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Pharmacopeial Impurities (EP / USP / BP)

Lovastatin EP Impurity A

Reference StandardAvailable on request

Lovastatin EP Impurity A (CAS 73573-88-3) supplier Zemixal. Request a quote with price, lead time and documents. Quotes within one business day.

Pack sizes
Lovastatin EP Impurity A chemical structure
CAS number73573-88-3
FormulaC23H34O5
Molar mass390.5 g/mol
Physical formSolid
HS code38229090
InChIKeyAJLFOPYRIVGYMJ-INTXDZFKSA-N
IUPAC name[(1S,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (2S)-2-methylbutanoate

About Lovastatin EP Impurity A

Lovastatin EP Impurity A is supplied by Zemixal as a characterised reference material for Lovastatin analysis. Key data (Reference Standard): CAS 73573-88-3, formula C23H34O5 and molar mass 390.5 g/mol. It is handled as a solid.

Typical applications

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

Safe handling

Hazard communication follows GHS (Danger: H317, H351, H360 and H362). Our SDS lists exposure controls and first-aid measures.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and custom quantities are quoted on request. 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 A
Product nameLovastatin EP Impurity A
Catalogue numberZX-022033
CAS number73573-88-3
IUPAC name[(1S,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (2S)-2-methylbutanoate
Molecular formulaC23H34O5
Molar mass390.5 g/mol
Exact mass390.2406
GradeReference Standard
Physical formSolid
XLogP33.9
H-bond donors / acceptors1 / 5
Topological polar surface area72.8 Ų
HS code38229090
InChIKeyAJLFOPYRIVGYMJ-INTXDZFKSA-N
SMILESCC[C@H](C)C(=O)O[C@H]1CCC=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@@H]3C[C@H](CC(=O)O3)O
PubChem CID64715
SynonymsMevastatin, Pravastatin Deshydroxy Impurity, Lovastatin - Impurity A, compactin, Mevastatine, CS 500, ML236B lactone, 7-(1,2,6,7,8,8a-Hexahydro-2-methyl-8-(2-methylbutyryloxy)naphthyl)-3-hydroxyheptan-5-olide, 6-demethylmevinolin, Compactin (penicillium), (+)-Compactin

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 Danger

  • H317May cause an allergic skin reaction
  • H351Suspected of causing cancer
  • H360May damage fertility or the unborn child
  • H362May cause harm to breast-fed children
  • H373May causes damage to organs through prolonged or repeated exposure
  • H412Harmful to aquatic life with long lasting effects

Precautionary statements P203, P260, P261, P263, P264, P270, P272, P273, P280, P302 + P352, P318, P319, P321, P333 + P317, P362 + P364, 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 A
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 A

Which CAS number identifies Lovastatin EP Impurity A?
Lovastatin EP Impurity A is registered under CAS 73573-88-3. You may also see it listed as Mevastatin, Pravastatin Deshydroxy Impurity, Lovastatin - Impurity A. Our catalogue number for this item is ZX-022033.
What are the formula and molar mass of Lovastatin EP Impurity A?
For Lovastatin EP Impurity A, its formula is C23H34O5 and its molar mass is 390.5 g/mol. The systematic (IUPAC) name is [(1S,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-oxooxan-2-yl]ethyl]-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] (2S)-2-methylbutanoate. InChIKey AJLFOPYRIVGYMJ-INTXDZFKSA-N lets you match it in any structure database.
How is Lovastatin EP Impurity A used in pharmaceutical QC?
Lovastatin EP Impurity A 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 A?
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 A?
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 A to my country?
Yes. Because Lovastatin EP Impurity A 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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