(1R)-Endo-(+)-fenchyl alcohol

CAS : 2217-02-9

Ref. 3D-FE34598

Informations sur le produit

• Nom: (1R)-Endo-(+)-fenchyl alcohol
• Synonymes: (+)-Fenchol, (+)-Fenchol~1,3,3-Trimethyl-2-norbornanol, (+)-Fenchyl alcohol, (+)-α-Fenchol, (+)-α-Fenchyl alcohol, (1R)-endo-(+)-Fenchyl alcohol, (1R,2R,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol, (1R,2S,4S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol, (2R)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-ol, 1,3,3-Trimethyl-2-norbornanol, <span class="text-smallcaps">D</span>-Fenchol, <span class="text-smallcaps">D</span>-Fenchyl alcohol, Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R,2R,4S)-, Bicyclo[2.2.1]heptan-2-ol, 1,3,3-trimethyl-, (1R-endo)-
• CAS: 2217-02-9

Description

(1R)-Endo-(+)-fenchyl alcohol is a chemotype of terpenes. Terpenes are hydrocarbons that are the major constituent of many essential oils and resins. The most well-known terpene is limonene, which is found in the rinds of citrus fruits. Terpenes are important for their flavors and aromas. They also have a variety of industrial uses, such as in fragrances and flavorings, paints, varnishes, and coatings. This particular chemotype has an equilibration time of 1-2 minutes at room temperature and can be prepared by evaporation or headspace techniques. (1R)-Endo-(+)-fenchyl alcohol has been detected in the aroma of grapefruit peel oil with a sensitivity of 0.5 ng/l air sample. It can be quantified using gas chromatography with flame ionization detection at 0.1 μg/l air sample or

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 154.25 g/mol
• Formule: C₁₀H₁₈O
• Degré de pureté: Min. 97%
• Couleur/Forme: White Powder