Basic Description

Synonyms	NADP disodium salt \| Nadide phosphate disodium \| Triphosphopyridine nucleotide disodium salt \| NADP \| NADP Disodium \| Disodium NADP
Specifications & Purity	≥97%
Biochemical and Physiological Mechanisms	NADP and NADPH form a redox pair. NADP is the oxidised form of NADPH. NADP/NADPH is a coenzyme that supports redox reactions via the transport of electrons in a vast array of applications.
Storage Temp	Store at -20°C,Argon charged
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description	A participant coenzyme in aerobic and anaerobic oxidation Nicotinamide adenine dinucleotide phosphate (NADP) and NADPH form a redox pair. NADP/NADPH is a coenzyme that supports redox reactions via the transport of electrons in a vast array of applications, especially anaerobic reactions such as lipid and nucleic acid synthesis. NADP/NADPH is a coenzyme couple in various cytochrome P450 systems and oxidase/reductase reaction systems, such as the thioredoxin reductase/thioredoxin system.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class (5'->5')-dinucleotides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	(5'->5')-dinucleotides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	(5'->5')-dinucleotides
Alternative Parents	Purine nucleotide sugars Purine ribonucleoside diphosphates Purine ribonucleoside 2',5'-bisphosphates Nicotinamide nucleotides Pentose phosphates Glycosylamines 6-aminopurines Monosaccharide phosphates Organic pyrophosphates Nicotinamides Aminopyrimidines and derivatives Monoalkyl phosphates Imidolactams Pyridinium derivatives N-substituted imidazoles Tetrahydrofurans Vinylogous amides Heteroaromatic compounds Primary carboxylic acid amides Amino acids and derivatives Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic oxides Primary amines Hydrocarbon derivatives Organopnictogen compounds Organic sodium salts Organic zwitterions
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	(5'->5')-dinucleotide - Purine nucleotide sugar - Purine ribonucleoside diphosphate - Purine ribonucleoside bisphosphate - Purine ribonucleoside 2',5'-bisphosphate - Nicotinamide-nucleotide - Pyridine nucleotide - Pentose-5-phosphate - Pentose phosphate - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Pyridine carboxylic acid or derivatives - Imidazopyrimidine - Purine - Nicotinamide - Monoalkyl phosphate - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyridine - Pyridinium - Pyrimidine - Vinylogous amide - Azole - Tetrahydrofuran - Imidazole - Heteroaromatic compound - Primary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Organic alkali metal salt - Azacycle - Oxacycle - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Alcohol - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic salt - Organic zwitterion - Amine - Organonitrogen compound - Organooxygen compound - Organic sodium salt - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as (5'->5')-dinucleotides. These are dinucleotides where the two bases are connected via a (5'->5')-phosphodiester linkage.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504761129
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504761129
IUPAC Name	disodium;[(2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-[[[[(2R,3S,4R,5R)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-hydroxyphosphoryl]oxymethyl]-4-hydroxyoxolan-3-yl] phosphate
INCHI	InChI=1S/C21H28N7O17P3.2Na/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32;;/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39);;/q;2*+1/p-2/t10-,11-,13-,14-,15-,16-,20-,21-;;/m1../s1
InChIKey	WSDDJLMGYRLUKR-WUEGHLCSSA-L
Smiles	C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)N4C=NC5=C(N=CN=C54)N)OP(=O)([O-])[O-])O)O)O)C(=O)N.[Na+].[Na+]
Isomeric SMILES	C1=CC(=C[N+](=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)N4C=NC5=C(N=CN=C54)N)OP(=O)([O-])[O-])O)O)O)C(=O)N.[Na+].[Na+]
WGK Germany	3
PubChem CID	2734411
Molecular Weight	787.37

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

26 results found

Lot Number	Certificate Type	Date	Item
C2526649	Certificate of Analysis	Feb 18, 2025	N113163
C2526659	Certificate of Analysis	Feb 18, 2025	N113163
C2526660	Certificate of Analysis	Feb 18, 2025	N113163
C2526661	Certificate of Analysis	Feb 18, 2025	N113163
C2526662	Certificate of Analysis	Feb 18, 2025	N113163
J2424653	Certificate of Analysis	Oct 16, 2024	N113163
A2513246	Certificate of Analysis	Oct 16, 2024	N113163
J2424654	Certificate of Analysis	Oct 16, 2024	N113163
J2424652	Certificate of Analysis	Oct 16, 2024	N113163
F2103102	Certificate of Analysis	May 25, 2024	N113163
F2403104	Certificate of Analysis	May 25, 2024	N113163
F2403105	Certificate of Analysis	May 25, 2024	N113163
F2403102	Certificate of Analysis	May 25, 2024	N113163
F2403103	Certificate of Analysis	May 25, 2024	N113163
G23041037	Certificate of Analysis	Jun 14, 2023	N113163
G23041038	Certificate of Analysis	Jun 14, 2023	N113163
G23041039	Certificate of Analysis	Jun 14, 2023	N113163
G23041040	Certificate of Analysis	Jun 14, 2023	N113163
E2408046	Certificate of Analysis	Jun 14, 2023	N113163
G2322038	Certificate of Analysis	Jun 14, 2023	N113163
K2215857	Certificate of Analysis	Nov 04, 2022	N113163
K2215820	Certificate of Analysis	Nov 04, 2022	N113163
K2215861	Certificate of Analysis	Nov 04, 2022	N113163
K2215834	Certificate of Analysis	Nov 04, 2022	N113163
K2215762	Certificate of Analysis	Nov 04, 2022	N113163
G2206379	Certificate of Analysis	Jun 29, 2022	N113163

Show more⌵

Chemical and Physical Properties

Solubility	Soluble in water (50 mg/ml), 0.001% aqueous buffer, pH 7.0, methanol, and ethanol (less soluble). Insoluble in ether, and ethyl acetate.
Sensitivity	Heat sensitive ;Moisture sensitive
Molecular Weight	787.400 g/mol
XLogP3
Hydrogen Bond Donor Count	6
Hydrogen Bond Acceptor Count	21
Rotatable Bond Count	12
Exact Mass	787.039 Da
Monoisotopic Mass	787.039 Da
Topological Polar Surface Area	373.000 Å²
Heavy Atom Count	50
Formal Charge	0
Complexity	1280.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	8
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	3

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Fei Qiu, Yijun Yan, Junlan Zeng, Jian-Ping Huang, Lingjiang Zeng, Wei Zhong, Xiaozhong Lan, Min Chen, Sheng-Xiong Huang, Zhihua Liao. (2021) Biochemical and Metabolic Insights into Hyoscyamine Dehydrogenase. ACS Catalysis, 11 (5): (2912–2924).
2. Lijun Geng, Xudong Yu, Yajuan Li, Yanqiu Wang, Yongquan Wu, Jujie Ren, Fengfeng Xue, Tao Yi. (2019) Instant hydrogel formation of terpyridine-based complexes triggered by DNA via non-covalent interaction. Nanoscale, 11 (9): (4044-4052).
3. Yunkai Sun, Xiaoxia Wu, Pei Zuo, Zhao Liu, Xuepei Miao, Jian Liu, Hairuo Wen. (2024) Synthesis and mutagenic risk of avanafil's potential genotoxic impurities. RSC Advances, 14 (30): (21432-21438).

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

=

Concentration

x

Volume

x

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

x

Volume 1 (V1)

=

Concentration 2 (C2)

x

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

=

Mass (in vial)

÷

Desired Reconstitution Concentration

SKU	Size	Availability	Price
N113163-50mg	50mg	3	$9.90
N113163-250mg	250mg	5	$19.90
N113163-1g	1g	2	$29.90
N113163-5g	5g	2	$99.90
N113163-25g	25g	2	$319.90
N113163-100g	100g	4	$829.90

NADP, Disodium Salt - 97%, high purity , CAS No.24292-60-2