Description

Cerivastatin Sodium is a synthetic, highly potent HMG-CoA reductase inhibitor. This active pharmaceutical ingredient (API) is critical for the research and development of lipid-lowering therapeutics. It is primarily utilized by pharmaceutical companies and research institutions engaged in metabolic disorder studies and drug formulation.

Application

• Pharmaceutical API: Primary use as the active ingredient in the formulation of cholesterol-lowering medications.
• Biochemical Research: A key tool for studying the HMG-CoA reductase pathway, enzyme inhibition kinetics, and cholesterol biosynthesis in vitro.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical laboratories.
• Metabolic Disorder Studies: Used in preclinical research to investigate hyperlipidemia, atherosclerosis, and related cardiovascular conditions.
• Process Development: Employed in the development and optimization of synthetic routes and purification processes for statin-class drugs.

Basic Information

Product Name	Cerivastatin Sodium
CAS No.	143201-11-0
Molecular Formula	C26H33FNO5•Na
Molecular Weight	481.54 g/mol
Synonyms	Cerivastatin Sodium Salt; (3R,5S,6E)-7-[4-(4-Fluorophenyl)-2,6-diisopropyl-5-(methoxymethyl)pyridin-3-yl]-3,5-dihydroxyhept-6-enoic Acid Sodium Salt; Rivastatin Sodium; BAY w 6228; Lipobay (Brand Name); ZD 4522 Sodium; Sodium (E,3R,5S)-7-[4-(4-fluorophenyl)-5-(methoxymethyl)-2,6-di(propan-2-yl)pyridin-3-yl]-3,5-dihydroxyhept-6-enoate
EINECS	Contact for details

Quality Control

Our Cerivastatin Sodium is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets high-grade pharmaceutical standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

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 material is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0% (on anhydrous basis)
Water Content (KF)	≤2.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.