Therapeutic Uses
Anti-Cancer / Oncology
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
4-(5-((2-chloroethyl)amino)-1-methyl-1H-benzo[d]imidazol-2-yl)butanoic acid hydrochloride
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Bendamustine Deschloroethyl Acid Impurity 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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Bendamustine Deschloroethyl Acid Impurity usage and description
Bendamustine Deschloroethyl Acid Impurity is a chemical compound that is commonly used in the pharmaceutical industry as an intermediate in the synthesis of the drug Bendamustine. It is a byproduct that is formed during the synthesis of Bendamustine and is known to be a potent impurity that can significantly affect the quality and efficacy of the final drug product.
The chemical formula of Bendamustine Deschloroethyl Acid Impurity is C15H17ClN2O2, and its molecular weight is 296.76 g/mol. It is a white to off-white crystalline powder that is sparingly soluble in water but soluble in organic solvents like methanol, ethanol, and acetone.
Bendamustine Deschloroethyl Acid Impurity is a known genotoxic impurity and can cause DNA damage in cells. Therefore, it is essential to control its presence in the final drug product to ensure its safety and efficacy. The acceptable limit of Bendamustine Deschloroethyl Acid Impurity in Bendamustine drug products is typically set at 0.1% or lower.
In conclusion, Bendamustine Deschloroethyl Acid Impurity is a critical impurity that needs to be monitored and controlled during the synthesis of Bendamustine drug products. Its chemical properties and potential genotoxicity make it an important consideration for pharmaceutical companies looking to manufacture high-quality and effective drug products.