Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
2-Descarboxy-2-Cyano Telmisartan; Telmisartan Cyano Analog
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
Telmisartan EP Impurity G 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.
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.
Telmisartan EP Impurity G usage and description
Telmisartan EP Impurity G, also known as 4'-Hydroxy Telmisartan, is a chemical compound that is commonly used in the production of Telmisartan, a medication used to treat hypertension or high blood pressure. Telmisartan EP Impurity G is a metabolite of Telmisartan and is formed when the medication is broken down in the liver.
Telmisartan EP Impurity G is a white crystalline powder that is sparingly soluble in water and soluble in ethanol. It has a molecular weight of 516.64 g/mol and a chemical formula of C33H30N4O4. Telmisartan EP Impurity G is typically used as a reference standard in pharmaceutical laboratories to aid in the identification and analysis of Telmisartan and its related substances.
Telmisartan EP Impurity G is also used in the development and validation of analytical methods for detecting and quantifying Telmisartan and its metabolites in biological samples. It is important to monitor these levels in patients who are taking Telmisartan to ensure proper dosing and to prevent potential adverse effects.
Overall, Telmisartan EP Impurity G plays a critical role in the development and quality control of Telmisartan and its related medications. Its usage and chemical information are important for the pharmaceutical industry and healthcare professionals who prescribe and administer these medications to patients.