2-[8-Isopropyl-6-methylbicyclo[2.2.2]oct-5-en-2-yl]-1,3-dioxolane (CAS N° 68901-32-6)​

Photo credits: ScenTree SAS

2-[8-Isopropyl-6-methylbicyclo[2.2.2]oct-5-en-2-yl]-1,3-dioxolane

Citrus > Zesty > Grapefruit > Green Fruits

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)​

Photo credits: ScenTree SAS

Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.

Do you sell any of the raw materials? Would you like to let our users know?
Send an email to fournisseurs@scentree.coto learn about our advertising opportunities.

Information Générales

General Presentation

  • CAS N° :

    68901-32-6
  • EINECS number :

    272-669-9
  • FEMA number :

    Donnée indisponible.
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    Donnée indisponible.
  • Volatility :

    Base
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    1,008
  • Refractive Index @20°C :

    1,488 - 1,493
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,0018 mmHg @25°C
  • Flash Point :

    140°C (284°F)
  • Molecular formula :

    C15H24O2
  • Molecular Weight :

    236,35 g/mol
  • Log P :

    5,3
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

  • Detection Threshold :

    39,91 ng/l air
Utilisation

Chemistry & Uses

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.

Natural availability :

Glycolierral® is not available in its natural state.

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.

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.

Stability :

Unstable in alkaline products, except soaps.

Other comments :

Data not available.

I am a chocolate hazelnut cookie. I come out of the oven. Impossible to refuse me.
This website is using cookies
Our website uses cookies for statistics, performance, and security. These anonymous data allow us to give you an optimal navigation experience. You can always disable cookies in your browser settings.