Description

Moexipril Hydrochloride is a potent, long-acting angiotensin-converting enzyme (ACE) inhibitor used in its active form. This high-purity active pharmaceutical ingredient (API) is critical for the formulation of effective antihypertensive and heart failure medications. It is primarily required by pharmaceutical manufacturers and research institutions engaged in cardiovascular drug development and production. Consistent quality and reliable supply are paramount for ensuring the safety and efficacy of the final dosage forms.

Application

• Pharmaceutical API: Primary active ingredient in prescription medications for the treatment of hypertension (high blood pressure).
• Cardiovascular Drug Formulation: Used in the development and commercial manufacturing of tablets and other solid oral dosage forms.
• Combination Therapies: May be formulated in fixed-dose combination drugs with other antihypertensive agents like hydrochlorothiazide.
• Clinical Research: Serves as a reference standard and raw material in pharmacokinetic, pharmacodynamic, and stability studies.
• Generic Drug Production: Essential for manufacturers producing bioequivalent versions of branded moexipril hydrochloride medications.

Basic Information

Product Name	Moexipril Hydrochloride
CAS No.	82586-52-5
Molecular Formula	C27H34N2O7 • HCl
Molecular Weight	535.03 g/mol
Synonyms	Moexipril HCl; (3S)-2-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)-3-phenylpropyl]amino]-1-oxopropyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-3-isoquinolinecarboxylic acid hydrochloride; Moexiprilum; UNII-5I6J4B5P6F; RS-10085-197; Moexipril Hydrochloride (USP); Moexipril Hydrochloride (EP)
EINECS	Contact for details

Quality Control

Our Moexipril Hydrochloride is manufactured under strict quality management systems. Each batch is tested to ensure it meets stringent specifications for identity, purity, and potency, aligning with major pharmacopeial standards such as USP and EP. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing results for assay, related substances, residual solvents, and other critical parameters to guarantee supply reliability and regulatory compliance for our global B2B clients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a 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 crystalline powder
Identification (IR)	Conforms
Identification (HPLC)	Conforms
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 2.0%
Water (KF)	NMT 1.0%
Residue on Ignition	NMT 0.1%
Heavy Metals	NMT 20 ppm
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.