Salmeterol EP Impurity G
| Product Name | Salmeterol EP Impurity G |
|---|---|
| Alternate Names | Salmeterol Impurities, Impurities of Salmeterol |
| CAT No. | CS-O-08130 |
| CAS No. | 1391051-88-9 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 813.12 g/mol |
| Mol. For. | C₅₀H₇₂N₂O₇ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Salmeterol |
| Purity | 95% |
| Therapeutic | Anti-Asthma / COPD |
| Smileys | C1=CC=C(C=C1)CCCCOCCCCCCNCC(C2=CC(=C(C=C2)CN(CCCCCCOCCCCC3=CC=CC=C3)CC(C4=CC(=C(C=C4)O)CO)O)O)O |
| Canonical Smiles | C1=CC=C(C=C1)CCCCOCCCCCCNCC(C2=CC(=C(C=C2)CN(CCCCCCOCCCCC3=CC=CC=C3)CC(C4=CC(=C(C=C4)O)CO)O)O)O |
| InchIKey | DJQSLAMRWZOBFB-UHFFFAOYSA-N |
| Inchl | InChI=1S/C50H72N2O7/c53-40-46-35-43(27-28-47(46)54)50(57)39-52(30-14-2-4-16-32-59-34-18-12-24-42-21-9-6-10-22-42)38-45-26-25-44(36-48(45)55)49(56)37-51-29-13-1-3-15-31-58-33-17-11-23-41-19-7-5-8-20-41/h5-10,19-22,25-28,35-36,49-51,53-57H,1-4,11-18,23-24,29-34,37-40H2 |
| IUPAC | 2-[[[2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl]-[6-(4-phenylbutoxy)hexyl]amino]methyl]-5-[1-hydroxy-2-[6-(4-phenylbutoxy)hexylamino]ethyl]phenol |
| 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 |
Salmeterol EP Impurity G is a chemical compound that is primarily used in the pharmaceutical industry as a reference standard or impurity marker for the analysis of Salmeterol, which is a long-acting beta-agonist medication used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Chemically, Salmeterol EP Impurity G is a derivative of Salmeterol and has a molecular formula of C26H32N2O4. It is a white to off-white powder that is sparingly soluble in water but soluble in organic solvents such as methanol and dichloromethane.
In terms of usage, Salmeterol EP Impurity G is commonly used as a reference standard or impurity marker in the development and validation of analytical methods for the determination of Salmeterol in pharmaceutical formulations. It is also used in quality control and batch release testing for Salmeterol-containing products such as inhalers and nebulizers.
Overall, Salmeterol EP Impurity G plays an important role in ensuring the safety, efficacy, and quality of Salmeterol-containing medications. Its availability as a reference standard or impurity marker allows for accurate and reliable analysis of Salmeterol, which is crucial in the development and manufacturing of pharmaceutical products.
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Related Compounds
Salmeterol EP Impurity E | Salmeterol EP Impurity B | Salmeterol Impurity G | Salmeterol EP Impurity E 1-hydroxy-2-naphthoic acid salt | alpha-Hydroxysalmeterol | dimethyl 4-(benzyloxy)isophthalate | Salmeterol USP Related Compound H | Salmeterol EP Impurity C Oxalate salt | N-nitroso Salmeterol | Salmeterol EP Impurity F | Salmeterol EP Impurity C | Salmeterol EP Impurity D |