Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 928-95-0
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EINECS number : 213-191-2
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FEMA number : 2562
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Density : 0,845
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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
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Price Range : €
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Appearance : Colorless liquid
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FLAVIS number : 02.157
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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 : 159°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C6H12O
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Log P : Donnée indisponible.
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Molecular Weight : 100,16 g/mol
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Fusion Point : -40°C
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Flash Point : 55°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Trans-2-Hexenol has a much less powerful smell than trans-2-Hexenal, which has a strong green apple smell. It can then be more easily used in all types of compositions.
Stability :
Stable in perfumes and diverse functional bases
Uses in perfumery :
Trans-2-Hexenol is used in green notes and unripe fruit accords. Also used in stem notes for floral accords. Makes a honeysuckle more vegetal and fresh. Allows you to nuance floral notes. Gives a fresh appearance to jasmine, freesia or peony.
Year of discovery :
Data not available.
Isomerism :
Trans-2-Hexenol has a more fruity, apple-like smell than cis-3-Hexenol, which is purely green. This is why it is more often used in fruity accords than cis-3-Hexenol, that is used in flowery accords. Cis-2-Hexenol has a very green smell and also more fruity than cis-3-Hexenol.
Synthesis precursor :
Trans-2-Hexenol is a precursor to the synthesis of trans-2-Hexenyl acetate and other esters made from this alcohol.
Natural availability :
Trans-2-Hexenol is found naturally in Roman Chamomile EO and Violet Leaf Absolute, and can therefore be naturally extracted, although synthetic trans-2-Hexenol is more often used.
Synthesis route :
Trans-2-Hexenol is synthesized by the same route as cis-3-Hexenol, or by an isomerization in an acid medium of cis-3-Hexenol.
Regulations & IFRA
This ingredient is not restricted
