Witch Hazel

Botanical Overview

Witch Hazel (Hamamelis virginiana) is a flowering plant in the Hamamelidaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. This species belongs to the Hamamelidaceae family, a group of flowering plants.

General Description

Hamamelis virginiana, known as witch-hazel, common witch-hazel, American witch-hazel and beadwood, is a species of flowering shrub native to eastern North America, from Nova Scotia west to Minnesota, and south to central Florida to eastern Texas.

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

Family Context

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

Geographic Distribution

Witch Hazel has been recorded in 10 countries and territories worldwide, including Belgium, Canada, Germany, Estonia, France, and others.

Traditional Uses

Witch Hazel has been traditionally used for skin and wound care, pain and inflammation, and nervous system disorders, among other applications.

Skin and wound care.

  • Skin
  • 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.

  • Inflammation
  • Anodyne

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.

Nervous system disorders.

  • Sedative

Nervous system support involves taking the herb as a warm tea, often in the evening or before bed. The calming compounds interact with neurotransmitter systems to promote relaxation and restful sleep.

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Phenolic: antioxidant compounds that neutralize free radicals
  • 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: Belgium, Canada, Germany, Estonia, France, Mexico, Poland, Sweden, United States, Unknown.

Complete Use Records

CategoryCultural Context
AstringentElsewhere, Italian, US(Appalachia)
BruiseElsewhere, US, US(Amerindian)
PilesChina, US
SedativeDutch, US(Appalachia)
SkinChina, US(Amerindian)
TonicDanish, US(Appalachia)
Ache(Back)US(Amerindian)
AlterativeChina
AntidiarrheicElsewhere
AntisepticGerman
CancerGermany
ChewstickUS(Amerindian)
CosmeticChina
EyeUS(Amerindian)
HemorrhoidsElsewhere
HemostatFrench
HemostaticElsewhere
InflammationUS(Amerindian)
MedicineUS(Appalachia)
MyalgiaUS(Appalachia)
PoulticeUS(Amerindian)
RefrigerantSpanish
ScalpElsewhere
SprainUS
Steam-BathUS(Appalachia)
TumorUS(Amerindian)
Varicose VeinsElsewhere
WitchhazelElsewhere
WoundElsewhere
AnodyneEnglish

Complete Chemical Inventory

CompoundFormulaMW
6-METHYLHEPTADIEN-3,5-ON(2)
ACETALDEHYDEC₂H₄O44.05 Da
AFZELINC₂₁H₂₀O₁₀432.4 Da
ALCOHOLS
ALPHA-IONONEC₁₃H₂₀O192.30 Da
ASTRAGALINC₂₁H₂₀O₁₁448.4 Da
BETA-IONONEC₁₃H₂₀O192.30 Da
CATECHIN-3-GALLATEC₂₂H₁₈O₁₀442.4 Da
CATECHIN-TANNIN
CHOLINEC₅H₁₄NO+104.17 Da
D-GALLOCATCHEIN
ELLAGITANNINC₄₄H₃₂O₂₇992.7 Da
ESTERS
GALLIC-ACIDC₇H₆O₅170.12 Da
GALLO-TANNIN
HAMAMELIDINE
HAMAMELIN
HAMAMELITANNINC₂₀H₂₀O₁₄484.4 Da
HAMAMELOSEC₆H₁₂O₆180.16 Da
ISOQUERCITRINC₂₁H₂₀O₁₂464.4 Da
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
L-EPICATECHINC₁₅H₁₄O₆290.27 Da
L-EPIGALLOCATECHINC₁₅H₁₄O₇306.27 Da
LEUCOCYANIDINC₁₅H₁₄O₇306.27 Da
LEUCODELPHINIDINC₁₅H₁₄O₈322.27 Da
MYRICETINC₁₅H₁₀O₈318.23 Da
MYRICETIN-3-GLUCOSIDE
N-HEXEN-2-AL
PHENOLC₆H₆O94.11 Da
PHLOBAPHENE

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


References & Further Reading

External Research Links

Data Sources