Porfiromycin API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in oncology pharmaceutical formulations and anticancer research. Porfiromycin is a mitomycin analogue and bioreductive alkylating antineoplastic agent that exhibits potent cytotoxic activity by forming DNA cross-links and inhibiting DNA synthesis in rapidly dividing cancer cells. It has been investigated for the treatment of solid tumors, bladder cancer, gastrointestinal cancers, breast cancer, and other malignant neoplasms. Its exceptional purity, 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 Porfiromycin 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 manufacturing technologies and stringent quality management systems to ensure superior purity, consistency, and compliance with international pharmaceutical quality standards.
Every batch of Porfiromycin 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, microbial limits, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical specifications.
Our Porfiromycin API is available in Research Grade and Pharmaceutical Grade, making it suitable for injectable oncology formulations, anticancer pharmaceutical research, 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, temperature-controlled logistics, competitive pricing, and responsive technical support, we ensure reliable worldwide delivery of premium-quality Porfiromycin API.
If you are looking for a trusted Porfiromycin 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 | Purple to Violet Crystalline Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | ≥ 98.0% |
| Loss on Drying | NMT 2.0% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 5.5 – 7.0 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.0% |
| Water Content | NMT 2.0% |
| Specific Rotation | +110° to +125° (c = 0.5, Water) |
| Melting Point | 175°C – 182°C |
| Solubility | Soluble in Water and Methanol; Slightly Soluble in Ethanol; Practically Insoluble in Chloroform |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Porfiromycin API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 801-52-9) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Porfiromycin 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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