Camphor

Also known as: Ho Leaf

Botanical Overview

Camphor (Cinnamomum camphora) is a flowering plant in the Lauraceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The laurel family (Lauraceae) includes trees and shrubs with aromatic, leathery leaves that are typically alternate. The flowers are small and greenish, and the fruits are drupes or berries. Many species produce essential oils rich in aromatic compounds like camphor and eucalyptol.

General Description

It is known by various names, most notably the camphor tree, camphorwood or camphor laurel.

ⓘ Information
Description adapted from Wikipedia (CC BY-SA 4.0).

Family Context

The Lauraceae family is primarily tropical and subtropical. Notable medicinal members include:

Geographic Distribution

Camphor has been recorded in 10 countries and territories worldwide, including Australia, Brazil, China, Japan, South Korea, and others.

Traditional Uses

Camphor has been traditionally used for digestive health, skin and wound care, and pain and inflammation, among other applications.

Digestive health.

  • Carminative
  • Diarrhea
  • Vermifuge

For digestive complaints, the herb is typically prepared as a tea or decoction taken before meals. The bitter compounds stimulate digestive secretions and improve nutrient absorption. Some traditions use the powdered root or leaves in small doses as a stomachic tonic.

Skin and wound care.

  • Wound

For skin conditions, the fresh or dried plant is applied topically as a poultice, wash, or compress. A strong decoction can be used to clean wounds and sores. The antimicrobial properties help prevent infection while promoting tissue repair.

Pain and inflammation.

  • Anodyne
  • Rheumatism
  • Arthritis
  • Inflammation
  • Neuralgia

For pain and inflammation, preparations are applied both topically as compresses and taken internally. A warm poultice draws blood to the area and promotes healing, while internal preparations address systemic inflammation.

Active Compounds

Phytochemical research has identified 30 compounds in this species, including a diverse array of phytochemical classes (see the Complete Chemical Inventory below for the full list).

The identified compounds include the following categories:

  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
ⓘ Information
Information on this page is compiled from Dr. Duke’s Phytochemical and Ethnobotanical Databases (USDA ARS), a public domain resource. Consult a healthcare professional before using any herbal preparation.

Distribution and Conservation

Reported distribution: Australia, Brazil, China, Japan, South Korea, New Zealand, Reunion, Taiwan, United States, South Africa.

Complete Use Records

CategoryCultural Context
StimulantElsewhere, Nepal, Turkey
AnodyneChina, Turkey
CirculationChina, Elsewhere
RheumatismChina, Elsewhere
AbdomenChina
AnalepticElsewhere
AnthelminthicNepal
AntisepticElsewhere
ArthritisChina
Beri-BeriChina
CalmativeElsewhere
CamphorElsewhere
CarminativeNepal
ConvulsionChina
DermatophytosisChina
DiarrheaElsewhere
EnergyChina
FavusChina
FumigantTurkey
HysteriaElsewhere
InflammationElsewhere
MyocarditisElsewhere
NeuralgiaElsewhere
RubefacientElsewhere
SedativeElsewhere
Ache(Tooth)China
TraumaChina
TumorItaly
VermifugeChina
WoundChina

Complete Chemical Inventory

CompoundFormulaMW
(+)-CAMPHENEC₁₀H₁₆136.23 Da
(-)-CAMPHENEC₁₀H₁₆136.23 Da
(-)-LINALOLC₁₀H₁₈O154.25 Da
(Z)-OCIMENOLC₁₀H₁₆O152.23 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
3,5-DIMETHYL-4,6-DI-O-METHYLPHLORACETOPHENONE
3,7-DIMETHYL-OCTA-1,5-DIEN-3,7-DIOL
3,7-DIMETHYL-OCTA-1,7-DIEN-3,6-DIOLC₁₀H₁₈O₂170.25 Da
5-DODECANYL-4-HYDROXY-4-METHYL-2-CYCLOPENTENONE
ACETALDEHYDEC₂H₄O44.05 Da
ACETIC-ACIDC₂H₄O₂60.05 Da
ALPHA-BISABOLOLC₁₅H₂₆O222.37 Da
ALPHA-CALACORENEC₁₅H₂₀200.32 Da
ALPHA-HEXANAL
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ALPHA-TERPINYL-ACETATEC₁₂H₂₀O₂196.29 Da
AZULENEC₁₀H₈128.17 Da
BETA-BISABOLOLC₁₅H₂₆O222.37 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-ELEMENEC₁₅H₂₄204.35 Da
BETA-HEXANAL
BETA-MYRCENEC₁₀H₁₆136.23 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BETA-SELINENEC₁₅H₂₄204.35 Da
BISABOLENEC₁₅H₂₄204.35 Da
BORNEOLC₁₀H₁₈O154.25 Da
CADINADIENE

Data from PubChem (NIH/NLM, public domain).


References & Further Reading

External Research Links

Data Sources