M.F.
CโโHโโNโOโ
Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at freezer (-20ยฐC) for long term storage
Synonyms
Enalapril EP Impurity A, 1356932-13-2
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Enalapril 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.
Enalapril EP Impurity A usage and description
Enalapril EP Impurity A is a chemical compound that is commonly used in the pharmaceutical industry. It is a by-product or intermediate in the synthesis of Enalapril, which is a medication used in the treatment of hypertension and heart failure. Enalapril EP Impurity A is a white to off-white crystalline powder that is soluble in organic solvents such as ethanol, methanol, and acetonitrile.
The usage of Enalapril EP Impurity A is primarily as a reference standard in the quality control of Enalapril formulations. It is also used in research and development studies to evaluate the purity and stability of Enalapril. The impurity is considered to be a potential contaminant in the manufacturing process of Enalapril, and therefore its identification and quantification is essential to ensure the safety and efficacy of the final product.
From a chemical perspective, Enalapril EP Impurity A is a dipeptide derivative that contains an alanine and a proline residue. It is known to be an impurity that arises during the synthesis of Enalapril and is formed by the condensation of two precursor molecules. The impurity has a molecular weight of 373.43 g/mol and a molecular formula of C16H22N2O4.
In conclusion, Enalapril EP Impurity A is an essential reference standard in the quality control of Enalapril formulations. Its identification and quantification are critical for ensuring the safety and efficacy of the medication. Its chemical structure and properties make it a useful intermediate in the synthesis of Enalapril, but it is also considered a potential contaminant in the manufacturing process.