Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Azilsartan Metabolite I; CS-AQ-00132 ;1-[[2'-(Aminoiminomethyl)[1,1'-biphenyl]-4-yl]methyl]-2-ethoxy-1H-benzimidazole-7-carboxylic Acid
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
Azilsartan impurity L is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
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While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
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Azilsartan impurity L usage and description
Azilsartan impurity L is a chemical compound that is often used in the pharmaceutical industry as a reference standard for quality control purposes. This impurity is a derivative of Azilsartan, which is a medication used to treat high blood pressure. Azilsartan impurity L is considered to be an important reference standard for quality control because it is used to verify the purity and identity of Azilsartan products.
The chemical formula of Azilsartan impurity L is C25H23N3O4, and its molecular weight is 433.47 g/mol. This impurity is a yellowish-brown powder that is soluble in organic solvents such as methanol and acetonitrile. It has a melting point of approximately 220-230°C.
Azilsartan impurity L is primarily used for analytical purposes, such as the development and validation of analytical methods for the determination of Azilsartan in pharmaceutical formulations. It is also used for the identification and quantification of impurities in Azilsartan products. Additionally, Azilsartan impurity L is used as a standard for the evaluation of the stability of Azilsartan formulations.
In conclusion, Azilsartan impurity L is an important reference standard for quality control in the pharmaceutical industry. Its chemical properties and analytical applications make it a valuable tool in the development and validation of analytical methods for the determination of Azilsartan products.
