Quinacrine API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in antimalarial, antiprotozoal, and immunomodulatory pharmaceutical formulations. Quinacrine, also known as Mepacrine, is a synthetic acridine derivative that has been utilized for the treatment of malaria, giardiasis, lupus erythematosus, rheumatoid arthritis, and other parasitic or autoimmune disorders. It is also extensively studied in oncology, antimicrobial, and molecular biology research due to its DNA intercalating and immunomodulatory properties. Its excellent purity, stability, and batch-to-batch consistency make it suitable for formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research.
MEDIOCON INC is a trusted Quinacrine 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 international distributors. Our GMP-compliant manufacturing facilities employ advanced production technologies and rigorous quality management systems to ensure superior purity, consistency, and compliance with international pharmaceutical standards.
Every batch of Quinacrine 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 thoroughly evaluated before commercial release to ensure compliance with stringent pharmaceutical quality specifications.
Our Quinacrine API is available in USP, EP, BP, IP, Research Grade, and Pharmaceutical Grade, making it suitable for antimalarial formulations, antiparasitic drug development, analytical testing, formulation development, quality control laboratories, stability studies, pharmaceutical process validation, and research applications. 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 seamless 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 Quinacrine API.
If you are looking for a trusted Quinacrine 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 | Yellow to Yellowish-Green Crystalline Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 1.0% |
| Residue on Ignition | NMT 2.0% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 5.0 – 7.0 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.0% |
| Water Content | NMT 1.0% |
| Specific Rotation | Not Applicable (Achiral Compound) |
| Melting Point | 228°C – 235°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 Quinacrine API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 83-89-6) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Quinacrine 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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