Doxylamine EP Impurity B is chemically (1RS)-1-phenyl-1-(pyridin-2-yl)ethan-1-ol (as per EP) ; 1-Phenyl-1-(pyridin-2-yl)ethan-1-ol (as per USP). It is also known as Doxylamine Alcohol (USP). Doxylamine EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Doxylamine EP Impurity B 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 Doxylamine.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. These products are for analytical purpose only and not for human use.
Poids
0,45 Kg (450 g)
Volume
0,0015 m³ (1500 cm³)
Largeur
0,1 m (10 cm)
Longueur
0,1 m (10 cm)
Hauteur
0,15 m (15 cm)
Les dimensions, le poids et le volume sont bruts (emballage inclus)
