2-[8-Isopropyl-6-methylbicyclo[2.2.2]oct-5-en-2-yl]-1,3-dioxolane
Glycoacétal® ; 2-(5-methyl-2-propan-2-yl-8-bicyclo[2.2.2]oct-5-enyl)-1,3-dioxolane ; 8-isopropyl-6-methylbicyclooctenyldioxolane ; 2-(8-iso propyl-6-methylbicyclo(2.2.2)oct-5-en-2-yl)-1,3-dioxolane
![2-[8-Isopropyl-6-methylbicyclo[2.2.2]oct-5-en-2-yl]-1,3-dioxolane (CAS N° 68901-32-6)](/static/scentree_detailed_pages/images/30131_1.PNG "2-[8-Isopropyl-6-methylbicyclo[2.2.2]oct-5-en-2-yl]-1,3-dioxolane (CAS N° 68901-32-6)")
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General Presentation
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CAS N° : : 68901-32-6
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EINECS number : 272-669-9
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FEMA number : Donnée indisponible.
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Density : 1,008
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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 : Base
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Price Range : €€€
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Appearance : Colorless liquid
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FLAVIS number : Donnée indisponible.
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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 :
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Detection Threshold : 39,91 ng/l air
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Molecular formula : C15H24O2
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Log P : 5,3
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Molecular Weight : 236,35 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 140°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Stability :
Unstable in alkaline products, except soaps.
Uses in perfumery :
Glycolierral® is used in woody, fruity-rhubarb, aldehydic, white flowers, gardenia, orris and lily of the valley notes.
Year of discovery :
Data not available.
Isomerism :
Glycolierral® has no isomer commonly used in perfumery.
Synthesis precursor :
Glycolierral® is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Glycolierral® is not available in its natural state.
Synthesis route :
Glycolierral® is an acetal obtained by reaction between ethylene glycol and Ivyal, another compound of olfactory interest with the smell of cut grass.
Regulations & IFRA
This ingredient is not restricted
