NINGBO INNO PHARMCHEM CO., LTD. specializes in the supply of high-quality pharmaceutical intermediates, and Naltrexone Powder is a prime example of our commitment to excellence. This article explores the chemical properties of Naltrexone Powder (CAS: 16590-41-3) and its critical role in pharmaceutical manufacturing.

Naltrexone Powder is characterized by its distinct white powder appearance and a purity exceeding 99%, as verified through HPLC analysis. This high level of purity is non-negotiable for its use as an Active Pharmaceutical Ingredient (API) or intermediate in drug production. The stability of Naltrexone Powder, with a shelf life of two years, ensures its viability for manufacturers over extended periods.

As an opioid receptor antagonist, Naltrexone Powder is indispensable in the synthesis of pharmaceuticals targeting addiction. Its primary function is to block the effects of opioids, thereby aiding individuals in overcoming dependence. This makes it a crucial component in the formulation of medications for both opioid use disorder (OUD) and alcohol use disorder (AUD). The consistent supply of Naltrexone powder is paramount for pharmaceutical production pipelines.

The precise chemical specifications, including its molecular formula (C20H23NO4) and molecular weight (341.41), are meticulously documented to meet regulatory requirements. Pharmaceutical companies rely on these detailed specifications when sourcing Naltrexone powder for their production processes. The manufacturing capacity for Naltrexone powder is also a key consideration for ensuring a stable supply chain.

NINGBO INNO PHARMCHEM CO., LTD. is a trusted source for Naltrexone Powder, providing reliable access to this vital pharmaceutical intermediate. Our dedication to quality control and adherence to pharmaceutical standards ensures that our clients receive products that meet the highest benchmarks. Understanding the chemical properties and reliable supply of Naltrexone powder is crucial for pharmaceutical innovation and patient care.