Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Paracetamol EP Impurity C, 3964-54-3
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
Yes -Refer MSDS for accurate information
Paracetamol EP Impurity C 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
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Paracetamol EP Impurity C usage and description
Paracetamol EP Impurity C is a chemical substance that is used in the production of the popular pain relief medication, Paracetamol. It is also known as 4-Amino-3-chlorophenol and is classified as an organic compound with a molecular formula of C6H6ClNO.
The chemical is an impurity that is present in small amounts in the Paracetamol drug substance. It is a by-product formed during the manufacturing process of Paracetamol and is removed during the purification process. However, it is still important to monitor and control the levels of this impurity to ensure the safety and efficacy of the Paracetamol medication.
There are strict regulations and guidelines set by regulatory bodies such as the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA) that dictate the acceptable levels of impurities present in pharmaceutical products. The maximum limit of Paracetamol EP Impurity C in Paracetamol drug substance is set at 0.05%.
In conclusion, while Paracetamol EP Impurity C is an impurity in the production of Paracetamol, it is important to monitor its levels to ensure the safety and efficacy of the final medication. The strict regulations and guidelines set by regulatory bodies ensure that pharmaceutical products are safe for human consumption.
