmalonic acids, respectively. This may lead to overestimation of these keto acids, if they were not oximated in the original sample, and the mistaken reporting of the 2-hydroxymalonates.

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Year:  1999        PMID: 10518283     DOI: 10.1023/a:1005510224963

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  2 in total

1.  Branched-chain alpha-keto acids isolated as oxime derivatives: relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease.

Authors:  G Lancaster; O A Mamer; C R Scriver
Journal:  Metabolism       Date:  1974-03       Impact factor: 8.694

2.  Trimethylsilylation of malonate ester enols.

Authors:  O A Mamer; S S Tjoa
Journal:  Clin Chem       Date:  1973-01       Impact factor: 8.327

  2 in total

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