Quinapril Hydrochloride API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in the formulation of antihypertensive and cardiovascular medications. Quinapril Hydrochloride is an Angiotensin-Converting Enzyme (ACE) inhibitor indicated for the treatment of hypertension, congestive heart failure, and cardiovascular disorders. By inhibiting ACE, it reduces the formation of angiotensin II, resulting in vasodilation and improved cardiovascular function. Its superior purity, excellent stability, and consistent batch-to-batch quality make it ideal for pharmaceutical formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Quinapril Hydrochloride API manufacturer and bulk supplier in India, supplying premium-quality pharmaceutical ingredients to pharmaceutical companies, biotechnology organizations, contract manufacturing organizations (CMOs), formulation developers, research laboratories, and global distributors. Our GMP-compliant manufacturing facilities employ advanced production technologies and stringent quality management systems to ensure exceptional purity, consistency, and compliance with international pharmaceutical standards.
Every batch of Quinapril Hydrochloride API manufactured by MEDIOCON INC undergoes comprehensive analytical testing using validated quality control methods. Critical quality parameters including identity, assay, impurity profile, moisture content, pH, melting point, specific rotation, residual solvents, particle size distribution, heavy metals, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical specifications.
Our Quinapril Hydrochloride API is available in USP, EP, BP, IP, and Pharmaceutical Grade, making it suitable for tablet and capsule formulations, cardiovascular pharmaceutical products, analytical testing, formulation development, quality control laboratories, stability studies, process validation, and pharmaceutical research. We also provide complete regulatory documentation, including Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), Technical Data Sheet (TDS), and supporting regulatory documents, ensuring smooth procurement and regulatory compliance.
With a strong commitment to quality, innovation, and customer satisfaction, MEDIOCON INC has established itself as a dependable global supplier of pharmaceutical raw materials. Through secure packaging, competitive pricing, efficient logistics, and responsive technical support, we ensure reliable worldwide delivery of premium-quality Quinapril Hydrochloride API.
If you are looking for a trusted Quinapril Hydrochloride API manufacturer, exporter, and bulk supplier, MEDIOCON INC provides pharmaceutical-grade ingredients backed by complete documentation, consistent quality, and timely worldwide supply.
| Parameter | Specification |
|---|---|
| Appearance | White to Off-White Crystalline Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 1.0% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 3.5 – 5.5 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.5% |
| Water Content | NMT 2.0% |
| Specific Rotation | −35° to −45° (c = 1, Methanol) |
| Melting Point | 118°C – 125°C |
| Solubility | Freely Soluble in Water and Methanol; Slightly Soluble in Ethanol |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Quinapril Hydrochloride API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 82586-55-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Quinapril Hydrochloride API Manufacturer & Bulk Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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