1215605-14-3

1215605-14-3 structure
1215605-14-3 structure
  • Name: Sodium 3-methyl-2-oxobutanoate-13C4,d3
  • Chemical Name: 2-Keto-3-(methyl-d3)-butyric acid-1,2,3,4-13C4 sodium salt
  • CAS Number: 1215605-14-3
  • Molecular Formula: 13CH313CH(CD3)13CO13CO2Na
  • Molecular Weight: 145.09
  • Catalog: Research Areas Others
  • Create Date: 2022-11-21 22:15:10
  • Modify Date: 2024-04-03 12:52:08
  • Sodium 3-methyl-2-oxobutanoate-13C4,d3 is the deuterium and 13C labeled Sodium 3-methyl-2-oxobutanoate[1]. Sodium 3-methyl-2-oxobutanoate is a precursor of pantothenic acid in Escherichia coli[2][3][4].

Name 2-Keto-3-(methyl-d3)-butyric acid-1,2,3,4-13C4 sodium salt
Synonyms MFCD05664338
Description Sodium 3-methyl-2-oxobutanoate-13C4,d3 is the deuterium and 13C labeled Sodium 3-methyl-2-oxobutanoate[1]. Sodium 3-methyl-2-oxobutanoate is a precursor of pantothenic acid in Escherichia coli[2][3][4].
Related Catalog
In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

[2]. MAAS WK, et al. alpha-Ketoisovaleric acid, a precursor of pantothenic acid in Escherichia coli. J Bacteriol. 1953 Apr;65(4):388-93.  

[3]. Schauder P, et al. Oral administration of alpha-ketoisovaleric acid or valine in humans: blood kinetics and biochemical effects. J Lab Clin Med. 1984 Apr103(4):597-605.  

[4]. Coitinho AS, et al. Pharmacological evidence that alpha-ketoisovaleric acid induces convulsions through GABAergic and glutamatergic mechanisms in rats. Brain Res. 2001 Mar 9894(1):68-73.  

Melting Point 227-230 °C (lit.) (lit.)
Molecular Formula 13CH313CH(CD3)13CO13CO2Na
Molecular Weight 145.09
Appearance solid