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HomeProduct name listValencene

Valencene

Synonym(s):(+)-Valencene;(3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene

  • CAS NO.:4630-07-3
  • Empirical Formula: C15H24
  • Molecular Weight: 204.35
  • MDL number: MFCD00075884
  • EINECS: 225-047-6
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-11-19 15:53:33
Valencene  Structural

What is Valencene ?

Description

(+)-Valencene is a sesquiterpene that has been found in C. sativa and is an aromatic component of orange essence oil. (+)-Valencene (50 μM) induces heme oxgenase-1 (HO-1) expression in macrophages and inhibits the expression of inducible nitric oxide synthase (iNOS), the production of nitric oxide (NO), and the release of high-mobility group box-1 (HMGB1) in RAW 264.7 cells stimulated with LPS. It also increases the survival rate in a mouse model of sepsis induced by cecal ligation and puncture. (+)-Valencene has been used in the synthesis of nootkatone .

Chemical properties

clear colorless to yellowish liquid

Occurrence

Reported found in citrus fruits, orange peel, orange juice, bitter orange peel oil, lemon peel oil, grapefruit juice, grapefruit peel oil, kumquat peel oil, leaves and stalk of celery, clove stem, Thymus vulgaris L., fresh mango, globe artichoke, cardamom, mangosteen and cocoa.

The Uses of Valencene

Valencene is a sesquiterpene and an essential oil component found in a variety of plants, and has been shown to have functional antioxidant, antiradical and antimicrobial properties.

The Uses of Valencene

(+)-Valencene can be used as a precursor to prepare:

  • (+)-Nootkatone (a sesquiterpene) by dark singlet oxygenation.
  • Benzoyloxyvalencene by reacting with tert-butyl peroxy benzoate via Kharasch?Sosnovsky allylic oxidation method.
  • (+)-Lineariifolianone, a natural product.

What are the applications of Application

(+)-Valencene is an aroma component of citrus fruit and citrus-derived odorants

Definition

ChEBI: A carbobicyclic compound and sesquiterpene that is 1,2,3,4,4a,5,6,7-octahydronaphthalene which is substituted a prop-1-en-2-yl group at position 3 and by methyl groups at positions 4a and 5 (the 3R,4aS,5R diastereoisomer).

Preparation

By a Wolf–Kishner reduction of nootkatone.

General Description

Valencene is the major sesquiterpene aroma constituent of orange peel oil. It is mainly used as a starting material to synthesize nootkatone, an important flavor compound of grapefruit.

Properties of Valencene

Boiling point: 274 °C(lit.)
Density  0.92 g/mL at 25 °C(lit.)
refractive index  n20/D 1.504(lit.)
FEMA  3443 | VALENCENE
Flash point: >230 °F
storage temp.  2-8°C
solubility  Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form  Oil
color  Colourless
Specific Gravity 0.92
Odor at 10.00 % in dipropylene glycol. sweet fresh citrus grapefruit woody orange asprin dry green oily
optical activity [α]22/D +90°, neat
Hydrolytic Sensitivity 1: no significant reaction with aqueous systems
JECFA Number 1337
BRN  3539153
Stability: Light Sensitive
EPA Substance Registry System Naphthalene, 1,2,3,5,6,7,8,8a-octahydro-1,8a-dimethyl-7-(1-methylethenyl)-, (1R,7R,8aS)- (4630-07-3)

Safety information for Valencene

Signal word Danger
Pictogram(s)
ghs
Health Hazard
GHS08
GHS Hazard Statements H304:Aspiration hazard
Precautionary Statement Codes P331:Do NOT induce vomiting.
P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P405:Store locked up.
P501:Dispose of contents/container to..…

Computed Descriptors for Valencene

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