Lovastatin EP Impurity E

Name: Lovastatin EP Impurity E
Brand: Vaqora Chemicals
SKU: VQ-026525

About Lovastatin EP Impurity E

Listed under CAS 77517-29-4, Lovastatin EP Impurity E is a pharmacopeial impurity of Lovastatin available from Vaqora Chemicals. Its molecular formula is C24H38O5 and its molecular weight is 406.6 g/mol. Alternative names: Lovastatin - Impurity E and Dihydromevinolin.

It is supplied as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. Handle it with standard laboratory precautions and appropriate personal protective equipment.

This Lovastatin impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Our customers for this product work in pharmaceutical manufacturing and academic and industrial research.

Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Lovastatin 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 Lovastatin

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

Lovastatin impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product name	Lovastatin EP Impurity E
Catalogue No.	VQ-026525
CAS Number	77517-29-4
IUPAC name	[(1S,3S,4aR,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl] (2S)-2-methylbutanoate
Molecular formula	C₂₄H₃₈O₅
Molecular weight	406.6 g/mol
Exact mass	406.2719
Grade	Reference Standard
HSN code	38229090
InChIKey	IFIFFBWHLKGTMO-LDIGTXGYSA-N
SMILES	CC[C@H](C)C(=O)O[C@H]1C[C@H](C[C@H]2[C@@H]1[C@H]([C@H](C=C2)C)CC[C@@H]3C[C@H](CC(=O)O3)O)C
PubChem CID	196514

Physical properties
Physical form	Solid
LogP (XLogP3)	5
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 E?

The CAS Registry Number of Lovastatin EP Impurity E is 77517-29-4. It is also known as Lovastatin - Impurity E, Dihydromevinolin, 4a,5-Dihydromevinolin.

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

Lovastatin EP Impurity E has the molecular formula C24H38O5 and a molecular weight of 406.6 g/mol. Its IUPAC name is [(1S,3S,4aR,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-3,7-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl] (2S)-2-methylbutanoate.

What is Lovastatin EP Impurity E used for?

Lovastatin EP Impurity E 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 E can I order?

We supply Lovastatin 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 Lovastatin EP Impurity E?

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

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