Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(2S)-1-((2S)-2-((1-ethoxy-1-oxo-4-phenylbutan-2-yl)amino)propanoyl)pyrrolidine-2-carboxylic acid
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Enalapril EP impurity A (mixture of diastereomers) is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Enalapril EP impurity A (mixture of diastereomers) usage and description
Enalapril EP impurity A (mixture of diastereomers) is an organic compound that is used in the pharmaceutical industry as a reference standard for the development and quality control of the active pharmaceutical ingredient Enalapril. Enalapril is a medication that is used to treat high blood pressure, heart failure, and other cardiovascular conditions. The impurity A of Enalapril is a mixture of diastereomers, which are stereoisomers that are not mirror images of each other but have different arrangements of atoms in their structures.
The chemical formula of Enalapril EP impurity A is C18H22N2O4 and its molecular weight is 330.38 g/mol. The impurity A of Enalapril is a white to off-white crystalline powder that is soluble in water and organic solvents such as methanol, ethanol, and acetonitrile. It has a melting point range of 119-125°C.
Enalapril EP impurity A is typically used in the pharmaceutical industry as a reference standard to ensure the purity and potency of the active pharmaceutical ingredient Enalapril. It is also used in research studies to investigate the pharmacological properties and toxicity of Enalapril and its related compounds. The impurity A of Enalapril is a valuable tool in the development and quality control of Enalapril-based medications, and its chemical information is essential for ensuring the safety and efficacy of these drugs.
