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Cilastatin EP Impurity B

SZ CAT No:SZ-C073004
CAS No
NA
Mol.F.
C21H34N2O6S
Mol.Wt.
442.6
Inv. Status
Synthesis on demand

Chemical Name :

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Usage Note:

Cilastatin EP Impurity B is chemically (Z)-7-[[(2R)-2-carboxy-2-[[(1RS)-1-methyl-3-oxobutyl]amino]ethyl]sulfanyl]-2-[[[(1S)-2,2-dimethylcyclopropyl]carbonyl]amino]hept-2-enoic acid (as per EP). Cilastatin EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Cilastatin EP Impurity B 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 Cilastatin.

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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Cilastatin EP Impurity B for Method Validation

Cilastatin Reference Standard

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Cilastatin EP Impurity B 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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