Cefepime Hydrochloride EP Impurity F

Cefepime Hydrochloride EP Impurity F, also known as (6R,7R)-7-(4-Formyl-3,5-dimethyl-1-piperazinyl)-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hydrochloride, is an impurity of the antibiotic drug Cefepime Hydrochloride. It is a white to off-white crystalline powder with a molecular formula of C18H24N8O4S2.HCl and a molecular weight of 526.01 g/mol. Cefepime Hydrochloride EP Impurity F is a by-product that is formed during the synthesis of Cefepime Hydrochloride. It is important to monitor the levels of this impurity as it can affect the quality and efficacy of the final drug product. In pharmaceutical manufacturing, Cefepime Hydrochloride EP Impurity F is used as a reference standard for the identification and quantification of this impurity in the drug substance and drug product. The usage of Cefepime Hydrochloride EP Impurity F is strictly limited to laboratory and research purposes. It should not be used for human or veterinary applications. Proper handling and disposal of this material are necessary to prevent environmental contamination and health hazards. Cefepime Hydrochloride EP Impurity F should be stored in a cool, dry place away from heat, light, and moisture. It should also be kept out of the reach of children and unauthorized personnel.