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VAQORACHEMICALS
Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Lovastatin EP Impurity B

Synonyms: Lovastatin Hydroxy Acid Sodium Salt · Lovastatin EP Impurity B Sodium · Lovastatin - Impurity B (Sodium Salt) · Lovastatin Hydroxy Impurity Sodium Salt

CAS No.75225-50-2
FormulaC24H37NaO6
Mol. weight444.50
Catalogue No.VQ-023008
PurityReference Standard
HSN38229090

Lovastatin EP Impurity B (CAS 75225-50-2) – Lovastatin impurity standard. C24H37NaO6, MW 444.5. Order from Vaqora Chemicals with COA and global delivery.

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

About Lovastatin EP Impurity B

Lovastatin EP Impurity B is a pharmacopeial impurity of Lovastatin carrying the CAS registry number 75225-50-2. Formula C24H37NaO6, molecular weight 444.5 g/mol. Common synonyms include Lovastatin Hydroxy Acid Sodium Salt and Lovastatin EP Impurity B Sodium.

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. Under GHS it is labelled “Warning”, so handle it with suitable PPE and consult the SDS.

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.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export 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 B
Catalogue No.VQ-023008
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
Molecular weight444.5 g/mol
Exact mass444.2488
GradeReference Standard
HSN 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
Physical properties
Physical formSolid
H-bond donors / acceptors2 / 6
TPSA107 Ų
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)

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed

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

The CAS Registry Number of Lovastatin EP Impurity B is 75225-50-2. It is also known as Lovastatin Hydroxy Acid Sodium Salt, Lovastatin EP Impurity B Sodium, Lovastatin - Impurity B (Sodium Salt).

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

Lovastatin EP Impurity B has the molecular formula C24H37NaO6 and a molecular weight of 444.5 g/mol. Its 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.

What is Lovastatin EP Impurity B used for?

Lovastatin EP Impurity B 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 B can I order?

We supply Lovastatin EP Impurity B 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 B?

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

Yes. Lovastatin EP Impurity B 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 B

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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
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Related products

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

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