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Cefazolin EP Impurity G (Triethylamine salt) - Image 1

Cefazolin EP Impurity G (Triethylamine salt)

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Description

Chemical Name: (5aR,6R)-6-[(1H-Tetrazol-1-ylacetyl)amino]-5a,6-dihydro-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazine-1,7(4H)-dione compound with triethylamine (1:1) (as per EP);N-{(5aR,6R)-1,7-Dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl}-2-(1H-tetrazol-1-yl)acetamide compound with triethylamine (1:1) (as per USP)
Synonym: Cefazolin lactone

Shipping Temperature:
Ambient

HSN Code:
38229010

Country of Origin: India

Smiles: O=C(OC1)C2=C1CS[C@@]([C@@H]3NC(CN4C=NN=N4)=O)([H])N2C3=O.CCN(CC)CC

Additional Information

Cefazolin EP Impurity G (Triethylamine salt) is chemically (5aR,6R)-6-[(1H-Tetrazol-1-ylacetyl)amino]-5a,6-dihydro-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazine-1,7(4H)-dione compound with triethylamine (1:1) (as per EP);N-{(5aR,6R)-1,7-Dioxo-1,3,4,5a,6,7-hexahydroazeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl}-2-(1H-tetrazol-1-yl)acetamide compound with triethylamine (1:1) (as per USP).
It is also known as Cefazolin lactone.
Cefazolin EP Impurity G (Triethylamine salt) is supplied with detailed characterization data compliant with regulatory guideline. Cefazolin EP Impurity G (Triethylamine salt) 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. ISP Standards products are for analytical purpose only and not for human use.

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