Cefalotin Sodium Impurity – C
(6R,7R)-3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (7-ACA)
| Chemical Name | (6R,7R)-3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (7-ACA) |
|---|---|
| CAS No. | 957-68-6 |
| Molecular Formula | C10H12N2O5S |
| Molecular Weight | 272.28 |
| Chemical Structure |
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Cefalotin Sodium Impurity – C
Cefalotin Sodium Impurity – C is a known related substance / impurity of Cefalotin Sodium, as listed in the EP reference standard. Chemically, it is described as (6R,7R)-3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (7-ACA). It has the molecular formula C10H12N2O5S and a molecular weight of 272.28 g/mol. This impurity standard supports HPLC method validation, forced degradation studies, and routine quality control testing of Cefalotin Sodium. Supplied as a certified, high-purity reference standard suitable for HPLC, GC, and LC-MS analysis.
Cefalotin Sodium impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.
We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Cefalotin Sodium impurities that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related impurities.
This related products or Impurities are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.
BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.
BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.
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