Black Mustard

Botanical Overview

Black Mustard (Brassica nigra) is a flowering plant in the Brassicaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The mustard family (Brassicaceae) includes herbs with alternate leaves and four-petaled flowers arranged in cross-like clusters. The fruits are typically elongated capsules called siliques. Most species produce glucosinolates and isothiocyanates, pungent sulfur-containing compounds with anticancer and antimicrobial properties.

General Description

It is cultivated for its dark-brown-to-black seeds, which are commonly used as a spice.

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

Family Context

The Brassicaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Black Mustard has been recorded in 10 countries and territories worldwide, including Belgium, Germany, Spain, France, United Kingdom, and others.

Traditional Uses

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

Digestive health.

  • Carminative
  • Stomachic
  • Laxative

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.

  • Pneumonia

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Sterol: cholesterol-like compounds with anti-inflammatory properties
  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Emetic. 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, Germany, Spain, France, United Kingdom, Israel, Netherlands, Sweden, Ukraine, United States.

Complete Use Records

CategoryCultural Context
RubefacientChina, Chinese, Elsewhere, Spain, Turkey
EmeticChina, Elsewhere, Iraq, Turkey
DiureticChina, Turkey
PneumoniaElsewhere, Japan
RheumatismChina, Japan
StimulantChina, Turkey
Ache(Foot)China
AnodyneChinese
ApertifChina
ArthritisChina
CarminativeChina
CounterirritantTurkey
HerpesVenezuela
Lymphoma(Neck)US
Mustard-PlasterElsewhere
PoulticeJapan
SciaticaElsewhere
Sclerosis(Spleen)Syria
ScurvyTurkey
StomachicTurkey
Tumor(Viscera)Belgium
VesicantTurkey
NeuralgiaJapan
DandruffElsewhere
LaxativeTurkey
LumbagoChina
PleurisyElsewhere

Complete Chemical Inventory

CompoundFormulaMW
2,4-METHYLENE-CHOLESTEROLC₂₈H₄₆O398.7 Da
2-BUTYL-GLUCOSINOLATEC₁₁H₂₁NO₉S₂375.4 Da
2-METHYL-BUTYL-GLUCOSINOLATE
2-PHENYLETHYL-GLUCOSINOLATEC₁₅H₂₀NO₉S₂-422.5 Da
2-PHENYLETHYL-ISOTHIOCYANATEC₉H₉NS163.24 Da
3,7-DIGLUCOSIDE-ISORHAMNETIN
3-METHYLTHIOPROPYL-GLUCOSINOLATEC₁₁H₂₁NO₉S₃407.5 Da
3-O-BETA-D-GLUCOSIDE-ISORHAMNETIN
3-SOPHOROSIDE-7-GLUCOSIDE-ISORHAMNETIN
3-SOPHOROSIDE-ISORHAMNETIN
ALLYL-CYANIDEC₄H₅N67.09 Da
ALLYL-ISOTHIOCYANATEC₄H₅NS99.16 Da
ALLYL-RHODANIDE
ALLYL-THIOCYANATEC₄H₅NS99.16 Da
ALPHA-LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
ASTRAGALINC₂₁H₂₀O₁₁448.4 Da
BETA-CAROTENEC₄₀H₅₆536.9 Da
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CALCIUMCa40.08 Da
CARBOHYDRATES
CHLOROGENIC-ACIDC₁₆H₁₈O₉354.31 Da
COPPERCu63.55 Da
CYSTINEC₆H₁₂N₂O₄S₂240.3 Da
ERUCIC-ACIDC₂₂H₄₂O₂338.6 Da
FATC₁₆H₃₂O₂256.42 Da
FERULIC-ACIDC₁₀H₁₀O₄194.18 Da
FIBER

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


References & Further Reading

External Research Links

Data Sources