Methotrexate EP Impurity H
| Product Name | Methotrexate EP Impurity H |
|---|---|
| Alternate Names | Methotrexate Impurities, Impurities of Methotrexate |
| CAT No. | CS-T-32162 |
| CAS No. | 67022-39-3 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 468.5 g/mol |
| Mol. For. | C21H24N8O5 |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Methotrexate |
| Purity | 95% |
| Therapeutic | Immunosuppressants |
| Smileys | NC1=NC(N)=NC2=NC=C(CN(C3=CC=C(C(N[C@H](C(O)=O)CCC(OC)=O)=O)C=C3)C)N=C12 |
| 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 |
Methotrexate EP Impurity H is a chemical substance that is used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Methotrexate drugs. Methotrexate is a widely used chemotherapy drug that is primarily used for the treatment of cancer and autoimmune diseases such as rheumatoid arthritis and psoriasis. Methotrexate EP Impurity H is an important tool for quality control and assurance in the production of Methotrexate drugs.
The chemical formula for Methotrexate EP Impurity H is C20H23N7O6 and it has a molecular weight of 465.44 g/mol. The substance is a yellow to orange powder that is soluble in water and methanol. It is stable under normal storage conditions and has a purity of at least 98%.
Methotrexate EP Impurity H is typically used in pharmaceutical laboratories for analytical testing and method development. It is also used in the development and validation of analytical techniques such as high-performance liquid chromatography (HPLC) and gas chromatography (GC). The substance is also important for the development of new drugs and drug formulations, as it helps to ensure the quality and purity of Methotrexate drugs.
In conclusion, Methotrexate EP Impurity H is a crucial reference standard for the pharmaceutical industry. Its usage in analytical testing and quality assurance ensures the safe and effective production of Methotrexate drugs for the treatment of cancer and autoimmune diseases.
Get an Instant Quote
Related Compounds
Methotrexate EP Impurity F | Methotrexate EP Impurity D | N-Dinitroso Methotrexate Impurity 2 | R-Methotrexate di sodium | Methotrexate diethyl ester | Methotrexate Nitroso Impurity 1 | Methotrexate Nitroso Impurity 1 | Methotrexate Dimethylamide | Methotrexate EP Impurity G | Methotrexate EP Impurity C | Methotrexate EP Impurity B | N-nitroso Methotrexate Impurity 2 | Methotrexate EP Impurity I | Methotrexate EP Impurity B Disodium salt | Methotrexate EP Impurity A | N-nitroso Methotrexate Ethylester impurity | Methotrexate - Impurity E (HCl Salt) | Methotrexate EP Impurity B (MonoHydrate) | N-Nitroso Methotrexate EP Impurity-L (1) | Methotrexate EP Impurity E | Methotrexate EP Impurity J | Methotrexate EP Impurity L | N-Desmethyl Methotrexate dinitroso impurity | N-Nitroso Methotrexate EP Impurity-L (2) | N-Nitroso Methotrexate EP Impurity-B | N, N-Dinitroso Methotrexate EP Impurity L |