Description

Tenivastatin Calcium is a synthetic, selective inhibitor of HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis. This high-purity active pharmaceutical ingredient (API) is critical for the development and production of next-generation lipid-lowering therapeutics. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on cardiovascular disease treatment and metabolic disorder research.

Application

• Pharmaceutical API: Primary active ingredient in the formulation of cholesterol-lowering medications (statins).
• Biochemical Research: Used as a reference standard and tool compound in studies of cholesterol metabolism and HMG-CoA reductase enzyme kinetics.
• Drug Development: Serves as a key intermediate in the synthesis and preclinical development of novel statin-based therapies.
• Analytical Standard: Employed for method development, validation, and quality control testing in analytical laboratories.

Basic Information

Product Name	Tenivastatin Calcium
CAS No.	530112-57-3
Molecular Formula	C25H37F2NO6•1/2Ca
Molecular Weight	502.56 (for free acid, C25H38F2NO6)
Synonyms	Tenivastatin Calcium Salt; (3R,5S)-7-[2-Cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-dihydroxyhept-6-enoic Acid Calcium Salt; Tenivastatin Ca; Tenivastatin Hemicalcium Salt; BAY 62-9953; BAY-62-9953
EINECS	Contact for details

Quality Control

Our Tenivastatin Calcium 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 stringent pharmaceutical-grade specifications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with relevant guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥98.0% (anhydrous basis)
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Water Content (KF)	≤5.0%
Residue on Ignition	≤0.5%
Heavy Metals	≤20 ppm

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