Therapeutic Uses
Anti-Migraines
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
1-Descarboxy ketolac
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Ketorolac 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.
Ketorolac EP Impurity I usage and description
Ketorolac EP Impurity I is a chemical compound that is used as a reference standard in the pharmaceutical industry. It is a synthetic compound that is related to the nonsteroidal anti-inflammatory drug Ketorolac, which is used to treat pain and inflammation in the body. Ketorolac EP Impurity I is a byproduct of the synthesis of Ketorolac, and it is present in small amounts in the final product.
In the pharmaceutical industry, Ketorolac EP Impurity I is used as a reference standard to ensure the quality and purity of Ketorolac. It is used in analytical methods such as high-performance liquid chromatography (HPLC) and gas chromatography (GC) to identify and quantify impurities in Ketorolac.
Ketorolac EP Impurity I is a white to off-white powder with a molecular weight of 238.28 g/mol. Its chemical name is (±)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid, and its chemical formula is C14H13NO3.
In conclusion, Ketorolac EP Impurity I is a useful reference standard in the pharmaceutical industry. Its chemical information and usage are important for ensuring the quality and purity of Ketorolac, which is a widely used drug for pain relief and inflammation treatment.
