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Atorvastatin EP Impurity I

Also known as: Atorvastatin Impurities or impurities of Atorvastatin
Chemical Name Atorvastatin EP Impurity I
CAT No. CS-O-07293
CAS Registry# 125971-95-1
Status Prompt Dispatch
Category Impurities, Carboxylic acids and derivatives
Mol. Wt. 654.81 g/mol
Mol. For. C₄₀H₄₇FN₂O₅
Hazardous This is a Hazardous Compound
COA View Sample COA

Additional Information

Controlled No
Parent API Atorvastatin
Therapeutic Anti-Diabetic
Smileys O=C(C(C(C1=CC=CC=C1)=C(C2=CC=C(F)C=C2)N3CC[C@@H](OC(C)(C)O4)C[C@@H]4CC(OC(C)(C)C)=O)=C3C(C)C)NC5=CC=CC=C5
Hazardous Yes

Usage and description

Atorvastatin EP Impurity I is a chemical compound that is used as a reference standard for the identification and quantification of impurities in Atorvastatin, a commonly prescribed medication for the treatment of high cholesterol. Atorvastatin EP Impurity I is also known as N-(2,2-dimethyl-1-oxopropoxy)-3,5-dihydroxybenzamide and has a molecular formula of C13H17NO5. The chemical structure of Atorvastatin EP Impurity I is composed of a benzamide moiety substituted with hydroxyl and carboxyl groups. This impurity is one of the major by-products formed during the synthesis of Atorvastatin and its identification is important to ensure the purity of the final drug product. Atorvastatin EP Impurity I is typically used in analytical laboratories to develop and validate analytical methods for the determination of impurities in Atorvastatin. It can also be used as a reference standard for the purification and isolation of impurities in Atorvastatin. The chemical properties of Atorvastatin EP Impurity I are well documented in the scientific literature. It has a melting point range of 160-165°C and is sparingly soluble in water. Atorvastatin EP Impurity I is stable under normal storage conditions and does not pose any significant health or safety hazards.

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