104809-32-7 | Beta-nicotinamide adenine dinucleotide, reduced dipotassium salt

Packsize	Purity	Availability	Price	Discounted Price
25mg	95%	in stock	$76.00	$53.00

Description

• Catalog Number: AE16801
• Chemical Name: Beta-nicotinamide adenine dinucleotide, reduced dipotassium salt
• CAS Number: 104809-32-7
• Molecular Formula: C21H27K2N7O14P2
• Molecular Weight: 741.6217020000003
• MDL Number: MFCD00079494
• SMILES: O[C@@H]1[C@H](O)[C@H](O[C@H]1N1C=CCC(=C1)C(=O)N)COP(=O)(OP(=O)(OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2N)[O-])[O-].[K+].[K+]

Upstream Synthesis Route

**Application in Chemical Synthesis:**In chemical synthesis, β-Nicotinamide adenine dinucleotide, reduced dipotassium salt (NADH) serves as a vital cofactor for various enzyme-catalyzed redox reactions. This potent electron donor participates in a wide range of biochemical processes, playing a crucial role in energy production and metabolism within living cells. NADH's ability to act as a reducing agent makes it a valuable component in enzymatic reactions involved in the biosynthesis of essential molecules such as fatty acids, amino acids, and nucleotides. Its presence facilitates the conversion of precursors into complex compounds, thereby enabling the efficient production of key biomolecules. Furthermore, NADH is instrumental in the regeneration of antioxidants such as glutathione, providing cellular protection against oxidative stress and ensuring the maintenance of redox balance. This property makes it indispensable in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals that require precise control over oxidation-reduction reactions. Overall, the utilization of NADH in chemical synthesis enhances the efficiency and selectivity of various enzymatic transformations, making it a versatile tool for the production of valuable compounds in both industrial and research settings.