Tedizolid Dimer Impurity

Tedizolid Dimer Impurity is a process-related impurity formed during the synthesis of tedizolid. It is used in pharmaceutical quality control as a reference standard to detect and quantify dimeric by-products that may form during manufacturing. Monitoring this impurity is essential to ensure the purity, safety, and consistency of the final tedizolid product. Although it has no therapeutic use, its identification and control are critical for meeting regulatory requirements and maintaining high-quality drug production standards.