Pneumocandin B0 API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used as a key antifungal intermediate in the production of echinocandin-class antifungal drugs, particularly Caspofungin Acetate. Pneumocandin B0 is a naturally occurring cyclic lipopeptide obtained through the fermentation of Glarea lozoyensis and serves as the principal starting material for semi-synthetic antifungal agents. Its exceptional purity, chemical stability, and batch-to-batch consistency make it suitable for pharmaceutical manufacturing, formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Pneumocandin B0 API manufacturer and bulk supplier in India, supplying premium-quality pharmaceutical ingredients and advanced intermediates to pharmaceutical companies, biotechnology organizations, contract manufacturing organizations (CMOs), formulation developers, research laboratories, and international distributors. Our GMP-compliant manufacturing facilities employ advanced fermentation and purification technologies along with stringent quality management systems to ensure superior purity, consistency, and compliance with international pharmaceutical standards.
Every batch of Pneumocandin B0 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, endotoxin levels, microbial limits, particle size distribution, heavy metals, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical quality specifications.
Our Pneumocandin B0 API is available in Research Grade and Pharmaceutical Grade, making it suitable for antifungal API manufacturing, Caspofungin intermediate production, 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 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 and advanced intermediates. Through validated packaging, competitive pricing, efficient logistics, and dedicated technical support, we ensure reliable worldwide delivery of premium-quality Pneumocandin B0 API.
If you are looking for a trusted Pneumocandin B0 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 Off-White Lyophilized Powder |
| Identification | HPLC, LC-MS & IR Complies |
| Assay (HPLC) | ≥ 98.0% |
| Loss on Drying | NMT 3.0% |
| Residue on Ignition | NMT 0.5% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 5.5 – 7.5 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 2.0% |
| Water Content | NMT 3.0% |
| Specific Rotation | +28° to +38° (c = 1, Methanol) |
| Melting Point | 185°C – 195°C |
| Solubility | Freely 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 Pneumocandin B0 API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 135575-42-7) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Pneumocandin B0 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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