Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Oxymetazoline USP Related Compound A ; Oxymetazoline BP Impurity A
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Oxymetazoline EP Impurity A 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.
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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
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Oxymetazoline EP Impurity A usage and description
Oxymetazoline EP Impurity A is a chemical compound that is commonly used as a reference standard in the pharmaceutical industry. This impurity is a byproduct of the synthesis process of Oxymetazoline, which is a nasal decongestant used to relieve symptoms of congestion, itching, and sneezing caused by allergies or the common cold.
Chemically, Oxymetazoline EP Impurity A is a derivative of imidazole and has a molecular formula of C12H14N2O2. Its exact chemical structure and properties are important to understand for the accurate identification and quantification of Oxymetazoline impurities during drug development and manufacturing processes.
The usage of Oxymetazoline EP Impurity A is essential in ensuring the safety and efficacy of Oxymetazoline-based products. It is used as a reference standard in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC) to quantify the amount of impurity in a given sample. This impurity is also used as a benchmark to ensure that the manufacturing process of Oxymetazoline is within acceptable limits.
In conclusion, Oxymetazoline EP Impurity A plays a crucial role in the pharmaceutical industry as a reference standard for the analysis and quality control of Oxymetazoline-based products. Its chemical information and properties are essential for accurate identification and quantification of impurities during drug development and manufacturing processes.
