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Metabolites & Degradation ProductsReference StandardAvailable on request

Sofosbuvir impurity I

Synonyms: Ethyl Sofosbuvir Analog · Ethoxy Sofosbuvir Impurity, Sofosbuvir impurity I · Sofosbuvir ethyl ester impurity · Sofosbuvir Impurity 19

CAS No.2164516-85-0
FormulaC21H27FN3O9P
Mol. weight515.40
Catalogue No.VQ-023783
PurityReference Standard
HSN38229090

Sofosbuvir impurity I (CAS 2164516-85-0) – Sofosbuvir impurity standard. C21H27FN3O9P, MW 515.4. From Vaqora Chemicals, with COA and worldwide delivery.

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50 mg
100 mg
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About Sofosbuvir impurity I

Sofosbuvir impurity I (CAS 2164516-85-0) is a metabolite or degradation product of Sofosbuvir offered by Vaqora Chemicals. With the molecular formula C21H27FN3O9P, it has a molar mass of 515.4 g/mol. It is also known as Ethyl Sofosbuvir Analog or Sofosbuvir ethyl ester impurity.

It is supplied as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Good laboratory practice and suitable PPE are recommended during handling.

It is used in metabolite identification, stability-indicating method development and impurity profiling of Sofosbuvir, as well as in QC testing and ANDA/DMF documentation. It is used across pharmaceutical manufacturing and academic and industrial research.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide.

Typical applications

  • Metabolite identification
  • Stability-indicating methods
  • Impurity profiling

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Related to Sofosbuvir

View every impurity, metabolite and intermediate we list for Sofosbuvir.

Sofosbuvir impurities

Specifications & identifiers

Chemical identifiers
Product nameSofosbuvir impurity I
Catalogue No.VQ-023783
CAS Number2164516-85-0
IUPAC nameethyl (2S)-2-[[[(2R,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate
Molecular formulaC21H27FN3O9P
Molecular weight515.4 g/mol
Exact mass515.1469
GradeReference Standard
HSN code38229090
InChIKeyHRGZELWFPQCNNG-NQVPMCNCSA-N
SMILESCCOC(=O)[C@H](C)N[P@](=O)(OC[C@@H]1[C@H]([C@@]([C@@H](O1)N2C=CC(=O)NC2=O)(C)F)O)OC3=CC=CC=C3
PubChem CID131704518
Physical properties
Physical formSolid
LogP (XLogP3)0.6
H-bond donors / acceptors3 / 11
TPSA153 Ų
SynonymsEthyl Sofosbuvir Analog, Ethoxy Sofosbuvir Impurity, Sofosbuvir impurity I, Sofosbuvir ethyl ester impurity, Sofosbuvir Impurity 19, Sofosbuvir O-Desisopropyl O-Ethyl Ester

Documents

Frequently asked questions

What is the CAS number of Sofosbuvir impurity I?

The CAS Registry Number of Sofosbuvir impurity I is 2164516-85-0. It is also known as Ethyl Sofosbuvir Analog, Ethoxy Sofosbuvir Impurity, Sofosbuvir impurity I, Sofosbuvir ethyl ester impurity.

What is the molecular formula and molecular weight of Sofosbuvir impurity I?

Sofosbuvir impurity I has the molecular formula C21H27FN3O9P and a molecular weight of 515.4 g/mol. Its IUPAC name is ethyl (2S)-2-[[[(2R,3R,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyloxolan-2-yl]methoxy-phenoxyphosphoryl]amino]propanoate.

What is Sofosbuvir impurity I used for?

Sofosbuvir impurity I is supplied as a characterised reference material related to Sofosbuvir. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.

Which grade and pack sizes of Sofosbuvir impurity I can I order?

We supply Sofosbuvir impurity I in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Sofosbuvir impurity I?

Yes. Every lot of Sofosbuvir impurity I is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.

Can Sofosbuvir impurity I be shipped internationally?

Yes. We export Sofosbuvir impurity I worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.

Enquire about Sofosbuvir impurity I

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