Quazepam API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in the formulation of sedative-hypnotic and anxiolytic medications. Quazepam is a benzodiazepine derivative primarily indicated for the treatment of insomnia, sleep initiation disorders, sleep maintenance disorders, and anxiety-related sleep disturbances. It enhances the activity of gamma-aminobutyric acid (GABA) in the central nervous system, promoting sedation and improving sleep quality. Its high purity, excellent stability, and batch-to-batch consistency make it ideal for pharmaceutical formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Quazepam 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 utilize advanced manufacturing technologies and stringent quality management systems to ensure exceptional purity, consistency, and compliance with international pharmaceutical quality standards.
Every batch of Quazepam 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 specifications.
Our Quazepam API is available in USP, EP, BP, IP, and Pharmaceutical Grade, making it suitable for tablet formulations, capsule formulations, analytical testing, formulation development, quality control laboratories, stability studies, pharmaceutical process validation, and authorized 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 Quazepam API.
If you are looking for a trusted Quazepam 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 Pale Yellow Crystalline Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 0.5% |
| Residue on Ignition | NMT 0.2% |
| 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 | 238°C – 242°C |
| Solubility | Slightly Soluble in Water; Freely Soluble in Methanol, Ethanol, Chloroform, and Acetone |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Quazepam API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 36735-22-5) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Quazepam 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.
Export Markets
Quality & Compliance