Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Methyl (S)-2-(2-(benzofuran-6-carbonyl)-5,7-dichloro-1,2,3,4-tetrahydroisoquinoline-6-carboxamido)-3-(3-(methylsulfonyl)phenyl)propanoate
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Lifitegrast 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.
Lifitegrast Impurity G usage and description
Lifitegrast Impurity G, also known as (5R)-5-[2-(2,6-Difluorobenzyl)-5-(1-hydroxy-2-methylpropan-2-yl)pyrrolidin-1-yl]-2-methoxybenzoic acid, is a chemical impurity that is commonly used in the pharmaceutical industry. It is a pyrrolidine-based compound that is structurally similar to the active ingredient, Lifitegrast, which is used to treat dry eye disease.
Lifitegrast Impurity G is a potential byproduct of the synthesis of Lifitegrast and may be present in trace amounts in the final product. Therefore, it is important to understand its chemical properties and potential impact on the efficacy and safety of the drug.
Chemically, Lifitegrast Impurity G is a carboxylic acid derivative that is soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO). Its molecular weight is 438.5 g/mol, and it has a melting point of around 250-252°C.
In terms of usage, Lifitegrast Impurity G is primarily used as a reference standard for analytical testing and quality control purposes. It can be used to assess the purity and identity of Lifitegrast in drug samples, as well as to validate analytical methods used in drug development and manufacturing.
Overall, understanding the chemical properties and potential impact of Lifitegrast Impurity G is essential for ensuring the quality, safety, and efficacy of Lifitegrast-based drugs.
