Therapeutic Uses
Anti-Thrombotics
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(1S,2S,3R,5S)-3-[7-[[(1R,2S)-2-(3,4-Difluorophenyl)cyclopropyl]amino]-5-(propylsulfinyl)-3H-1,2,3-triazolo[4,5-d]pyrimidin-3-yl]-5-(2-hydroxyethoxy)-1,2-cyclopentanediol (ACI)
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Ticagrelor Impurity L (Mixture of Diastereomers) 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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Ticagrelor Impurity L (Mixture of Diastereomers) usage and description
Ticagrelor Impurity L is a chemical compound that is commonly used as a reference standard in the manufacturing of Ticagrelor, which is a popular antiplatelet medication used in the treatment of various cardiovascular disorders. Ticagrelor Impurity L is a derivative of the active pharmaceutical ingredient Ticagrelor, and it is used to ensure the quality, purity, and consistency of the final drug product.
Chemically, Ticagrelor Impurity L is known as 3-(4-((4-((3R,4R)-4-(4-fluorophenyl)-3,4-dimethyl-1-piperidinyl)-3-methoxyphenyl)amino)-3-methoxyphenyl)propanoic acid. It is a white crystalline powder that is soluble in organic solvents such as methanol and acetonitrile. The chemical formula of Ticagrelor Impurity L is C32H40FNO5, and its molecular weight is 537.67 g/mol.
Ticagrelor Impurity L is used in the quality control process of Ticagrelor because it is a known impurity that can occur during the manufacturing process. By using Ticagrelor Impurity L as a reference standard, manufacturers can ensure that the final drug product contains a specific level of impurities, which is important for ensuring the safety and efficacy of the medication. Overall, Ticagrelor Impurity L is an essential tool for pharmaceutical manufacturers in the production of high-quality Ticagrelor.