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Lidocaine EP Impurity C
| Chemical Name | Lidocaine EP Impurity C |
|---|---|
| CAT No. | CS-T-18564 |
| CAS Registry# | 2198-53-0 |
| Status | Available for Immediate Dispatch |
| Category | Impurities, Organic reagents |
| Mol. Wt. | 163.22 g/mol |
| Mol. For. | C₁₀H₁₃NO |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
Additional Information
| Controlled | No |
|---|---|
| Parent API | Lidocaine |
| Smileys | CC1=C(C(=CC=C1)C)NC(=O)C |
| Canonical Smiles | CC1=C(C(=CC=C1)C)NC(=O)C |
| InchIKey | NRPTXWYBRKRZES-UHFFFAOYSA-N |
| Inchl | InChI=1S/C10H13NO/c1-7-5-4-6-8(2)10(7)11-9(3)12/h4-6H,1-3H3,(H,11,12) |
| IUPAC | N-(2,6-dimethylphenyl)acetamide |
| Hazardous | Yes |
Usage and description
Lidocaine EP Impurity C is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the analysis and characterization of Lidocaine. It is a type of impurity that is often found in Lidocaine formulations, and is used as a marker to ensure that the purity of the drug is maintained during the manufacturing process.
Chemically, Lidocaine EP Impurity C is known as 2,6-dimethylaniline, and it is a colorless liquid with a faint, sweet odor. It is soluble in water and ethanol, and has a melting point of -10°C.
When used in the pharmaceutical industry, Lidocaine EP Impurity C is typically added to a sample of Lidocaine and then analyzed using various techniques, such as gas chromatography or high-performance liquid chromatography. This allows researchers to determine the amount of impurities present in the drug, and to ensure that it meets the necessary quality standards.
Overall, Lidocaine EP Impurity C is an important tool for pharmaceutical researchers and manufacturers, as it allows them to ensure that Lidocaine is produced to the highest standards of quality and purity.
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