Leuprolide Acetate EP Impurity G

Leuprolide Acetate EP Impurity G is a chemical compound that belongs to the class of gonadotropin-releasing hormone (GnRH) analogs. It is commonly used as an impurity reference standard for the quality control and analysis of Leuprolide Acetate, a medication used in the treatment of prostate cancer, endometriosis, and infertility. The Leuprolide Acetate EP Impurity G is a synthetic peptide with a molecular weight of 1201.43 Daltons, and its chemical structure is similar to that of Leuprolide Acetate. The usage of Leuprolide Acetate EP Impurity G is essential in the pharmaceutical industry, as it helps to ensure the purity and quality of Leuprolide Acetate. It is used in the development and validation of analytical methods for the quantification of impurities in Leuprolide Acetate, as well as in the quality control of the drug substance and drug product. The impurity reference standard is used to ensure that the final product meets the required regulatory standards. In terms of chemical information, Leuprolide Acetate EP Impurity G is a peptide that contains 14 amino acids. Its chemical formula is C₆₀H₈₆N₁₈O₁₅, and its molecular structure includes a cyclic hexapeptide ring and a side-chain carboxylic acid group. The compound has a high solubility in water and is stable under normal storage conditions. The accurate characterization and quantification of Leuprolide Acetate EP Impurity G are crucial to ensure the safety and efficacy of Leuprolide Acetate-based medications.