M.F.
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HโโClโNโOโ
Therapeutic Uses
Anti-Fungals
Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
Synonyms
2-Butyl-4-(4-(4-(4-(((2S,4S)-4-((R)-(2,4-dichlorophenyl)(1H-1,2,4-triazol-1-yl)methyl)-1,3-dioxolan-2-yl)methoxy)phenyl)piperazin-1-yl)phenyl)-2,4-dihydro-3H1,2,4-triazol-3-one
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Refer MSDS for complete information
Itraconazole EP Impurity F 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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Itraconazole EP Impurity F usage and description
Itraconazole EP Impurity F is a chemical compound that is commonly used in the pharmaceutical industry as an impurity standard during the testing and analysis of Itraconazole drug formulations. It is a synthetic compound that is chemically related to Itraconazole, which is an antifungal medication used to treat a variety of fungal infections.
Chemically, Itraconazole EP Impurity F is known as 2,4-dichloro-1H-pyrrole-3-carboxylic acid, and it is commonly used as a reference standard during the quality control testing process of Itraconazole formulations. It is also used during the development and validation of analytical methods used to quantify Itraconazole in various drug formulations.
The usage of Itraconazole EP Impurity F is strictly regulated by various international organizations such as the United States Pharmacopeia (USP) and the European Pharmacopoeia (EP) to ensure that it is pure, safe, and effective for its intended use. It is important for pharmaceutical companies to ensure that their Itraconazole formulations meet the strict quality standards set by these organizations to ensure the safety and efficacy of the medication.
In conclusion, Itraconazole EP Impurity F plays a crucial role in the quality control testing and analysis of Itraconazole drug formulations. It is an important chemical reference standard that ensures the purity, safety, and efficacy of Itraconazole medication.