The Neomycin Sulfate System Suitability Mixture is a composite USP reference material comprising defined proportions of neomycin components. It is used to assess the resolution and performance of chromatographic systems during neomycin analysis. This standard ensures assay reproducibility and accuracy in pharmaceutical quality control environments.
The USP biologics antibiotics category includes a wide range of antimicrobial agents that are essential in treating bacterial infections. These antibiotics are derived from various natural sources or synthesized to combat specific pathogens effectively. The USP provides comprehensive standards, reference materials, and analytical procedures to ensure the identity, quality, purity, and consistency of antibiotic therapeutics throughout their lifecycle.
The United States Pharmacopeia (USP) provides quality standards for biologics to ensure their safety, efficacy, and quality throughout the manufacturing process. These standards assist manufacturers in adhering to regulatory requirements and help safeguard public health by reducing risks associated with biologics.
| MDL number | MFCD00037007 |
|---|---|
| UNSPSC Code | 41116107 |
| NACRES | NA.24 |
| SMILES string | [S](=O)(=O)(O)O.N[C@H]1[C@H](O[C@H]([C@H]([C@@H]1O)O)CN)O[C@@H]2[C@H](O[C@H]([C@@H]2O)O[C@H]3[C@@H]([C@H](C[C@H]([C@@H]3O)N)N)O[C@H]4O[C@@H]([C@H]([C@@H]([C@H]4N)O)O)CN)CO |
| InChI | 1S/C23H46N6O13.H2O4S/c24-2-7-13(32)15(34)10(28)21(37-7)40-18-6(27)1-5(26)12(31)20(18)42-23-17(36)19(9(4-30)39-23)41-22-11(29)16(35)14(33)8(3-25)38-22;1-5(2,3)4/h5-23,30-36H,1-4,24-29H2;(H2,1,2,3,4)/t5-,6+,7-,8+,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+;/m1./s1 |
| InChI key | OIXVKQDWLFHVGR-WQDIDPJDSA-N |
| API family | neomycin |
| form | solid |
| manufacturer/tradename | USP |
| web metadata keyword.default | USP Biologics |
| application(s) | USP Biologicspharmaceutical (small molecule) |
| format | neat |
| storage temp. | −20°C |
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