Pixantrone API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in oncology pharmaceutical formulations for the treatment of aggressive non-Hodgkin lymphoma (NHL) and other hematological malignancies. Pixantrone is an aza-anthracenedione antineoplastic agent designed to interfere with DNA replication by inhibiting topoisomerase II and inducing DNA damage in rapidly dividing cancer cells while minimizing cardiotoxicity compared to conventional anthracyclines. Its exceptional purity, excellent chemical stability, and batch-to-batch consistency make it suitable for pharmaceutical formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Pixantrone 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 superior purity, consistency, and compliance with international pharmaceutical quality standards.
Every batch of Pixantrone 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, heavy metals, particle size distribution, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical specifications.
Our Pixantrone API is available in USP, EP, Research Grade, and Pharmaceutical Grade, making it suitable for injectable oncology formulations, analytical testing, formulation development, quality control laboratories, stability studies, pharmaceutical process validation, and anticancer 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 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 dedicated technical support, we ensure reliable worldwide delivery of premium-quality Pixantrone API.
If you are looking for a trusted Pixantrone 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 | Dark Blue to Blue-Violet Crystalline Powder |
| Identification | IR, HPLC, LC-MS & UV Complies |
| Assay (HPLC) | ≥ 99.0% |
| Loss on Drying | NMT 1.0% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 4.5 – 6.5 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.0% |
| Water Content | NMT 1.0% |
| Specific Rotation | Not Applicable (Achiral Compound) |
| Melting Point | 255°C – 265°C |
| Solubility | Soluble in Water, Methanol and Dimethyl Sulfoxide (DMSO); 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 Pixantrone API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 856415-75-1) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Pixantrone 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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