Methotrexate EP Impurity E

Product Name Methotrexate EP Impurity E
Alternate Names Methotrexate Impurities, Impurities of Methotrexate
CAT No. CS-T-14358
CAS No. 19741-14-1
Category Impurities
Stock IN-Stock
Mol. Wt. 325.33 g/mol
Mol. For. C₁₅H₁₅N₇O₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Methotrexate
Therapeutic Immunosuppressants
Smileys CN(CC1=CN=C2C(=N1)C(=NC(=N2)N)N)C3=CC=C(C=C3)C(=O)O
Canonical Smiles CN(CC1=CN=C2C(=N1)C(=NC(=N2)N)N)C3=CC=C(C=C3)C(=O)O
InchIKey LWCXZSDKANNOAR-UHFFFAOYSA-N
Inchl InChI=1S/C15H15N7O2/c1-22(10-4-2-8(3-5-10)14(23)24)7-9-6-18-13-11(19-9)12(16)20-15(17)21-13/h2-6H,7H2,1H3,(H,23,24)(H4,16,17,18,20,21)
IUPAC 4-[(2,4-diaminopteridin-6-yl)methyl-methylamino]benzoic acid
Controlled No
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Methotrexate EP Impurity E is a chemical compound that is used in the manufacturing of Methotrexate. Methotrexate is a chemotherapy drug that is used to treat various forms of cancer and autoimmune diseases. Methotrexate EP Impurity E is a byproduct that is produced during the synthesis of Methotrexate. It is a white to off-white powder that is insoluble in water and soluble in organic solvents. Methotrexate EP Impurity E is classified as an impurity because it is not the desired product of the chemical reaction. However, it is still an important chemical compound because it can affect the purity and potency of Methotrexate. Therefore, the amount of Methotrexate EP Impurity E in the final drug product must be minimized to ensure the safety and efficacy of the drug. Chemically, Methotrexate EP Impurity E is known as N-(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)amino}benzoyl)-L-glutamic acid. It has a molecular formula of C20H23N7O6 and a molecular weight of 469.44 g/mol. Methotrexate EP Impurity E is a derivative of pteridine and glutamic acid, which are important components of the Methotrexate synthesis pathway. In conclusion, Methotrexate EP Impurity E is an important chemical compound in the manufacturing of Methotrexate. While it is classified as an impurity, it must be carefully controlled to ensure the safety and efficacy of the final drug product. Its chemical properties make it an essential component of the Methotrexate synthesis pathway.

Related Compounds

Methotrexate EP Impurity B | Methotrexate EP Impurity B (MonoHydrate) | Methotrexate - Impurity E (HCl Salt) | Methotrexate EP Impurity B Disodium salt | Methotrexate diethyl ester | Methotrexate EP Impurity I | N-nitroso Methotrexate Impurity 2 | N-nitroso Methotrexate Ethylester impurity | Methotrexate Nitroso Impurity 1 | N-Nitroso Methotrexate EP Impurity-L (2) | Methotrexate EP Impurity G | N-Nitroso Methotrexate EP Impurity-L (1) | N-Desmethyl Methotrexate dinitroso impurity | Methotrexate EP Impurity A | N, N-Dinitroso Methotrexate EP Impurity L | Methotrexate EP Impurity H | Methotrexate EP Impurity J | Methotrexate EP Impurity L | N-Nitroso Methotrexate EP Impurity-B | Methotrexate EP Impurity F | Methotrexate Dimethylamide | Methotrexate Nitroso Impurity 1 | N-Dinitroso Methotrexate Impurity 2 | Methotrexate EP Impurity C | Methotrexate EP Impurity D | R-Methotrexate di sodium |

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