Description

Moexipril is an angiotensin-converting enzyme (ACE) inhibitor, a critical active pharmaceutical ingredient (API) in the treatment of hypertension and congestive heart failure. Its primary value lies in its proven efficacy for cardiovascular conditions, making it a cornerstone in therapeutic regimens. This high-purity compound is essential for pharmaceutical manufacturers engaged in the production of finished dosage forms, such as tablets, requiring a reliable and compliant API supply chain.

Application

• Primary Pharmaceutical Ingredient: As the key active component in antihypertensive and heart failure medications.
• Finished Dosage Form Manufacturing: Direct compression or granulation processes for tablet formulation.
• Generic Drug Production: Sourcing for manufacturers developing bioequivalent versions of branded moexipril medications.
• Clinical Research & Development: Use as a reference standard or raw material in new drug development studies.
• Contract Manufacturing: Supply to CDMOs (Contract Development and Manufacturing Organizations) for client-specific production.
• Regulatory Submissions: Providing API with supporting documentation (DMF, CEP) for regulatory filings with agencies like the FDA and EMA.

Basic Information

Product Name	Moexipril
CAS No.	103775-10-6
Molecular Formula	C27H34N2O7 • C2H4O2
Molecular Weight	535.6 g/mol (as acetate salt)
Synonyms	Moexipril Hydrochloride; Moexipril Acetate; Moexiprilum; UNII-4C6Y5C0W5U; (3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid hydrochloride; Moexipril HCl; RS-10085
EINECS	Contact for details

Quality Control

Our Moexipril is manufactured under strict quality management systems, targeting compliance with major pharmacopoeial standards such as USP and EP. Each batch undergoes comprehensive analytical testing including identification, assay, impurity profiling, and residual solvent analysis. A Certificate of Analysis (COA) documenting all test results is provided with every shipment to ensure full traceability and quality assurance for our B2B partners.

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 (moisture-sensitive) nature, the container must be kept tightly sealed in a low-humidity environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms
Identification (HPLC)	Conforms
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Residual Solvents (GC)	Complies with ICH Q3C

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