(1R,2R)-2-Amino-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(pyrrolidin-1-yl)propan-1-ol
Eliglustat Impurity 12 is listed by Simson Pharma as a impurity standards for laboratory research, analytical development and quality-control workflows.
Suitability is method- and purpose-specific. Before use, verify the product name, catalogue number, chemical identifiers, storage requirements and the information reported in the current product or batch documentation. Your laboratory remains responsible for method qualification or validation.
Eliglustat Impurity 12 for method validation Eliglustat Impurity 12 reference standard Eliglustat Impurity 12 for ANDA filing Eliglustat Impurity 12 for forced degradation studies Eliglustat Impurity 12 identification standard Eliglustat Impurity 12 for DMF filing Eliglustat Impurity 12 HPLC standard Eliglustat Impurity 12 supplier Eliglustat Impurity 12 manufacturer Eliglustat Impurity 12 distributor
