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Applications
USP Rivaroxaban Assay and Organic Impurities - System Suitability Solution run on AgilentĀ® 1260
28024
Separation Mode: Reversed Phase
Reversed Phase
C18
HPLC
Pharmaceutical
Pharmaceutical
Therapeutic / Clinical

USP Rivaroxaban Assay and Organic Impurities - System Suitability Solution run on AgilentĀ® 1260

Analytes
1Related Compound B
2Related Compound D
3Related Compound G
4Rivaroxaban
5Related Compound J
Details
LC Conditions (App ID: 28024)
Column:
Brand Name:
Luna Omega
Part No:
Phase Name:
C18
System:
Agilent Technologies 1200 Series Agilent Technologies 1200 Series
Sample Note:
Solution B: 5.3mM sodium hexane sulfonate, 3.77mM phosphoric acid in water Diluent: Acetonitrile and solution B (40:60) System suitability solution: 0.5 mg/mL of USP Rivaroxaban RS and 0.5 Āµg/mL each of USP Rivaroxaban Related Compound B RS, USP Rivaroxaban Related Compound D RS, USP Rivaroxaban Related Compound G RS, and USP Rivaroxaban Related Compound J RS in Diluentā€‹ peak no. 1 analyte name: rivaroxaban related compound G RT (min): 14.099 conc.: 0.5ug/mL peak no. 2 analyte name: rivaroxaban RT (min): 15.66 conc.: 0.5mg/mL
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