113-24-6 | Sodium pyruvate

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$16.00	$11.00
25g	98%	in stock	$18.00	$12.00
100g	98%	in stock	$25.00	$17.00
500g	98%	in stock	$42.00	$29.00
1000g	98%	in stock	$73.00	$51.00

Description

• Catalog Number: AB78764
• Chemical Name: Sodium pyruvate
• CAS Number: 113-24-6
• Molecular Formula: C3H3NaO3
• Molecular Weight: 110.0439
• MDL Number: MFCD00002586
• SMILES: CC(=O)C(=O)[O-].[Na+]

Computed Properties

• Complexity: 88.2
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

Sodium 2-oxopropanoate, also known as sodium pyruvate, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a precursor in the synthesis of various important compounds. One of its key applications is as a building block in the formation of amino acids, which are essential molecules for protein synthesis and biological functions.Furthermore, sodium 2-oxopropanoate plays a crucial role in the Krebs cycle, a central metabolic pathway in cells where it is involved in the production of energy through the oxidation of carbohydrates, fats, and proteins. Its ability to participate in key biochemical reactions makes it a valuable tool in research laboratories studying cellular metabolism and energy production.Moreover, sodium 2-oxopropanoate is utilized in the pharmaceutical industry for the development of new drugs and medicines. Its incorporation into drug molecules can enhance their stability, solubility, and bioavailability, thereby improving their therapeutic effects. Additionally, it is employed in cosmetic formulations for its antioxidant properties and potential skin benefits.Overall, sodium 2-oxopropanoate is a fundamental compound in chemical synthesis, with wide-ranging applications in organic chemistry, biochemistry, pharmaceuticals, and cosmetics. Its versatility and reactivity make it an indispensable tool for scientists and researchers in various fields.

Literature

• Carbonic anhydrase inhibitors. Inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with aliphatic and aromatic carboxylates.

  Bioorganic & medicinal chemistry 20090401

• Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with carboxylates.

  Bioorganic & medicinal chemistry letters 20050201

• Cloning of a lactate dehydrogenase gene from Clostridium acetobutylicum B643 and expression in Escherichia coli.

  Applied and environmental microbiology 19901201