Sacubitril Impurity 22 is a known related compound associated with the synthesis, degradation, or manufacturing process of Sacubitril. It is commonly used as a reference standard for impurity profiling and analytical studies.

Sacubitril Impurity 22 helps pharmaceutical companies identify, quantify, and monitor impurities, ensuring product quality and regulatory compliance.

Sacubitril Impurity 22 can be analyzed using HPLC, UPLC, LC-MS, GC-MS (where applicable), and other advanced chromatographic and spectroscopic techniques.

Yes, Sacubitril Impurity 22 is widely used as a reference standard for qualitative and quantitative analysis of impurities in pharmaceutical products.

It assists in establishing specificity, accuracy, precision, linearity, detection limits, and quantification limits during analytical method validation studies.

Sacubitril Impurity 22 can be sourced from Chemicea, a trusted supplier of pharmaceutical impurities, reference standards, metabolites, and analytical research materials for the pharmaceutical industry.

Sacubitril Impurity 22 may form during the synthesis, purification, storage, or degradation of the parent drug substance under specific process or environmental conditions.

Chemicea provides COA, H-NMR, MASS, HPLC, and TGA reports as standard with Sacubitril Impurity 22. Additional reports such as CNMR, IR, UV, DEPT, Water Content, and CHNS can be provided upon request, subject to availability.

The CAS number for Sacubitril Impurity 22 is 1012341-48-8.