Common Violet

Also known as: Sweet Violet

Botanical Overview

Common Violet (Viola odorata) is a flowering plant in the Violaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. This species belongs to the Violaceae family, a group of flowering plants.

General Description

The small hardy herbaceous perennial is commonly known as wood violet, sweet violet, English violet, common violet, florist’s violet, or garden violet. The plant is native to Eurasia. The leaves and flowers are edible and have been used to make fragrances.

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

Family Context

The Violaceae family is widely distributed. Notable medicinal members include:

  • Pansy — 22 documented uses

Geographic Distribution

Common Violet has been recorded in 10 countries and territories worldwide, including Belgium, Switzerland, Germany, Denmark, France, and others.

Traditional Uses

Common Violet has been traditionally used for digestive health, respiratory conditions, and urinary tract health, among other applications.

Digestive health.

  • Laxative
  • Purgative

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.

Respiratory conditions.

  • Expectorant
  • Cough
  • Pectoral
  • Catarrh

Respiratory conditions are addressed through steam inhalation of the herb’s vapors or internal use as a warm tea. The hot infusion acts as an expectorant, helping to loosen phlegm and clear congestion. Some traditions combine it with honey for coughs.

Urinary tract health.

  • Diuretic

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

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:

  • Sterol: cholesterol-like compounds with anti-inflammatory properties
ⓘ 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.
⚠ Caution
Traditional records: This plant has documented uses including Emetic, Poison, Purgative. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Belgium, Switzerland, Germany, Denmark, France, United Kingdom, Netherlands, Poland, Russia, Sweden.

Complete Use Records

CategoryCultural Context
CancerAustralia, Czechoslovakia, Mexico, Pakistan, Peru, South Africa, West Indies
EmollientElsewhere, Mexico, Turkey
ExpectorantElsewhere, Haiti, Turkey
BiliousElsewhere, Kurdistan
CoughEurasia, Spain
EmeticDominican Republic, Mexico
LaxativeElsewhere, Mexico
LungElsewhere, Iraq
PectoralDominican Republic, Venezuela
PoisonElsewhere, US
PurgativeElsewhere, Turkey
AntisepticTurkey
AntitussiveElsewhere
AperientTurkey
CatarrhElsewhere
DiaphoreticElsewhere
EyeElsewhere
FeverElsewhere
FungicideElsewhere
LiqueurEurasia
PerfumeEurasia
SedativeTurkey
BactericideElsewhere
DepurativeElsewhere
DiureticElsewhere
NervineTurkey
SudorificTurkey
CatharticElsewhere
TeaEurasia
TumorChile

Complete Chemical Inventory

CompoundFormulaMW
2,6-NONADIEN-1-ALC₉H₁₄O138.21 Da
2,6-NONADIEN-1-OLC₉H₁₆O140.22 Da
3-BETA-FRIEDELANOL
ALDEHYDEC₂₀H₃₀O₅350.4 Da
ALPHA-IONONEC₁₃H₂₀O192.30 Da
ALPHA-IRONEC₁₄H₂₂O206.32 Da
BENZYL-ALCOHOLC₇H₈O108.14 Da
BETA-IONONEC₁₃H₂₀O192.30 Da
BETA-IRONEC₁₄H₂₂O206.32 Da
BETA-NITROPROPIONIC-ACID
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
CYANINC₂₇H₃₁O₁₆+611.5 Da
D-DIHYDRO-ALPHA-IONONE
D-DIHYDRO-BETA-IONONE
DIETHYL-PHTHALATEC₁₂H₁₄O₄222.24 Da
ENANTHIC-ACIDC₇H₁₄O₂130.18 Da
EUGENOLC₁₀H₁₂O₂164.20 Da
FERULIC-ACIDC₁₀H₁₀O₄194.18 Da
FRIEDELINC₃₀H₅₀O426.7 Da
GAULTHERINC₁₉H₂₆O₁₂446.4 Da
HEPTENOLC₇H₁₄O114.19 Da
ISOBORNEOLC₁₀H₁₈O154.25 Da
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
L-ZINGIBERENEC₁₅H₂₄204.35 Da
MALIC-ACIDC₄H₆O₅134.09 Da
METHYL-SALICYLATEC₈H₈O₃152.15 Da
MYROSIN
N-2-OCTEN-1-OL(?)
N-HEPTENOL
N-HEPTYL-ACID

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


References & Further Reading

External Research Links

Data Sources