(1R-cis)-N-[2-amino-4-chloro-6-[[4-(hydroxymethyl)-2-cyclopenten-1-yl]amino]-5-pyrimidinyl]-formamide
Abacavir EP Impurity E 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.
Buy 208762-35-0 Purchase 208762-35-0 Order 208762-35-0 Enquire 208762-35-0 208762-35-0 price 208762-35-0 supplier 208762-35-0 manufacturer 208762-35-0 exporter Abacavir EP Impurity E for method validation Abacavir EP Impurity E reference standard Abacavir EP Impurity E for ANDA filing Abacavir EP Impurity E for forced degradation studies Abacavir EP Impurity E identification standard Abacavir EP Impurity E for DMF filing Abacavir EP Impurity E HPLC standard Abacavir EP Impurity E supplier Abacavir EP Impurity E manufacturer Abacavir EP Impurity E distributor
