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o-Methyl Atorvastatin Calcium Salt CAS NO 887196-29-4
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CAS No.:887196-29-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
o-Methyl Atorvastatin Calcium Salt is a key pharmaceutical intermediate in the synthesis of atorvastatin, the active ingredient in leading cholesterol-lowering medications. This compound is critical for research and development, enabling precise structural modifications and metabolic studies. It is primarily utilized by pharmaceutical manufacturers, R&D laboratories, and fine chemical suppliers focused on cardiovascular drug development and generic API production.
Application
- Pharmaceutical Intermediate: A crucial building block in the synthetic pathway for Atorvastatin API.
- Research & Development: Used in metabolic and pharmacokinetic studies to understand drug behavior.
- Process Chemistry: Serves as a reference standard and starting material for process optimization and scale-up.
- Analytical Standard: Employed as a high-purity standard for HPLC, LC-MS, and other analytical method development.
- Generic Drug Manufacturing: Essential for companies developing bioequivalent versions of cholesterol-lowering drugs.
- Academic Research: Used in universities and institutes for medicinal chemistry and organic synthesis projects.
Basic Information
| Product Name | o-Methyl Atorvastatin Calcium Salt |
| CAS No. | 887196-29-4 |
| Molecular Formula | C39H36CaF2N2O6 (or corresponding hydrate/adduct) |
| Molecular Weight | Contact for details |
| Synonyms | Atorvastatin o-Methyl Ester Calcium Salt; (3R,5R)-7-[2-(4-Fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-3,5-dihydroxyheptanoic Acid Methyl Ester Calcium Salt; o-Methyl Atorvastatin Ca Salt; Atorvastatin Impurity; Atorvastatin Related Compound; Atorvastatin Methyl Ester Calcium; CAS 887196-29-4 |
| EINECS | Contact for details |
Quality Control
Our o-Methyl Atorvastatin Calcium Salt is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by spectroscopic methods, to ensure it meets the stringent requirements for pharmaceutical intermediates. A Certificate of Analysis (COA) detailing all specifications and test results is provided with every shipment.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment. For long-term storage, consider desiccated conditions.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Water Content (KF) | ≤ 5.0% |
| Residual Solvents (GC) | Complies with ICH guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






