Lovastatin EP Impurity F

Name: Lovastatin EP Impurity F
Brand: Vaqora Chemicals
SKU: VQ-026527

About Lovastatin EP Impurity F

Listed under CAS 1048973-04-1, Lovastatin EP Impurity F is a pharmacopeial impurity of Lovastatin available from Vaqora Chemicals. With the molecular formula C24H34O5, it has a molar mass of 402.5 g/mol. Common synonyms include Lovastatin - Impurity F.

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.

This Lovastatin impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. It is used across pharmaceutical manufacturing and academic and industrial research.

Vaqora Chemicals supplies Lovastatin EP Impurity F 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 Lovastatin

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

Lovastatin impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product name	Lovastatin EP Impurity F
Catalogue No.	VQ-026527
CAS Number	1048973-04-1
IUPAC name	[(1S,3R,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (E)-2-methylbut-2-enoate
Molecular formula	C₂₄H₃₄O₅
Molecular weight	402.5 g/mol
Exact mass	402.2406
Grade	Reference Standard
HSN code	38229090
InChIKey	JSVUTGMIKPKXNQ-ORSWIJFBSA-N
SMILES	C/C=C(\C)/C(=O)O[C@H]1C[C@H](C=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@@H]3C[C@H](CC(=O)O3)O)C
PubChem CID	155929072

Physical properties
Physical form	Solid
LogP (XLogP3)	4.1
H-bond donors / acceptors	1 / 5
TPSA	72.8 Å²

Documents

Safety Data Sheet (SDS)16-section GHS · on request Certificate of AnalysisTypical / batch COA · on request Specification sheetTDS / MOA · on request

Frequently asked questions

What is the CAS number of Lovastatin EP Impurity F?

The CAS Registry Number of Lovastatin EP Impurity F is 1048973-04-1. It is also known as Lovastatin - Impurity F.

What is the molecular formula and molecular weight of Lovastatin EP Impurity F?

Lovastatin EP Impurity F has the molecular formula C24H34O5 and a molecular weight of 402.5 g/mol. Its IUPAC name is [(1S,3R,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (E)-2-methylbut-2-enoate.

What is Lovastatin EP Impurity F used for?

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

We supply Lovastatin EP Impurity F 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 Lovastatin EP Impurity F?

Yes. Every lot of Lovastatin EP Impurity F 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 Lovastatin EP Impurity F be shipped internationally?

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