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Roxithromycin EP Impurity G

Roxithromycin EP Impurity G Watermark

Roxithromycin EP Impurity G

SZ CAT No:CL-RTC-02
CAS No:425365-64-6
Mol.F:C42H78N2O16
Mol.Wt.:867.1
Chemical Name:(3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-((((2-methoxyethoxy)methoxy)methoxy)imino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one
SMILES: CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C(=N\OCOCOCCOC)/[C@H](C)[C@@H](O)[C@]1(C)O
Inventory Status:Custom synthesis

This impurity is related to Roxithromycin EP Impurity G is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.

Roxithromycin EP Impurity G is used as a reference standard in analytical research. It ensures consistency of formulations.

Chemical Name:(3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-((((2-methoxyethoxy)methoxy)methoxy)imino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one
Country of Origin: India
Product Category: Impurity Reference Standard
API NAME: Roxithromycin
Molecular Formula: C42H78N2O16
Molecular Weight: 867.1
Storage: Store in a cool, dry place.

product
Roxithromycin EP Impurity G
Qty: -, Pack Size: -, Total Qty: -(mg)
CAT No:CL-RTC-02
CAS No:425365-64-6
Mol.F:C42H78N2O16
Mol.Wt:867.1
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