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Losartan Acetyloxy Impurity
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Disclaimer
The product information provided on this website by ISPStandards is based on the best available understanding at the time of publication. Customers are responsible for verifying the accuracy of this information before making a purchase. ISPStandards may update product details as new information or specifications become available, without prior notice.
- Product Overview
- Description
- Technical Data
Description
Chemical Name: 5-(4′-(Acetyloxymethyl)(1,1′-biphenyl)-2-yl)-1H-tetrazole
Synonym: Candesartan Acetyloxy Impurity
Shipping Temperature:
Ambient
HSN Code:
38229010
Country of Origin: India
Smiles: O=C(OCC1=CC=C(C2=CC=CC=C2C3=NN=NN3)C=C1)C
Additional Information
Losartan Acetyloxy Impurity is chemically 5-(4′-(Acetyloxymethyl)(1,1′-biphenyl)-2-yl)-1H-tetrazole.
It is also known as Candesartan Acetyloxy Impurity.
Losartan Acetyloxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Losartan Acetyloxy Impurity 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 Losartan.
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.
Development and validation of a stability-indicating HPLC method for the simultaneous determination of Losartan potassium, hydrochlorothiazide, and their degradation products