Tofacitinib impurity L
| Product Name | Tofacitinib impurity L |
|---|---|
| CAT No. | CS-AQ-00041 |
| CAS No. | 1675248-19-7 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 330.38 g/mol |
| Mol. For. | C₁₆H₂₂N₅O₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Therapeutic | Anti-Cancer / Oncology |
| Canonical Smiles | CC1CCN(CC1N(C)C2=NC=NC3=C2C=CN3)C(=O)CC(=O)N |
| InchIKey | CRDMXSMPTHMXRD-PWSUYJOCSA-N |
| Inchl | InChI=1S/C16H22N6O2/c1-10-4-6-22(14(24)7-13(17)23)8-12(10)21(2)16-11-3-5-18-15(11)19-9-20-16/h3,5,9-10,12H,4,6-8H2,1-2H3,(H2,17,23)(H,18,19,20)/t10-,12+/m1/s1 |
| IUPAC | 3-[(3R,4R)-4-methyl-3-[methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]piperidin-1-yl]-3-oxopropanamide |
| Controlled | No |
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| 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 |
Tofacitinib impurity L is a chemical substance that is used in the pharmaceutical industry as a reference standard for the analysis of Tofacitinib. Tofacitinib is a medication that is used to treat rheumatoid arthritis, psoriatic arthritis, and ulcerative colitis. It works by inhibiting the activity of a group of enzymes called Janus kinases (JAKs), which play a crucial role in the immune system.
Tofacitinib impurity L is a synthetic organic compound that has a molecular formula of C19H19N5O2S. It is classified as an impurity because it is a byproduct of the synthesis of Tofacitinib. It is important to control the presence of impurities in pharmaceutical products because they can affect the safety and efficacy of the medication. In the case of Tofacitinib, impurities can interfere with the binding of the drug to JAKs, reducing its effectiveness.
Chemically, Tofacitinib impurity L is a pyridine derivative that contains a sulfonamide group. It has a molecular weight of 381.45 g/mol and a melting point of 220-223°C. Tofacitinib impurity L is soluble in organic solvents such as methanol, ethanol, and acetonitrile. Its chemical structure is determined by various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.
In conclusion, Tofacitinib impurity L is an important reference standard used in the analysis of Tofacitinib. Its chemical information is crucial for the quality control of Tofacitinib and ensuring the safety and efficacy of the medication.
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