Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Cefadroxil impurity A; 4-Hydroxy-D-(-)-2-phenylglycine; Cefadroxil impurity A; Amoxicillin EP Impurity I
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Amoxicillin EP Impurity I 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 I usage and description
Amoxicillin EP Impurity I is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard in quality control testing of Amoxicillin drug formulations. It is also used in research and development of new drugs, and in the development of analytical methods for the detection and quantification of Amoxicillin and its related compounds.
Chemically, Amoxicillin EP Impurity I is a degradation product of Amoxicillin, which is an antibiotic in the penicillin group of drugs. It is a white to off-white powder that is soluble in water and ethanol. The chemical name of Amoxicillin EP Impurity I is (2S,5R,6R)-6-{[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid.
Amoxicillin EP Impurity I is used as a reference standard in the analysis of Amoxicillin drug formulations for purity, stability, and quality. It is also used in the development of analytical methods for the detection and quantification of Amoxicillin and its related compounds. The use of this reference standard ensures the accuracy and reliability of the analytical results obtained during quality control testing.
In conclusion, Amoxicillin EP Impurity I is a vital chemical compound in the pharmaceutical industry, and its usage in quality control testing of Amoxicillin drug formulations plays a significant role in ensuring the safety and efficacy of the drug.
