Menthyl isovalerate

Available forms:COA

pd_proNo:439598-5c98ce54-5eec-45c1-b22e-b6fd06689ff8

pd_productuse:

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Detailed introduction

Export Top Purity Menthyl isovalerate 16409-46-4 In Stock

  • Molecular Formula:C15H28 O2
  • Molecular Weight:240.386
  • Appearance/Colour:COA 
  • Vapor Pressure:0.00724mmHg at 25°C 
  • Melting Point:1.3°C (estimate) 
  • Refractive Index:1.452 
  • Boiling Point:269.5°Cat760mmHg 
  • Flash Point:113 ºC 
  • PSA:26.30000 
  • Density:0.909 
  • LogP:4.03650 

Menthyl isovalerate(Cas 16409-46-4) Usage

Preparation

Prepared by heating a mixture of l-menthol and isovaleric acid at 100 to 110°C in the presence of trace concentrated H2SO4 or at 100°C in the presence of HCl.

Hazard

Low toxicity by ingestion and skin contact. A moderate skin contact irritant.

Taste threshold values

Taste characteristics at 80 ppm: fruity, sweet, with a tutti-fruitti background.

InChI:InChI=1/C15H28O2/c1-10(2)8-15(16)17-14-9-12(5)6-7-13(14)11(3)4/h10-14H,6-9H2,1-5H3

16409-46-4 Relevant articles

PREPARATION OF MENTHYL ISOVALERATE BY CARBONYLATION OF ISOBUTYLENE

El'man, A. R.,Matveev, V. M.,Slivinskii, E. V.,Loktev, S. M.

, p. 217 - 221 (1990)

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SYNTHESES BASED ON MONOCARBON MOLECULES. I. SYNTHESIS OF MENTHYL ISOVALERATE BY HYDROCARBALKOXYLATION OF ISOBUTYLENE WITH CARBON MONOXIDE AND MENTHOL IN THE PRESENCE OF PALLADIUM-PHOSPHINE COMPLEXES

Suerbayev, Kh.A.,Tsukanov, I.A.,El'man, A.R.,Zhubanov, K.A.

, p. 1072 - 1074 (2007/10/02)

The kinetics of isobutylene carbalkoxyla...

16409-46-4 Process route

carbon monoxide
201230-82-2

carbon monoxide

menthol
89-78-1

menthol

isobutene
115-11-7,15220-85-6

isobutene

menthyl isovalerate
16409-46-4,89-47-4

menthyl isovalerate

Conditions
Conditions Yield
With palladium diacetate; hydrogen; toluene-4-sulfonic acid; triphenylphosphine; In xylene; at 100 ℃; for 2h; under 13680 Torr;
99.7%
With hydrogen; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; xylene; at 130 ℃; for 21h; under 33440 Torr; Product distribution; var. reactions conditions;
62%
With hydrogen; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; xylene; at 130 ℃; for 21h; under 33440 Torr;
62%
With palladium diacetate; hydrogen; toluene-4-sulfonic acid; triphenylphosphine; In xylene; at 100 ℃; for 2h; under 13680 Torr; other rate of hydrocarboxylation, var. component ratio, var. solvents;
3-methylbutyric acid
503-74-2

3-methylbutyric acid

(-)-menthol
2216-51-5

(-)-menthol

menthyl isovalerate
16409-46-4,89-47-4

menthyl isovalerate

Conditions
Conditions Yield
With sulfuric acid; at 100 - 110 ℃; -isovalerate;
With mineral acid; at 70 - 80 ℃; isovaleric acid l-menthyl ester;

16409-46-4 Upstream products

  • 503-74-2
    503-74-2

    3-methylbutyric acid

  • 2216-51-5
    2216-51-5

    (-)-menthol

  • 108-12-3
    108-12-3

    isopentanoyl chloride

  • 201230-82-2
    201230-82-2

    carbon monoxide

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