In the pharmaceutical industry, the quality and reliability of active pharmaceutical ingredients (APIs) and intermediates are paramount. Levamisole Hydrochloride, a synthetic organic compound, plays a significant role in this landscape, not only for its direct therapeutic applications but also as a crucial intermediate in the synthesis of various pharmaceuticals. Understanding its essential properties and the intricacies of sourcing this compound is vital for manufacturers aiming to produce safe and effective medications.

Levamisole Hydrochloride is typically presented as a white or off-white crystalline powder. Its chemical formula is C11H12N2S, with a molecular weight of 240.752. Key specifications often include a purity exceeding 99%, ensuring its suitability for pharmaceutical use. The compound is stable under recommended storage conditions, typically in a cool, dry place, and maintains a shelf life of up to two years. These characteristics are fundamental to its handling and integration into complex manufacturing processes. The consistent availability of Levamisole HCl chemical properties and specifications from reliable suppliers is a critical factor for pharmaceutical production continuity.

The primary application driving the demand for Levamisole Hydrochloride as a pharmaceutical intermediate stems from its well-established anthelmintic and immunomodulatory properties. Manufacturers utilize it as a foundational element in producing veterinary drugs and human pharmaceuticals designed to combat parasitic infections and modulate immune responses. The stringent requirements for pharmaceutical-grade materials mean that sourcing decisions must prioritize suppliers who adhere to international quality standards, such as GMP (Good Manufacturing Practice), HSE, ISO 9001, USP, and BP certifications, as noted in industry data.

For businesses looking to purchase Levamisole Hydrochloride for their production lines, meticulous vendor selection is essential. This involves evaluating supplier capabilities, including production capacity, quality control protocols, and their ability to provide necessary documentation like Certificates of Analysis (COA) and Material Safety Data Sheets (MSDS). The ability to buy Levamisole Hydrochloride in bulk quantities, coupled with assurance of consistent quality, ensures that manufacturing processes are not disrupted. This focus on sourcing the right Levamisole HCl raw material directly impacts the quality and efficacy of the final pharmaceutical products.

In essence, Levamisole Hydrochloride's role as a pharmaceutical intermediate underscores the importance of chemical precision and reliable supply chains. By adhering to rigorous standards for its properties and sourcing, the pharmaceutical industry can continue to leverage this versatile compound for the development of essential medicines.