Amoxicillin EP Impurity L
| VS CAT No | VS-A025013 |
| CAS No | 1789703-32-7 |
| Mol.F. | C24H29N5O7S2 |
| Mol.Wt. | 563.6 |
| Inv. Status | Custom Synthesis |
Chemical Name: (2S,5R,6R)-6-[[(2S,5R,6R)-6-[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid (as per EP)
Synonym: 6-APA Amoxicillin Amide ; Amoxicillin Related Compound L
Shipping Temperature: Ambient
Country of Origin: India
Smiles: O=C([C@@H](C(C)(C)S[C@]1([H])[C@@H]2NC([C@@H](C(C)(C)S[C@]3([H])[C@@H]4NC([C@H](N)C5=CC=C(O)C=C5)=O)N3C4=O)=O)N1C2=O)O
Amoxicillin EP Impurity L is chemically (2S,5R,6R)-6-[[(2S,5R,6R)-6-[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid (as per EP). It is also known as 6-APA Amoxicillin Amide ; Amoxicillin Related Compound L. Amoxicillin EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Amoxicillin EP Impurity L 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 Amoxicillin.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. Vsquare products are for analytical purpose only and not for human use.