Salbutamol EP Impurity C, also known as Salbutamol BP Impurity C; Levalbuterol Related Compound B; Albuterol Related Compound A, in various pharmacopoeias, is a highly characterized standard. It meets strict regulatory requirements set by USP, EMA, JP, and BP, making it a crucial component in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Salbutamol/ Levalbuterol. Salbutamol EP Impurity C / Salbutamol BP Impurity C / Albuterol Related Compound A / Levalbuterol Related Compound B / Salbutamol Deshydroxy Impurity (CAS No: 18910-68-4) or 4-(2-(tert-butylamino)-1-hydroxyethyl)-2-methylphenol, is formulated as a racemic mixture of the R- and S-isomers and a moderately selective beta(2)-receptor agonist that is used to treat asthma, bronchitis, COPD.
References
Lavorini, Federico, et al. Clinical and Functional Responses to Salbutamol Inhaled via Different Devices in Asthmatic Patients with Induced Bronchoconstriction.†British Journal of Clinical Pharmacology, vol. 58, no. 5, Nov. 2004, pp. 512–20, https://doi.org/10.1111/j.1365-2125.2004.02185.x.
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