Cymbopogon schoenanthus

Details Top

Internal ID UUID64402f81ca43a034768296
Scientific name Cymbopogon schoenanthus
Authority Spreng.
First published in Pl. Min. Cogn. Pug. 2: 15 (1815)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Steam‑distilled essential oil, commonly marketed as “Schoenanthus oil” or a lemongrass‑type oil, obtained from the fresh or air‑dried above‑ground plant material (yield ≈ 0.5–1.5 % w/w).
- Dried leaves and stems sold as a culinary herb/spice for flavoring.

Industrial and craft applications:
- The essential oil is incorporated into natural insect‑repellent formulations (aerosol sprays, skin lotions, candles, and mosquito coils) because of its high citronellal content (≈ 60–80 %).
- It serves as a fragrance component in soaps, detergents, surface cleaners, and other household products, providing a fresh citrus‑herbaceous note.
- The stiff, dry stems are locally used for basic thatching of small structures, for weaving simple mats, and for making brooms or cordage, exploiting their moderate tensile strength.

Food and beverages (non‑medicinal):
- Fresh or dried leaves and stems are chopped or ground and added to soups, stews, rice dishes, and spice blends, especially in Horn‑of‑Africa cuisines and in Arabian‑Peninsula cooking, where they impart a lemon‑like aroma.
- The dried material is also employed as a tea‑flavoring additive, contributing a citrus‑herbaceous note without medicinal claims.

Fragrance and cosmetics:
- The oil functions as a top‑note fragrance in perfumery and in personal‑care products such as body washes, shampoos, lotions, and deodorants, where its bright citrus profile is valued for lasting freshness.

Properties relevant to use:
- Chemical profile: citronellal (≈ 60–80 %), geraniol (≈ 5–10 %), citronellol (≈ 4–8 %), and minor sesquiterpenes; the high citronellal level confers strong insect‑repellent activity and a characteristic lemon‑citrus odor.
- Physical properties: oil density ≈ 0.880 g mL⁻¹ at 20 °C; refractive index ≈ 1.465; ester value typical of lemongrass‑type oils.
- Mechanical properties: stems possess moderate tensile strength suitable for coarse weaving and simple structural applications.

Standards and regulation:
- Schoenanthus oil produced for commercial use typically conforms to ISO 4730 (Oil of Lemongrass) for chemical specifications such as citronellal content, refractive index, and acid value.
- Fragrance and cosmetic applications are governed by IFRA guidelines on safe usage limits and by the EU Cosmetic Regulation (EC) No 1223/2009, which requires labeling of fragrance allergens.

Sustainability and sourcing:
- The species is harvested from wild, semi‑arid populations across sub‑Saharan Africa and the Arabian Peninsula; limited cultivation exists in Kenya and Sudan to supply essential‑oil markets.
- Sustainable practices include cutting stems above ground to allow regeneration, rotating harvesting sites, and encouraging small‑scale cultivation to reduce pressure on wild stands.
- Monitoring of wild populations is recommended to prevent over‑exploitation, particularly where the oil is a primary income source for local communities.

Synonyms Top

Scientific name Authority First published in
Andropogon circinnatus Hochst. & Steud. ex Steud. Syn. Pl. Glumac. 1(4-5): 387. 1854 [1855 publ. 20-21 Jul 1854]
Andropogon eriophorus Willd. Sp. Pl., ed. 4 [Willdenow] 4(2): 910. 1806 [Apr 1806]
Andropogon laniger Munro J. Linn. Soc., Bot. 19: 409 (1882)
Andropogon schoenanthus var. versicolor (Nees ex Steud.) Hack. Monogr. Phan. 6: 610. 1889
Cymbopogon arabicus Nees ex Steud. Syn. Pl. Glumac. 1(4-5): 387. 1854 [1855 publ. 20-21 Jul 1854]
Cymbopogon citriodorus Link Enum. Hort. Berol. Alt. 1: 107 (1821)
Lagurus schoenanthus Steud. Nomencl. Bot. : 461 (1821)
Sorghum schoenanthus Kuntze Revis. Gen. Pl. 2: 792 (1891)
Trachypogon schoenanthus Nees Linnaea 7: 281. 1832
Andropogon schoenanthus L. Sp. Pl. : 1046 (1753)
Andropogon lanigerum Desf. Fl. Atlant. 2: 379 1800

Common names Top

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Language Common/alternative name
English camel grass
Afrikaans kameelgras
Arabic إذخر مكي
Arabic إذخر
Arabic حشيشة الجمل
Arabic أبوركية
Arabic حلفابر
Czech voňatka šašinová
Persian گورگیاه
grc σχοῖνος
Hausa nobe
Malayalam നാന്മുഖപ്പുല്ല്
Dutch kameelgras
Polish palczatka wełnista

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cymbopogon schoenanthus subsp. proximus (Hochst. ex A.Rich.) Maire & Weiller Fl. Afrique N. 1: 287 (1952)
Cymbopogon schoenanthus subsp. schoenanthus

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) 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
  • Africa
    • East Tropical Africa
      • Kenya
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Ivory Coast
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Central African Republic
    • Western Indian Ocean
      • Réunion
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iran
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000861106
UNII RJJ0F54DE8
USDA Plants CYSC8
Tropicos 25510896
INPN 629510
KEW urn:lsid:ipni.org:names:397010-1
The Plant List kew-406274
Open Tree Of Life 913224
NCBI Taxonomy 79841
IPNI 397010-1
iNaturalist 506860
GBIF 2705269
Freebase /m/04f0bkm
EPPO CYGSH
EOL 1114865
USDA GRIN 12821
Wikipedia Cymbopogon_schoenanthus

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Ovicidal, larvicidal and adulticidal activity of black pepper (Piper nigrum L.) essential oil and tea tree oil (Melaleuca alternifolia) against Haemonchus contortus Mohamed HI, Arafa WM, Ahmed OM, El-Dakhly KM J Parasit Dis 13-Feb-2024
PMCID:PMC10908739
doi:10.1007/s12639-024-01650-w
PMID:38440752
Ethnobotanical study on medicinal plants in Melit area (North Darfur), Western Sudan Muhakr MA, Ahmed IM, El hassan GO, Yagi S J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765873
doi:10.1186/s13002-023-00646-9
PMID:38172804
Synergistic Stabilization of Nanoemulsion Using Nonionic Surfactants and Salt-Sensitive Cellulose Nanocrystals Liu L, Abiol KA, Friest MA, Fisher KD Polymers (Basel) 12-Dec-2023
PMCID:PMC10747914
doi:10.3390/polym15244682
PMID:38139935
Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district Qari SH, Alqethami A, Qumsani AT Saudi Pharm J 02-Dec-2023
PMCID:PMC10733703
doi:10.1016/j.jsps.2023.101881
PMID:38130903
An Overview of Cancer in Djibouti: Current Status, Therapeutic Approaches, and Promising Endeavors in Local Essential Oil Treatment Abdoul-Latif FM, Ainane A, Houmed Aboubaker I, Mohamed J, Ainane T Pharmaceuticals (Basel) 16-Nov-2023
PMCID:PMC10674319
doi:10.3390/ph16111617
PMID:38004482
Optimization and antifungal efficacy against brown rot fungi of combined Salvia rosmarinus and Cedrus atlantica essential oils encapsulated in Gum Arabic Annemer S, Ez-zoubi A, Ez zoubi Y, Satrani B, Stambouli H, Assouguem A, Ullah R, Bouayoun T, Fettoukh N, Farah A Sci Rep 09-Nov-2023
PMCID:PMC10636173
doi:10.1038/s41598-023-46858-7
PMID:37945688
Sustainable Pest Management Using Novel Nanoemulsions of Honeysuckle and Patchouli Essential Oils against the West Nile Virus Vector, Culex pipiens, under Laboratory and Field Conditions Hikal WM, Baz MM, Alshehri MA, Bahattab O, Baeshen RS, Selim AM, Alhwity L, Bousbih R, Alshourbaji MS, Ahl HA Plants (Basel) 25-Oct-2023
PMCID:PMC10650709
doi:10.3390/plants12213682
PMID:37960039
The Cytokinins BAP and 2-iP Modulate Different Molecular Mechanisms on Shoot Proliferation and Root Development in Lemongrass (Cymbopogon citratus) Cárdenas-Aquino MD, Camas-Reyes A, Valencia-Lozano E, López-Sánchez L, Martínez-Antonio A, Cabrera-Ponce JL Plants (Basel) 21-Oct-2023
PMCID:PMC10610249
doi:10.3390/plants12203637
PMID:37896100
In vitro and in vivo anthelmintic efficacy of peppermint (Mentha x piperita L.) essential oil against gastrointestinal nematodes of sheep Štrbac F, Krnjajić S, Stojanović D, Ratajac R, Simin N, Orčić D, Rinaldi L, Ciccone E, Maurelli MP, Cringoli G, Bosco A Front Vet Sci 10-Aug-2023
PMCID:PMC10472939
doi:10.3389/fvets.2023.1232570
PMID:37662995
Chemical Composition, In Vitro Antioxidant Activities, and Inhibitory Effects of the Acetylcholinesterase of Liparis nervosa (Thunb.) Lindl. Essential Oil Zhao J, Xu Z, Gao P, Liu X Biomolecules 07-Jul-2023
PMCID:PMC10377283
doi:10.3390/biom13071089
PMID:37509125
Phytochemical Screening and Antimicrobial Activity of Methanolic Extract of Cymbopogon schoenanthus (L.) (azkhar) Collected from Afif City, Saudi Arabia Mokhtar LM, Salim IA, Alotaibi SN, Awaji EA, Alotaibi MM, Doman AO Life (Basel) 27-Jun-2023
PMCID:PMC10381605
doi:10.3390/life13071451
PMID:37511826
Biological activity of cinnamaldehyde, citronellal, geraniol and anacardic acid on Haemonchus contortus isolates susceptible and resistant to synthetic anthelmintics Frota GA, dos Santos VO, Rodrigues JF, Oliveira BR, Albuquerque LB, de Vasconcelos FR, Silva AC, Teixeira M, de Brito ES, dos Santos JM, Vieira LD, Monteiro JP Rev Bras Parasitol Vet 19-Jun-2023
PMCID:PMC10321719
doi:10.1590/S1984-29612023027
PMID:37341288
Chemical Composition of Essential Oil of Cymbopogon schoenanthus (L.) Spreng from Burkina Faso, and Effects against Prostate and Cervical Cancer Cell Lines Bayala B, Coulibaly LL, Djigma F, Bunay J, Yonli A, Traore L, Baron S, Figueredo G, Simpore J, Lobaccaro JM Molecules 05-Jun-2023
PMCID:PMC10254514
doi:10.3390/molecules28114561
PMID:37299034
Current State of Knowledge Regarding WHO High Priority Pathogens—Resistance Mechanisms and Proposed Solutions through Candidates Such as Essential Oils: A Systematic Review Romanescu M, Oprean C, Lombrea A, Badescu B, Teodor A, Constantin GD, Andor M, Folescu R, Muntean D, Danciu C, Dalleur O, Batrina SL, Cretu O, Buda VO Int J Mol Sci 04-Jun-2023
PMCID:PMC10253476
doi:10.3390/ijms24119727
PMID:37298678
Insight into the phytochemical profile and antimicrobial activities of Amomum subulatum and Amomum xanthioides: an in vitro and in silico study Alruhaili MH, Almuhayawi MS, Gattan HS, Alharbi MT, Nagshabandi MK, Jaouni SK, Selim S, AbdElgawad H Front Plant Sci 20-Apr-2023
PMCID:PMC10157186
doi:10.3389/fpls.2023.1136961
PMID:37152127

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Bicyclo[5.2.0]nonane, 2-methylene-4,8,8-trimethyl-4-vinyl- 564746 Click to see CC1(CC2C1CCC(CC2=C)(C)C=C)C 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
4-Carene, (1S,3R,6R)-(-)- 530422 Click to see 136.23 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6R)-rel- 85568 Click to see 154.25 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
2-Methyl-5-(1-methylethenyl)cyclohexanol 12072 Click to see 154.25 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
o-Mentha-1(7),8-dien-3-ol 564552 Click to see 152.23 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
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/10.1016/J.APJTM.2016.06.009
a Farnesol 3327 Click to see 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
alpha-Santalene 94164 Click to see 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
Bulnesol 90785 Click to see 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
Cyclosativene 519960 Click to see 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
Eudesm-7(11)-en-4-ol 6432454 Click to see 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
Hinesol 289964 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
Dihydroagarofuran 21593552 Click to see 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
beta-Chamigrene 442353 Click to see 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1S,7S,8aR)-1,2,3,4,6,7,8,8a-Octahydro-1,8a-dimethyl-7-(1-methylethenyl)naphthalene 656496 Click to see 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(-)-7-Epi-alpha-selinene 10726905 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Bicyclo(5.3.0)decane, 2-methylene-5-(1-methylvinyl)-8-methyl- 564533 Click to see 204.35 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Andrographolide 5318517 Click to see CC12CCC(C(C1CCC(=C)C2CC=C3C(COC3=O)O)(C)CO)O 350.40 unknown https://doi.org/10.1016/J.APJTM.2016.06.009
> Organoheterocyclic compounds / Piperidines
2-Piperidineethanamine 27568 Click to see 128.22 unknown https://doi.org/10.1016/J.APJTM.2016.06.009

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