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Cefazolin EP Impurity A

SZ目录编号:SZ-C016002
CAS 号30246-33-4
分子式C11H12N4O3S3
分子量344.4
投资状态In Stock
Rel. CAS No66659-21-0 (Na salt) ; 88739-52-0 (K salt) ; 98493-37-9 (HCl salt)

化学名称: (6R,7R)-7-Amino-3-[[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP) ; (6R,7R)-7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per USP)

异名: Cefazolin Deacylated (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: O=C(C(N12)=C(CSC3=NN=C(C)S3)CS[C@]2([H])[C@H](N)C1=O)O

Cefazolin EP Impurity A is chemically (6R,7R)-7-Amino-3-[[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP) ; (6R,7R)-7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per USP). It is also known as Cefazolin Deacylated (USP). Cefazolin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Cefazolin EP Impurity A 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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