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Lisinopril EP Impurity J

N° de SZ CAT:SZ-L027012
Número CAS2566937-60-6
Mol.F.C37H53N5O8
Peso Molecular695.9
Status de FaturaLimited Stock

Nome Químico: (2S)-1-[(2S)-6-[(2S)-6-Amino-2-[[(1S)-1-carboxy-3-phenylpropyl]amino]hexanamido]-2-[[(1S)-1-carboxy-3-phenylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid (as per EP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C([C@H]1N(C([C@@H](N[C@H](C(O)=O)CCC2=CC=CC=C2)CCCCNC([C@@H](N[C@H](C(O)=O)CCC3=CC=CC=C3)CCCCN)=O)=O)CCC1)O

Lisinopril EP Impurity J is chemically (2S)-1-[(2S)-6-[(2S)-6-Amino-2-[[(1S)-1-carboxy-3-phenylpropyl]amino]hexanamido]-2-[[(1S)-1-carboxy-3-phenylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid (as per EP). Lisinopril EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Lisinopril EP Impurity J 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 Lisinopril.

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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