Cymbopogon flexuosus

Details Top

Internal ID UUID64402f7e80b3a798639745
Scientific name Cymbopogon flexuosus
Authority (Nees ex Steud.) Will.Watson
First published in Gaz. N. W. Ind. 10: 392 (1882)

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.

In India, warm infusions of fresh or dried leaves are taken to ease mild colds and fever, and crushed leaf sheaths are sometimes applied as a poultice for headaches; Ayurvedic pharmacopoeias record similar preparations. In Thailand and Malaysia, a classic decoction of lemongrass sheaths with ginger is given for stomach upset, coughs, and colds, often as a household remedy. In Sri Lanka and across parts of Southeast Asia, the leaf infusion is valued as a gentle digestive tonic. These uses are documented in the Herbal Pharmacopoeia of the Indian Herbal Association, the WHO monographs on selected medicinal plants, and the Spice and Medicinal Plants of Sri Lanka by Jayaweera.

For a practical recipe: make a mild tea by simmering about 6–8 g of fresh cut leaf (about 2–3 cm pieces) in 500 mL of water for 10 minutes, then steep, covered, off heat for 5–7 minutes and strain. Alternatively, use 2 g dried leaf per 200 mL water and steep for 10 minutes. If you prefer a 1:5 tincture, macerate 20 g of dried leaf in 100 mL of 45–50% ethanol for 2–3 weeks in the dark, shaking occasionally, then press and filter. Safety note: use moderate amounts; essential‑oil components can be skin‑irritating; avoid in early pregnancy and on broken skin unless advised by a practitioner.

Active constituents reported for Cymbopogon flexuosus are the essential‑oil components citral (neral and geranial), geraniol, myrcene, citronellal, limonene, and often β‑caryophyllene, with the oil being primarily citral‑rich; these fit the profile used traditionally for mild respiratory and digestive support.

Modern relevance is strong: research on essential oil and extracts continues, and commercial teas, oils, and dietary supplements featuring lemongrass remain widely available in global markets.

General Uses Top

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Common products:
Citral-rich essential oil (cooking grade) and high-purity citral (neral and geranial mixture).

Industrial and craft applications:
Natural fragrance component in household cleaners, detergents, air care, and fabric care. Citral as a fragrance ingredient and intermediate for aroma-chemical synthesis (e.g., ionones) in fine fragrance and flavor formulations.

Food and beverages (non-medicinal):
Flavoring agent in beverages, confectionery, and savory foods at typical usage levels; major contributor of lemon-like aroma. Food-grade essential oil or citral preparations may be used as flavoring.

Fragrance and cosmetics:
Perfume and cosmetic ingredient (e.g., soaps, lotions, shampoos) for lemon-like top-note; fragrance dosage limited in leave-on applications due to IFRA standards for citral.

Properties relevant to use:
Typical commercial oil contains 65–85% citral (neral:geranial ≈ 1:1) with a characteristic lemon odor; density ~0.89–0.92 g/mL (20 °C); refractive index ~1.483–1.490 (20 °D). Citral readily undergoes acid-catalyzed cyclization to α- and β-ionone, enabling aroma-chemical derivatization.

Standards and regulation:
IFRA standards limit citral in certain product types to address sensitization risk. Flavor use complies with national food-additive regulations (e.g., FEMA GRAS/US; EU Flavouring Regulation). Agricultural practice is guided by ISO 3215 for Cymbopogon cultivation and harvesting where applicable.

Sustainability and sourcing:
Primarily cultivated in India and other tropical regions; products are obtained by steam distillation of fresh or partly dried leaves and stems. Supply is influenced by crop agronomy and oil-yield seasonality; traceability supports quality and regulatory compliance.

Synonyms Top

Scientific name Authority First published in
Andropogon ampliflorus Steud. Syn. Pl. Glumac. 1: 388 (1854)
Andropogon flexuosus Nees Syn. Pl. Glumac. 1(4-5): 388. 1854 [1855 publ. 20-21 Jul 1854]
Andropogon nardus var. flexuosus (Steud.) Hack. Monogr. Phan. 6: 603 1889
Cymbopogon flexuosus var. arunachalis S.C.Nath & K.K.Sarma Biochem. Syst. Ecol. 30: 159 (2002)
Cymbopogon flexuosus var. assamensis S.C.Nath & K.K.Sarma Biochem. Syst. Ecol. 30: 160 (2002)
Cymbopogon flexuosus var. sikkimensis Bor J. Bombay Nat. Hist. Soc. 52: 162. 1954
Cymbopogon travancorensis Bor J. Bombay Nat. Hist. Soc. 52: 174 (1954)
Andropogon nardus subsp. flexuosus (Nees ex Steud.) Hack. Monogr. Phan. 6: 603. 1889 (1889)
Andropogon flexuosus Nees ex Steud. Syn. Pl. Glumac. [Steudel] 1: 388 (1854)

Common names Top

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Language Common/alternative name
English east indian lemongrass
Spanish cymbopogon travancorensis
Spanish andropogon nardus subsp. flexuosus
Spanish andropogon ampliflorus
Spanish andropogon flexuosus
Arabic إذخر متعرج
Bulgarian Източноиндийска лимонова трева
bho जरकुस
Hindi नीबू घास
Hindi लेमन ग्रास
Hindi नींबू घास
Kannada ನಿಂಬೆ ಹುಲ್ಲು
Malayalam ഇഞ്ചിപ്പുല്ല്
Polish palczatka pogięta
Vietnamese sả dịu
Chinese 東印度香茅
Chinese 东印度柠檬草
Chinese 曲序香茅

Subspecies (abbr. subsp./ssp.) Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000860994
UNII 0MK18YOA5G
USDA Plants CYFL2
Tropicos 25547502
KEW urn:lsid:ipni.org:names:396927-1
The Plant List kew-406169
Open Tree Of Life 186966
NCBI Taxonomy 79835
IPNI 396926-1
iNaturalist 427431
GBIF 2705270
Freebase /m/0fz4yk
EPPO CYGFL
EOL 1115597
USDA GRIN 12804
Wikipedia Cymbopogon_flexuosus

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_027790015.1 ASM2779001v1 Contig Bangalore Unniversity 2023-01-09 14.23 520.20 Mb

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
Design of three-component essential oil extract mixture from Cymbopogon flexuosus, Carum carvi, and Acorus calamus with enhanced antioxidant activity Assaggaf H, Jeddi M, Mrabti HN, Ez-zoubi A, Qasem A, Attar A, Goh BH, Tan SL, Bouyahya A, Goh KW, Hachlafi NE Sci Rep 22-Apr-2024
PMCID:PMC11035653
doi:10.1038/s41598-024-59708-x
PMID:38649707
Silicon nanoparticles vs trace elements toxicity: Modus operandi and its omics bases Mukarram M, Ahmad B, Choudhary S, Konôpková AS, Kurjak D, Khan MM, Lux A Front Plant Sci 03-Apr-2024
PMCID:PMC11021597
doi:10.3389/fpls.2024.1377964
PMID:38633451
Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry Oliveira GD, McManus C, Vale IR, dos Santos VM Pathogens 18-Mar-2024
PMCID:PMC10974541
doi:10.3390/pathogens13030260
PMID:38535603
Isolation and characterization of novel bioplasticizers from rose (Rosa damascena Mill.) petals and its suitability investigation for poly (butylene adipate-co-terephthalate) biofilm applications Edayadulla N, Divakaran D, Chandraraj SS, Suyambulingam I, Jayamani E, Sanjay MR, Siengchin S 3 Biotech 12-Mar-2024
PMCID:PMC10933221
doi:10.1007/s13205-024-03956-1
PMID:38486820
Influence of Lemongrass Essential Oil (Cymbopogon flexuosus) Supplementation on Diabetes in Rat Model Júnior AS, Aidar FJ, Silva LA, de B. Silva T, de Almeida SF, Teles DC, de L. Junior W, Schimieguel DM, de Souza DA, Nascimento AC, Camargo EA, dos Santos JL, de O. e Silva AM, de S. Nunes R, Borges LP, Lira AA Life (Basel) 04-Mar-2024
PMCID:PMC10971504
doi:10.3390/life14030336
PMID:38541661
Pathogenesis, Prophylaxis, and Treatment of Candida auris Preda M, Chivu RD, Ditu LM, Popescu O, Manolescu LS Biomedicines 01-Mar-2024
PMCID:PMC10968176
doi:10.3390/biomedicines12030561
PMID:38540174
Molecular Characterization and Phylogenetic Analysis of Centipedegrass [Eremochloa ophiuroides (Munro) Hack.] Based on the Complete Chloroplast Genome Sequence Wang H, Zhang Y, Zhang L, Wang J, Guo H, Zong J, Chen J, Li D, Li L, Liu J, Li J Curr Issues Mol Biol 19-Feb-2024
PMCID:PMC10888139
doi:10.3390/cimb46020106
PMID:38392224
Lemongrass (Cymbopogon flexuosus) growth rate, essential oil yield and composition as influenced by different soil conditioners under two watering regimes Mwithiga G, Maina S, Muturi P, Gitari J Heliyon 02-Feb-2024
PMCID:PMC10867615
doi:10.1016/j.heliyon.2024.e25540
PMID:38370218
Exploring the Clinical Applications of Lemongrass Essential Oil: A Scoping Review Kusuma IY, Perdana MI, Vágvölgyi C, Csupor D, Takó M Pharmaceuticals (Basel) 25-Jan-2024
PMCID:PMC10892616
doi:10.3390/ph17020159
PMID:38399374
Tetraclinis articulata (Vahl) Mast.: Volatile constituents, antioxidant, antidiabetic and wound healing activities of its essential oil Khatib S, Mahdi I, Drissi B, Fahsi N, Bouissane L, Sobeh M Heliyon 17-Jan-2024
PMCID:PMC10839871
doi:10.1016/j.heliyon.2024.e24563
PMID:38317922
Fighting Microbial Infections from Escherichia coli O157:H7: The Combined Use of Three Essential Oils of the Cymbopogon Genus and a Derivative of Esculentin-1a Peptide Scotti R, Casciaro B, Stringaro A, Maggi F, Colone M, Gabbianelli R Antibiotics (Basel) 16-Jan-2024
PMCID:PMC10812396
doi:10.3390/antibiotics13010086
PMID:38247645
A literature review of bioactive substances for the treatment of periodontitis: In vitro, in vivo and clinical studies Kim TH, Heo SY, Chandika P, Kim YM, Kim HW, Kang HW, Je JY, Qian ZJ, Kim N, Jung WK Heliyon 11-Jan-2024
PMCID:PMC10826675
doi:10.1016/j.heliyon.2024.e24216
PMID:38293511
Drug resistance patterns and genotype associations of Trichomonas gallinae in meat pigeons (Columba livia): insights from Guangdong Province, China Cai H, Liu Y, Zhu Y, Fang S, Wang D, Yan Z, Shen H, Liao S, Qi N, Li J, Lin X, Hu J, Song Y, Chen X, Yin L, Zhang J, Lv M, Sun M Front Vet Sci 09-Jan-2024
PMCID:PMC10803545
doi:10.3389/fvets.2023.1343321
PMID:38264468
Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A J Nanobiotechnology 05-Jan-2024
PMCID:PMC10770920
doi:10.1186/s12951-023-02284-5
PMID:38183090
Mechanisms of pathogenicity for the emerging fungus Candida auris Horton MV, Holt AM, Nett JE PLoS Pathog 21-Dec-2023
PMCID:PMC10735027
doi:10.1371/journal.ppat.1011843
PMID:38127686

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
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1055/S-2006-961434
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1055/S-2006-961434
Isoelemicin 5318557 Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC 208.25 unknown https://doi.org/10.1055/S-2006-961434
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Dimethyl-2,4,6-octatriene 5368821 Click to see CC=C(C)C=CC=C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-960939
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1992.9698040
https://doi.org/10.1055/S-2006-961997
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1016/S0031-9422(00)80673-1
https://doi.org/10.1055/S-2006-961997
https://doi.org/10.1080/10412905.1994.9698332
Citronellal 7794 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-961997
https://doi.org/10.1080/10412905.1992.9698040
https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1080/10412905.1992.9698040
https://doi.org/10.1055/S-2006-961997
https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1016/S0031-9422(00)80673-1
https://doi.org/10.1055/S-2006-960939
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-960939
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-2006-961434
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1055/S-2006-961434
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-961434
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698332
D-Borneol 6552009 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961434
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1055/S-2006-961434
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698332
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-2006-961434
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-961434
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-960939
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-961434
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961434
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961434
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698332
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-960939
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961434
https://doi.org/10.1080/10412905.1994.9698332
https://doi.org/10.1055/S-2006-960939
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961434
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-960939
https://doi.org/10.1080/10412905.1994.9698332
Valerenal 6440942 Click to see 218.33 unknown https://doi.org/10.1055/S-2006-960939
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961434
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961434
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aS,7S,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 1715310 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)84290-9
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961434
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1994.9698332
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
4-Nonanone 78236 Click to see 142.24 unknown https://doi.org/10.1080/10412905.1994.9698332
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1994.9698332

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