Entecavir EP Impurity F

Product Name Entecavir EP Impurity F
Alternate Names Entecavir Impurities, Impurities of Entecavir
CAT No. CS-T-05539
CAS No. 649761-24-0
Category Impurities
Stock IN-Stock
Mol. Wt. 485.65 g/mol
Mol. For. C₂₇H₃₁N₅O₂Si
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Entecavir
Purity Not less than 90 %
Therapeutic Antiretroviral / Anti-HIV
Smileys C[Si](C)(C1CC(C(=C)C1COCC2=CC=CC=C2)N3C=NC4=C3N=C(NC4=O)N)C5=CC=CC=C5
Controlled No
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Entecavir EP Impurity F is a chemical compound that is used in the development and production of Entecavir, an antiviral medication used to treat chronic hepatitis B. Entecavir EP Impurity F is an impurity that is produced during the synthesis of Entecavir. It is a byproduct of the reaction between the starting materials used in the synthesis process. The chemical formula of Entecavir EP Impurity F is C12H14N2O3, with a molecular weight of 234.25 g/mol. Its chemical structure includes a pyrimidine ring and a carboxylic acid group. It is a white to off-white powder that is soluble in water and organic solvents. Entecavir EP Impurity F is used in the quality control of Entecavir production. It is important to ensure that the levels of impurities in the final product are within acceptable limits to ensure the safety and efficacy of the medication. Entecavir EP Impurity F is also used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC) to identify and quantify impurities in Entecavir. In conclusion, Entecavir EP Impurity F is an important chemical compound in the production and quality control of Entecavir. Its chemical information and usage in analytical methods make it a valuable tool in ensuring the safety and efficacy of the medication.

Related Compounds

Entecavir Lactose Adduct Impurity 1 | Entecavir Impurity 5 | Entecavir Impurity 2 | Entecavir impurity B | Entecavir Impurity 6 (ent-Entecavir-di-O-benzyl Ether) |

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