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Fórmula empírica (notación de Hill):
C12H22O2
Número CAS:
Peso molecular:
198.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-911-8
MDL number:
Assay:
97%
Form:
liquid
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Permítanos ayudarleInChI key
XHXUANMFYXWVNG-UHFFFAOYSA-N
InChI
1S/C12H22O2/c1-8(2)11-6-5-9(3)7-12(11)14-10(4)13/h8-9,11-12H,5-7H2,1-4H3
SMILES string
CC(C)C1CCC(C)CC1OC(C)=O
assay
97%
form
liquid
refractive index
n20/D 1.447 (lit.)
bp
228-229 °C (lit.)
density
0.922 g/mL at 25 °C (lit.)
functional group
ester
Quality Level
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General description
Menthyl acetate (MA), a monoterpene is one of the main constituent of the peppermint essential oil obtained from the leaves of Mentha piperita. It has been reported to show ambulation-promoting effect in mice. Its fumigant and repellent activity has been evaluated on first-instar nymphs of the bloodsucking bug Rhodnius prolixus. The decomposition of MA in an atmospheric flow reactor and a low-pressure flat flame has been investigated by molecular-beam mass spectrometry (MBMS).
Menthyl acetate is a monoterpene that is widely utilized as a flavoring agent in the food and beverage industry.
Menthyl acetate is a monoterpene that is widely utilized as a flavoring agent in the food and beverage industry.
Application
Menthyl acetate may be used in the preparation of 3-amino-2-hydroxyalkanoates via lithium amide-supported Mannich-type reaction of its lithium enolate with PMP-arylaldimines (PMP=p-methoxyphenyl) followed by in situ oxidation with oxaziridine.
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Asymmetric synthesis of 3-amino-2-hydroxyalkanoates by Mannich reaction of menthyl acetate with imines and subsequent oxidation.
Hata S and Tomioka K.
Tetrahedron, 63(35), 8514-8520 (2007)
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Journal of the Science of Food and Agriculture, 621-627 (2015)
T Umezu et al.
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The potential antifungal effects of Thymus vulgaris L., Thymus tosevii L., Mentha spicata L., and Mentha piperita L. (Labiatae) essential oils and their components against 17 micromycetal food poisoning, plant, animal and human pathogens are presented. The essential oils were
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A large number of cosmetics and topical pharmaceuticals contain compounds of natural origin. There is a rising concern if these compounds can interact with the activity of other topically applied components in these formulations. The current study demonstrates modulation of
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