Ceftiofur Disulfide Dimer (USP) INVENZA

Ceftiofur Disulfide Dimer (USP)

CAT No. IR-A06213
CAS No. 120905-00-2
Molecular Formula C28H28N10O10S6
Molecular Weight 857
Chemical Name
(6R,6`R,7R,7`R,Z)-3,3`-[Dithiobis(methylene)]bis{7-[(Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid}
Shipping Temperature Ambient temperature
HSN Code 29339990
Country of Origin India
Usage Note All products supplied by Invenza Research are intended exclusively for laboratory research, analytical testing, scientific investigations, and research and development purposes. These materials are not intended for human or animal consumption.
Product Description

Ceftiofur Disulfide Dimer (USP) (CAS No. 120905-00-2), chemically known as (6R,6`R,7R,7`R,Z)-3,3`-[Dithiobis(methylene)]bis{7-[(Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid}, is a well-characterized pharmaceutical impurity reference standard associated with Ceftiofur. It is widely used by pharmaceutical research laboratories, analytical scientists, contract research organizations (CROs), and quality control laboratories to support impurity identification, chromatographic method development, analytical method validation, and stability studies.

This reference standard plays an important role in ensuring accurate impurity profiling during the development and quality assessment of Ceftiofur-based pharmaceutical products. It is suitable for use in analytical techniques such as HPLC, LC-MS, UPLC, and other validated chromatographic methods where reliable impurity characterization is required.

Ceftiofur Disulfide Dimer (USP) has the molecular formula C28H28N10O10S6 and a molecular weight of 857 g/mol. It is also known by the chemical name (6R,6`R,7R,7`R,Z)-3,3`-[Dithiobis(methylene)]bis{7-[(Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid} and is identified by CAS No. 120905-00-2.

Researchers and analytical laboratories utilize this impurity reference standard during pharmaceutical development, quality control testing, method transfer, and regulatory compliance activities. Its use helps support the characterization and monitoring of related substances throughout the product lifecycle.

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Applications & Regulatory Use Cases

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