Table of Contents
- 1 What is the structure of methyl salicylate?
- 2 What is the Iupac name for methyl salicylate?
- 3 What is the mechanism of action of methyl salicylate formation?
- 4 How is methyl salicylate metabolized?
- 5 What is the condensed structural formula of ethanol?
- 6 What is the molar mass of methyl salicylate?
- 7 How do you make methyl salicylate?
- 8 What is the Iupac name of salol?
- 9 What products contain ester methyl salicylate?
- 10 What is the reaction between methanol and salicylic acid?
- 11 Is methyl salicylate alcohol?
What is the structure of methyl salicylate?
What is the Iupac name for methyl salicylate?
Methyl salicylate/IUPAC ID
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 In salicylic acid (on the right), the ester group has been replaced by a carboxylic acid group (-COOH).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 the mechanism of action of methyl salicylate formation?
Methyl salicylate is a salicylic acid derivative, and when combined with menthol, produces menthyl salicylate 6. Salicylates inhibit cyclooxygenase, thereby reducing the formation of prostaglandins, and cause platelet dysfunction Methyl salicylate is used topically as a counter-irritant.
How is methyl salicylate metabolized?
Minor metabolism may occur in various tissues but hepatic metabolism constitutes the majority of metabolic processes of absorbed methyl salicylate. It is mainly hydrolyzed to salicylic acid via hepatic esterase enzymes.
What is Salol structure?
What is the condensed structural formula of ethanol?
Classification of Alcohols
|Condensed Structural Formula||Class of Alcohol||Common Name|
|CH 3CH 2OH||primary||ethyl alcohol|
|CH 3CH 2CH 2OH||primary||propyl alcohol|
|(CH 3) 2CHOH||secondary||isopropyl alcohol|
|CH 3CH 2CH 2CH 2OH||primary||butyl alcohol|
What is the molar mass of methyl salicylate?
Methyl salicylate/Molar mass
How is methyl salicylate synthesis?
When salicylic acid is heated with methyl alcohol, the carboxyl group of salicylic acid is esterified producing a strong-smelling liquid ester (methyl salicylate). an alcohol and a carboxylic acid. The reaction is reversible and uses an acid as a catalyst.
How do you make methyl salicylate?
1) Dissolve 0.2 grams salicylic acid into 2.0 mL of methanol in a 5 mL round bottom flask. 2) Add 4-5 drops concentrated H2SO4 3) Add a few boiling chips to promote smooth boiling. 4) Reflux for 40 minutes. 5) After 40 minutes, remove and isolate product.
What is the Iupac name of salol?
|Preferred IUPAC name Phenyl 2-hydroxybenzoate|
|Other names Salol|
What is the formula of phenyl benzoate?
|Chemical Safety||Laboratory Chemical Safety Summary (LCSS) Datasheet|
|Synonyms||PHENYL BENZOATE 93-99-2 Benzoic acid phenyl ester Diphenylcarboxylate Benzoic acid, phenyl ester More…|
What products contain ester methyl salicylate?
Specific Products that Use Methyl Salicylate Bengay Icy Hot Cream Salonpas Pain Patch Analgesic Balm Adazin LidoPro Menthocin Patch with Lidocaine Soothee Patch Terocin Medrox
What is the reaction between methanol and salicylic acid?
When methyl salicylate is prepared from salicylic acid and methanol, an OH – is the leaving group from the salicylic acid. The presence of the acid provides a large amount of H+ ions to stabilize the leaving group to H2O , and speeds up the rate of the reaction .
Is methyl salicylate edible?
Methyl salicylate is essentially harmless in practice unless it is intentionally consumed at high concentrations. Edible substances containing wintergreen typically contain less than one percent, making it difficult for them to be sufficiently toxic.
Is methyl salicylate alcohol?
Methyl salicylate (oil of wintergreen ) is an organic ester. When an acid (containing the – COOH group) reacts with an alcohol (a compound containing an –OH group) formed an ester.