α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
- Product Name
- α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
- CAS No.
- 634908-42-2
- Chemical Name
- α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2
- Synonyms
- α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2;α-Ketoisovaleric acid, sodium salt (dimethyl-13C?, 99%);2-Keto-3-(methyl-13C)-butyric-4-13C acid sodium salt
- CBNumber
- CB910773751
- Formula Weight
- 0
- MOL File
- Mol file
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2 Property
- Melting point:
- 227-230°C (lit.)
- form
- solid
- color
- White to off-white
- CAS Number Unlabeled
- 3715-29-5
N-Bromosuccinimide Price
- Product number
- 571334
- Product name
- 2-Keto-3-(methyl-13C)-butyric-4-13C acid sodium salt
- Purity
- 99 atom % 13C, 97% (CP)
- Packaging
- 100MG
- Price
- $313.5
- Updated
- 2025/07/31
- Product number
- 571334
- Product name
- 2-Keto-3-(methyl-13C)-butyric-4-13C acid sodium salt
- Purity
- 99 atom % 13C, 97% (CP)
- Packaging
- 500MG
- Price
- $714.95
- Updated
- 2025/07/31
- Product number
- 571334
- Product name
- 2-Keto-3-(methyl-13C)-butyric-4-13C acid sodium salt
- Purity
- 99 atom % 13C, 97% (CP)
- Packaging
- 1G
- Price
- $1501
- Updated
- 2025/07/31
α-Keto Isovaleric Acid Sodium Salt Dimethyl-13C2 Chemical Properties,Usage,Production
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-13C2 Preparation Products And Raw materials
Raw materials
Preparation Products
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