Storage Condition
Keep in a tightly closed vial, store in freezer
Synonyms
Orlistat USP Related Compound A
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
Orlistat Impurity A 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
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Orlistat Impurity A usage and description
Orlistat Impurity A is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the development of drugs that target obesity and related conditions. It is a synthetic compound that is used to evaluate the purity and quality of Orlistat, a popular anti-obesity medication. Orlistat Impurity A is also used as an analytical reference standard for the determination of Orlistat in pharmaceutical preparations by high-performance liquid chromatography (HPLC).
Chemically, Orlistat Impurity A is known as N-formyl-L-leucine, and it has a molecular weight of 173.2 g/mol. The compound is a white to off-white powder that is soluble in water and organic solvents such as methanol and acetonitrile. It is stable under normal storage conditions and does not require any special handling or storage precautions.
In terms of usage, Orlistat Impurity A is primarily used by pharmaceutical companies as a reference standard in the development and quality control of Orlistat-based drugs. It is also used by regulatory agencies such as the US Food and Drug Administration (FDA) to ensure the safety and efficacy of Orlistat-based drugs before they are approved for use in the market.
In conclusion, Orlistat Impurity A is an important reference standard in the pharmaceutical industry that is used to ensure the quality and safety of Orlistat-based drugs. Its chemical properties and stability make it an ideal reference standard for use in drug development and quality control.
