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Roxithromycin EP Impurity I

N° de SZ CAT:SZ-R023007
Número CAS425365-66-8
Mol.F.C45H84N2O17
Peso Molecular925.2
Status de FaturaCustom Synthesis

Nome Químico: 2'-0-[(2-methoxyethoxy) methyl] erythromycin 9-(E)-[0-[(2- methoxy ethoxy) methyl] oxime]

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C(O[C@H](CC)[C@@](C)(O)[C@H](O)[C@H]/1C)[C@H](C)[C@](O[C@@]2([H])C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)([H])[C@H](C)[C@@H](O[C@@]3([H])[C@H](OCOCCOC)[C@@H](N(C)C)C[C@@H](C)O3)[C@](C)(O)C[C@@H](C)C1=N/OCOCCOC

Roxithromycin EP Impurity I is chemically 2'-0-[(2-methoxyethoxy) methyl] erythromycin 9-(E)-[0-[(2- methoxy ethoxy) methyl] oxime]. Roxithromycin EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Roxithromycin EP Impurity I 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 Roxithromycin.

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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