α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2 Basic information
- Product Name:
- α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
- Synonyms:
-
- α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
- 2-Keto-3-(methyl-13C)-butyric-4-13C acid sodium salt
- α-Ketoisovaleric acid, sodium salt (dimethyl-13C?, 99%)
- CAS:
- 634908-42-2
- MW:
- 0
- Mol File:
- Mol File
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2 Chemical Properties
- Melting point:
- 227-230°C (lit.)
- form
- solid
- color
- White to off-white
- CAS Number Unlabeled
- 3715-29-5
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2 Usage And Synthesis
Uses
3-Methyl-2-oxobutanoic acid-13C2 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
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2Supplier
- Tel
- 400-6206333 13167063860
- anhua.mao@aladdin-e.com
- Tel
- 021-61312847; 18021002903
- 3008007409@qq.com
- Tel
- 021-64400900 15800436310
- bessey@reertech.com
- Tel
- 21-20338288
- ordercn@merckgroup.com
- Tel
- 021-60936350
- scbt@scbt.com