Storage Condition
Store at refrigerator (2-8°C) for long term storage
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.
Lifitegrast Impurity D usage and description
Lifitegrast Impurity D is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the detection and quantification of impurities in Lifitegrast drug formulations. The compound is a known impurity of Lifitegrast and is often present in trace amounts in the final drug product.
Lifitegrast Impurity D is a white to off-white crystalline powder that has a molecular weight of 419.5 g/mol. Its chemical formula is C23H22N2O2 and its CAS number is 1628145-82-3. The compound is soluble in methanol, ethanol, and acetonitrile and has a melting point of 190-200°C.
The usage of Lifitegrast Impurity D is essential in the quality control of Lifitegrast formulations. The impurity can be detected and quantified using analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). The presence of impurities in drug formulations can affect the safety, efficacy, and stability of the final product. Therefore, it is important to monitor and control the levels of impurities in pharmaceuticals.
In conclusion, Lifitegrast Impurity D is an important reference standard that is used in the quality control of Lifitegrast drug formulations. Its chemical information and properties are essential in the detection and quantification of impurities in pharmaceuticals, ensuring the safety and efficacy of the final product.
