Name: Pyrophosphoric acid - Moligand™, ≥94%(T) , CAS No.2466-09-3
SKU: P639996
Availability: InStock

Pyrophosphoric acid - Moligand™, ≥94%(T) , CAS No.2466-09-3

CAS: 2466-09-3 Cat. No.: P639996 Formula: (HO)₂P(O)OP(O)(OH)₂ Molecular Weight: 177.98 EC Number: 219-574-0

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Pyrophosphoric acid - Moligand™, ≥94%(T) CAS No(2466-09-3) by Aladdin Scientific

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AVAILABLE TO ORDER

GRADE & PURITY Moligand™ ? ≥94%(T)

Synonyms

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Documents & Articles Citations of This Product Solution Calculators Reviews

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Why this grade

Moligand™, ≥94%(T) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

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

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Literature proof

Cited in 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Pyrophosphoric acid has been shown to enhance the rate of pyrophosphate hydrolysis by nonenzymatic catlysis and by inorganic pyrophoshatase. Pyrophosphoric acid can be used for the preparation of vanadyl pyrophosphato methoxide cluster anion. Pyrophosphoric Acid is used in anion binding of inorganic phosphates due to its ability to form complexes.
An enhanger of the rate of pyrophosphate hydrolysis by nonenzymatic catlysis and by inorganic pyrophoshatase

Specifications

Synonyms

Specifications & Purity

Moligand™, ≥94%(T)

Storage

Room temperature,Argon charged

Shipped In

Normal

Grade

Moligand™

Purity

≥94%(T)

Names and Identifiers

Pubchem Sid

504750450

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750450

Canonical Smiles

OP(=O)(O)OP(=O)(O)O

IUPAC Name

phosphono dihydrogen phosphate

InChIKey

XPPKVPWEQAFLFU-UHFFFAOYSA-N

INCHI

1S/H4O7P2/c1-8(2,3)7-9(4,5)6/h(H2,1,2,3)(H2,4,5,6)

Isomeric SMILES

OP(=O)(O)OP(=O)(O)O

WGK Germany

RTECS

JL6672500

UN Number

3260

Packing Group

Molecular Weight

177.98

Reaxy-Rn

3942075

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3942075&ln=

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

Kingdom Inorganic compounds
- Superclass Homogeneous non-metal compounds
  - Class Non-metal oxoanionic compounds
    - Subclass Non-metal pyrophosphates

Kingdom	Inorganic compounds
Superclass	Homogeneous non-metal compounds
Class	Non-metal oxoanionic compounds
Subclass	Non-metal pyrophosphates
Intermediate Tree Nodes	Not available
Direct Parent	Non-metal pyrophosphates
Alternative Parents	Inorganic oxides
Molecular Framework	Not available
Substituents	Non-metal pyrophosphate - Inorganic oxide
Description	This compound belongs to the class of inorganic compounds known as non-metal pyrophosphates. These are inorganic non-metallic compounds containing a pyrophosphate as its largest oxoanion.
External Descriptors	phosphorus oxoacid - acyclic phosphorus acid anhydride
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

3D Structure

Associated Targets(Human)

FDPS Tclin Farnesyl pyrophosphate synthase (2 Activities)

Discover Target: FDPS

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FDPS Tclin Farnesyl diphosphate synthase (1240 Activities)

Discover Target: FDPS

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OTC Tchem Ornithine carbamoyltransferase (24 Activities)

Discover Target: OTC

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

BLM Tchem Bloom syndrome protein (4248 Activities)

Discover Target: BLM

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)

Discover Target: pol

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Hepatitis C virus (23859 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

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.

10 results found

Lot Number	Certificate Type	Date	Item
I2617002	Certificate of Analysis	Sep 21, 2026	P639996
I2617003	Certificate of Analysis	Sep 21, 2026	P639996
F2615124	Certificate of Analysis	Jun 25, 2026	P639996
B24231084	Certificate of Analysis	Feb 28, 2024	P639996
B24231085	Certificate of Analysis	Feb 28, 2024	P639996
B24231086	Certificate of Analysis	Feb 28, 2024	P639996
B24231087	Certificate of Analysis	Feb 28, 2024	P639996
B24231088	Certificate of Analysis	Feb 28, 2024	P639996
F2519055	Certificate of Analysis	Feb 28, 2024	P639996
H2515073	Certificate of Analysis	Feb 28, 2024	P639996

Chemical and Physical Properties

Sensitivity	Moisture Sensitive
Melt Point(°C)	58-63℃
Molecular Weight	177.980 g/mol
XLogP3	-3.200
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	7
Rotatable Bond Count	2
Exact Mass	177.943 Da
Monoisotopic Mass	177.943 Da
Topological Polar Surface Area	124.000 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	147.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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	1

Documents & Articles

Molecular Mechanisms and Multidomain Applications of Inorganic Pyrophosphatase

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Inorganic pyrophosphatase

How to Choose Inorganic Acids: Making Descaling, Derusting, and Surface Treatment Controllable via pH and the “Fate of the Salts Formed” (with Tables 1–3)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Acids Inorganic Acids

The Methodological Value of TPS-Cl: The Logic of Selective Activation and Representative Transformations in Nucleoside and Nucleotide Chemistry

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

TPS-Cl 2,4,6-triisopropylbenzenesulfonyl chloride

Citations of This Product

How to Cite Aladdin Scientific Products? Citations Search

Solution Calculators

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Reviews

📚 Citations by Application

Spectroscopy sample preparation4

Drug / compound screening3

Other applications9

Organic synthesis — reaction medium7

Cytotoxicity screening1

Polymer synthesis & polymerization2

Industrial & non-pharma application2

Extraction & workup solvent4

View all 17 citations →

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Pyrophosphoric acid - Moligand™, ≥94%(T) , CAS No.2466-09-3

Storage & shipping

Quality documents

Literature proof

Overview

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Customer Reviews

📚 Citations by Application

Need help choosing the grade?