Description

Delapril is a high-purity active pharmaceutical ingredient (API) belonging to the class of angiotensin-converting enzyme (ACE) inhibitors. This compound is critical for the development and production of cardiovascular medications, offering a targeted mechanism of action. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in drug formulation, clinical research, and advanced chemical synthesis. Our supply of Delapril CAS NO 110508-93-5 is characterized by stringent quality control to ensure reliability for critical applications.

Application

• Pharmaceutical API: Primary use as the active ingredient in the formulation of prescription antihypertensive and heart failure medications.
• Reference Standard: Serves as a certified reference material (CRM) for quality control and analytical method validation in pharmaceutical laboratories.
• Biochemical Research: Used in pharmacological studies to investigate ACE inhibition mechanisms and cardiovascular disease pathways.
• Process Development: Employed in the research and scale-up of synthetic routes for novel ACE inhibitor derivatives.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of finished dosage forms.
• Academic Research: Utilized in university and institutional labs for teaching and advanced studies in medicinal chemistry.

Basic Information

Product Name	Delapril
CAS No.	110508-93-5
Molecular Formula	C26H30N2O5
Molecular Weight	450.53 g/mol
Synonyms	Delapril; Delapril Hydrochloride; (S)-1-[N-(1-Ethoxycarbonyl-3-phenylpropyl)-L-alanyl]-L-proline; Delaprilum; Adecut; CV-3317; Indalapril; REV-6000A
EINECS	Contact for details

Quality Control

Our Delapril is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. We provide full traceability and support regulatory submissions with detailed documentation. Certificates of Analysis (COA) are available upon request, detailing purity, identity, and impurity profiles.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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