What is the structure of methyl salicylate?

What is the structure of methyl salicylate?

Methyl salicylate/Formula

What does methyl salicylate look like?

It is the methyl ester of salicylic acid. It is a colorless, viscous liquid with a sweet, fruity odor reminiscent of root beer, but often associatively called “minty”, as it is an ingredient in mint candies.

What is the functional group of methyl salicylate?

In methyl salicylate (on the left) the benzene ring is substituted by two functional groups, a hydroxyl group (-OH) and an ester group (-COOCH3). In salicylic acid (on the right), the ester group has been replaced by a carboxylic acid group (-COOH).

What is structure of aspirin?


What is Salol structure?

Phenyl salicylate/Formula

What is the Colour of methyl salicylate?

Methyl salicylate is a liquid methyl ester of salicylic acid with a distinct characteristic odor. It is colorless or light pale in color, and commonly known as synthetic oil of wintergreen (made from the distillation of wintergreen leaves).

Is methyl salicylate the same as aspirin?

Methyl salicylate, if ingested, is very poisonous. Although aspirin is acetyl salicylate that is structurally close to methyl salicylate, after ingestion it is rapidly broken down into salicylic acid by blood and liver esterase; very little methyl salicylate is broken down to salicylic acid by the esterase in blood.

What is the appearance of salicylic acid?

Salicylic acid

Chemical formula C7H6O3
Molar mass 138.122 g/mol
Appearance Colorless to white crystals
Odor Odorless

What functional groups are in aspirin?

The common name of aspirin is acetylsalicylic acid and its IUPAC name is 2-Acetoxybenzoic acid. Between ester and carboxylic acid functional groups the highest priority functional group is carboxylic acid. Hence, in aspirin carboxylic acid is the principal functional group. Therefore, the correct option is B, -COOH.

What are the functional groups in salicylic acid?

The salicylic acid starting material has two unique functional groups: a carboxylic acid and a phenol.

What is the chemical formula for methyl salicylate?

Methyl salicylate PubChem CID 4133 Structure Find Similar Structures Chemical Safety Laboratory Chemical Safety Summary (LCSS Molecular Formula C8H8O3 Synonyms methyl salicylate Methyl 2-hydroxybenzoa

How is methyl salicylate used in everyday life?

The compound was first extracted and isolated from plant species Gaultheria procumbens in 1843. It can be manufactured synthetically and it used as a fragrance, in foods, beverages, and liniments. It forms a colorless to yellow or reddish liquid and exhibits a characteristic odor and taste of wintergreen.

Where does the COOH group of salicylic acid come from?

The COOH group of salicylic acid is esterified with methanol (CH3OH) in methyl salicylate (winter green oil), while the acid portion of the ester in acetylsalicylic acid (aspirin) is acetic acid, and salicylic acid contributes to the phenolic −OH community. Where does methyl salicylate come from? This is a derivative of salicylic acid.

How does menthol and methyl salicylate work together?

Methyl salicylate and menthol work in coordination by making the skin feel warm and cool. Such feelings on the skin distract individuals from the feelings of pains and ache of the joints and muscles. Wintergreen oil uses do not end there.