Sumatriptan EP Impurity H

Product Name Sumatriptan EP Impurity H
Alternate Names Sumatriptan Impurities, Impurities of Sumatriptan
CAT No. CS-O-08217
CAS No. 1391052-59-7
Category Impurities
Stock IN-Stock
Mol. Wt. 495.7 g/mol
Mol. For. C27H37N5O2S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Sumatriptan
Purity Not specified
Therapeutic Anti-Migraines
Smileys CN(C)CCC1=CN(CC2=CC=C3C(C(CCN(C)C)=CN3)=C2)C4=CC=C(C[S](NC)(=O)=O)C=C14
Canonical Smiles CNS(=O)(=O)CC1=CC2=C(C=C1)N(C=C2CCN(C)C)CC3=CC4=C(C=C3)NC=C4CCN(C)C
InchIKey RFUHQZCKISNFJJ-UHFFFAOYSA-N
Inchl InChI=1S/C27H37N5O2S/c1-28-35(33,34)19-21-7-9-27-25(15-21)23(11-13-31(4)5)18-32(27)17-20-6-8-26-24(14-20)22(16-29-26)10-12-30(2)3/h6-9,14-16,18,28-29H,10-13,17,19H2,1-5H3
IUPAC 1-[3-[2-(dimethylamino)ethyl]-1-[[3-[2-(dimethylamino)ethyl]-1H-indol-5-yl]methyl]indol-5-yl]-N-methylmethanesulfonamide
Controlled No
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Sumatriptan EP Impurity H is a chemical compound that is used in the pharmaceutical industry as a reference standard and impurity in the synthesis of Sumatriptan, a medication used for the treatment of migraines and cluster headaches. This impurity is also known as N-(2-(Dimethylamino)ethyl)-N-methyl-2-(phenylsulfonyl)acetamide and is classified as a benzene sulfonamide derivative. Chemically, Sumatriptan EP Impurity H has a molecular formula of C16H23N3O3S and a molecular weight of 337.44 g/mol. It is a fine white or off-white crystalline powder that is soluble in organic solvents such as methanol, ethanol, and ethyl acetate. The usage of Sumatriptan EP Impurity H in the pharmaceutical industry is crucial for ensuring the quality and purity of Sumatriptan. It is used as a reference standard for the analytical method development, validation, and quality control of Sumatriptan. It is also used as an impurity in the synthesis of Sumatriptan to determine the purity of the final product. In conclusion, Sumatriptan EP Impurity H is an important chemical compound in the pharmaceutical industry that plays a critical role in the quality control and synthesis of Sumatriptan. Its chemical information and usage are essential for ensuring the safety and efficacy of Sumatriptan as a medication for the treatment of migraines and cluster headaches.

Related Compounds

N,N-Dinitroso Sumatriptan | Sumatriptan EP Impurity F | Sumatriptan EP Impurity G | Sumatriptan EP Impurity B HCl salt | Sumatriptan Impurity 3 | Sumatriptan degradation impurity | Sumatriptan 3-Hydroxy-2-Oxo Impurity | Sumatriptan Aminophenyl Impurity | Sumatriptan EP Impurity D | Sumatriptan EP Impurity B | Sumatriptan EP Impurity C | Sumatriptan Hydrazine Impurity | Sumatriptan EP Impurity B HCl Salt | N-Nitroso sumatriptan | Sumatriptan N-Nitroso impurity | Sumatriptan EP Impurity E | N-Nitroso Desmethyl Sumatriptan impurity | Sumatriptan Succinate Related Compound C | Sumatriptan Succinate impurity II | Sumatriptan Succinate Related Compound A | Sumatriptan EP Impurity A | Sumatriptan C Dimer | Sumatriptan impurity 1 | Methyl (4-Nitrophenyl)methanesulfonate |

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