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422770

Menthyl acetate

97%

Synonym(s):

(±)-Menthol acetate, (±)-Menthyl acetate, dl-Menthyl acetate

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$72.76

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$174.25

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About This Item

Empirical Formula (Hill Notation):
C12H22O2
CAS Number:
Molecular Weight:
198.30
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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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

SMILES string

CC(C)C1CCC(C)CC1OC(C)=O

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

Inchi Key

XHXUANMFYXWVNG-UHFFFAOYSA-N

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1 of 4

This Item
45997484431166170
assay

97%

assay

≥99.9% (GC)

assay

≥99.5%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

refractive index

n20/D 1.447 (lit.)

refractive index

n20/D 1.361 (lit.), n20/D 1.362

refractive index

n20/D 1.402 (lit.)

refractive index

n20/D 1.541 (lit.)

bp

228-229 °C (lit.)

bp

57-58 °C (lit.)

bp

145-146 °C (lit.)

bp

265 °C (lit.)

density

0.922 g/mL at 25 °C (lit.)

density

0.934 g/mL at 25 °C

density

0.970 g/mL at 25 °C (lit.)

density

1.057 g/mL at 25 °C

form

liquid

form

-

form

-

form

powder

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.[1][2][3] It has been reported to show ambulation-promoting effect in mice.[4] Its fumigant and repellent activity has been evaluated on first-instar nymphs of the bloodsucking bug Rhodnius prolixus.[5] 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.[6]

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.[7]

pictograms

Environment

hcodes

pcodes

Hazard Classifications

Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup


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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)
Kinetic studies of methyl acetate pyrolysis and oxidation in a flow reactor and a low-pressure flat flame using molecular-beam mass spectrometry.
Yang X, et al.
Proceedings of the Combustion Institute, 35(1), 491-498 (2015)
T Umezu et al.
Pharmacology, biochemistry, and behavior, 69(3-4), 383-390 (2001-08-18)
Various plant-derived essential oils (EOs) have traditionally been used in the treatment of mental disorders, despite a lack of scientific evidence. In a previous study, we demonstrated that certain EOs possess behavioral effects, a finding that supports our original hypotheses
V Sfara et al.
Journal of medical entomology, 46(3), 511-515 (2009-06-06)
The aim of this study was to evaluate the fumigant and repellent activity of five essential oils (from eucalyptus, geranium, lavender, mint, and orange oil) and seven monoterpenes (eucalyptol, geraniol, limonene, linalool, menthone, linalyl acetate, and menthyl acetate) on first-instar
A review on peppermint oil.
Alankar, S.
Asian Journal of Pharmaceutical and Clinical Research, 2(2), 27-33 (2009)

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