Therapeutic Uses
Anti ulcer
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(4S)-2-[5-(4-Hydroxyphenyl)-3,6-dioxopiperazin-2-yl]-5,5-dimethylthiazolidine-4-carboxylic acid
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95 %
Hazard Compound
No -Refer MSDS for accurate information
Amoxicillin EP Impurity C is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Amoxicillin EP Impurity C usage and description
Amoxicillin EP Impurity C, also known as 2-Hydroxyethylthioethyl amoxicillin, is an organic compound that is used in the pharmaceutical industry as an impurity reference standard for the analysis of amoxicillin drug substances and products. The impurity is derived from the synthesis of amoxicillin, which is a β-lactam antibiotic used to treat bacterial infections. The presence of Amoxicillin EP Impurity C in amoxicillin drug substances and products can affect their quality and efficacy, and therefore, its quantification is important for ensuring the safety and effectiveness of amoxicillin-based medications.
Chemically, Amoxicillin EP Impurity C is a white to off-white crystalline powder with a molecular formula of C11H20N2O5S and a molecular weight of 288.35 g/mol. It is soluble in water and ethanol, and its melting point ranges from 98°C to 102°C. The impurity is structurally related to amoxicillin, containing a β-lactam ring and an amide group.
The usage of Amoxicillin EP Impurity C involves its quantification in amoxicillin drug substances and products using various analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). The impurity reference standard is used to establish the limit for its acceptable levels in amoxicillin-based medications, which is typically set at 0.2% or lower.
In conclusion, Amoxicillin EP Impurity C is an important reference standard used in the pharmaceutical industry for the analysis of amoxicillin drug substances and products. Its quantification is crucial for ensuring the safety and effectiveness of amoxicillin-based medications, and its chemical information and properties are important for its identification and characterization.
