For any organization involved in pharmaceutical manufacturing, a thorough understanding of the technical specifications for raw materials is non-negotiable. Lofexidine Hydrochloride (CAS 21498-08-8) is no exception. As a key Active Pharmaceutical Ingredient (API), its precise characteristics dictate its suitability and efficacy in various therapeutic formulations, particularly those aimed at managing opioid withdrawal symptoms.

The primary technical specification to consider when you look to buy Lofexidine Hydrochloride is its purity. Reputable manufacturers typically guarantee a purity of 99% for this compound. This high level of purity is essential to meet stringent regulatory requirements and ensure the safety and efficacy of the final drug product. The appearance of Lofexidine Hydrochloride is generally described as a white powder, which is a standard visual indicator for quality in many pharmaceutical raw materials.

Proper storage conditions are also critical for maintaining the integrity of Lofexidine Hydrochloride. Manufacturers recommend storing it in a well-closed container, protected from moisture, heat, and direct light. Maintaining low temperatures can further preserve its stability over time. Adherence to these storage guidelines is paramount throughout the supply chain, from the manufacturer's facility to the end-user's storage.

When sourcing Lofexidine Hydrochloride, it is advisable to obtain a detailed Certificate of Analysis (CoA) from the supplier. This document provides a comprehensive breakdown of the product’s specifications, including assay (purity), identification tests, and limits for impurities. For those seeking to purchase in bulk or establish a long-term supply agreement, understanding these technical details and confirming the manufacturer's compliance with international quality standards is a fundamental step. Engaging with experienced China suppliers can provide access to consistent quality and valuable technical support.