Therapeutic Uses
Anti ulcer
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Rabeprazole Sulfone N-Oxide
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
Rabeprazole 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.
Rabeprazole EP Impurity I usage and description
Rabeprazole EP Impurity I is a chemical compound that is used in the pharmaceutical industry as a reference standard for the analysis of rabeprazole, which is a proton pump inhibitor drug used for the treatment of gastroesophageal reflux disease, ulcers, and other gastrointestinal disorders. The impurity is also known as 1-(3-methoxypropoxy)-3-methylbenzene, and is a derivative of rabeprazole.
The chemical structure of Rabeprazole EP Impurity I includes a benzene ring, a methyl group, and a methoxypropoxy group. It has a molecular formula of C12H18O2 and a molecular weight of 194.27 g/mol. The compound is a white solid that is soluble in organic solvents such as methanol, acetonitrile, and dichloromethane.
In pharmaceutical analysis, Rabeprazole EP Impurity I is used as a standard for the identification and quantification of rabeprazole impurities in drug formulations. It is also used in the development and validation of analytical methods for the determination of rabeprazole in biological fluids such as plasma and urine.
Overall, Rabeprazole EP Impurity I plays a crucial role in ensuring the quality and safety of rabeprazole-containing pharmaceutical products. Its availability as a reference standard enables accurate and reliable analysis of rabeprazole impurities, which is important for the effective treatment of gastrointestinal disorders.
