Description

Moveltipril Calcium is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the efficacy and consistency of advanced therapeutic formulations. It is primarily utilized by manufacturers in the pharmaceutical and biotechnology sectors for the development and production of cardiovascular and other specialized medications.

Application

• Pharmaceutical Active Ingredient (API): Serves as a key component in the synthesis of prescription medications.
• Cardiovascular Drug Intermediate: Used in the research and production of drugs targeting hypertension and heart conditions.
• Biochemical Research: Employed as a reference standard or reagent in pharmacological and metabolic studies.
• Formulation Development: Integral in pre-formulation studies and the development of solid dosage forms like tablets and capsules.
• Process Chemistry: Acts as a critical building block in multi-step synthetic routes for complex molecules.

Basic Information

Product Name	Moveltipril Calcium
CAS No.	85921-53-5
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Moveltipril Calcium Salt; (S)-1-[(S)-6-Amino-2-[[(S)-1-carboxy-3-phenylpropyl]amino]-5-oxohexyl]-N-[(S)-1-carboxy-2-(4-hydroxyphenyl)ethyl]-L-prolinamide Calcium Salt; Calcium Moveltipril; Moveltipril Ca; SQ 29,852 Calcium Salt
EINECS	Contact for details

Quality Control

Our Moveltipril Calcium is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee traceability and compliance.

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
Assay (HPLC)	≥98.0%
Water Content (KF)	≤2.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Heavy Metals	≤20 ppm
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.