SalbutaMolIMpurityN;5-[[5-[2-[(1,1-DiMethylethyl)aMino]-1-hydroxyethyl]-2-hydroxyphenyl]Methyl]-α1-[[(1,1-diMethylethyl)aMino]Methyl]-4-hydroxy-1,3-benzenediMethanol;SalbutaMolDiMer;4-(2-(tert-butylamino)-1-hydroxyethyChemicalbookl)-2-(5-(2-(tert-butylamino)-1-hydroxyethyl)-2-hydroxybenzyl)-6-(hydroxymethyl)phenol;SalbutamolEPImpurityN;SalbutamolImpurity13(SalbutamolEPImpurityN);SalbutamolSulfateEPImpurityN;SalbutamolEPImpurityN(AlbuterolDimer)
Salbutamol Impurity L is a critical reference standard for the quality control of the beta-2 adrenergic agonist Salbutamol. It typically arises from synthetic by-products during the manufacturing process or via degradation pathways. The compound is characterized by its specific molecular structure, often used to validate HPLC methods in pharmaceutical production.
Store under inert atmosphere at low temperatures to prevent degradation. Handle with appropriate PPE in a fume hood due to potential sensitization risks. Strictly limit exposure to clinical environments; this material is not for human administration but serves solely as a laboratory reagent.