Salbutamol EP Impurity I
| Product Name | Salbutamol EP Impurity I |
|---|---|
| Alternate Names | Salbutamol Impurities, Impurities of Salbutamol |
| CAT No. | CS-T-48795 |
| CAS No. | 56796-66-8 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 329.43 g/mol |
| Mol. For. | C₂₀H₂₇NO₃ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Salbutamol |
| Smileys | CC(C)(C)NCC(C1=CC(=C(C=C1)OCC2=CC=CC=C2)CO)O |
| Canonical Smiles | CC(C)(C)NCC(C1=CC(=C(C=C1)OCC2=CC=CC=C2)CO)O |
| InchIKey | ICDQPCBDGAHBGG-UHFFFAOYSA-N |
| Inchl | InChI=1S/C20H27NO3/c1-20(2,3)21-12-18(23)16-9-10-19(17(11-16)13-22)24-14-15-7-5-4-6-8-15/h4-11,18,21-23H,12-14H2,1-3H3 |
| IUPAC | 2-(tert-butylamino)-1-[3-(hydroxymethyl)-4-phenylmethoxyphenyl]ethanol |
| 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 |
Salbutamol EP Impurity I is a chemical compound that is used in pharmaceutical research and development. It is an impurity that is found in salbutamol, which is a bronchodilator medication used to treat asthma and other respiratory conditions. Salbutamol EP Impurity I is used as a reference standard in quality control tests for salbutamol drug formulations. It is also used as a marker for purity and potency of the drug.
Chemically, Salbutamol EP Impurity I is known as (RS)-2-(tert-butylamino)-1-(4-hydroxy-3-hydroxymethylphenyl)ethanol. It is a white to off-white powder that is soluble in water and methanol. The molecular formula of Salbutamol EP Impurity I is C13H21NO3 and its molecular weight is 239.3 g/mol.
The use of Salbutamol EP Impurity I in pharmaceutical research and development is important for ensuring the safety and efficacy of salbutamol drug formulations. By using this impurity as a reference standard, researchers can accurately measure the purity and potency of the drug. This helps to ensure that patients receive a safe and effective medication for their respiratory conditions.
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Related Compounds
Salbutamol Impurity N Acetate Salt | Salbutamol Impurity O | Levalbuterol Related Compound E Hydrochloride | Salbutamol EP Impurity D | Salbutamol EP Impurity A | Salbutamol Acetonide Methyl Ether | Salbutamol EP Impurity B | Salbutamol EP Impurity C | Salbutamol diethyl ether | Salbutamol EP Impurity H | Salbutamol Impurity K | Salbutamol EP Impurity G | Salbutamol Glyoxal Impurity | Salbutamol EP Impurity D Sulfate salt | Salbutamol Impurity P | Colterol | Salbutamol EP Impurity L Hydrochloride | Salbutamol Related Compound 1 | Salbutamol EP Impurity K (hemihydrate) | Salbutamol Impurity L | N-Benzyl Salbutamol Hydrochloride | Salbutamol EP Impurity E | Salbutamol Acetonide |