Black Walnut

Botanical Overview

Black Walnut (Juglans nigra) belongs to the Juglandaceae family. Limited but reliable traditional records indicate this plant has recognized medicinal applications in one or more healing traditions. This species belongs to the Juglandaceae family, a group of flowering plants.

General Description

Black walnut is susceptible to thousand cankers disease, which provoked a decline of walnut trees in some regions. Black walnut is allelopathic, releasing chemicals from its roots and other tissues that may harm other organisms and give the tree a competitive advantage, but there is no scientific consensus that this is a primary competitive factor. Black walnut is an important tree commercially, as the wood is a deep brown color and easily worked. Walnut seeds (nuts) are cultivated for their distinctive and desirable taste. Walnut trees are grown for lumber and food, and processors have found additional markets for even the tough outer hulls by finely grinding them for use in products such as abrasive cleansers. Many cultivars have been developed for improved quality wood or nuts. In 2017, the United States Department of Agriculture valued U. S. walnut timber at $530 billion. A significant amount is grown in Missouri.

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

Family Context

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

Geographic Distribution

Black Walnut has been recorded in 10 countries and territories worldwide, including Austria, Belgium, Canada, Czech Republic, Germany, and others.

Traditional Uses

Black Walnut has been traditionally used for digestive health, skin and wound care, and reproductive health.

Digestive health.

  • 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.

  • Sore

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.

Reproductive health.

  • Syphilis

In traditional contexts, reproductive health applications typically involve internal preparations such as teas or decoctions. The herb may be taken at specific times during the menstrual cycle.

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
  • 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: Austria, Belgium, Canada, Czech Republic, Germany, France, United Kingdom, Italy, Netherlands, United States.

Complete Use Records

CategoryCultural Context
LeukemiaUS
MedicineUS(Appalachia)
SoreUS
SyphilisUS
TapewormUS
DiphtheriaUS
GargleUS
Hair-DyeElsewhere
InsecticideUS
VermifugeUS

Complete Chemical Inventory

CompoundFormulaMW
1,2,3-TRIMETHYL-BENZENEC₉H₁₂120.19 Da
1,2,4-TRIMETHYL-BENZENEC₉H₁₂120.19 Da
1,3-DIMETHYL-BENZENEC₈H₁₀106.16 Da
1,4-NAPHTHOQUINONEC₁₀H₆O₂158.15 Da
1-2-5-TRIMETHYLBENZENEC₉H₁₂120.19 Da
1-2-DIMETHYLBENZENE
1-4-DIMETHYLBENZENE
1-METHYLNAPHTHALENEC₁₁H₁₀142.20 Da
2-2-DIMETHYLDECAN-1-OL
2-6-10-TRIMETHYLDODECANEC₁₅H₃₂212.41 Da
2-ACETYL-1-HYDROXY-4-METHYL-BENZENE
2-HYDROXY-4-METHOXY-BENZALDEHYDEC₈H₈O₃152.15 Da
2-METHYLHEPTAN-2-THIOL
2-PHENYLETHANOLC₈H₁₀O122.16 Da
3-ETHYL-2-METHYLHEPTA-1,3-DIENE
3-METHYLTRIDECANEC₁₄H₃₀198.39 Da
5-HYDROXYTRYPTAMINEC₁₀H₁₂N₂O176.21 Da
5-NOR-PINEN-2-OL
6-PROPYLTRIDECANEC₁₆H₃₄226.44 Da
7-METHYLUNDECENE
ALANINEC₃H₇NO₂89.09 Da
ALPHA-HYDROJUGLONE-4-GLUCOSIDEC₁₆H₁₈O₈338.31 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALUMINUMAl26.981538 Da
ANTIMONYSb121.760 Da
ARACHIDIC-ACIDC₂₀H₄₀O₂312.5 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ARSENICAs74.92159 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH

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


References & Further Reading

External Research Links

Data Sources