Naltrexone EP Impurity D, with the CAS number 607732-61-6, is a chemical compound that is recognized as an impurity associated with the pharmaceutical drug naltrexone, which is primarily used in the treatment of opioid dependence and alcohol use disorder. This impurity is characterized by its structural similarity to naltrexone, featuring modifications that can affect its pharmacological properties. Typically, impurities like Naltrexone EP Impurity D are monitored during the manufacturing process to ensure the quality and safety of the final pharmaceutical product. The presence of such impurities can influence the efficacy and safety profile of the drug, making it crucial for regulatory compliance. In terms of physical properties, detailed information such as solubility, melting point, and spectral data would be necessary for a comprehensive understanding, but these specifics are often determined through analytical methods like HPLC or NMR. Overall, the characterization and control of impurities like Naltrexone EP Impurity D are essential in pharmaceutical development and quality assurance.

Naltrexone EP Impurity D

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Applications Degradation product of Naltrexone.
References Soni, S., et al.: J. Forensic Sci., 24, 437 (1979), Kambia, K., et al.: Biomed. Chromatogr., 14, 151 (2000),


2,2'-Bisnaltrexone (Naltrexone Impurity)

Naltrexone is a synthetic opioid receptor antagonist that binds to the opioid receptors in the brain and blocks the effects of heroin and other opiates. Naltrexone impurity D is an impurity found in naltrexone that has no therapeutic effect on humans. Naltrexone impurity D is also known as 3,4-dichloro-N-([1-(3-methylphenyl)ethyl]amino)-6-methylpyridine.

CAS 607732-61-6: Naltrexone EP Impurity D

2,2'-Bisnaltrexone (Naltrexone Impurity)

Ref: TR-B504500

Naltrexone impurity D

Ref: 3D-IN167082

Naltrexone EP Impurity D

Ref: ST-EA-CP-N57004