It is the sodium salt of aspirin. The carboxyl group in aspirin (COOH) is converted to COONa. This molecule is water-soluble.
Aspirin. the pain killer
Product depends on reaction conditions and quantity of sodium hydroxide used in the reaction. Initially sticky product [sodium salt of methyl salicylate] will form that on heating will effect saponification [hydrolysis of ester] resulting in sodium salicyale.
its an ionic compound / polar
Methyl salicylate and buckminsterfullerene.
minty and also sort of like plastic
ferric salicylate(Violet colour compound) and HCL are made
Injection of sodium salicylate sodium iodide
You can turn sodium hydroxide into sodium salicylate by reacting it with salicylic acid.
Aspirin, sodium salicylate, choline salicylate, and magnesium salicylate
no, but it dissolves
Is a product :)
Product depends on reaction conditions and quantity of sodium hydroxide used in the reaction. Initially sticky product [sodium salt of methyl salicylate] will form that on heating will effect saponification [hydrolysis of ester] resulting in sodium salicyale.
Yes. It is a salt commonly used as a food additive.
salicylic acid is non polar and will not dissolve in water. However, it is soluble in sodium bicarbonate solution because an acid-base reaction occurs. Salicylic acid turns to a salt called sodium salicylate. Sodium salicylate is composed of a cat ion (Na+) and of an anion (salicylate ion). Because of the negative charge in the salicylate ion and the positive charge of Na+, water molecules in the sodium bicarbonate solution and from the reaction are attracted to these ions and eventually dissolve them.
its an ionic compound / polar
Antipyretic drugs are those that reduce fever. Ibuprofen, naproxen sodium, ketoprofen, aspirin, magnesium salicylate, sodium salicylate, paracetamol, acetaminophen, metamizole, nabumetone, nimesulide, phenazone and quinine are antipyretic drugs.
I personally think it does. I was performing an experiment in the lab with solubility patterns, where most of the organic compound (p-toluidine, benzoic acid, 2-napthol, glucose) dissolved and the sodium chloride did not. sodium chloride had the specific Na+ charged group which is also found in the sodium salicylate. Then again, my knowledge is limited and correct experimentation will yield the right answer. Source: Undergrad, life science, U of T.
Benzyl salicylate is an ester.