Fosinopril EP Impurity D

N° de SZ CAT:	SZ-F022005
Número CAS	1356446-78-0
Mol.F.	C30H46NO7P
Peso Molecular	563.7
Status de Fatura	Custom Synthesis
Rel. CAS No	1356353-41-7 (sodium salt)

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Nome Químico: (2S,4R)-4-cyclohexyl-1-[[(R)-[(1S)-2-methyl-1-(propanoyloxy)propoxy](4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid (as per EP) ; (4R)-4-cyclohexyl-1-[(R)-[(S)-1-hydroxy-2-methylpropoxy](4-phenylbutyl)phosphinyl]acetyl-L-proline propionate (ester) (as per USP)

Sinônimo: Fosinopril USP Related Compound D

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=[P@@](CC(N1C[C@](C2CCCCC2)([H])C[C@]1(C(O)=O)[H])=O)(O[C@](OC(CC)=O)(C(C)C)[H])CCCCC3=CC=CC=C3

Fosinopril EP Impurity D is chemically (2S,4R)-4-cyclohexyl-1-[[(R)-[(1S)-2-methyl-1-(propanoyloxy)propoxy](4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid (as per EP) ; (4R)-4-cyclohexyl-1-[(R)-[(S)-1-hydroxy-2-methylpropoxy](4-phenylbutyl)phosphinyl]acetyl-L-proline propionate (ester) (as per USP). It is also known as Fosinopril USP Related Compound D. Fosinopril EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Fosinopril EP Impurity D 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 Fosinopril.

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.

Fosinopril EP Impurity D

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