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Baclofen EP Impurity F

SZ CAT No:SZ-B050015
CAS No
NA
Mol.F.
C10H11Cl2NO2 : H2O
Mol.Wt.
248.1 : 18.0
Inv. Status
In Stock
Rel. CAS No4846-95-1 (free base) ; 5819-46-5 (HCl salt) ; 5819-45-4 (Na salt)

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Usage Note:

Baclofen EP Impurity F is chemically (3RS)-4-amino-3-(3,4-dichlorophenyl)butanoic acid hydrate (as per EP). Baclofen EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Baclofen EP Impurity F 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 Baclofen.

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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Baclofen EP Impurity F for Method Validation

Baclofen Reference Standard

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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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