Therapeutic Uses
Anti-Thrombotics
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Dabigatran heptane-2-yl analog; O-(2-Heptyl) Dabigatran Ethyl Ester
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Dabigatran Etexilate EP Impurity F 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.
Dabigatran Etexilate EP Impurity F usage and description
Dabigatran Impurity E is a chemical compound that is used primarily in the pharmaceutical industry as a reference standard for quality control purposes. It is a known impurity of dabigatran, which is an anticoagulant drug used to prevent blood clots in patients with atrial fibrillation, deep vein thrombosis, and pulmonary embolism.
The chemical information of Dabigatran Impurity E includes its molecular formula, molecular weight, and purity level. Its molecular formula is C16H20N2O2, and its molecular weight is 272.34 g/mol. The purity level of Dabigatran Impurity E is typically around 98%, and it is a white to off-white powder that is soluble in organic solvents such as methanol and ethanol.
In terms of usage, Dabigatran Impurity E is used as a reference standard in the development and validation of analytical methods for the detection and quantification of dabigatran in various pharmaceutical products. It is also used in the characterization and analysis of dabigatran-related impurities and degradation products.
Overall, Dabigatran Impurity E plays a critical role in ensuring the quality and safety of dabigatran-based pharmaceutical products by providing a reliable and accurate reference standard for the analysis of dabigatran and its related impurities.
