Therapeutic Uses
Anti-Cancer / Oncology
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Nilotinib EP Impurity A
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
Yes -Refer MSDS for accurate information
Nilotinib Genotoxic Impurity 1 is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Nilotinib Genotoxic Impurity 1 usage and description
Nilotinib Genotoxic Impurity 1 is a chemical impurity that is frequently present in the anti-cancer drug Nilotinib. This impurity is classified as genotoxic, meaning that it has the potential to cause mutations in DNA, potentially leading to the development of cancer. Due to its genotoxic properties, Nilotinib Genotoxic Impurity 1 is considered to be a potentially harmful substance and must be closely monitored during the production of Nilotinib.
The usage of Nilotinib Genotoxic Impurity 1 is primarily to monitor the level of impurities in Nilotinib. It is essential to ensure that the drug is safe for human consumption and does not pose a significant risk to health. The amount of Nilotinib Genotoxic Impurity 1 present in Nilotinib must be kept below a certain level, as determined by regulatory authorities, to ensure that the drug is safe for use.
From a chemical perspective, Nilotinib Genotoxic Impurity 1 is a derivative of Nilotinib, containing a specific chemical structure that may contribute to its genotoxic properties. It is crucial to understand the chemical properties of this impurity to ensure that it is effectively monitored and controlled during the production of Nilotinib. Overall, the usage and chemical information of Nilotinib Genotoxic Impurity 1 are essential to ensure that Nilotinib is a safe and effective drug for those who need it.
