Flucloxacillin Sodium Monohydrate Impurity – D
3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid
| Chemical Name | 3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid |
|---|---|
| CAS No. | 3919-74-2 |
| Molecular Formula | C11H7ClFNO3 |
| Molecular Weight | 255.63 |
| Chemical Structure |
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Flucloxacillin Sodium Monohydrate Impurity – D
Flucloxacillin Sodium Monohydrate Impurity – D is identified as a process-related impurity of Flucloxacillin Sodium Monohydrate in accordance with EP specifications. Chemically, it is described as 3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylic acid. It has the molecular formula C11H7ClFNO3 and a molecular weight of 255.63 g/mol. It is used as a reference standard for impurity profiling, analytical method development, and quality control testing in pharmaceutical laboratories. Available with a Certificate of Analysis (CoA) as a high-purity reference standard suitable for HPLC and LC-MS applications.
Flucloxacillin Sodium Monohydrate 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 Flucloxacillin Sodium Monohydrate 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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