Citrus > Zesty > Bergamot > Agrestic > Lavender

Menthanyl acetate

2-(4-methylcyclohexyl)propan-2-yl acetate ; Dihydroterpenyl acetate ; Acetic acid dihydroterpenyl ester; Acetic acid para-menthan-8-yl ester ; Dihydroterpineol acetate

Menthanyl acetate (CAS N° 58985-18-5)​

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Information Générales

General Presentation

  • CAS N° : : 58985-18-5

  • EINECS number : 261-543-9

  • FEMA number : Donnée indisponible.

  • Density : 0,936

  • Optical rotation : Lorem Ipsum

  • Allergens : This ingredient does not contain any allergen.

  • Refractive Index @20°C : Lorem Ipsum

  • Volatility : Head/Heart

  • Price Range :

  • Appearance : Colorless to amber liquid

  • FLAVIS number : 09.617

  • JECFA number : Donnée indisponible.

Information on synthetic ingredients

  • Acid Value : Lorem Ipsum

  • Boiling Point : 220-230°C (à 985 hPa)

  • Detection Threshold : Donnée indisponible.

  • Molecular formula : C12H22O2

  • Log P : 4,26

  • Molecular Weight : 198,31 g/mol

  • Fusion Point : <-20°C

  • Flash Point : 96°C

  • Vapor pressure : Lorem Ipsum

Utilisation

Uses

Other comments :

In terms of smell, Menthanyl acetate is to be compared with Linalyl acetate and Terpinyl acetate, from which it derivates. It brings an additional lavender facet.

Stability :

acetates may form acetic acid through time

Uses in perfumery :

Menthanyl acetate is used in citrus accords in alliance with bergamot and lemon and in fougere accords in alliance with lavender. Brings a fresh note to woody accords. Used in air fresheners and detergents for its stability.

Year of discovery :

Data not available.

Isomerism :

Menthanyl acetate synthesis induces the occurence of a mixture of two positional isomers : one has its ester group attached to the cycle, and the other has it on an alpha position. Menthanyl acetate is a constitutional isomer of Citronellyl acetate, Verdox® and Vertenex®. However, Citronellyl acetate is reminiscent of pear and rose, and Verdox® and Vertenex® smell more like apple, pear, and are much woodier.

Synthesis precursor :

Menthanyl acetate is not a precursor to the synthesis of another compound of olfactory interest.

Natural availability :

Menthanyl acetate is naturally present in Peppermint EO, in very small quantities, not allowing to obtain it in its natural state.

Synthesis route :

Menthanyl acetate is prepared by a hydrogenation reaction of isomeric Terpinyl acetate, in the presence of a Raney nickel catalysis for example. It can also be synthesized by an esterification reaction of a mixture of isomeric para-menthanols, using a strong acid catalyst as sulfuric acid. This synthesis is giving birth to two positional isomers.

Utilisation

Regulations & IFRA

This ingredient is not restricted

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