Verapamil Impurity I, with the CAS number 2893-91-6, is a chemical compound that is recognized as an impurity associated with the pharmaceutical agent verapamil, which is primarily used as a calcium channel blocker in the treatment of hypertension and certain heart conditions. This impurity is typically characterized by its molecular structure, which may include specific functional groups that differentiate it from the parent compound. It is important to note that impurities like Verapamil Impurity I can affect the efficacy and safety of pharmaceutical formulations, necessitating rigorous quality control measures during drug manufacturing. The compound may exhibit distinct physical and chemical properties, such as solubility in various solvents, stability under different conditions, and specific reactivity profiles. Analytical techniques such as chromatography and mass spectrometry are often employed to identify and quantify impurities like this one in pharmaceutical products, ensuring compliance with regulatory standards. Understanding the characteristics of such impurities is crucial for maintaining the integrity of medicinal products.

VERAPAMIL IMPURITY I

2893-91-6: Verapamil Impurity I, with the CAS number 2893-91-6, is a chemical compound that is recognized as an impurity associated with the pharmaceutical agent verapamil, which is primarily used as a calcium channel blocker in the treatment of hypertension and certain heart conditions. This impurity is typically characterized by its molecular structure, which may include specific functional groups that differentiate it from the parent compound. It is important to note that impurities like Verapamil Impurity I can affect the efficacy and safety of pharmaceutical formulations, necessitating rigorous quality control measures during drug manufacturing. The compound may exhibit distinct physical and chemical properties, such as solubility in various solvents, stability under different conditions, and specific reactivity profiles. Analytical techniques such as chromatography and mass spectrometry are often employed to identify and quantify impurities like this one in pharmaceutical products, ensuring compliance with regulatory standards. Understanding the characteristics of such impurities is crucial for maintaining the integrity of medicinal products.

CAS 2893-91-6

VERAPAMIL IMPURITY I

Verapamil EP Impurity I

Ref: ST-EA-CP-V10009