Young Journal of Thermal Analysis and Calorimetry volume 120, pages789–794 (2015) A chromatography-free synthesis of racemic salbutamol hemisulfate AgatheVanoostLaurentPetit Tetrahedron Letters Methods for the preparation of salbutamol (review) Methods of Synthesis and Technology of the Production of Drugs; Published: October 1991; Volume 25, pages 733–739 Synthesis of the impurity F of salbutamol
Abstract
The synthesis provides access to multi-gram quantities of impurity F with good purity for
In order to confirm the structures 2 and also provide an easy
It is known that there are some impurities that could be produced during synthesis or
First synthesis of the diastereomeric mixture of Salbutamol dimer (2) is
Mol
SARP and TARP impurities (1 mg mL −1), were prepared by dissolving 100 mg of the
Inv
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Salbutamol has rapid, potent, and long-lasting bronchodilating activity with only slight inotropic or chronotropic effects
It is known that there are some impurities that could be produced during synthesis or during storage of the drug
Therefore, API impurity profiling is becoming increasingly important, as impurities in APIs can compromise drug safety and quality []
CAS No 156547-62-5; 41489-89-8 Mol
Keywords: Salbutamol sulphate, Impurities, Synthesis, Isolation and Characterization Introduction Salbutamol sulphate is a relatively selective 2-adrenergic agonist and is used as a bronchodilator
Also known as 3-Dehydroxy Salbutamol having CAS No 18910-68-4, C13H21NO2, 223
It is used in Salbutamol impurity profiling as per limits and threshold values
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Salbutamol Glyoxal Impurity
Status : Custom Synthesis
solution
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