Potent Pharmaceutical Ingredient
May cause harm to the unborn child; avoid contact with skin and inhalation of dust.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Benazepril (CAS 86541-74-4) is a pharmaceutical-grade active ingredient belonging to the class of angiotensin-converting enzyme (ACE) inhibitors. It functions by preventing the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor, thereby reducing blood pressure and systemic vascular resistance.
In the Indian pharmaceutical landscape, Benazepril is a critical component for manufacturers focused on the cardiovascular segment. With India's growing focus on chronic disease management, the demand for high-quality, compliant API intermediates remains steady among domestic formulation units and export-oriented pharmaceutical companies.
Procurement of Benazepril requires strict adherence to pharmacopeial standards (USP/BP/EP). Buyers should ensure that suppliers provide comprehensive COA (Certificate of Analysis) documentation, impurity profiles, and compliance with GMP (Good Manufacturing Practices) to meet the rigorous quality requirements of the Indian CDSCO and international regulatory bodies.
Benazepril pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Benazepril prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
Yes, our Benazepril is sourced from GMP-certified facilities compliant with international standards.
We provide a full COA, MSDS, and stability data with every shipment.
Yes, small quantities are available for R&D and analytical validation purposes.
While it is an API, please consult local regulations regarding veterinary drug formulation requirements.
Lead time is typically 2-4 weeks depending on batch availability and location.
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