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Cabergoline EP Impurity A

Also known as: Cabergoline Impurities or impurities of Cabergoline
Chemical Name Cabergoline EP Impurity A
CAT No. CS-O-31517
CAS Registry# 81409-74-7
Status Prompt Dispatch
Category Impurities
Mol. Wt. 296.4 g/mol
Mol. For. C18H20N2O2
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information

Controlled No
Parent API Cabergoline
Purity Not less than 95%
Therapeutic Anti-Parkinsons
Smileys C=CCN(C[C@H](C(O)=O)C1)[C@@](C2)([H])[C@@]1([H])C3=C4C2=CNC4=CC=C3
Hazardous Yes

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 (8β)-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.

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