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

Rosuvastatin EP Impurity D

Synonyms: Rosuvastatin lactone · Rosuvastatin-5S-lactone · ent-Rosuvastatin Lactone · Rosuvastatin 5 S-lactone

CAS No.503610-43-3
FormulaC22H26FN3O5S
Mol. weight463.50
Catalogue No.VQ-006678
PurityReference Standard
HSN38229090

Rosuvastatin EP Impurity D (CAS 503610-43-3) – Rosuvastatin impurity standard. C22H26FN3O5S, MW 463.5. COA included. Worldwide shipping from Vaqora Chemicals.

Pack sizesPrice on quotation · bulk available
10 mg
25 mg
50 mg
100 mg
Bulk / custom pack · kg to MT
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Batch COA with every lot
16-section GHS SDS
Export to 120+ countries
DG-compliant packing

About Rosuvastatin EP Impurity D

Listed under CAS 503610-43-3, Rosuvastatin EP Impurity D is a pharmacopeial impurity of Rosuvastatin available from Vaqora Chemicals. Formula C22H26FN3O5S, molecular weight 463.5 g/mol. Alternative names: Rosuvastatin lactone and Rosuvastatin-5S-lactone.

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. Under GHS it is labelled “Warning”, so handle it with suitable PPE and consult the SDS.

As a characterised impurity of Rosuvastatin, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Rosuvastatin EP Impurity D in 10 mg, 25 mg, 50 mg and 100 mg packs, each shipped with a Certificate of Analysis (COA), and exports 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.

Rosuvastatin impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameRosuvastatin EP Impurity D
Catalogue No.VQ-006678
CAS Number503610-43-3
IUPAC nameN-[4-(4-fluorophenyl)-5-[(E)-2-[(2S,4R)-4-hydroxy-6-oxooxan-2-yl]ethenyl]-6-propan-2-ylpyrimidin-2-yl]-N-methylmethanesulfonamide
Molecular formulaC22H26FN3O5S
Molecular weight463.5 g/mol
Exact mass463.1577
GradeReference Standard
HSN code38229090
InChIKeySOEGVMSNJOCVHT-VEUZHWNKSA-N
SMILESCC(C)C1=NC(=NC(=C1/C=C/[C@@H]2C[C@H](CC(=O)O2)O)C3=CC=C(C=C3)F)N(C)S(=O)(=O)C
PubChem CID29918986
Physical properties
Physical formSolid
LogP (XLogP3)2.4
H-bond donors / acceptors1 / 9
TPSA118 Ų
SynonymsRosuvastatin lactone, Rosuvastatin-5S-lactone, ent-Rosuvastatin Lactone, Rosuvastatin 5 S-lactone, Rosuvastatin-5-S-lactone

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant
GHS08 Health hazard
Health hazard

Signal word: Warning

Hazard statements

  • H315Causes skin irritation
  • H319Causes serious eye irritation
  • H335May cause respiratory irritation
  • H373May causes damage to organs through prolonged or repeated exposure

Precautionary statements: P260, P261, P264, P264 + P265, P271, P280, P302 + P352, P304 + P340, P305 + P351 + P338, P319, P321, P332 + P317, P337 + P317, P362 + P364, P403 + P233, P405, P501

Classification is indicative (aggregated GHS notifications) and may vary by grade and concentration. Always refer to the SDS supplied with your lot.

Documents

Frequently asked questions

What is the CAS number of Rosuvastatin EP Impurity D?

The CAS Registry Number of Rosuvastatin EP Impurity D is 503610-43-3. It is also known as Rosuvastatin lactone, Rosuvastatin-5S-lactone, ent-Rosuvastatin Lactone.

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

Rosuvastatin EP Impurity D has the molecular formula C22H26FN3O5S and a molecular weight of 463.5 g/mol. Its IUPAC name is N-[4-(4-fluorophenyl)-5-[(E)-2-[(2S,4R)-4-hydroxy-6-oxooxan-2-yl]ethenyl]-6-propan-2-ylpyrimidin-2-yl]-N-methylmethanesulfonamide.

What is Rosuvastatin EP Impurity D used for?

Rosuvastatin EP Impurity D 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 D can I order?

We supply Rosuvastatin EP Impurity D 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 D?

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

Yes. Rosuvastatin EP Impurity D is classified as hazardous, so it is packed in UN-approved packaging and shipped as dangerous goods under IATA/IMDG rules. We export worldwide on EXW, FOB, CIF and DAP terms.

Enquire about Rosuvastatin EP Impurity D

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Why buyers choose Vaqora

  • Batch-traceable lots with COA
  • R&D packs to multi-tonne supply
  • IATA / IMDG dangerous-goods packing
  • EXW, FOB, CIF, DAP Incoterms
  • Custom synthesis & sourcing
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Related products

Reference Standard
Rosuvastatin chemical structure
Rosuvastatin
CAS
287714-41-4
Formula
C22H28FN3O6S
MW
481.5 g/mol
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