Irinotecan Impurity 3, identified by its CAS number 200619-21-2, is a chemical compound associated with the anticancer drug irinotecan, which is used primarily in the treatment of colorectal cancer. This impurity is a byproduct that can arise during the synthesis of irinotecan and may affect the drug's efficacy and safety profile. The compound typically exhibits characteristics such as a specific molecular structure that includes a quinoline ring, which is common in many anticancer agents. Its chemical properties may include solubility in organic solvents, and it may display varying degrees of stability under different pH conditions. The presence of impurities like Irinotecan Impurity 3 is significant in pharmaceutical formulations, as they can influence the pharmacokinetics and pharmacodynamics of the primary drug. Regulatory agencies often require thorough characterization and quantification of such impurities to ensure the safety and effectiveness of the final pharmaceutical product. Understanding the properties of impurities is crucial for quality control in drug manufacturing processes.

Irinotecan Impurity 3

200619-21-2: Irinotecan Impurity 3, identified by its CAS number 200619-21-2, is a chemical compound associated with the anticancer drug irinotecan, which is used primarily in the treatment of colorectal cancer. This impurity is a byproduct that can arise during the synthesis of irinotecan and may affect the drug's efficacy and safety profile. The compound typically exhibits characteristics such as a specific molecular structure that includes a quinoline ring, which is common in many anticancer agents. Its chemical properties may include solubility in organic solvents, and it may display varying degrees of stability under different pH conditions. The presence of impurities like Irinotecan Impurity 3 is significant in pharmaceutical formulations, as they can influence the pharmacokinetics and pharmacodynamics of the primary drug. Regulatory agencies often require thorough characterization and quantification of such impurities to ensure the safety and effectiveness of the final pharmaceutical product. Understanding the properties of impurities is crucial for quality control in drug manufacturing processes.

CAS 200619-21-2

Irinotecan Impurity 3

Irinotecan Impurity 6

Ref: ST-EA-CP-I9026