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Camphene

2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane

3,3-Dimethyl-2-methylenenorcamphane · 3,3-Dimethyl-2-methylenenorbornane

Bicyclic monoterpenoid alkene · C₁₀H₁₆

Chemical structure of Camphene
2D structure PubChem / NCI CIR

Chemical info

CAS number CAS
5794-03-6
Molecular formula
C₁₀H₁₆
Molecular weight
136.23 g/mol
Aroma
Fresh camphoraceous, pine-woody, clean and sharp.

Safety

Low concern · Safe at standard use

Camphene is a simple monoterpene common in pine and mint oils. The compound presents low toxicity risk.

Skin. A 4 percent patch test on 25 volunteers caused no sensitization.

Oral. Acute oral LD50 in rats exceeds 5 g/kg; rabbit dermal LD50 exceeds 2.5 g/kg.

Reproductive. Rat developmental NOAEL is 1,000 mg/kg/day on gestation days 6–15. Maternal NOAEL is 250 mg/kg/day due to temporary reduced motor activity at the high dose.

Mutagenicity. Non-mutagenic in the Ames test. (±)-Camphene is non-genotoxic in Chinese hamster ovary cells.


Usage guidelines

Concern level
Low
Rat developmental NOAEL
1,000 mg/kg/day

Found in essential oils

Principal sources
Spruce (Norway)7.0 – 26.5 %
Fir needle (Siberian)24.2 %
Fir needle (Japanese)18.5 %
Fir (Douglas)16.7 %
Fir needle (silver)14.8 %
Valerian (European)0.1 – 14.4 %
Spruce (red)12.9 %
Pine (grey)2.8 – 12.1 %
Sage (Spanish)4.6 – 10.6 %
Cistus1.1 – 10.3 %
Rosemary2.8 – 10.0 %
Spruce (white)9.9 %
Fir needle (Canadian)3.5 – 9.7 %
Pine (Scots)1.6 – 9.4 %
Sage (Dalmatian)0 – 8.6 %
Spruce (black)8.1 %
Feverfew5.4 – 7.7 %
Lavender (Spanish)2.8 – 5.5 %
African bluegrass3.6 – 5.4 %
Pine (white)5.2 %
Thyme (borneol CT)5.0 %

Pharmacokinetics

Camphene is primarily metabolized through epoxidation and hydration. In rabbits, glucuronide conjugates of a hydroxyl derivative (camphenol) and the monoglucuronide of camphene glycol are excreted. After intravenous 0.6 mg/kg in a human subject, 3.6 percent was eliminated through expired air within three hours, mostly within five minutes.


Notes

Camphene contributes the fresh pine note to coniferous oils. The compound also shows cholesterol-lowering activity in preliminary rodent studies.