Description

Delapril Hydrochloride is a high-purity active pharmaceutical ingredient (API) primarily used as an angiotensin-converting enzyme (ACE) inhibitor. This compound is critical for the research, development, and manufacturing of cardiovascular medications, offering reliable therapeutic action. It is essential for pharmaceutical companies, research institutions, and contract manufacturing organizations (CMOs) focused on producing antihypertensive and heart failure treatments.

Application

• Pharmaceutical API: Primary active ingredient in the formulation of prescription antihypertensive drugs.
• Cardiovascular Research: Key reference standard and biochemical tool for studying ACE inhibition mechanisms and pharmacokinetics.
• Drug Development: Used in preclinical and clinical studies for developing new cardiovascular therapies and combination drugs.
• Generic Drug Manufacturing: Serves as the core API for producing generic versions of ACE inhibitor medications.
• Analytical Standard: High-purity grade used for quality control, method validation, and calibration in analytical laboratories.

Basic Information

Product Name	Delapril Hydrochloride
CAS No.	108428-40-6
Molecular Formula	C26H38N2O5•HCl
Molecular Weight	495.05 g/mol
Synonyms	Delapril HCl; (S)-1-[N-[(S)-1-Carboxy-3-phenylpropyl]alanyl]hexahydro-2-oxo-1H-azepine-1-acetic acid hydrochloride; Delapril Hydrochloride (JP17); Adecut® (brand name); REV 6000A; Delapril Monohydrochloride; Delaprilum Hydrochloride
EINECS	Contact for details

Quality Control

Our Delapril Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity pharmaceutical standards, including identification, assay, and impurity profile analysis. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with in-house specifications and supporting regulatory submissions.

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 dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
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)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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