Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Nefopam Deoxy Impurity
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
Nefopam HCL 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.
Nefopam HCL Impurity D usage and description
Nefopam HCL Impurity D is a chemical compound that is commonly used in the pharmaceutical industry as an impurity in the manufacture of Nefopam hydrochloride. Nefopam hydrochloride is an analgesic drug that is used to treat moderate to severe pain. Impurity D is a by-product of the synthesis of Nefopam hydrochloride and is usually present in small amounts in the final drug product.
The chemical name of Nefopam HCL Impurity D is 4-(2-chlorophenyl)-1,2,3,4-tetrahydroisoquinoline and its molecular formula is C16H16ClN. It is a white to off-white crystalline powder that is sparingly soluble in water and soluble in organic solvents like methanol and ethanol.
The usage of Nefopam HCL Impurity D is strictly regulated in the pharmaceutical industry as it is considered a potential impurity that can affect the quality of the final drug product. Manufacturers of Nefopam hydrochloride are required to monitor the levels of Impurity D in their drug products to ensure that they meet the acceptable limits set by regulatory authorities.
Overall, Nefopam HCL Impurity D plays an important role in the manufacturing of Nefopam hydrochloride and its chemical properties and usage are closely monitored to ensure the safety and efficacy of the final drug product.
