Therapeutic Uses
Anti-Asthma / COPD
Storage Condition
Store at refrigerator (2-8ยฐC) for long term storage
Synonyms
Naproxen EP Impurity J, 21388-17-0
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Naproxen EP Impurity J is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
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Naproxen EP Impurity J usage and description
Naproxen EP Impurity J is a chemical compound that is used as a reference standard for the assays and impurity profiling of naproxen drugs. It is also known as Naproxen EP Impurity N or (2S)-2-(6-methoxynaphthalen-2-yl)propanoic acid. The compound is a white or off-white powder with a molecular weight of 242.28 g/mol and a melting point range of 130-135ยฐC.
In terms of its chemical properties, Naproxen EP Impurity J is best characterized as a derivative of naproxen, which is a nonsteroidal anti-inflammatory drug (NSAID) that is commonly used to treat pain, inflammation, and fever. Naproxen acts by inhibiting the production of prostaglandins, which are chemical messengers that cause inflammation and pain. The impurity J is a byproduct of the synthesis of naproxen, and its presence in pharmaceutical formulations can affect the purity and efficacy of the drug.
For this reason, Naproxen EP Impurity J is used as a reference standard in quality control testing of naproxen drugs. The compound is typically analyzed using chromatographic techniques such as high-performance liquid chromatography (HPLC) or gas chromatography (GC), and its concentration is quantified using a calibration curve. The use of reference standards such as Naproxen EP Impurity J ensures that the purity and potency of naproxen drugs are maintained, and that they are safe and effective for use in treating pain and inflammation.