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・ Mentzelia involucrata
・ Mentzelia laevicaulis
・ Mentzelia leucophylla
・ Mentzelia lindleyi
・ Mentzelia micrantha
・ Mentzelia mollis
・ Mentzelia montana
・ Mentzelia multiflora
・ Mentzelia nitens
・ Mentzelia oreophila
・ Mentha × gracilis
・ Mentheville
・ Menthidae
・ Menthofuran
・ Menthogen
Menthol
・ Menthol (data page)
・ Menthol cigarette
・ Mentholatum
・ Menthon-Saint-Bernard
・ Menthone
・ Menthonnex-en-Bornes
・ Menthonnex-sous-Clermont
・ Menthorpe
・ Menthorpe Gate railway station
・ Menthoxypropanediol
・ Menthyl acetate
・ Menthyl anthranilate
・ Menthyl isovalerate
・ Menti Nostrae


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Menthol : ウィキペディア英語版
Menthol

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Menthol is an organic compound made synthetically or obtained from corn mint, 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 (1''R'',2''S'',5''R'') 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 (1''R'',2''S'',5''R'') form (bottom left corner of the diagram below). The eight possible stereoisomers are:
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:

The (+)- and (–)-enantiomers of menthol are the most stable among these based on their cyclohexane conformations. With the ring itself in a chair conformation, all three bulky groups can orient in equatorial positions.
The two crystal forms for racemic menthol 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.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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