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Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Rosuvastatin EP Impurity E

Synonyms: Rosuvastatin Acid - Impurity E

CAS No.2226413-61-0
FormulaC38H46F2N6O9S2
Mol. weight832.90
Catalogue No.VQ-033668
PurityReference Standard
HSN38229090

Rosuvastatin EP Impurity E (CAS 2226413-61-0) – Rosuvastatin impurity standard. C38H46F2N6O9S2, MW 832.9. Vaqora Chemicals: COA, global shipping.

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25 mg
50 mg
100 mg
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16-section GHS SDS
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About Rosuvastatin EP Impurity E

Rosuvastatin EP Impurity E (CAS 2226413-61-0) is a pharmacopeial impurity of Rosuvastatin offered by Vaqora Chemicals. Formula C38H46F2N6O9S2, molecular weight 832.9 g/mol. Alternative names: Rosuvastatin Acid - Impurity E.

It is supplied as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.

Pharmaceutical QC and development laboratories use this impurity standard of Rosuvastatin to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.

Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Rosuvastatin EP Impurity E is dispatched with a Certificate of Analysis (COA) to destinations worldwide.

Typical applications

  • Pharmacopeial method verification
  • Impurity profiling
  • QC release testing
  • ANDA / DMF filings

Industries

Related to Rosuvastatin

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

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Specifications & identifiers

Chemical identifiers
Product nameRosuvastatin EP Impurity E
Catalogue No.VQ-033668
CAS Number2226413-61-0
IUPAC name(E,3R,5S)-7-[4-(4-fluorophenyl)-2-[[2-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-2-hydroxyethyl]sulfonyl-methylamino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoic acid
Molecular formulaC38H46F2N6O9S2
Molecular weight832.9 g/mol
Exact mass832.2736
GradeReference Standard
HSN code38229090
InChIKeyMWYNOQUFUVPRSK-KTLASYKKSA-N
SMILESCC(C)C1=NC(=NC(=C1/C=C/[C@H](C[C@H](CC(=O)O)O)O)C2=CC=C(C=C2)F)N(C)S(=O)(=O)CC(C3=C(N=C(N=C3C(C)C)N(C)S(=O)(=O)C)C4=CC=C(C=C4)F)O
PubChem CID145714326
Physical properties
Physical formSolid
LogP (XLogP3)3.2
H-bond donors / acceptors4 / 17
TPSA241 Ų

Documents

Frequently asked questions

What is the CAS number of Rosuvastatin EP Impurity E?

The CAS Registry Number of Rosuvastatin EP Impurity E is 2226413-61-0. It is also known as Rosuvastatin Acid - Impurity E.

What is the molecular formula and molecular weight of Rosuvastatin EP Impurity E?

Rosuvastatin EP Impurity E has the molecular formula C38H46F2N6O9S2 and a molecular weight of 832.9 g/mol.

What is Rosuvastatin EP Impurity E used for?

Rosuvastatin EP Impurity E is supplied as a characterised reference material related to Rosuvastatin. 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 Rosuvastatin EP Impurity E can I order?

We supply Rosuvastatin EP Impurity E 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 Rosuvastatin EP Impurity E?

Yes. Every lot of Rosuvastatin EP Impurity E 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 Rosuvastatin EP Impurity E be shipped internationally?

Yes. We export Rosuvastatin EP Impurity E worldwide by air and sea freight or express courier, on EXW, FOB, CIF, CFR or DAP Incoterms, with full export documentation.

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Why buyers choose Vaqora

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