Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
5-(4′-(Azidomethyl)-[1,1′-biphenyl]-2-yl)-1H-tetrazole
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Refer MSDS for accurate information
Useful research chemical for a range of applications
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.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Irbesartan Impurity 15 usage and description
Irbesartan Impurity 15 is a chemical compound that is used in the pharmaceutical industry as a reference standard for the analysis and characterization of Irbesartan, which is a medication used to treat high blood pressure. This impurity is a byproduct of the synthesis of Irbesartan and is typically present in small amounts in the final drug product.
Irbesartan Impurity 15 is also known as 2-n-Butyl-1,3-diazaspiro[4.4]non-1-en-4-one and has a molecular formula of C12H20N2O. It is a white to off-white powder that is sparingly soluble in water and ethanol. This impurity is considered to be a potential genotoxic impurity and is subject to strict regulatory guidelines in the pharmaceutical industry.
To ensure the safety and efficacy of Irbesartan, it is essential to monitor and control the levels of Irbesartan Impurity 15 in the final drug product. This is achieved through the use of analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). By measuring the levels of this impurity, pharmaceutical manufacturers can ensure that Irbesartan meets the required quality standards and is safe for human consumption.
In conclusion, Irbesartan Impurity 15 plays a critical role in the analysis and control of Irbesartan drug products. Its chemical properties and potential genotoxicity make it a critical impurity to monitor and control in the pharmaceutical industry.
