Therapeutic Uses
Anti-Migraines
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
rac 1-Methoxy Ketorolac; 5-Benzoyl-1-methoxy-2,3-dihydro-1H-pyrrolizine-1-carboxylic Acid
Application Notes
Useful research chemical for a range of applications
Hazard Compound
Yes -Refer MSDS for accurate information
Ketorolac EP Impurity D 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 D usage and description
Ketorolac EP Impurity D, also known as 5-Bromo-2-methyl-3-(2-oxo-1,3-dioxolan-4-yl) pyridine, is a chemical compound that is commonly used as an impurity reference standard in the pharmaceutical industry. It is a heterocyclic organic compound that consists of a pyridine ring with a bromine atom and a methyl group attached to it. The compound has a molecular weight of 297.1 g/mol and a melting point of 84-87°C.
Ketorolac EP Impurity D is primarily used in the quality control of Ketorolac Tromethamine, which is a nonsteroidal anti-inflammatory drug (NSAID) used to treat moderate to severe pain. It is used as a reference standard to ensure that the Ketorolac Tromethamine drug product meets the required purity standards. The impurity is also used in the development and validation of analytical methods for the identification and quantification of Ketorolac EP Impurity D in pharmaceutical products.
The chemical information of Ketorolac EP Impurity D is important for regulatory compliance and quality control purposes. It is essential to ensure that the impurity is within acceptable limits as per the guidelines set by regulatory authorities. The compound is typically analyzed using techniques such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) to determine its purity and identity.
In conclusion, Ketorolac EP Impurity D is an important reference standard in the pharmaceutical industry, which is used to ensure the quality and purity of Ketorolac Tromethamine drug products. Its chemical information is crucial for quality control and regulatory compliance purposes.
