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 reliable therapeutic efficacy. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in drug formulation and advanced clinical studies.

Application

• Pharmaceutical API: Primary active ingredient in antihypertensive and heart failure medications.
• Reference Standard: Used in analytical laboratories for quality control, method development, and validation.
• Research & Development: Key intermediate in the synthesis of novel ACE inhibitor derivatives and pharmacokinetic studies.
• Formulation Development: Employed in the creation of various dosage forms, including tablets and capsules.
• Clinical Trial Material: Sourced for use in Phase I-IV clinical trials under Good Manufacturing Practice (GMP) standards.

Basic Information

Product Name	Delapril
CAS No.	83435-66-9
Molecular Formula	C26H30N2O5
Molecular Weight	450.53 g/mol
Synonyms	Delapril Hydrochloride; Delapril HCl; (S)-1-[N-[(S)-1-Carboxy-3-phenylpropyl]alanyl]hexahydro-2H-azepin-2-one; Acepril; Adecut; CV-3317; Indalapril; REV-6000A
EINECS	Contact for details

Quality Control

Our Delapril is manufactured under strict quality systems to ensure it meets the rigorous standards required for pharmaceutical applications. Each batch is tested against comprehensive specifications, including identity, purity, and impurity profiles, using validated analytical methods such as HPLC and IR spectroscopy. A Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and compliance.

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 nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	98.0% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Loss on Drying	≤ 1.0%
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.