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Pharmacopeial Impurities (EP / USP / BP)

Lovastatin EP Impurity C

Reference StandardAvailable on request

Buy Lovastatin EP Impurity C (CAS 109273-98-5) from Zemixal. Lab and bulk packs, batch COA, fast global delivery. Packs from 10 mg.

Pack sizes
Lovastatin EP Impurity C chemical structure
CAS number109273-98-5
FormulaC24H34O4
Molar mass386.5 g/mol
Physical formSolid
HS code38229090
InChIKeySPIVMHAGTHFLMO-OCAGQIGWSA-N
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

About Lovastatin EP Impurity C

Analytical teams working on Lovastatin use Lovastatin EP Impurity C as a qualified comparison standard. For your records (Reference Standard), the material is defined by CAS 109273-98-5, formula C24H34O4 and molar mass 386.5 g/mol. It is handled as a solid.

Where it is used

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

Storage and safety notes

Classified under GHS with signal word Warning and hazard statements H302 and H351. Read the SDS before first use.

Available as 10 mg, 25 mg, 50 mg and 100 mg. Larger or split packs can be arranged. Every shipment includes a certificate of analysis with characterisation data. Add it to your quote list and our team replies with price, lead time and shipping options within one business day.

Reference standards for Lovastatin

See every impurity, metabolite and related compound we list for this API.

Lovastatin standards

Typical uses

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

Applications

Pharmaceutical Manufacturing and QCResearch Labs and Universities

Grade guides

Ph. Eur. Grade (European Pharmacopoeia)

Specifications and identifiers

Specifications of Lovastatin EP Impurity C
Product nameLovastatin EP Impurity C
Catalogue numberZX-025456
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
Molar mass386.5 g/mol
Exact mass386.2457
GradeReference Standard
Physical formSolid
XLogP35.4
H-bond donors / acceptors0 / 4
Topological polar surface area52.6 Ų
HS 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
SynonymsAnhydro Lovastatin Lactone, Lovastatin - Impurity C, Dehydromonacolin K, Dehydro Lovastatin, Anhydrolovastatin, Dehydrolovastatin

Lot values are stated on the batch certificate of analysis. Ask for a typical COA with your quotation.

Safety and GHS hazards

GHS07 Irritant or harmful
Irritant or harmful
GHS08 Health hazard
Health hazard

Signal word Warning

  • H302Harmful if swallowed
  • H351Suspected of causing cancer

Precautionary statements P203, P264, P270, P280, P301 + P317, P318, P330, P405, P501

Classification summarised from public GHS notifications. It can vary with grade and concentration, so always follow the SDS supplied with your lot.

Pack sizes

Pack sizes of Lovastatin EP Impurity C
10 mgQuoted on request
25 mgQuoted on request
50 mgQuoted on request
100 mgQuoted on request

Need a different size? Bulk drums and custom packing are quoted on request through the quote form on this page.

Questions about Lovastatin EP Impurity C

Which CAS number identifies Lovastatin EP Impurity C?
Lovastatin EP Impurity C is registered under CAS 109273-98-5. You may also see it listed as Anhydro Lovastatin Lactone, Lovastatin - Impurity C, Dehydromonacolin K. Our catalogue number for this item is ZX-025456.
What are the formula and molar mass of Lovastatin EP Impurity C?
For Lovastatin EP Impurity C, its formula is C24H34O4 and its molar mass is 386.5 g/mol. The systematic (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. InChIKey SPIVMHAGTHFLMO-OCAGQIGWSA-N lets you match it in any structure database.
How is Lovastatin EP Impurity C used in pharmaceutical QC?
Lovastatin EP Impurity C is a characterised reference material linked to Lovastatin. Laboratories use it to identify and quantify this impurity during method development and validation, stability work, batch release testing and regulatory submissions.
What grade and pack sizes are available for Lovastatin EP Impurity C?
This listing is Reference Standard grade. Standard packs are 10 mg, 25 mg, 50 mg, 100 mg. Larger quantities and custom packing can be quoted on request.
Which documents come with Lovastatin EP Impurity C?
Each lot ships with a batch certificate of analysis and a 16-section GHS safety data sheet. A typical COA or specification sheet can be shared with the quotation before you order.
Can Zemixal ship Lovastatin EP Impurity C to my country?
Yes. Because Lovastatin EP Impurity C is classed as hazardous, it travels in UN-approved packaging as dangerous goods under IATA or IMDG rules, with the export paperwork your broker needs.

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