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Esketamine EP Impurity A | CAS 6740-87-0 - Request Quote

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Esketamine EP Impurity A

SZ CAT No:SZ-E061002
CAS No
6740-87-0
Mol.F.
C13H16ClNO
Mol.Wt.
237.7
Inv. Status
In Stock
Rel. CAS No90717-16-1 (HCl salt)

Chemical Name :

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Usage Note:

Esketamine EP Impurity A is chemically 1-[(2-Chlorophenyl)(methylimino)methyl]cyclopentanol (as per EP). Esketamine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Esketamine 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 Esketamine Hydrochloride.

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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Esketamine EP Impurity A for Method Validation

Esketamine Hydrochloride Reference Standard

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Esketamine EP Impurity A Identification Standards

Esketamine EP Impurity A for DMF Filing

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

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

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