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Oseltamivir EP Impurity A | CAS 1364932-19-3 - Request Quote

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Oseltamivir EP Impurity A

SZ CAT No:SZ-O003002
CAS No
1364932-19-3
Mol.F.
C14H24N2O4
Mol.Wt.
284.4
Inv. Status
In Stock
Shipping Condition Room Temperature

Chemical Name :

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Usage Note:

Oseltamivir EP Impurity A is chemically (3R,4R,5S)-5-acetamido-4-amino-3-(1-ethylpropoxy)cyclohex-1-ene-1-carboxylic acid (as per EP). It is also known as Oseltamivir Acid. Oseltamivir EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Oseltamivir EP Impurity A 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 Oseltamivir.

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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Oseltamivir EP Impurity A for Method Validation

Oseltamivir Reference Standard

Oseltamivir EP Impurity A for ANDA Filing

Oseltamivir EP Impurity A for Forced Degradation Studies

Oseltamivir EP Impurity A Identification Standards

Oseltamivir EP Impurity A 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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