Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Candesartan Cilexetil EP impurity B, 869631-11-8
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Candesartan Cilexetil EP impurity B 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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Candesartan Cilexetil EP impurity B usage and description
Candesartan Cilexetil EP impurity B, also known as (2-[(2'-carboxybiphenyl-4-yl)methyl]-1H-benzimidazol-6-yl)acetic acid, is a chemical impurity that is commonly found in pharmaceutical products that contain Candesartan Cilexetil. This impurity can be formed during the synthesis of Candesartan Cilexetil and can be present in small amounts in the final product.
Candesartan Cilexetil EP impurity B is a white or off-white crystalline powder that is sparingly soluble in water and soluble in methanol and acetonitrile. It has a molecular weight of 361.4 g/mol and a melting point range of 235-240°C.
The usage of Candesartan Cilexetil EP impurity B is not recommended in pharmaceutical formulations as it is considered an impurity. However, it is important to monitor the levels of this impurity in Candesartan Cilexetil formulations as it can affect the purity and quality of the final product. Regulatory agencies such as the United States Pharmacopeia (USP) have set limits on impurities in pharmaceutical products, including Candesartan Cilexetil, to ensure the safety and efficacy of the product.
In conclusion, Candesartan Cilexetil EP impurity B is an impurity that can be present in pharmaceutical products containing Candesartan Cilexetil. It is important to monitor and control the levels of this impurity to ensure the quality and safety of the final product.
