Mace

Also known as: Nutmeg, Muskatnussbaum (Ger.), nogal moscado (Sp.), nuez moscada (Sp.)

Botanical Overview

Commonly known as Mace, this species belongs to the Myristicaceae family. Traditional healers across continents have independently recognized the medicinal value of this species, leading to one of the most extensive ethnobotanical records available. This species belongs to the Myristicaceae family, a group of flowering plants.

General Description

This aromatic tree is economically significant as the primary source of two distinct spices: nutmeg, derived from its seed, and mace, obtained from the seed’s aril.

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

Family Context

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

Geographic Distribution

Mace has been recorded in 10 countries and territories worldwide, including Brazil, Indonesia, India, Sri Lanka, Malaysia, and others.

Traditional Uses

Mace has been traditionally used for digestive health, respiratory conditions, and skin and wound care, among other applications.

Digestive health.

  • Carminative
  • Stomachic
  • Dysentery
  • Dyspepsia

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.

  • Asthma

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.

Skin and wound care.

  • Leprosy

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.

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:

  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Narcotic, Abortifacient. 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: Brazil, Indonesia, India, Sri Lanka, Malaysia, Singapore, Trinidad, Tanzania, United States, Unknown.

Complete Use Records

CategoryCultural Context
CarminativeChina, Elsewhere, Moluccas, Turkey
MalariaElsewhere, Malaya, Trinidad
AstringentChina, Elsewhere
LeprosyElsewhere, Malaya
NarcoticChina, Elsewhere
RheumatismElsewhere, Malaya
SciaticaElsewhere, Malaya
StimulantElsewhere, Haiti
TonicChina, Elsewhere
StomachicChina, Turkey
AbortifacientTurkey
AphrodisiacElsewhere
AsthmaTrinidad
BactericideElsewhere
BladderElsewhere
CancerNew Zealand
DigestiveElsewhere
DysenteryElsewhere
DysmenorrheaTrinidad
DyspepsiaMalaya
FeverTrinidad
FluTrinidad
GastromegalyMalaya
HalitosisElsewhere
InfectionHaiti
InflammationElsewhere
IntestineDominican Republic
LinimentTurkey
OsteosisMalaya
ParturitionMalaya

Complete Chemical Inventory

CompoundFormulaMW
(+)-BETA-PINENEC₁₀H₁₆136.23 Da
(+)-BORNEOLC₁₀H₁₈O154.25 Da
(+)-LIMONENEC₁₀H₁₆136.23 Da
(+)-LINALOOLC₁₀H₁₈O154.25 Da
(+)-MYRISFRAGRANSINC₂₀H₂₂O₄326.4 Da
(+)-PINENEC₁₀H₁₆136.23 Da
(-)-EPICATECHINC₁₅H₁₄O₆290.27 Da
1,8-CINEOLC₁₀H₁₈O154.25 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
1-(3,4,5-TRIMETHOXYPHENYL)-2-(4-ALLYL-2,6-DIME...PROPAN-1-OL
1-(3,4,5-TRIMETHOXYPHENYL)-2-(4-ALLYL-2,6-DIMETHOX...PROPANE
1-(3,4-METHYLENEDIOXYPHENYL)-2-(4-ALLYL-2,...PROPYL-ACETATE
1-(3,4-METHYLENEDIOXYPHENYL)-2-(4-ALLYL-2,...PROPYL-BENZOATE
1-(4-HYDROXY-3-METHOXYPHENYL)-2-(4-ALLYL-2,6DI...PROPAN-1-OL
1-(5-ACETOXY-3,4-DIMETHOXYPHENYL)-2-(4-ALLY...PROPYL-ACETATE
2-(4-ALLYL-2,6-DIMETHOXYPHENOXY)-1-(3,4,5-TRIMETHOXYPHENYL)-PROPANE
2-(4-ALLYL-2,6-DIMETHOXYPHENOXY)-1-(3,4-METHYLENEDIOXYPHENYL)-1-PROPANOLC₂₁H₂₄O₆372.4 Da
2-(4-ALLYL-2,6-DIMETHOXYPHENOXY)-1-(3,4-METHYLENEDIOXYPHENYL)-ACETIC-ACID-PROPYL-ESTER
2-(4-ALLYL-2,6-DIMETHOXYPHENOXY)-1-(4-ACETOXY-3-METHOXYPHENYL)-ACETIC-ACID-PROPYL-ESTER
2-(4-ALLYL-2,6-DIMETHOXYPHENOXY)-1-(4-HYDROXY-3-METHOXYPHENYL)-1-PROPANOLC₂₁H₂₆O₆374.4 Da
3-METHYL-ACETATE-DEC-4-EN-1-OL
3-METHYL-DEC-4-EN-1-OL
5-METHOXYDEHYDRODI-ISOEUGENOL
5-METHOXYEUGENOLC₁₁H₁₆O₃196.24 Da
6-METHOXYDIHYDROISOEUGENOL
ACETIC-ACIDC₂H₄O₂60.05 Da
ALPHA-BERGAMOTENEC₁₅H₂₄204.35 Da
ALPHA-COPAENEC₁₅H₂₄204.35 Da
ALPHA-CUBEBENEC₁₅H₂₄204.35 Da
ALPHA-FARNESENEC₁₅H₂₄204.35 Da

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


References & Further Reading

External Research Links

Data Sources