Menthol: Difference between revisions

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'''Menthol''' is a natural compound obtained from [[mint]] oils or produced synthetically. It has a characteristic minty smell and cooling sensation, and is widely used in [[cosmetics]], [[food]], and [[medicine]] for its therapeutic properties.
{{Short description|Organic compound used as flavoring and in medicinal applications}}


== History ==
[[File:Mentholisomere.svg|thumb|right|Menthol isomers]]
Menthol was first isolated from [[peppermint]] oil in 1771 by Hieronymus David Gaubius. It was initially used in the treatment of [[gastrointestinal]] disorders, but its uses have since expanded to include a wide range of applications in [[pharmaceuticals]] and [[cosmetics]].
[[File:Menthol_structures.svg|thumb|left|Menthol structures]]


== Properties ==
'''Menthol''' is an organic compound made synthetically or obtained from the oils of corn mint, peppermint, or other mints. It is a waxy, crystalline substance, clear or white in color, which is solid at room temperature and melts slightly above. The main form of menthol occurring in nature is (−)-menthol, which is assigned the (1R,2S,5R) configuration.
Menthol is a waxy, crystalline substance that is clear or white in color. It is soluble in [[alcohol]] and [[propylene glycol]], but not in [[water]]. It has a melting point of 31-36 degrees Celsius.


== Uses ==
==Chemical Structure and Properties==
Menthol is used in a variety of products for its cooling and soothing properties. It is a common ingredient in [[cough drops]], [[toothpaste]], and [[pain relief]] creams. It is also used in [[cigarettes]] to provide a minty flavor and reduce the harshness of the smoke.
Menthol is a [[terpene]] alcohol with the chemical formula C<sub>10</sub>H<sub>20</sub>O. It has three asymmetric carbon atoms in the cyclohexane ring, which allows for the existence of eight stereoisomers. The most common isomer in nature is (−)-menthol, which has a specific configuration that contributes to its characteristic cooling sensation.


== Health effects ==
[[File:Menthol-from-xtal-1999-chair-3D-balls.png|thumb|right|Menthol 3D structure]]
Menthol has been shown to have analgesic, antipruritic, and anti-irritant effects. It is used in [[medicine]] to soothe sore throats, reduce inflammation, and relieve minor aches and pains. However, it can also cause skin irritation and allergic reactions in some people.


== See also ==
Menthol is known for its ability to trigger the cold-sensitive TRPM8 receptors in the skin, which is why it is often used in products designed to provide a cooling sensation.
* [[Mint (plant)]]
* [[Peppermint]]
* [[Eucalyptus oil]]
* [[Camphor]]


== References ==
==Sources and Production==
<references />
Menthol can be extracted from [[mint]] oils, such as peppermint oil, or it can be synthesized. The synthetic production of menthol involves several chemical processes, including the Haarmann-Reimer process, which is a well-known method for industrial synthesis.


[[Category:Monoterpenes]]
[[File:Haarmann-Reimer_process.svg|thumb|left|Haarmann-Reimer process]]
[[Category:Cooling flavors]]
[[Category:Herbs]]
[[Category:Medicinal plants]]
[[Category:Pharmaceuticals]]


{{stub}}
===Natural Sources===
<gallery>
Menthol is primarily obtained from the essential oils of mint plants, particularly peppermint (''Mentha piperita'') and corn mint (''Mentha arvensis''). These plants are cultivated in various regions around the world, with India being one of the largest producers of natural menthol.
File:Mentholisomere.svg|Menthol isomers
 
File:Menthol structures.svg|Menthol structures
===Synthetic Production===
File:Menthol-from-xtal-1999-chair-3D-balls.png|Menthol 3D structure
Synthetic menthol is produced through several methods, including the hydrogenation of thymol and the Haarmann-Reimer process. These methods allow for the large-scale production of menthol to meet global demand.
File:Menthol Crystals close up.jpg|Menthol crystals close up
 
File:Menthol crystals.jpg|Menthol crystals
[[File:Menthol_synthesis.png|thumb|right|Menthol synthesis]]
File:Menthol biosynthesis image.gif|Menthol biosynthesis
 
File:Menthol synthesis.png|Menthol synthesis
==Applications==
File:Haarmann-Reimer process.svg|Haarmann-Reimer process
Menthol is widely used in various applications due to its cooling properties and pleasant aroma. It is a common ingredient in [[oral hygiene]] products, [[cough drops]], [[topical analgesics]], and [[flavoring]] agents in food and beverages.
File:Menthol reactions.png|Menthol reactions
 
</gallery>
===Medicinal Uses===
<gallery>
In medicine, menthol is used as a topical analgesic to relieve minor aches and pains. It is also used in [[cough suppressant]]s and [[decongestant]]s due to its ability to provide a cooling sensation and relieve throat irritation.
File:Menthol Crystals.JPG|Menthol Crystals
 
File:Menthol crystals.jpg|Menthol Crystals
===Flavoring and Fragrance===
File:Mentholisomere.svg|Menthol Isomers
Menthol is used as a flavoring agent in [[chewing gum]], [[candy]], and [[toothpaste]]. Its refreshing aroma makes it a popular choice in [[perfumes]] and [[cosmetics]].
File:Menthol structures.svg|Menthol Structures
 
File:Menthol-from-xtal-1999-chair-3D-balls.png|Menthol 3D Structure
==Biosynthesis==
File:Menthol Crystals close up.jpg|Menthol Crystals Close Up
The biosynthesis of menthol in plants involves several enzymatic steps starting from [[geranyl diphosphate]], a common precursor in the biosynthesis of monoterpenes.
File:Menthol crystals.jpg|Menthol Crystals
 
File:Menthol biosynthesis image.gif|Menthol Biosynthesis
[[File:Menthol_biosynthesis_image.gif|thumb|left|Menthol biosynthesis]]
File:Menthol synthesis.png|Menthol Synthesis
 
File:Haarmann-Reimer process.svg|Haarmann-Reimer Process
==Physical Properties==
File:Menthol reactions.png|Menthol Reactions
Menthol is a crystalline substance that is solid at room temperature. It has a melting point of approximately 36 °C (97 °F) and a boiling point of 212 °C (414 °F). It is slightly soluble in water but highly soluble in organic solvents such as alcohol and ether.
</gallery>
 
[[File:Menthol_Crystals_close_up.jpg|thumb|right|Menthol crystals close up]]
[[File:Menthol_crystals.jpg|thumb|left|Menthol crystals]]
 
==Related Pages==
* [[Mint (herb)]]
* [[Essential oil]]
* [[Terpene]]
* [[Cooling sensation]]
 
[[Category:Terpenes]]
[[Category:Flavoring agents]]
[[Category:Analgesics]]

Latest revision as of 11:23, 23 March 2025

Organic compound used as flavoring and in medicinal applications


Menthol isomers
Menthol structures

Menthol is an organic compound made synthetically or obtained from the oils of corn mint, peppermint, or other mints. It is a waxy, crystalline substance, clear or white in color, which is solid at room temperature and melts slightly above. The main form of menthol occurring in nature is (−)-menthol, which is assigned the (1R,2S,5R) configuration.

Chemical Structure and Properties[edit]

Menthol is a terpene alcohol with the chemical formula C10H20O. It has three asymmetric carbon atoms in the cyclohexane ring, which allows for the existence of eight stereoisomers. The most common isomer in nature is (−)-menthol, which has a specific configuration that contributes to its characteristic cooling sensation.

Menthol 3D structure

Menthol is known for its ability to trigger the cold-sensitive TRPM8 receptors in the skin, which is why it is often used in products designed to provide a cooling sensation.

Sources and Production[edit]

Menthol can be extracted from mint oils, such as peppermint oil, or it can be synthesized. The synthetic production of menthol involves several chemical processes, including the Haarmann-Reimer process, which is a well-known method for industrial synthesis.

File:Haarmann-Reimer process.svg
Haarmann-Reimer process

Natural Sources[edit]

Menthol is primarily obtained from the essential oils of mint plants, particularly peppermint (Mentha piperita) and corn mint (Mentha arvensis). These plants are cultivated in various regions around the world, with India being one of the largest producers of natural menthol.

Synthetic Production[edit]

Synthetic menthol is produced through several methods, including the hydrogenation of thymol and the Haarmann-Reimer process. These methods allow for the large-scale production of menthol to meet global demand.

File:Menthol synthesis.png
Menthol synthesis

Applications[edit]

Menthol is widely used in various applications due to its cooling properties and pleasant aroma. It is a common ingredient in oral hygiene products, cough drops, topical analgesics, and flavoring agents in food and beverages.

Medicinal Uses[edit]

In medicine, menthol is used as a topical analgesic to relieve minor aches and pains. It is also used in cough suppressants and decongestants due to its ability to provide a cooling sensation and relieve throat irritation.

Flavoring and Fragrance[edit]

Menthol is used as a flavoring agent in chewing gum, candy, and toothpaste. Its refreshing aroma makes it a popular choice in perfumes and cosmetics.

Biosynthesis[edit]

The biosynthesis of menthol in plants involves several enzymatic steps starting from geranyl diphosphate, a common precursor in the biosynthesis of monoterpenes.

File:Menthol biosynthesis image.gif
Menthol biosynthesis

Physical Properties[edit]

Menthol is a crystalline substance that is solid at room temperature. It has a melting point of approximately 36 °C (97 °F) and a boiling point of 212 °C (414 °F). It is slightly soluble in water but highly soluble in organic solvents such as alcohol and ether.

File:Menthol Crystals close up.jpg
Menthol crystals close up
File:Menthol crystals.jpg
Menthol crystals

Related Pages[edit]