Adenosine 5′-diphosphate monopotassium salt dihydrate - ≥95% , CAS No.72696-48-1

CAS: 72696-48-1 Cat. No.: A130017 Molecular Weight: 501.32 PubChem CID: 71299721
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Synonyms
ADP | ADP-K
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Size
Status
Price
Qty
100mg
A130017-100mg
2
$9.90
250mg
A130017-250mg
3
$9.90
1g
A130017-1g
2
$31.90
5×1g
A130017-5×1g
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$133.90
10g
A130017-10g
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$158.90
25g
A130017-25g
1
$281.90
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Adenosine 5′-Diphosphate Potassium Salt is a nucleotide that is widely distributed in nature. Adenosine 5′-Diphosphate Potassium Salt is an activator of P2Y.
A nucleotide that is widely distributed in nature.


application:

Adenosine 5′-diphosphate is a P2Y receptor agonist. Adenosine 5′-diphosphate has been used to study the release, neuronal effects and removal of extracellular β-nicotinamide adenine dinucleotide (β-NAD+) in the rat brain. Adenosine 5′-diphosphate has also been used to compare prasugrel versus clopidogrel antiplatelet therapy after acute coronary syndrome.

Specifications

Synonyms
ADP | ADP-K
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
P2Y receptor agonist.
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥95%
Names and Identifiers
Canonical SmilesC1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)[O-])O)O)N.O.O.[K+]
IUPAC Namepotassium;[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] hydrogen phosphate;dihydrate
InChIKeyHFCXEPLDPMALMF-MSQVLRTGSA-M
INCHI1S/C10H15N5O10P2.K.2H2O/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20;;;/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20);;2*1H2/q;+1;;/p-1/t4-,6-,7-,10-;;;/m1.../s1
Isomeric SMILES C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)OP(=O)(O)[O-])O)O)N.O.O.[K+]
WGK Germany 3
PubChem CID 71299721
Molecular Weight 501.32

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClassPurine nucleotides
SubclassPurine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPurine ribonucleoside diphosphates
Alternative Parents Purine ribonucleoside monophosphates  Pentose phosphates  Glycosylamines  6-aminopurines  Organic pyrophosphates  Monosaccharide phosphates  Aminopyrimidines and derivatives  Monoalkyl phosphates  Imidolactams  N-substituted imidazoles  Oxolanes  Heteroaromatic compounds  Secondary alcohols  1,2-diols  Oxacyclic compounds  Azacyclic compounds  Organic zwitterions  Hydrocarbon derivatives  Primary amines  Organic potassium salts  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Pyrimidine - Alkyl phosphate - Azole - Oxolane - Imidazole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Organic alkali metal salt - Azacycle - Oxacycle - Amine - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Primary amine - Organic oxygen compound - Organic salt - Organic zwitterion - Organic potassium salt - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as purine ribonucleoside diphosphates. These are purine ribobucleotides with diphosphate group linked to the ribose moiety.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

8 results found

Lot NumberCertificate TypeDateItem
C2215248Certificate of AnalysisDec 16, 2025 A130017
C2215249Certificate of AnalysisDec 16, 2025 A130017
A1823106Certificate of AnalysisOct 17, 2025 A130017
A2206628Certificate of AnalysisOct 13, 2025 A130017
A2206629Certificate of AnalysisOct 13, 2025 A130017
D1911027Certificate of AnalysisFeb 06, 2023 A130017
E1520037Certificate of AnalysisJan 05, 2023 A130017
B2321382Certificate of AnalysisNov 30, 2021 A130017
Chemical and Physical Properties
SolubilitySoluble in water (50 mg/ml).
Molecular Weight501.320 g/mol
XLogP3
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count16
Rotatable Bond Count6
Exact Mass501.006 Da
Monoisotopic Mass501.006 Da
Topological Polar Surface Area237.000 Ų
Heavy Atom Count30
Formal Charge0
Complexity650.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count4
Citations of This Product
References
1. Guannan Zhang, Anping Zhu, Shihong Wang, Qianshan Chen, Bing Liu, Jun Zhou, Zhaoyang Wu.  (2022)  Stabilizing liquid crystal droplets with hydrogel films and its application in monitoring adenosine triphosphate.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2022.130122]
2. Shun Hu, Xiaona Li, Kai Wang, Qiuhua Wu, Guolin Zhang, Xue Liu.  (2020)  Sensor array based on carbon dots for ATP-related physiological phosphates detecting and ATP hydrolysis monitoring.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2020.127851]
3. Guimei Wang, Xiaoxue Jiang, Nanyan Fu.  (2019)  Near-infrared squaraine fluorescent probe for imaging adenosine 5′-triphosphate in live cells.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2019.107698]
4. Gong Bi, Huang Shuai, Ye Niu, Yuan Xue, Ma Huiling.  (2018)  Pre-harvest ethylene control affects vase life of cut rose ‘Carola’ by regulating energy metabolism and antioxidant enzyme activity.  Horticulture Environment and Biotechnology,  59  (6): (835-845).  [PMID:] [10.1007/s13580-018-0053-8]
5. Pang Jiawei, Lu Yuexiang, Gao Xinyu, Song Panshu, Yang Fengyi, Liu Yueying.  (2018)  On-off-on luminescent pyrophosphate probe based on the use of Mn-doped ZnS quantum dots and using Eu(III) as a mediator.  MICROCHIMICA ACTA,  185  (10): (1-8).  [PMID:30259119] [10.1007/s00604-018-3003-3]
6. Lingzhi Zhao, Liu Zhao, Yanqing Miao, Chunye Liu, Chenxiao Zhang.  (2016)  Construction of a Turn Off-On-Off Fluorescent System Based on Competitive Coordination of Cu2+ between 6,7-Dihydroxycoumarin and Pyrophosphate Ion for Sensitive Assay of Pyrophosphatase Activity.  Journal of Analytical Methods in Chemistry,      [PMID:27766179] [10.1155/2016/4306838]
7. Pei Jin Xie, Ming Li Ye, Zhong Yang Hu, Guang Wen Pan, Yan Zhu, Jia Jie Zhang.  (2011)  Determination of levels of adenosine phosphates in blood by ion chromatography.  CHINESE CHEMICAL LETTERS,      [PMID:] [10.1016/j.cclet.2011.09.008]
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