Bilastine Impurity 11 is a known related compound associated with the synthesis, degradation, or manufacturing process of Bilastine. It is commonly used as a reference standard for impurity profiling and analytical studies.

Bilastine Impurity 11 helps pharmaceutical companies identify, quantify, and monitor impurities, ensuring product quality and regulatory compliance.

Bilastine Impurity 11 can be analyzed using HPLC, UPLC, LC-MS, GC-MS (where applicable), and other advanced chromatographic and spectroscopic techniques.

Yes, Bilastine Impurity 11 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.

Bilastine Impurity 11 can be sourced from Chemicea, a trusted supplier of pharmaceutical impurities, reference standards, metabolites, and analytical research materials for the pharmaceutical industry.

Bilastine Impurity 11 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 Bilastine Impurity 11. Additional reports such as CNMR, IR, UV, DEPT, Water Content, and CHNS can be provided upon request, subject to availability.

The CAS number for Bilastine Impurity 11 is 202189-77-3.