Search Results for " Almotriptan "
Almotriptan EP Impurity D (Oxalate)
| N° de SZ CAT: | SZ-A087003 |
| Número CAS | 1018676-03-3 |
| Mol.F. | C15H21N3O2S : C2H2O4 |
| Peso Molecular | 307.4 : 90.0 |
| Status de Fatura | Out of Stock, Synthesis on demand |
| Rel. CAS No | 181178-24-5 (free base) ; 1246860-79-6 (HCl salt) ; 1246860-78-5 (HBr salt) ; 1246860-65-0 (hemifumarate salt) |
Nome Químico: 2-[5-[(Pyrrolidine-1-sulfonyl)methyl]-1H-indol-3-yl]ethan-1-amine oxalate (as per EP) ; 2-{5-[(Pyrrolidin-1-ylsulfonyl)methyl]-1H-indol-3-yl}ethanamine oxalate (As per USP)
Sinônimo: Almotriptan USP Related Compound B ; Almotriptan Didesmethyl Impurity
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: NCCC1=CNC2=CC=C(C[S](=O)(N3CCCC3)=O)C=C12.O=C(O)C(O)=O
Almotriptan EP Impurity D (Oxalate) is chemically 2-[5-[(Pyrrolidine-1-sulfonyl)methyl]-1H-indol-3-yl]ethan-1-amine oxalate (as per EP) ; 2-{5-[(Pyrrolidin-1-ylsulfonyl)methyl]-1H-indol-3-yl}ethanamine oxalate (As per USP). It is also known as Almotriptan USP Related Compound B ; Almotriptan Didesmethyl Impurity. Almotriptan EP Impurity D (Oxalate) is supplied with detailed characterization data compliant with regulatory guideline. Almotriptan EP Impurity D (Oxalate) can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Almotriptan.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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