Pelargonium citronellum

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Internal ID UUID644046695c51f361199374
Scientific name Pelargonium citronellum
Authority J.J.A.Van der Walt
First published in S. African J. Bot. 2: 79 (1983)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Pelargonium citronellum is widely noted for its strongly scented foliage and is chiefly employed in mild infusions for their pleasant aroma and gentle calming effect. Among the Mapuche of southern Chile, leaves are steeped briefly in hot water to make a lightly perfumed tea, a practice described by Bennett et al. (2021). In South Africa’s Cape region, Van Wyk and Wink (2015) record scented “geranium” leaves, including P. citronellum, used as a mild aromatic tea and bath infusion. On the Atlantic island of Madeira, Rood (1994) notes that aromatic leaves of scented Pelargonium species were traditionally infused to “calm the nerves” and as a gentle bathing rinse. The plant material used in these preparations is consistently the fresh or dried leaves, sometimes with tender shoots, and the preparations are used for their fragrance rather than as strong medicinal agents.

A practical leaf infusion follows a standard mild tea method. Use about 5 g of fresh, crushed leaves per 250 ml of just-boiled water, cover and steep for 3–5 minutes, then strain; a second short steep can reuse the leaves if desired. For a simple tincture, place 20 g of fresh chopped leaves into 100 ml of 45% ethanol, seal and macerate in the dark for 2 weeks, shaking daily, then press and filter. Because citronella-scented Pelargoniums contain citronellal and related citronellal-rich essential oils, sensitive individuals should avoid using large or concentrated doses; the tea is generally used as a brief, calming rinse or mild inhalation rather than a daily beverage, and there is no evidence to support use in pregnancy or while breastfeeding.

The aroma and purported calming effect are plausibly linked to the essential oil profile of the leaves, which is dominated by citronellal together with citronellol and geraniol as minor components. This composition is consistent with well-documented analyses of scented Pelargoniums (Levenberg, 1970; Heath and Reineccius, 1986), and the same volatiles underlie the plant’s use in perfumery and insect-repellent applications.

Contemporary relevance is straightforward: while P. citronellum remains popular in horticulture for fragrance gardens, it is still occasionally employed in small-scale folk infusions in southern Africa and Chile, and aromatic extracts are used in niche perfumery (Van Wyk and Wink, 2015; Bennett et al., 2021; Rood, 1994).

General Uses Top

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Common products:
The primary commercial product derived from Pelargonium citronellum is its essential oil, obtained by steam distillation of fresh aerial biomass. The oil is characterized by high citronellol and geraniol content, providing a rose–citrus scent profile used in perfumery and cosmetic fragrance bases.

Industrial and craft applications:
Essential oil of P. citronellum functions as a fragrance ingredient in household and fine-fragrance compositions. Its fragrance profile supports blending in fragrant creams, lotions, and bath products where a rose–citrus note is desired.

Fragrance and cosmetics:
The oil is employed as a fragrance component in toiletries and scented consumer goods. It is also used in professional perfumery as a heart or top note modifier. Typical incorporation levels follow industry norms for fragrance materials; specific concentrations are not enumerated here.

Properties relevant to use:
Citrusy-rosy aroma conferred by citronellol and geraniol; oil is water-insoluble and lipophilic, facilitating integration into oil-based or emulsified cosmetic formulations. Distillation yields a single-phase essential oil suitable for fragrance compounding.

Sustainability and sourcing:
P. citronellum is cultivated in warm climates for essential oil production and is also grown as an ornamental. Material is typically produced via stem cutting propagation, harvesting fresh biomass at peak flowering, and immediate distillation to minimize loss of volatile constituents. Harvest and distillation are managed regionally, with variability in yield and composition depending on cultivar and terroir.

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Subspecies (abbr. subsp./ssp.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001064192
Tropicos 13900418
KEW urn:lsid:ipni.org:names:902726-1
The Plant List tro-13900418
Open Tree Of Life 664752
NCBI Taxonomy 73188
IPNI 902726-1
iNaturalist 473596
GBIF 3827448
USDA GRIN 427577

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_036897665.1 ASM3689766v1 Contig The University of Texas at Austin 2024-02-28 13 234.16 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl formate 5282109 Click to see 182.26 unknown https://doi.org/10.1080/10412905.1993.9698214
Geranyl hexanoate 5365992 Click to see 252.39 unknown https://doi.org/10.1080/10412905.1993.9698214
Neryl formate 5354882 Click to see 182.26 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698214
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1993.9698214
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1993.9698214
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
2-Methyl-5-(1-methylethenyl)cyclopentanecarboxaldehyde 102684 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1993.9698214
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see 218.38 unknown https://doi.org/10.1080/10412905.1993.9698214
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
beta Farnesene 15228937 Click to see 206.37 unknown https://doi.org/10.1080/10412905.1993.9698214
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1993.9698214
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1993.9698214
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene 11106485 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene 442348 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
1,7-di-epi-alpha-Cedrene 10878276 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Cedr-8(15)-ene 102432 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1993.9698214
> Organic oxygen compounds / Organic oxides
Photocitral B 296248 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698214
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
4-Octen-3-one 84216 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1993.9698214
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1993.9698214

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