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Pharmacopeial Impurities (EP / USP / BP)

Lovastatin EP Impurity B

Reference StandardAvailable on request

Order Lovastatin EP Impurity B (CAS 75225-50-2) online at Zemixal: C24H37NaO6, COA and SDS with every lot, worldwide shipping.

Pack sizes
Lovastatin EP Impurity B chemical structure
CAS number75225-50-2
FormulaC24H37NaO6
Molar mass444.5 g/mol
Physical formSolid
HS code38229090
InChIKeyLXZBFUBRYYVRQJ-AXHZAXLDSA-M
IUPAC namesodium (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate

About Lovastatin EP Impurity B

Analytical teams working on Lovastatin use Lovastatin EP Impurity B as a qualified comparison standard. Key data (Reference Standard): CAS 75225-50-2, formula C24H37NaO6 and molar mass 444.5 g/mol. It is handled as a solid.

Use cases we see most often

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

Storage and safety notes

It carries the GHS signal word Warning (H302), so wear gloves and eye protection and work with good ventilation.

Order it in 10 mg, 25 mg, 50 mg and 100 mg packs or ask for a bulk quotation. You receive a certificate of analysis with characterisation data with each order. Request pricing online and we confirm availability, documentation and freight to your country.

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 B
Product nameLovastatin EP Impurity B
Catalogue numberZX-022034
CAS number75225-50-2
IUPAC namesodium (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate
Molecular formulaC24H37NaO6
Molar mass444.5 g/mol
Exact mass444.2488
GradeReference Standard
Physical formSolid
H-bond donors / acceptors2 / 6
Topological polar surface area107 Ų
HS code38229090
InChIKeyLXZBFUBRYYVRQJ-AXHZAXLDSA-M
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](C[C@H](CC(=O)[O-])O)O)C.[Na+]
PubChem CID16760544
SynonymsLovastatin Hydroxy Acid Sodium Salt, Lovastatin EP Impurity B Sodium, Lovastatin - Impurity B (Sodium Salt), Lovastatin Hydroxy Impurity Sodium Salt, Lovastatin Sodium, Sodium mevinolinate, MSD-803, sodium salt, MB-530B, Lovastatin sodium salt, Lovastatin Hydroxy Acid, Sodium Salt, Mevinolin sodium, Lovastatin hydroxy acid (sodium)

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

Signal word Warning

  • H302Harmful if swallowed

Precautionary statements P264, P270, P301 + P317, P330, 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 B
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 B

Which CAS number identifies Lovastatin EP Impurity B?
Lovastatin EP Impurity B is registered under CAS 75225-50-2. You may also see it listed as Lovastatin Hydroxy Acid Sodium Salt, Lovastatin EP Impurity B Sodium, Lovastatin - Impurity B (Sodium Salt). Our catalogue number for this item is ZX-022034.
What are the formula and molar mass of Lovastatin EP Impurity B?
For Lovastatin EP Impurity B, its formula is C24H37NaO6 and its molar mass is 444.5 g/mol. The systematic (IUPAC) name is sodium (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate. InChIKey LXZBFUBRYYVRQJ-AXHZAXLDSA-M lets you match it in any structure database.
How is Lovastatin EP Impurity B used in pharmaceutical QC?
Lovastatin EP Impurity B 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 B?
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 B?
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 B to my country?
Yes. Because Lovastatin EP Impurity B 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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