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L-Menthol
[CAS# 2216-51-5]

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Complete supplier list of L-Menthol
Identification
Classification Flavors and spices >> Synthetic spice >> Alcoholic spice >> Alicyclic alcohol
Name L-Menthol
Synonyms L-p-Menthan-3-ol; (1R,2S,5R)-(-)-Menthol; (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol
Molecular Structure CAS # 2216-51-5, L-Menthol, L-p-Menthan-3-ol, (1R,2S,5R)-(-)-Menthol, (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol
Molecular Formula C10H20O
Molecular Weight 156.26
CAS Registry Number 2216-51-5
EC Number 218-690-9
FEMA 2665
SMILES C[C@@H]1CC[C@H]([C@@H](C1)O)C(C)C
Properties
Density 0.9±0.1 g/cm3, Calc.*, 0.89 g/mL (Expl.)
Melting point 41-44 ºC (Expl.)
Index of Refraction 1.457, Calc.*, 1.534 (Expl.)
Boiling Point 215.4±8.0 ºC (760 mmHg), Calc.*, 212 ºC (Expl.)
Flash Point 93.3 ºC, Calc.*, 93 ºC (Expl.)
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Serious eye damageEye Dam.1H318
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Acute toxicityAcute Tox.4H302
SDS Available
up Discovory and Applicatios
L-Menthol is a naturally occurring organic compound widely recognized for its distinct minty aroma and cooling sensation. It is an alcohol derived from mint plants, particularly peppermint (Mentha × piperita), and has been used for centuries in various cultural and medicinal applications. The compound is commonly found in essential oils and is a major component of peppermint oil, contributing to its characteristic fragrance and flavor.

The discovery of L-menthol can be traced to ancient times, where it was likely used in traditional remedies for its soothing properties. The isolation and identification of menthol as a distinct compound occurred in the 19th century, when scientists began to study the chemical makeup of essential oils. Its structure was determined to be a cyclic monoterpene alcohol, which explained its unique sensory properties, including its cooling effect when applied to the skin or mucous membranes.

L-Menthol has a variety of applications, both in the pharmaceutical and non-pharmaceutical industries. It is perhaps best known for its use in medicinal products, where it is employed for its analgesic, antispasmodic, and decongestant properties. Menthol is a common ingredient in topical creams and ointments designed to relieve muscle pain, minor aches, and the symptoms of conditions such as arthritis. When applied to the skin, menthol induces a cooling sensation, which provides a temporary relief from pain by acting as a counterirritant. This cooling effect is also useful in the treatment of sore throats and nasal congestion, where menthol is often included in throat lozenges, cough drops, and nasal inhalers to ease breathing and reduce discomfort.

In addition to its medicinal uses, L-menthol is a popular ingredient in a wide range of consumer products, including cosmetics, oral care products, and food and beverages. It is commonly used in toothpaste and mouthwashes due to its refreshing flavor and ability to mask unpleasant tastes, as well as its antibacterial properties. The compound is also utilized in chewing gum, confectionery, and beverages, where it imparts a minty flavor and is prized for its cooling sensation.

L-Menthol is also employed in the production of perfumes and air fresheners, where it enhances the fragrance profiles of various products. Its fresh, minty scent makes it a popular component in fragrances intended to evoke a clean, invigorating atmosphere. Moreover, menthol is used as a flavoring agent in some alcoholic beverages, such as mentholated liqueurs, and in some non-alcoholic beverages for its distinct taste.

Another key application of L-menthol is in the tobacco industry. It is often added to menthol cigarettes to impart a refreshing, cooling effect when smoked. Mentholated cigarettes have been marketed as a smoother alternative to regular tobacco cigarettes, and L-menthol plays a significant role in the sensory experience of smoking. Despite its popularity, mentholated cigarettes have been the subject of regulatory scrutiny due to health concerns associated with smoking.

The use of L-menthol is generally considered safe when applied in appropriate concentrations in consumer products. However, in high concentrations, menthol can cause skin irritation or mucous membrane discomfort. It is important for manufacturers to adhere to safety guidelines when incorporating menthol into products to ensure its proper use. Regulatory bodies, such as the U.S. Food and Drug Administration (FDA), have established limits on the amount of menthol that can be used in food, cosmetics, and pharmaceutical products to ensure consumer safety.

In conclusion, L-menthol is a versatile and widely used compound with a rich history and a broad range of applications. From its medicinal uses in topical creams and throat lozenges to its role in food, beverages, and cosmetics, L-menthol is valued for its cooling, refreshing properties. It continues to be an essential ingredient in numerous consumer products, owing to its ability to provide relief, enhance flavor, and improve the sensory experience.

References

2024. Field effectiveness of some essential oil emulsions against the whitefly Bemisia tabaci (GENN.) that infest potato plants in Egypt. Journal of Plant Diseases and Protection, 131(5).
DOI: 10.1007/s41348-024-00944-8

2024. Mentha spp. essential oils: toxicity to Alphitobius diaperinus, activity against poultry pathogenic bacteria, and Beauveria bassiana compatibility. Environmental science and pollution research international, 31(22).
DOI: 10.1007/s11356-024-33484-7

2024. Variability of the Constituent Composition of Mentha piperita L. Essential Oil. Pharmaceutical Chemistry Journal, 58(2).
DOI: 10.1007/s11094-024-03142-w
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