Therapeutic Uses
Anti-Diabetic
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
sodium (3R,5R)-7-((1S,2S,6R,8S,8aR)-8-((2,2-dimethylbutanoyl)oxy)-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl)-3,5-dihydroxyheptanoate
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
Simvastatin EP 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
always, we appreciate your support.
Simvastatin EP Impurity A usage and description
Simvastatin EP Impurity A is a chemical compound that is used in the pharmaceutical industry as a reference standard during the quality control of Simvastatin, a commonly prescribed medication for lowering cholesterol levels in the bloodstream. Simvastatin EP Impurity A is a by-product of the synthesis of Simvastatin, and its presence in Simvastatin preparations can affect the stability and efficacy of the medication. Therefore, it is important to monitor the levels of Simvastatin EP Impurity A in Simvastatin formulations to ensure their safety and effectiveness.
The chemical formula of Simvastatin EP Impurity A is C25H38O5, and its molecular weight is 418.57 g/mol. It is a white to off-white powder that is sparingly soluble in water and soluble in organic solvents such as methanol and ethanol.
The chemical structure of Simvastatin EP Impurity A is similar to that of Simvastatin, with the exception of an additional hydroxyl group at position 3 of the butyrolactone ring. This structural difference can affect the pharmacological properties of Simvastatin EP Impurity A and its interaction with other compounds.
In conclusion, Simvastatin EP Impurity A is an important reference standard for the quality control of Simvastatin preparations. Its chemical properties and structure play a crucial role in the stability and efficacy of Simvastatin, and its careful monitoring is essential for ensuring the safety and effectiveness of Simvastatin-based medications.
