Formoterol Fumarate EP Impurity D
| Product Name | Formoterol Fumarate EP Impurity D |
|---|---|
| Alternate Names | Formoterol Impurities, Impurities of Formoterol |
| CAT No. | CS-O-14076 |
| CAS No. | 1795133-96-8 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 358.43 g/mol |
| Mol. For. | C₂₀H₂₆N₂O₄ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Formoterol |
| Therapeutic | Anti-Asthma / COPD |
| Smileys | O=CNC1=CC(C(O)CN(C)C(C)CC2=CC=C(OC)C=C2)=CC=C1O |
| Canonical Smiles | CC(CC1=CC=C(C=C1)OC)N(C)CC(C2=CC(=C(C=C2)O)NC=O)O |
| InchIKey | IORGIYWNPKTFPA-UHFFFAOYSA-N |
| Inchl | InChI=1S/C20H26N2O4/c1-14(10-15-4-7-17(26-3)8-5-15)22(2)12-20(25)16-6-9-19(24)18(11-16)21-13-23/h4-9,11,13-14,20,24-25H,10,12H2,1-3H3,(H,21,23) |
| IUPAC | N-[2-hydroxy-5-[1-hydroxy-2-[1-(4-methoxyphenyl)propan-2-yl-methylamino]ethyl]phenyl]formamide |
| 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 |
Formoterol Fumarate EP Impurity D is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard or impurity marker for the analysis of Formoterol Fumarate. It has a molecular formula of C19H23NO4 and a molecular weight of 329.4 g/mol. This impurity is usually found in small amounts in Formoterol Fumarate drug substance, and its presence can affect the quality, purity, and efficacy of the final product. Therefore, it is essential to monitor and control its levels during drug development and manufacturing.
Formoterol Fumarate EP Impurity D is typically characterized and quantified using high-performance liquid chromatography (HPLC) or gas chromatography (GC) techniques. It is also used as a reference standard for the development of analytical methods for the determination of Formoterol Fumarate in drug products, raw materials, and biological samples.
In conclusion, Formoterol Fumarate EP Impurity D plays a vital role in the quality control and assurance of Formoterol Fumarate drug products. Its accurate identification and quantification are critical in ensuring the safety, purity, and efficacy of the final pharmaceutical product.
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Related Compounds
Formoterol Fumarate EP Impurity I | C-Demethyl N-Benzyl Formoterol O-Benzyl Ether | Formoterol Fumarate EP Impurity C | Formoterol Fumarate Dihydrate EP Impurity I (S,R-isomer) ((S,R)-Formoterol) | Formoterol related compound I | Formoterol Fumarate EP Impurity F | Formoterol impurity B fumarate salt | Formoterol impurity C fumarate salt | Formoterol Impurity 1 | Formoterol impurity F fumarate salt | Formoterol Impurity D | Formoterol Impurity 2 | rac-O-Benzyl N-Phenyl Formoterol(Mixture of Diastereomers) | Arformoterol Unknown Impurity at 0.97RRT Impurity | N-(5-((R)-2-(benzyl((R)-1-(4-methoxyphenyl)propan-2-yl)amino)-1-hydroxyethyl)-2-hydroxyphenyl)formamide | Formoterol Fumarate EP Impurity B | Formoterol impurity D fumarate salt | N-nitroso Formoterol | Formoterol Fumarate Dihydrate - Impurity H (Freebase) | Formoterol Fumarate EP Impurity E | Formoterol Fumarate EP Impurity A | Formoterol Imine Impurity | Formoterol Fumarate dihydrate Impurity | Formoterol impurity E fumarate salt | Formoterol Fumarate Dihydrate EP Impurity I (R,S-isomer) ((R,S)-Formoterol) | Formoterol Fumarate EP Impurity H | Formoterol EP Impurity A Fumarate | Formoterol EP Impurity C | Formoterol Related Compound C | Formoterol Impurity G | Arformoterol Impurity 1 | Formoterol Impurity G Hydrochloride | Formoterol Ethyl Ether Impurity | Formoterol Impurity 13 |