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Candesartan N1-Ethyl Impurity  | CAS 1246817-38-8 - Request Quote

Picture of Candesartan N1-Ethyl Impurity 

Candesartan N1-Ethyl Impurity 

SZ CAT No:SZ-C011036
CAS No
1246817-38-8
Mol.F.
C26H24N6O3 
Mol.Wt.
468.5
Inv. Status
Synthesis on demand

Chemical Name :

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Usage Note:

Candesartan N1-Ethyl Impurity  is chemically 2-Ethoxy-1-[[2'-(1-ethyl-1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-benzimidazole-7-carboxylic acid ;. It is also known as N1-Ethyl Candesartan (Acid) ; . Candesartan N1-Ethyl Impurity  is supplied with detailed characterization data compliant with regulatory guideline. Candesartan N1-Ethyl 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 Candesartan.

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

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Candesartan N1-Ethyl Impurity  for Method Validation

Candesartan Reference Standard

Candesartan N1-Ethyl Impurity  for ANDA Filing

Candesartan N1-Ethyl Impurity  for Forced Degradation Studies

Candesartan N1-Ethyl Impurity  Identification Standards

Candesartan N1-Ethyl Impurity  for DMF Filing

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SynZeal will update these details as per new developments or findings in product specifications without further notice.

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