Rose Geranium

Also known as: Scented Geranium

Botanical Overview

Rose Geranium (Pelargonium graveolens) is a species in the Geraniaceae family. This species belongs to the Geraniaceae family, a group of flowering plants. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 30 compounds in this species, suggesting potential medicinal value.

General Description

Common names include rose geranium, sweet scented geranium, old-fashioned rose geranium, and rose-scent geranium.

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

Family Context

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

Geographic Distribution

Rose Geranium has been recorded in 10 countries and territories worldwide, including Brazil, China, Spain, France, Mexico, and others.

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:

  • Alkaloid: nitrogenous compounds with diverse pharmacological activities

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. The limited documentation available for this species represents an opportunity for ethnobotanical research.

ⓘ 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: Brazil, China, Spain, France, Mexico, New Zealand, Sweden, United States, South Africa, Unknown.

Complete Chemical Inventory

CompoundFormulaMW
1,3-PENTADIENEC₅H₈68.12 Da
10-EPI-GAMMA-EUDESMOLC₁₅H₂₆O222.37 Da
11-NORBOURBONANONE
11-SELINEN-4-ALPHA-OL
2-FURFURALC₅H₄O₂96.08 Da
2-HEXANONEC₆H₁₂O100.16 Da
2-METHYL-3-BUTEN-2-OLC₅H₁₀O86.13 Da
2-METHYL-3-BUTENAL
2-METHYL-3-PENTANONEC₆H₁₂O100.16 Da
2-METHYL-BUTANAL-TRANS-2-METHYL-3-BUTENAL
2-METHYL-BUTANOLC₅H₁₂O88.15 Da
2-METHYL-PROPANALC₄H₈O72.11 Da
2-METHYLBUTYL-FORMATEC₆H₁₂O₂116.16 Da
2-METHYLOPROPYL-FORMATE
2-PENTANONEC₅H₁₀O86.13 Da
2-PROPANOLC₃H₈O60.10 Da
3-HEXEN-1-OLC₆H₁₂O100.16 Da
3-METHYL-2-BUTANONEC₅H₁₀O86.13 Da
3-METHYL-BUTANOLC₅H₁₂O88.15 Da
3-METHYL-CYCLO-PENTANONE
3-METHYLBUTYL-FORMATEC₁₂H₂₄O₄232.32 Da
4-METHYL-2-PENTANONEC₆H₁₂O100.16 Da
6-OXO-6,7-DIHYDROCITRONELLIC-ACID
7-HYDROXY-6,7-DIHYDROGERANIOL
7-HYDROXYDIHYDROCITRONELLOLC₁₀H₂₂O₂174.28 Da
ACETALDEHYDEC₂H₄O44.05 Da
ACETIC-ACIDC₂H₄O₂60.05 Da
ACETONEC₃H₆O58.08 Da
ALCOHOLS
ALPHA-BOURBONENEC₁₅H₂₄204.35 Da

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


References & Further Reading

External Research Links

Data Sources