2-Keto-3-methylbutyric acid-13C5 sodium salt
2-Keto-3-methylbutyric acid-13C5 sodium salt Basic information
- Product Name:
- 2-Keto-3-methylbutyric acid-13C5 sodium salt
- Synonyms:
-
- 2-Ketoisovaleric acid-13C5 sodium salt
- 3-Methyl-2-oxobutanoic acid-13C5 sodium salt
- α-Keto-3-methylbutyric acid-13C5 sodium
- α-Ketoisovaleric acid-13C5 sodium salt
- [13C5]-2-Keto-3-methylbutyric acid sodium salt
- ALPHA-KETOISOVALERIC ACID, SODIUM SALT (13C5, 98%)
- α-Ketoisovaleric Acid, Sodium Salt (13C5, 98%)
- α-Keto Isovaleric Acid Sodium Salt 13C5
- CAS:
- 1173018-24-0
- MF:
- C5H7NaO3
- MW:
- 143.14205
- Mol File:
- 1173018-24-0.mol
2-Keto-3-methylbutyric acid-13C5 sodium salt Chemical Properties
- Melting point:
- 227-230°C
- solubility
- DMSO (Slightly), Water (Slightly)
- form
- Solid
- color
- White to Off-White
- CAS Number Unlabeled
- 3715-29-5
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-37/38-41
- Safety Statements
- 26-36/37/39
- WGK Germany
- 3
2-Keto-3-methylbutyric acid-13C5 sodium salt Usage And Synthesis
Uses
Sodium 3-methyl-2-oxobutanoate-13C5 is the 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].
References
[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. DOI:10.1177/1060028018797110
[2] MAAS WK, et al. alpha-Ketoisovaleric acid, a precursor of pantothenic acid in Escherichia coli. J Bacteriol. 1953 Apr;65(4):388-93. DOI:10.1128/jb.65.4.388-393.1953
[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. PMID:6366097
[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. DOI:10.1016/s0006-8993(00)03321-7
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