Amisulpride EP Impurity E
| Chemical Name | Amisulpride EP Impurity E |
|---|---|
| Alternate Names | Amisulpride Impurities, Impurities of Amisulpride |
| CAT No. | CS-P-08910 |
| CAS Registry# | 71675-87-1 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 259.28 g/mol |
| Mol. For. | C₁₀H₁₃NO₅S |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Amisulpride |
| Canonical Smiles | CCS(=O)(=O)C1=C(C=C(C(=C1)C(=O)O)OC)N |
| InchIKey | OJVNCXHGGYYOPH-UHFFFAOYSA-N |
| Inchl | InChI=1S/C10H13NO5S/c1-3-17(14,15)9-4-6(10(12)13)8(16-2)5-7(9)11/h4-5H,3,11H2,1-2H3,(H,12,13) |
| IUPAC | 4-amino-5-ethylsulfonyl-2-methoxybenzoic acid |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
Amisulpride EP Impurity E is a chemical compound that is used in the pharmaceutical industry as a reference standard for quality control purposes. The compound is classified as an impurity, which means it is a byproduct or contaminant that is present in small quantities in the main product. Amisulpride EP Impurity E is typically used to ensure that the main product, amisulpride, is of high quality and meets regulatory standards.
Amisulpride EP Impurity E is also known as N-[(1-ethylpyrrolidin-2-yl)methyl]benzamide. It has a molecular weight of 236.33 g/mol and a molecular formula of C14H20N2O. The compound is a white to off-white powder that is soluble in organic solvents such as methanol and ethanol.
The chemical information on Amisulpride EP Impurity E is important for pharmaceutical companies to ensure that they are producing high-quality drugs that are safe and effective for patients. The impurity may have an impact on the stability and efficacy of the main product, which makes it important to monitor its presence and levels in the drug formulation. The use of reference standards like Amisulpride EP Impurity E is critical to maintaining the quality and safety of pharmaceutical products.
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Related Compounds
Amisulpride EP impurity B | Amisulpride ethanethiol Impurity | Amisulpride EP impurity A | Amisulpride EP impurity D | N-Methyl Amisulpride | Amisulpride Impurity 5 | Amisulpride Impurity 3 | Amisulpride EP impurity C |