The main impurties are probably the unreacted reactants. i.e salicylic acid and some acetic anhydride (ethanoic anhydride)
What is the effect of impurity of aspirin in humans body
yes
unreacted salicylic acid
Pyridine is used in the synthesis of aspirin as a catalyst to help facilitate the esterification reaction between salicylic acid and acetic anhydride. Its basic properties help neutralize the acidic byproducts formed during the reaction, which improves the yield of aspirin. Additionally, pyridine can also help dissolve the reactants and promote the formation of the desired product.
Phosphoric acid is used in the synthesis of aspirin as a catalyst to facilitate the esterification reaction between salicylic acid and acetic anhydride. It helps increase the reaction rate and yield of aspirin.
No, aspirin synthesis is not an esterification reaction. It involves the reaction of salicylic acid with acetic anhydride to form acetylsalicylic acid (aspirin) and acetic acid through an acetylation reaction. Esterification typically involves the reaction of an alcohol with a carboxylic acid to form an ester.
Synthesis of acetyl chloride via the reaction of acetic acid with sulphuric acid
Aspirin (acetyl salycilic acid) is prepared from salycilic acid and acetic anhydride; salicylic acid is prepared from sodium phenoxide and carbon dioxide (Kolbe synthesis).
Certain Eicosanoids--M.S. Exercise Physiology
if dissolved in water, it can be called an impurity.
During the synthesis of aspirin, the bonds that break are the ester bonds in acetic anhydride and salicylic acid. New bonds that form are ester bonds between the acetyl group and the hydroxyl group of salicylic acid to produce aspirin.
Aspirin (acetlysalicylic acid) is an irreversible inhibitor of the cyclo-oxygenase (COX-I and COX-II) enzymes which are responsible for the conversion of arachidonic acid into the prostaglandins. It is supposed that this happens due to the acetylation effects of aspirin.