Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 58985-18-5
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EINECS number : 261-543-9
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FEMA number : Donnée indisponible.
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Density : 0,936
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : €
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Appearance : Colorless to amber liquid
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FLAVIS number : 09.617
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JECFA number : Donnée indisponible.
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 220-230°C (à 985 hPa)
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H22O2
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Log P : 4,26
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Molecular Weight : 198,31 g/mol
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Fusion Point : <-20°C
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Flash Point : 96°C
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Vapor pressure : Lorem Ipsum
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.
Regulations & IFRA
This ingredient is not restricted