Description

Delapril is a high-purity active pharmaceutical ingredient (API) belonging to the class of angiotensin-converting enzyme (ACE) inhibitors. It is a critical intermediate in the synthesis of advanced cardiovascular medications, offering reliable performance in complex pharmaceutical manufacturing processes. This compound is essential for research institutions and pharmaceutical companies engaged in the development and production of antihypertensive drugs and related therapeutic agents.

Application

• Pharmaceutical Intermediate: Primary use as a key building block in the synthesis of finished dosage forms of ACE inhibitor drugs.
• Active Pharmaceutical Ingredient (API): Serves as the core therapeutic agent in formulated cardiovascular medications.
• Research & Development: Utilized in pharmacological studies, bioavailability research, and the development of new drug delivery systems.
• Reference Standard: Acts as a certified reference material (CRM) for quality control and analytical method validation in pharmaceutical laboratories.
• Process Chemistry: Employed in scale-up and optimization studies for commercial pharmaceutical synthesis.

Basic Information

Product Name	Delapril
CAS No.	110508-92-4
Molecular Formula	C26H30N2O5
Molecular Weight	450.53 g/mol
Synonyms	Delapril; (S)-1-[N-[(S)-1-Carboxy-3-phenylpropyl]alanyl]hexahydro-2-oxo-1H-azepine-1-acetic acid; Delaprilum; Delapril Hydrochloride (salt form); Acepril; Adecut; CV-3317; NVP-CV3317
EINECS	Contact for details

Quality Control

Our Delapril is manufactured under strict quality management systems to ensure it meets the stringent requirements of the pharmaceutical industry. Each batch is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. A Certificate of Analysis (COA) documenting compliance with in-house specifications is provided with every shipment. We support compliance with cGMP, ICH Q7, and other relevant regulatory guidelines for active pharmaceutical ingredients.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

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 ≤ 1.5% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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