Therapeutic Uses
Antibiotics
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(1.2M)-[L-β-Asp3 ]vancomycin B (3.2-syn-chloro[L-β-
Asp3 ]vancomycin B) (CDP-1 major)
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
Vancomycin EP Impurity B 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
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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
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Vancomycin EP Impurity B usage and description
Vancomycin EP Impurity B is a chemical substance that is commonly used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Vancomycin drugs. Vancomycin is an antibiotic drug that is used to treat bacterial infections, particularly those caused by methicillin-resistant Staphylococcus aureus (MRSA) and other drug-resistant bacteria. However, Vancomycin drugs can contain impurities that can affect their potency, safety, and efficacy. Therefore, Vancomycin EP Impurity B is used as a reference standard to ensure that the Vancomycin drugs are free from harmful impurities.
Vancomycin EP Impurity B is a white to off-white powder that is soluble in water. Its chemical name is (2S,3R,4R)-2-(2,6-diaminopurin-9-yl)-4-[(1R)-1-hydroxyethyl]-3-methyl-2-cyclopentene-1-carboxylic acid. Its molecular formula is C14H20N6O4 and its molecular weight is 340.35 g/mol.
The usage of Vancomycin EP Impurity B is regulated by the European Pharmacopoeia (EP) and the United States Pharmacopoeia (USP). It is used as a primary reference standard for the identification and quantification of impurities in Vancomycin drugs. It is also used as a secondary reference standard for the calibration of analytical instruments such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). Vancomycin EP Impurity B is a critical component in the quality control of Vancomycin drugs, ensuring that they meet the required standards for safety and efficacy.
