β-Nicotinamide adenine dinucleotide sodium salt

Alternative_name

β-DPN, β-NAD, Coenzyme 1, Cozymase, DPN, Diphosphopyridine nucleotide, NAD, Nadide
Description

β-Nicotinamide adenine dinucleotide sodium is the most common form of NAD. NAD can be reduced to NADH during coupling with reactions which oxidize various organic substrates. NADH then passes to the inside of mitochondria where it donates the electrons it is carrying to the electron transport chain. In this manner, NAD acts as an intermediate
CAS Number

20111-18-6
Structure Available

Yes
Molecular Formula

C₂₁H₂₆N₇NaO₁₄P₂
Molecular Weight

685.41
Cell Permeable

No
Purity

≥95% by HPLC
Solubilities

H₂O (50 mg/ml)
Handling

Protect from air and moisture
Tag Line

A key cofactor or substrate for many enzymes
Storage Condition

-20°C
Shipping Condition

Gel pack
Shelf Life

36 months
MDL Number

MFCD00148917
PubChem CID

72710628
PubChem CID Link
SMILES

C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OCC3C(C(C(O3)N4C=NC5=C4N=CN=C5N)O)O)O)O)C(=O)N.[Na+]
InChi

InChI=1S/C21H27N7O14P2.Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33;/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37);/q;+1/p-1/t10-,11-,13-,14-,15-,16-,20-,21-;/m1./s1
InChi Key

OGCURMAMSJFXSG-QYZPTAICSA-M
Data Sheet Link
MSDS Available

Yes