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Dalvastatin CAS NO 132100-55-1


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CAS No.:132100-55-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Dalvastatin is a synthetic organic compound belonging to the statin class, known for its role as a key pharmaceutical intermediate. Its primary value lies in enabling the synthesis of advanced cholesterol-lowering agents, ensuring high-purity pathways for active pharmaceutical ingredient (API) manufacturing. This product is essential for research institutions and pharmaceutical companies engaged in the development and production of cardiovascular therapeutics and metabolic disorder treatments.

Application

  • Pharmaceutical Intermediate: A critical building block in the synthesis of HMG-CoA reductase inhibitors (statins) for cholesterol management.
  • Research & Development: Used in medicinal chemistry for the discovery and optimization of new lipid-regulating drug candidates.
  • Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in multi-step chemical processes to manufacture final drug substances.
  • Biochemical Research: Employed in studies investigating the mechanism of action of statins and their effects on metabolic pathways.
  • Reference Standard: Utilized as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Product Name Dalvastatin
CAS No. 132100-55-1
Molecular Formula C23H34FNO4
Molecular Weight 407.52 g/mol
Synonyms Dalvastatin; (3R,5S)-7-[2-Cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-dihydroxyhept-6-enoic acid; (E)-7-[2-Cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-dihydroxyhept-6-enoic acid; BMS-180431; SQ-33600; A synthetic statin derivative
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Quality Control

Our Dalvastatin is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical applications. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to current Good Manufacturing Practices (cGMP) principles, and our quality standards are designed to meet the rigorous requirements of pharmaceutical intermediate specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

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%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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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