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Atorvastatin EP Impurity J - Image 1

Atorvastatin EP Impurity J

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Description

Chemical Name: (2E,5S)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-5-hydroxyhept-2-enoic acid (as per EP);
(S,E)-7-[2-(4-Fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl]-5-hydroxyhept-2-enoic acid (as per USP);
Atorvastatin 3-Deoxy-Hept-2-Enoic Acid (USP)

Synonym: 2,3-Anhydro Atorvastatin ; Dehydro Atorvastatin Acid

Shipping Temperature:
Ambient

HSN Code:
38229010

Country of Origin: India

Smiles: OC(/C=C/C[C@H](O)CCN1C(C(C)C)=C(C(NC2=CC=CC=C2)=O)C(C3=CC=CC=C3)=C1C4=CC=C(F)C=C4)=O

Additional Information

Atorvastatin EP Impurity J is chemically (2E,5S)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-(propan-2-yl)-1H-pyrrol-1-yl]-5-hydroxyhept-2-enoic acid (as per EP);
(S,E)-7-[2-(4-Fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl]-5-hydroxyhept-2-enoic acid (as per USP);
Atorvastatin 3-Deoxy-Hept-2-Enoic Acid (USP)
.
It is also known as 2,3-Anhydro Atorvastatin ; Dehydro Atorvastatin Acid.
Atorvastatin EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Atorvastatin EP Impurity J can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Atorvastatin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.

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