M.F.
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Therapeutic Uses
Anti-Parkinsons
Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
Synonyms
Cabergoline EP Impurity A, 81409-74-7
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95%
Hazard Compound
No -Refer MSDS for accurate information
Cabergoline 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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Cabergoline EP Impurity A usage and description
Cabergoline EP Impurity A is a chemical substance that is commonly used in pharmaceutical research and development as a reference standard for the analysis of Cabergoline, a dopamine receptor agonist drug used to treat hyperprolactinemia and Parkinson's disease. Cabergoline EP Impurity A is a known impurity of Cabergoline, and its identification and quantification in Cabergoline samples is important for ensuring the quality and purity of the drug.
Chemically, Cabergoline EP Impurity A is a derivative of ergoline, a class of alkaloids found in plants such as rye fungus, and it is also structurally related to Cabergoline. Its chemical name is (8ฮฒ)-Cabergoline-6-methyl-9,10-didehydroergoline-8-carboxamide. Cabergoline EP Impurity A is a white to off-white powder with a molecular weight of 384.5 g/mol.
In pharmaceutical research, Cabergoline EP Impurity A is used as a reference standard for the development and validation of analytical methods for the identification and quantification of Cabergoline and its impurities. It is also used for quality control purposes to ensure the purity of Cabergoline samples. Cabergoline EP Impurity A is typically analyzed using high-performance liquid chromatography (HPLC) or gas chromatography (GC) techniques.
