Search Results for " Baclofen "
Baclofen EP Impurity A Lactose Adduct
| SZ CAT No: | SZ-B050048 |
| CAS No | NA |
| Mol.F. | C22H30ClNO11 |
| Mol.Wt. | 519.9 |
| Inv. Status | Synthesis on demand |
Chemical Name: 4-(4-chlorophenyl)-1-((3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)pyrrolidin-2-one
Synonym: Baclofen USP Related Compound A Lactose Adduct
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: OC[C@H]1OC(N2C(CC(C3=CC=C(Cl)C=C3)C2)=O)[C@H](O)[C@@H](O)[C@@H]1O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4O
Baclofen EP Impurity A Lactose Adduct is chemically 4-(4-chlorophenyl)-1-((3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)pyrrolidin-2-one. It is also known as Baclofen USP Related Compound A Lactose Adduct. Baclofen EP Impurity A Lactose Adduct is supplied with detailed characterization data compliant with regulatory guideline. Baclofen EP Impurity A Lactose Adduct 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 Baclofen.
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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