Therapeutic Uses
Anti-Hypertensives
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Enalapril Homophenylalanine Impurity; DL-Homophenylalanine
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Refer MSDS for complete information
Lisinopril 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
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Lisinopril EP Impurity A usage and description
Lisinopril EP Impurity A is a chemical compound used in the pharmaceutical industry as a reference standard or a quality control agent for the analysis of Lisinopril. Lisinopril is an ACE inhibitor medication used to treat hypertension and congestive heart failure. Lisinopril EP Impurity A is a synthetic compound that is not found naturally in the body. The chemical name of Lisinopril EP Impurity A is (2S,4S)-4-[(1-carboxy-3-phenylpropyl)amino]-2-(cyclohexylamino) butanoic acid.
The usage of Lisinopril EP Impurity A is primarily in the analytical field. It is used as a reference standard to compare the purity of Lisinopril drug samples. This impurity is used to ensure that the drug is of high quality and free of any potential contaminants that may negatively affect its efficacy. The presence of this impurity in a sample can also be used to identify the source of any impurities.
Chemically, Lisinopril EP Impurity A is a cyclic peptide with a molecular weight of 428.57 g/mol. It is a white to off-white powder with a melting point between 120-130°C. The compound has a solubility of 20mg/mL in water and 10mg/mL in ethanol. It is stable at room temperature and under normal storage conditions.
Overall, Lisinopril EP Impurity A is a vital reference standard for the pharmaceutical industry to ensure the quality and purity of Lisinopril drug samples. It is an essential tool for the analysis of the drug and identification of any potential impurities.
