Menthyl Acetate

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pd_proNo:486630-91c9a88f-c2d6-4a0d-89b5-9faea95a7b4c

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Detailed introduction

Good factory supply good Menthyl Acetate 89-48-5

  • Molecular Formula:C12H22O2
  • Molecular Weight:198.305
  • Vapor Pressure:0.0707mmHg at 25°C 
  • Melting Point:37 - 38oC 
  • Refractive Index:n20/D 1.447(lit.)  
  • Boiling Point:222.2 °C at 760 mmHg 
  • Flash Point:87 °C 
  • PSA:26.30000 
  • Density:0.932 g/cm3 
  • LogP:3.01030 

Menthyl acetate(Cas 89-48-5) Usage

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).

InChI:InChI=1/C12H22O2/c1-8(2)11-6-5-9(3)7-12(11)14-10(4)13/h8-9,11-12H,5-7H2,1-4H3/t9-,11+,12-/m0/s1

89-48-5 Relevant articles

Solvent-free Acetylation Procedure

Bhat, Sujata V.,Gupta, Manisha O.,Yadav, Jyoti K.,Vaze, Kedar R.

, p. 590 - 594 (2021/10/07)

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A Method For Preparing (Meth)Acrylic Acid Ester Based Compound

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Paragraph 0071-0072, (2021/05/07)

The invention relates to a method for pr...

Continuous-Flow Chemo and Enzymatic Synthesis of Monoterpenic Esters with Integrated Purification

Adarme, Carlos A.A.,Le?o, Raquel A.C.,de Souza, Stefania P.,Itabaiana, Ivaldo,de Souza, Rodrigo O.M.A.,Rezende, Claudia M.

, p. 39 - 46 (2018/05/22)

Monoterpenic esters are very important f...

Production of l-menthyl acetate through kinetic resolution by?Candida cylindracea lipase: effects of alkaloids as additives

Belkacemi, Fatima Zohra,Merabet-Khelassi, Mounia,Aribi-Zouioueche, Louisa,Riant, Olivier

, p. 6847 - 6860 (2018/07/15)

Abstract: Enzymatic transesterification ...

89-48-5 Process route

menthol
89-78-1

menthol

acetic anhydride
108-24-7

acetic anhydride

2-isopropyl-5-methylcyclohexyl acetate
89-48-5,2230-87-7,2552-91-2,2623-23-6,5157-89-1,16409-45-3,20777-36-0,20777-45-1,29066-34-0,42241-42-9,50539-17-8,55058-46-3,79199-84-1,146502-80-9

2-isopropyl-5-methylcyclohexyl acetate

Conditions
Conditions Yield
With lithium perchlorate; at 25 ℃; for 22h;
98%
With silica gel; for 0.05h; Microwave irradiation; neat (no solvent);
98%
With SBA-15-Ph-Pr-SO3H; at 20 ℃; for 0.416667h;
98%
4-N,N-dimethylaminopyridinium saccharinate; at 25 ℃; Product distribution / selectivity;
98%
With C12H8N2*2CH4O3S; at 30 ℃; for 2h;
98%
With poly(N,N'-dibromo-N-ethylnaphthyl-2,7-sulfonamide); In neat (no solvent); at 20 ℃; for 0.5h;
97%
With poly(4-vinylpyridine) supported copper(II) oxide nanoparticles; In neat (no solvent); at 20 ℃; for 0.05h; chemoselective reaction;
95%
With lanthanum(III) nitrate; at 20 ℃; for 0.25h;
94%
With 1-butyl-3-methylimidazolium tetrachloridoferrate(III); at 20 ℃; for 1.16667h; Ionic liquid;
94%
With rice husk ash; at 80 ℃; for 1h; Green chemistry;
93%
With 20CuO-ZnO nanocatalyst; In dichloromethane; at 20 ℃; for 1h; Green chemistry;
89%
With benzyltriphenylphosphonium tribromide; In chloroform; for 0.216667h; Reflux;
87%
With camphor-10-sulfonic acid; Graphite; In neat (no solvent); at 20 ℃; for 0.5h;
82%
With 1H-imidazole; at 20 ℃; for 24h; Green chemistry;
75%
magnesium bromide; In dichloromethane; at 20 ℃; for 3h;
72%
With pyridine; In dichloromethane;
With bismuth(lll) trifluoromethanesulfonate; at 0 ℃; for 1.5h;
97 % Chromat.
With sulfonated ordered mesoporous carbon (CMK-5-SO3H); In neat (no solvent); at 20 ℃; for 0.166667h; Green chemistry;
98 %Chromat.
With cesium 12-tungstophosphate; at 20 ℃; for 0.5h; Time; Catalytic behavior; Green chemistry;
With immobilized enzyme Novozym 435?; at 150 ℃; Enzymatic reaction;
vinyl acetate
108-05-4,9003-20-7

vinyl acetate

menthol
89-78-1

menthol

2-isopropyl-5-methylcyclohexyl acetate
89-48-5,2230-87-7,2552-91-2,2623-23-6,5157-89-1,16409-45-3,20777-36-0,20777-45-1,29066-34-0,42241-42-9,50539-17-8,55058-46-3,79199-84-1,146502-80-9

2-isopropyl-5-methylcyclohexyl acetate

Conditions
Conditions Yield
iodine; at 20 ℃; for 4.5h;
94%
With 2,2'-(phenylimino)bis[ethanol]; diethylzinc; In hexane; toluene; at 20 ℃; for 24h;
91%
With pseudomonas fuorescens lipase immobilized on multiwall carbon nano-tubes; at 50 ℃; for 12h; Green chemistry;
44%

89-48-5 Upstream products

  • 108-24-7
    108-24-7

    acetic anhydride

  • 1181819-05-5
    1181819-05-5

    menthol

  • 89-78-1
    89-78-1

    [1-α]-5-methyl-2-[1-methylethyl]-cyclohexanol

  • 108-05-4
    108-05-4

    vinyl acetate

89-48-5 Downstream products

  • 89-78-1
    89-78-1

    menthol

  • 2216-51-5
    2216-51-5

    (-)-menthol

  • 5157-89-1
    5157-89-1

    D-menthyl acetate

  • 15356-60-2
    15356-60-2

    (1S,2R,5S)-(+)-menthol

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