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Cadinene

(1S-cis)-1,2,3,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)-naphthalene (δ-)

Cadina 1(10),4-diene (δ-) · Cadina 4,10(15)-diene (γ-)

Bicyclic sesquiterpenoid alkene · C₁₅H₂₄

Chemical structure of Cadinene
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
483-76-1
Molecular formula
C₁₅H₂₄
Molecular weight
204.35 g/mol
Aroma
Warm woody, faintly earthy, a base note in wood oils.

Safety

Low concern · Safe at standard use

Cadinene exists in multiple isomeric forms, with γ- and δ-cadinene most common; together they occur in over 150 essential oils.

Skin. A 10 percent patch test on 25 volunteers gave no irritation or sensitization.

Oral. Acute oral LD50 in rats exceeds 5 g/kg; rabbit dermal LD50 exceeds 5 g/kg.

Cancer. δ-Cadinene shows moderate in vitro cytotoxicity against two human carcinoma cell lines.


Usage guidelines

Concern level
Low
CYP induction
CYP2B1 and CYP3A2

Found in essential oils

Principal sources
Siam wood15.6 – 32.6 %
Cade (rectified)24.2 %
Hinoki wood10.8 – 12.5 %
Cedrela11.7 %
Ylang-ylang0.2 – 10.8 %
Cubebtr – 9.5 %
Pine (Scots)tr – 9.5 %
Pepper (pink)4.7 – 9.1 %
Rhododendron9.1 %
Cedarwood (Port Orford)8.2 %
Copaiba1.7 – 7.7 %
Cangerana7.4 %
Peta7.4 %
Manuka4.8 – 7.2 %
Balsam poplar6.9 %
Muhuhu6.5 %
Cananga6.0 %
Hop5.5 %
Katrafay1.0 – 5.0 %
Vassoura5.1 %

Notes

The name cadinene derives from the genus Juniperus, where the compound was first isolated. Other isomers including γ1-, γ2-, ε-, σ-, τ- and ω-cadinene have also been reported. ω-Cadinene was originally named δ-cadinene, causing some historical confusion.