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· · COA & SDS available for every product · Same-day shipping on in-stock items Cidofovir - ≥98% , Human herpesvirus 1 DNA polymerase inhibitor, CAS No.113852-37-2, Human herpesvirus 1 DNA polymerase inhibitor
Synonyms
Cidofovir [INN] | CIDOFOVIR [WHO-DD] | NCGC00184994-03 | Vistide | [1-(4-amino-2-oxo-pyrimidin-1-yl)-3-hydroxy-propan-2-yl]oxymethylphosphonic acid | AKOS015854828 | BCP03734 | Forvade | NSC742135 | NSC-742135 | [(S)-2-(4-Amino-2-oxo-2H-pyrimidin-1-yl)-1-
Storage
Store at 2-8°C,Protected from light
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light Ships Wet ice 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.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Cidofovir suppresses virus replication by selective inhibition of viral DNA synthesis.
Specifications Synonyms
Cidofovir [INN] | CIDOFOVIR [WHO-DD] | NCGC00184994-03 | Vistide | [1-(4-amino-2-oxo-pyrimidin-1-yl)-3-hydroxy-propan-2-yl]oxymethylphosphonic acid | AKOS015854828 | BCP03734 | Forvade | NSC742135 | NSC-742135 | [(S)-2-(4-Amino-2-oxo-2H-pyrimidin-1-yl)-1-
Specifications & Purity
≥98%
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Human herpesvirus 1 DNA polymerase inhibitor
Product Properties Names and Identifiers Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508816561
Canonical Smiles
C1=CN(C(=O)N=C1N)CC(CO)OCP(=O)(O)O
IUPAC Name
[(2S)-1-(4-amino-2-oxopyrimidin-1-yl)-3-hydroxypropan-2-yl]oxymethylphosphonic acid
InChIKey
VWFCHDSQECPREK-LURJTMIESA-N
INCHI
1S/C8H14N3O6P/c9-7-1-2-11(8(13)10-7)3-6(4-12)17-5-18(14,15)16/h1-2,6,12H,3-5H2,(H2,9,10,13)(H2,14,15,16)/t6-/m0/s1
Isomeric SMILES
C1=CN(C(=O)N=C1N)C[C@@H](CO)OCP(=O)(O)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8331690&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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Diazines Subclass Pyrimidines and pyrimidine derivatives Intermediate Tree Nodes Not available Direct Parent Pyrimidones Alternative Parents Aminopyrimidines and derivatives Imidolactams Hydropyrimidines Organic phosphonic acids Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents Aminopyrimidine - Pyrimidone - Hydropyrimidine - Imidolactam - Organophosphonic acid - Organophosphonic acid derivative - Heteroaromatic compound - Azacycle - Organic oxide - Organopnictogen compound - Primary amine - Primary alcohol - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyrimidones. These are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. External Descriptors pyrimidone - phosphonic acids Data sources 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.
3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility 25°C: DMSO <1 mg/mL; Water <1 mg/mL; Ethanol <1 mg/mL Sensitivity Light sensitive；Moisture sensitive Molecular Weight 279.190 g/mol XLogP3 -3.600 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 6 Exact Mass 279.062 Da Monoisotopic Mass 279.062 Da Topological Polar Surface Area 146.000 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 417.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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
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