α-Keto Isovaleric Acid Sodium Salt 13C D6

Product Name α-Keto Isovaleric Acid Sodium Salt 13C D6
CAT No. CS-R-00562
CAS No. 3715-29-5 (Unlabeled)
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys O=C(C([O-])=O)C(C([2H])([2H])[2H])([2H])[13CH]([2H])[2H].[Na+]
Canonical Smiles CC(C)C(=O)C(=O)[O-].[Na+]
InchIKey WIQBZDCJCRFGKA-UHFFFAOYSA-M
Inchl InChI=1S/C5H8O3.Na/c1-3(2)4(6)5(7)8;/h3H,1-2H3,(H,7,8);/q;+1/p-1
IUPAC sodium;3-methyl-2-oxobutanoate
Controlled No
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α-Keto Isovaleric Acid Sodium Salt 13C D6, also known as α-Keto-3-methylbutyric acid sodium salt 13C D6, is a stable isotope-labeled compound that is commonly used in biochemical research and medical diagnosis. The compound is a derivative of the natural α-ketoisovaleric acid, which is synthesized in the human body during the catabolism of branched-chain amino acids (BCAAs) such as leucine, isoleucine, and valine. α-Keto Isovaleric Acid Sodium Salt 13C D6 is used in biochemical studies to investigate the metabolic pathways of BCAAs and their role in various physiological processes. It is also used as a diagnostic marker for metabolic disorders such as maple syrup urine disease, an inherited disorder that affects the breakdown of BCAAs in the body. The compound is chemically stable and has a molecular formula of C5H4D6NaO3. It is synthesized by replacing the hydrogen atoms in the α-ketoisovaleric acid molecule with deuterium atoms. This stable isotope-labeled compound is important in metabolic studies as it allows for accurate tracking of metabolic pathways and identification of metabolic intermediates. In summary, α-Keto Isovaleric Acid Sodium Salt 13C D6 is a valuable tool in biochemical research and medical diagnosis. Its stable isotope labeling allows for accurate tracking of metabolic pathways and identification of metabolic intermediates.

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