Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Xylazine EP impurity A; Bupivacaine EP Impurity F
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
Lidocaine impurity A 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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Lidocaine impurity A usage and description
Lidocaine impurity A is a byproduct of the synthesis of Lidocaine, a widely used local anesthetic. It is a white or off-white crystalline powder that is sparingly soluble in water and soluble in organic solvents like methanol and ethanol. The chemical formula of Lidocaine impurity A is C14H22N2O, and its molecular weight is 234.34 g/mol.
Lidocaine impurity A is considered a minor impurity and is typically present in small amounts in Lidocaine preparations. However, its presence can affect the purity and potency of Lidocaine, and therefore, it is essential to monitor its levels during the manufacturing process.
In terms of usage, Lidocaine impurity A is not intended for direct use in any medical or pharmaceutical application. Instead, it is used as a reference standard for analytical testing and quality control purposes. Its primary use is in the development and validation of analytical methods to detect and quantify impurities in Lidocaine preparations.
In conclusion, Lidocaine impurity A is an important chemical compound that plays a significant role in ensuring the quality and safety of Lidocaine preparations. Its chemical and physical properties, as well as its usage and role in the manufacturing process, make it a crucial reference standard for analytical testing and quality control in the pharmaceutical industry.
