Roselle

Also known as: Indian Sorrel, Jamaica Sorrel, Kharkadi, Red Sorrel, Sorrel, Malventee (Ger.), Rosella (Ger.)

Botanical Overview

Roselle (Hibiscus sabdariffa) is a flowering plant in the Malvaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. The mallow family (Malvaceae) includes herbs, shrubs, and trees with alternate leaves, often with stellate hairs. The flowers are typically showy with five petals and numerous stamens fused into a column. Many species produce mucilage and have demulcent and emollient properties.

General Description

In the 16th and early 17th centuries it was spread to Asia and the West Indies, where it has since become naturalized in many places. The stems are used for the production of bast fibre and the calyces are commonly steeped to make an infusion popular in many places around the world.

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

Family Context

The Malvaceae family is widely distributed worldwide. Notable medicinal members include:

Geographic Distribution

Roselle has been recorded in 10 countries and territories worldwide, including Australia, Burkina Faso, Benin, Brazil, Cameroon, and others.

Traditional Uses

Roselle has been traditionally used for digestive health, urinary tract health, and nervous system disorders, among other applications.

Digestive health.

  • Dyspepsia
  • 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.

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.

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:

  • Terpene: aromatic compounds with anti-inflammatory and antimicrobial 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.

Distribution and Conservation

Reported distribution: Australia, Burkina Faso, Benin, Brazil, Cameroon, India, Mexico, Nigeria, United States, Zambia.

Complete Use Records

CategoryCultural Context
DiureticDominican Republic, Elsewhere, India, Mexico
TonicElsewhere, Haiti, Mexico, Turkey
DemulcentElsewhere, Mexico, Turkey
EmollientHaiti, India, Turkey
RefrigerantIndia, Mexico, Turkey
AntisepticIndia, Iraq
CoffeeElsewhere, Panama(Cuna)
DigestiveIndia, Iraq
HypertensionIndia, Iraq
ScurvyHaiti, Turkey
TeaPanama(Cuna), Turkey
HeartIndia, Iraq
AphrodisiacTurkey
AstringentTurkey
CancerSudan
CataplasmDominican Republic
CholereticIndia
DebilityElsewhere
DyspepsiaElsewhere
FeverMexico
HangoverGuatemala
LaxativeIndia
NervesIndia
ResolventHaiti
SedativeIndia
StranguryElsewhere
BiliousIndia
CholagogueTurkey
DysuriaElsewhere

Complete Chemical Inventory

CompoundFormulaMW
(+)-ALLOOXYCITRONIC-ACID-LACTONE
(E)-2-HEPTENALC₇H₁₂O112.17 Da
(E)-2-HEXENALC₆H₁₀O98.14 Da
(Z)-3-HEXENOLC₆H₁₂O100.16 Da
1,4-CINEOLEC₁₀H₁₈O154.25 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
1-HEXANOLC₆H₁₄O102.17 Da
1-METHYL-4-(1-METHYLETHYL)-3-CYCLOHEXENOL
2,2-DIMETHYL-HEXANAL
2,3-DIMETHYLBUTANEC₆H₁₄86.18 Da
2,6-DIMETHYL-5,7-OCTADIEN-2-OLC₁₀H₁₈O154.25 Da
2-ETHENYLTETRAHYDRO-2,6,6-TRIMETHYL-2H-PYRANC₁₀H₁₈O154.25 Da
2-ETHYL-FURANC₆H₈O96.13 Da
2-HEXENOLC₆H₁₂O100.16 Da
2-METHYL-6-METHYLENE-7-OCTEN-2-OLC₁₀H₁₈O154.25 Da
2-PENTYL-FURANC₉H₁₄O138.21 Da
3-METHYL-1-BUTANOLC₅H₁₂O88.15 Da
4-METHYL-1-(1-METHYLETHYL)-3-CYCLOHEXEN-1-OL-ACETATE
5-METHYL-2-FURALDEHYDEC₆H₆O₂110.11 Da
6,10,14-TRIMETHYL-2-PENTADECANONEC₁₈H₃₆O268.5 Da
ACETIC-ACIDC₂H₄O₂60.05 Da
ACIDS
ALLOHYDROXYCITRIC-ACIDC₆H₈O₈208.12 Da
ALPHA-4-DIMETHYL-3-CYCLOHEXYL-1-ACETALDEHYDE
ALPHA-FARNESENEC₁₅H₂₄204.35 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ALPHA-TERPINYL-ACETATEC₁₂H₂₀O₂196.29 Da
ALPHA-TOCOPHEROLC₂₉H₅₀O₂430.7 Da
ALUMINUMAl26.981538 Da
ANISALDEHYDEC₈H₈O₂136.15 Da

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


References & Further Reading

External Research Links

Data Sources