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Picture of Cefazolin EP Impurity I

Cefazolin EP Impurity I

SZ CAT No:SZ-C016009
CAS No1675244-99-1
Mol.F.C14H16N8O5S3
Mol.Wt.472.5
Inv. StatusCustom Synthesis

Chemical Name: 2-[Carboxy[(1H-tetrazol-1-ylacetyl)amino]methyl]-5-[[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-5,6-dihydro-2H-1,3-thiazine-4-carboxylic acid (as per EP); 2-((2-(1H-tetrazol-1-yl)acetamido)(carboxy)methyl)-5-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-5,6-dihydro-2H-1,3-thiazine-4-carboxylic acid (as per USP)

Synonym: Cefazoloic Acid (EP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: O=C(C1=NC(C(C(O)=O)NC(CN2N=NN=C2)=O)SCC1CSC3=NN=C(C)S3)O

Cefazolin EP Impurity I is chemically 2-[Carboxy[(1H-tetrazol-1-ylacetyl)amino]methyl]-5-[[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-5,6-dihydro-2H-1,3-thiazine-4-carboxylic acid (as per EP); 2-((2-(1H-tetrazol-1-yl)acetamido)(carboxy)methyl)-5-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-5,6-dihydro-2H-1,3-thiazine-4-carboxylic acid (as per USP) . It is also known as Cefazoloic Acid (EP). Cefazolin EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Cefazolin EP Impurity I 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 Cefazolin.

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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