Import Docetaxel — Buy in Bulk from Supplier in China

Docetaxel is a semi-synthetic taxane-class chemotherapy agent with the molecular formula C47H51NO14 and a molecular weight of 853.90 g/mol. It is supplied as a white to off-white crystalline powder, with CAS number 33069-62-4, and is intended for formulation into injectable solutions for oncology use. The product is manufactured under controlled conditions to meet pharmaceutical-grade purity standards.

The compound is derived from 10-deacetylbaccatin III, extracted from the needles of the European yew tree, and modified through multi-step synthesis. Typical purity levels in pharmaceutical-grade docetaxel exceed 98.5%, with strict limits on related substances such as paclitaxel and other taxane impurities. The supplier does not provide HPLC chromatograms or specific impurity profiles, but industry standards require total impurities to be below 2.0%.

Docetaxel is purchased by global pharmaceutical manufacturers for inclusion in branded and generic cancer treatments, primarily for breast, non-small cell lung, and prostate cancers. Buyers require GMP-compliant manufacturing, batch traceability, and full regulatory documentation. Packaging is typically in 1g or 5g amber glass vials under nitrogen, with bulk supply options available. MOQ and lead time are subject to supplier confirmation.

Hubei Honch Pharmaceutical Co., Ltd. is located in Wuchang District, Wuhan, Hubei Province, and operates as a supplier of active pharmaceutical ingredients. The company’s address is registered in a commercial building, suggesting administrative and operational presence. The supplier is classified as imported and harbor-tier, indicating verified business registration and physical location, though no certifications, export volume, or client list are disclosed.

The listing states the product is manufactured under stringent quality controls but does not confirm GMP certification, FDA or EMA inspection history, or audit reports. No information is provided on facility size, production capacity, or quality control laboratory capabilities. Buyers must request GMP documentation, batch release certificates, and regulatory dossiers directly from the supplier before initiating procurement.