For researchers and developers in the pharmaceutical industry, understanding the detailed chemical profile of key intermediates is fundamental to successful synthesis and product development. Darunavir Impurity A, identified by CAS number 169280-56-2, is a critical compound in this regard. NINGBO INNO PHARMCHEM CO.,LTD. provides this essential material, offering comprehensive insights into its properties and scientific significance.

The chemical structure of Darunavir Impurity A is defined by its molecular formula: C20H29N3O3S, with a molecular weight of 391.53. It typically presents as a white crystal powder, a characteristic that aids in its identification and handling during laboratory processes. The high purity level, specified as ≥98% MIN, along with compliance to major pharmacopeial standards such as USP, BP, EP, and FCC, underscores its suitability for demanding pharmaceutical applications. For those looking to buy Darunabin intermediate, these details are crucial for ensuring research integrity.

As a leading pharmaceutical intermediate, Darunavir Impurity A is indispensable for the synthesis of Darunavir. Its precise chemical makeup allows for the controlled progression through complex synthetic pathways, ultimately contributing to the production of an effective antiviral drug. Beyond its direct role in synthesis, it also serves as a valuable pharmaceutical impurity reference standard. This allows for critical quality control measures, enabling precise quantification of impurities in finished pharmaceutical products.

NINGBO INNO PHARMCHEM CO.,LTD. is committed to supporting scientific advancement by being a reliable 4-AMINO-N-[(2R,3S)-3-AMINO-2-HYDROXY-4-PHENYLBUTYL]-N-ISOBUTYLBENZENE-1-SULFONAMIDE supplier. We understand the nuances of pharmaceutical research and provide this vital Darunavir synthesis intermediate with competitive pricing and accessible support. Our aim is to equip researchers and manufacturers with the high-quality materials they need to drive innovation in drug development.

In conclusion, the chemical profile of Darunavir Impurity A is a critical aspect for any professional involved in the research and manufacturing of Darunavir. By understanding its properties and significance, researchers can leverage this intermediate effectively to advance antiviral therapies and ensure the highest quality in pharmaceutical products.