Worldwide shipping · 120+ destinationsCOA & GHS SDS with every lotMon–Sat, 09:30–18:30 IST
VAQORACHEMICALS
Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Lovastatin EP Impurity C

Synonyms: Anhydro Lovastatin Lactone · Lovastatin - Impurity C · Dehydromonacolin K · Dehydro Lovastatin

CAS No.109273-98-5
FormulaC24H34O4
Mol. weight386.50
Catalogue No.VQ-026524
PurityReference Standard
HSN38229090

Lovastatin EP Impurity C (CAS 109273-98-5) – Lovastatin impurity standard. C24H34O4, MW 386.5. Buy from Vaqora Chemicals with COA and worldwide shipping.

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

About Lovastatin EP Impurity C

Listed under CAS 109273-98-5, Lovastatin EP Impurity C is a pharmacopeial impurity of Lovastatin available from Vaqora Chemicals. Its molecular formula is C24H34O4 and its molecular weight is 386.5 g/mol. Common synonyms include Anhydro Lovastatin Lactone and Lovastatin - Impurity C.

The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. It carries the GHS signal word “Warning” with 2 hazard statements. Review the Safety Data Sheet before use.

This Lovastatin impurity supports analytical method development and validation (AMV), batch release testing and the impurity sections of ANDA and DMF filings. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.

We offer Lovastatin EP Impurity C in 10 mg, 25 mg, 50 mg and 100 mg packs with a batch-specific COA, and ship to customers 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 nameLovastatin EP Impurity C
Catalogue No.VQ-026524
CAS Number109273-98-5
IUPAC name[(1S,3R,7S,8S,8aR)-3,7-dimethyl-8-[2-[(2R)-6-oxo-2,3-dihydropyran-2-yl]ethyl]-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (2S)-2-methylbutanoate
Molecular formulaC24H34O4
Molecular weight386.5 g/mol
Exact mass386.2457
GradeReference Standard
HSN code38229090
InChIKeySPIVMHAGTHFLMO-OCAGQIGWSA-N
SMILESCC[C@H](C)C(=O)O[C@H]1C[C@H](C=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@@H]3CC=CC(=O)O3)C
PubChem CID71315317
Physical properties
Physical formSolid
LogP (XLogP3)5.4
H-bond donors / acceptors0 / 4
TPSA52.6 Ų
SynonymsAnhydro Lovastatin Lactone, Lovastatin - Impurity C, Dehydromonacolin K, Dehydro Lovastatin, Anhydrolovastatin, Dehydrolovastatin

Safety & hazard information (GHS)

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

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed
  • H351Suspected of causing cancer

Precautionary statements: P203, P264, P270, P280, P301 + P317, P318, P330, 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 Lovastatin EP Impurity C?

The CAS Registry Number of Lovastatin EP Impurity C is 109273-98-5. It is also known as Anhydro Lovastatin Lactone, Lovastatin - Impurity C, Dehydromonacolin K.

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

Lovastatin EP Impurity C has the molecular formula C24H34O4 and a molecular weight of 386.5 g/mol. Its IUPAC name is [(1S,3R,7S,8S,8aR)-3,7-dimethyl-8-[2-[(2R)-6-oxo-2,3-dihydropyran-2-yl]ethyl]-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (2S)-2-methylbutanoate.

What is Lovastatin EP Impurity C used for?

Lovastatin EP Impurity C 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 C can I order?

We supply Lovastatin EP Impurity C 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 C?

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

Yes. Lovastatin EP Impurity C 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 Lovastatin EP Impurity C

We reply within one business day with price, pack options, lead time and documentation.

By submitting you agree to our privacy policy. We never share your details.

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
How ordering works

Related products

Reference Standard
Keto Lovastatin chemical structure
Keto Lovastatin
CAS
96497-73-3
Formula
C24H34O6
MW
418.5 g/mol
VQ-038164

More in Pharmacopeial Impurities (EP / USP / BP) →