Menthol

Not to be confused with methanol.

Menthol
(-)-Menthol	(-)-Menthol
File:Menthol.jpg
IUPAC name (1R,2S,5R)-2-isopropyl-5-methylcyclohexanol
Other names 3-p-Menthanol, Hexahydrothymol, Menthomenthol, peppermint camphor
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers
CAS number	89-78-1 Y
ChemSpider	15803
RTECS number	OT0350000, racemic
SMILES
style="background: #F8EABA; text-align: center;" colspan="2" | Properties
Molecular formula	C10H20O
Molar mass	156.27 g mol−1
Appearance	White or colorless crystalline solid
Density	0.890 g·cm−3, solid (racemic or (−)-isomer)
Melting point	36–38 °C (311 K), racemic 42–45 °C (318 K), (−)-form (α) 35-33-31 °C, (−)-isomer
Boiling point	212 °C (485 K)
Solubility in water	Slightly soluble, (−)-isomer
style="background: #F8EABA; text-align: center;" colspan="2" | Hazards
MSDS	External MSDS
R-phrases	R37/38, R41
S-phrases	S26, S36
Flash point	93 °C
style="background: #F8EABA; text-align: center;" colspan="2" | Related compounds
Related alcohols	Cyclohexanol, Pulegol, Dihydrocarveol, Piperitol
Related compounds	Menthone, Menthene, Thymol, p-Cymene, Citronellal
Y (what is this?)  (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Menthol is an organic compound made synthetically or obtained from peppermint or other mint oils. 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 has local anesthetic and counterirritant qualities, and it is widely used to relieve minor throat irritation. Menthol also acts as a weak kappa Opioid receptor agonist.

Structure

Natural menthol exists as one pure stereoisomer, nearly always the (1R,2S,5R) form (bottom left corner of the diagram below). The other seven stereoisomers are:

Structures of menthol isomers

In the natural compound, the isopropyl group is in the trans orientation to both the methyl and hydroxyl groups. Thus it can be drawn in any of the ways shown:

Menthol chair conformation

In the ground state all three bulky groups in the chair are equatorial, making (−)-menthol and its enantiomer the most stable two isomers out of the eight.

There are two crystal forms for racemic menthol; these have melting points of 28 °C and 38 °C. Pure (−)-menthol has four crystal forms, of which the most stable is the α form, the familiar broad needles.

Biological properties

Menthol's ability to chemically trigger the cold-sensitive TRPM8 receptors in the skin is responsible for the well known cooling sensation that it provokes when inhaled, eaten, or applied to the skin. In this sense it is similar to capsaicin, the chemical responsible for the spiciness of hot peppers (which stimulates heat sensors, also without causing an actual change in temperature).

Menthol has analgesic properties that are mediated through a selective activation of κ-opioid receptors. Menthol also enhances the efficacy of ibuprofen in topical applications via vasodilation, which reduces skin barrier function.

Occurrence

Mentha arvensis is the primary species of mint used to make natural menthol crystals and natural menthol flakes. This species is primarily grown in the Uttar Pradesh region in India.

(−)-Menthol (also called l-menthol or (1R,2S,5R)-menthol) occurs naturally in peppermint oil (along with a little menthone, the ester menthyl acetate and other compounds), obtained from Mentha x piperita. Japanese menthol also contains a small percentage of the 1-epimer, (+)-neomenthol.

Biosynthesis of menthol was investigated in M. x piperita, and all enzymes involved in its biosynthesis have been identified and characterized.

Production

As with many widely-used natural products, the demand for menthol greatly exceeds the supply from natural sources. Menthol is manufactured as a single enantiomer (94% ee) on the scale of 3,000 tons per year by Takasago International Corporation. The process involves an asymmetric synthesis developed by a team led by Ryoji Noyori: <imagemap> Image:Menthol synthesis.png|

rect 6 14 131 92 myrcene rect 136 46 201 63 diethylamine rect 468 110 628 180 citronellal rect 387 112 458 135 zinc bromide

desc bottom-left

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The process begins by forming an allylic amine from myrcene, which undergoes asymmetric isomerisation in the presence of a BINAP rhodium complex to give (after hydrolysis) enantiomerically pure R-citronellal. This is cyclised by a carbonyl-ene-reaction initiated by zinc bromide to isopulegol which is then hydrogenated to give pure (1R,2S,5R)-menthol.

Racemic menthol can be prepared simply by hydrogenation of thymol, and menthol is also formed by hydrogenation of pulegone.

Applications

Menthol is included in many products for a variety of reasons. These include:

• In non-prescription products for short-term relief of minor sore throat and minor mouth or throat irritation
  • Examples: lip balms and cough medicines
• As an antipruritic to reduce itching
• As a topical analgesic to relieve minor aches and pains such as muscle cramps, sprains, headaches and similar conditions, alone or combined with chemicals like camphor, eucalyptus oil or capsaicin. In Europe it tends to appear as a gel or a cream, while in the US patches and body sleeves are very frequently used
  • Examples: Tiger Balm, or IcyHot patches or knee/elbow sleeves
• In decongestants for chest and sinuses (cream, patch or nose inhaler)
  • Examples: Vicks Vaporub, Mentholatum
• In certain medications used to treat sunburns, as it provides a cooling sensation (then often associated with aloe)
• As an additive in certain cigarette brands, for flavor, to reduce the throat and sinus irritation caused by smoking.
• Commonly used in oral hygiene products and bad-breath remedies like mouthwash, toothpaste, mouth and tongue-spray, and more generally as a food flavor agent; e.g. in chewing gum, candy
• In a soda to be mixed with water to obtain a very low alcohol drink or pure (brand Ricqlès which contains 80% alcohol in France). The alcohol is also used to alleviate nausea, in particular motion sickness, by pouring a few drops on a lump of sugar.
• As a pesticide against tracheal mites of honey bees
• In perfumery, menthol is used to prepare menthyl esters to emphasize floral notes (especially rose)
• In first aid products such as "mineral ice" to produce a cooling effect as a substitute for real ice in the absence of water or electricity (Pouch, Body patch/sleeve or cream)
• In various patches ranging from fever-reducing patches applied to children's foreheads to "foot patches" to relieve numerous ailments (the latter being much more frequent and elaborate in Asia, especially Japan: some varieties use "functional protrusions", or small bumps to massage ones feet as well as soothing them and cooling them down)
• In some beauty products such as hair-conditioners, based on natural ingredients (e.g. St. Ives)

In organic chemistry, menthol is used as a chiral auxiliary in asymmetric synthesis. For example, sulfinate esters made from sulfinyl chlorides and menthol can be used to make enantiomerically pure sulfoxides by reaction with organolithium reagents or Grignard reagents. Menthol reacts with chiral carboxylic acids to give diastereomic menthyl esters, which are useful for chiral resolution.

Reactions

Menthol reacts in many ways like a normal secondary alcohol. It is oxidised to menthone by oxidising agents such as chromic acid or dichromate, though under some conditions the oxidation can go further and break open the ring. Menthol is easily dehydrated to give mainly 3-menthene, by the action of 2% sulfuric acid. PCl₅ gives menthyl chloride.

Reactions of menthol

History

There is evidence that menthol has been known in Japan for more than 2000 years, but in the West it was not isolated until 1771, by Hieronymus David Gaubius. Early characterizations were done by Oppenheim, Beckett, Moriya, and Atkinson.

Compendial status

• United States Pharmacopeia 23
• Japanese Pharmacopoeia 15
• Food Chemical Codex

Toxicology and MSDS data

Currently no reported nutrient or herb interactions involve menthol. (−)-Menthol has low toxicity: Oral (rat) LD₅₀: 3300 mg/kg; Skin (rabbit) LD₅₀: 15800 mg/kg.

Further reading

• E. E. Turner, M. M. Harris, Organic Chemistry, Longmans, Green & Co., London, 1952.
• Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
• The Merck Index, 7th edition, Merck & Co, Rahway, New Jersey, USA, 1960.
• Perfumer & Flavorist, December, 2007, Vol. 32, No.12, Pages 38–47

See also

• Camphor
• Menthol cigarettes
• Pulegone
• Vaporizer
• Vapor pressure

External links

• Colacot T. J. Platinum Metals Review 2002, 46(2), 82-83.
• Ryoji Noyori Nobel lecture (2001)
• Menthol Information
• Cooler than Menthol
• A review of menthol from the Science Creative Quarterly

ar:منثول