MEDIOCON INC is a trusted global supplier of Nitracrine API, providing high-quality pharmaceutical reference materials and research chemicals for pharmaceutical research, analytical testing, process development, and laboratory applications. Our products are manufactured under stringent quality standards to ensure excellent purity, consistency, and reliability.
Nitracrine is an investigational antitumor agent belonging to the acridine derivative class. It has been extensively studied for its DNA-intercalating properties and selective cytotoxic activity against hypoxic tumor cells. Nitracrine has attracted considerable attention in oncology research because of its ability to interfere with DNA replication and enhance the sensitivity of tumor cells to radiation therapy. Although it is primarily used for research purposes, it remains an important compound for pharmaceutical development, analytical method validation, stability studies, and cancer research applications.
MEDIOCON INC supplies premium-quality Nitracrine suitable for research laboratories, pharmaceutical manufacturers, universities, contract research organizations (CROs), and analytical laboratories worldwide.
| Parameter | Specification |
|---|---|
| Appearance | Yellow to Orange Crystalline Powder |
| Identification | IR & HPLC Compliant |
| Assay (HPLC) | ≥99.0% |
| Loss on Drying | 1.0% |
| Residue on Ignition | 0.20% |
| Heavy Metals | 10 ppm |
| Individual Impurity | 0.50% |
| Total Impurities | 1.50% |
| Water Content | 1.0% |
| Melting Point | 250–255°C |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Nitracrine API Manufacturer & Supplier (CAS 3697-42-5) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Nitracrine API Manufacturer & Supplier 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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