Details Top

Internal ID UUID643fe4c03e6d5450127594
Scientific name Ocimum africanum
Authority Lour.
First published in Fl. Cochinch. : 370 (1790)

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.

Ethnobotanical Uses

Across eastern and southern Africa, Ocimum africanum has been prepared as a simple liquid medicine for feverish colds and coughs. In South Africa, the Zulu and Venda communities traditionally decoct the leaves and sometimes include aerial parts, drinking the liquid while warm to break fevers and calm coughs (van Wyk and Gericke, 2018; Watt and Breyer-Brandwijk, 1962). In Kenya, fresh leaves are infused to treat colds and fevers, and elders recommend a honey-tempered drink for coughs (Kokwaro, 2009; Onyango, 2013). In coastal Mozambique and neighboring areas, leaves are similarly made into a tea to reduce fever and ease respiratory complaints, reflecting a wide regional familiarity with this lemony-scented herb (Jansen, 1981; Verde et al., 2002).

A practical leaf tea is straightforward to prepare. For a fever and cough remedy, steep about 1 heaping tablespoon (roughly 5–8 g) of fresh, clean leaves in 250 ml of freshly boiled water, covered, for 8–12 minutes; strain and drink warm, up to 2–3 cups per day while symptoms persist. If fresh leaves are scarce, use 3–5 g of dried herb per 250 ml of water and infuse 10–15 minutes. The tea is considered mild when used in these amounts; as with all strong-smelling labiates, people with known allergic reactions to basil or mint should avoid it, and evidence on safety in pregnancy and nursing is limited—many authorities advise caution and professional guidance during those periods.

Phytochemical studies of this species repeatedly report the essential-oil chemotype of high linalool with geraniol, citral, and camphor in modest proportions, accompanied by flavonoids such as apigenin and luteolin, and phenolic acids including rosmarinic acid. These constituents are well documented for O. africanum and plausibly account for the mild antispasmodic and soothing actions traditionally sought (Jirovetz et al., 2003; Chagonda et al., 2000; Grayer et al., 1996; Dandlen et al., 2010). The essential oil profile is similar to lemon balm (Melissa officinalis) and suggests antimicrobial support, while rosmarinic acid provides antioxidant potential compatible with the gentle remedy profile.

Today the herb is still occasionally encountered in local markets in Mozambique and South Africa, where it is sold as a leafy green and medicinal tea (Verde et al., 2002; van Wyk and Gericke, 2018). Contemporary pharmacological work on the essential oil and leaf extracts continues to corroborate its antimicrobial and antispasmodic effects, mirroring longstanding traditional indications but not replacing careful, dose-aware use by local practitioners (Jirovetz et al., 2003; Chagonda et al., 2000).

General Uses Top

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Common products:
- Cultivated as a culinary herb; leaves used fresh or dried as a flavoring/spice.
- Steam-distilled essential oil produced from leaves/flowering tops for fragrance and flavor use.

Food and beverages (non-medicinal):
- Leaves incorporated as a flavoring ingredient in foods, especially in Southeast Asian cuisine; leaves may be eaten raw or cooked.

Fragrance and cosmetics:
- Essential oil (high in citral) used in perfumery as a lemon-type fragrance component and as a flavoring agent.

Properties relevant to use:
- Essential oil composition is citral-dominated (neral and geranial), conferring strong lemon aroma suitable for perfumery and flavor applications.
- Plant is cultivated and harvested for oil production by steam distillation of aerial parts.

Standards and regulation:
- Essential oil quality is generally described in national or regional monographs (e.g., European or ISO standards) for basil/ lemon-basil oils; compliance is with established commerce norms for food-grade flavorings and fragrance-grade oils.

Synonyms Top

Scientific name Authority First published in
Ocimum americanum var. pilosum (Willd.) A.J.Paton Kew Bull. 47: 426 (1992)
Ocimum basilicum var. anisatum Benth. Labiat. Gen. Spec. 4. 1832
Ocimum citriodorum Vis. Index Seminum (PAD, Patavium) 1840: 9 (1840)
Ocimum graveolens A.Br. Flora 24: 265 1841
Ocimum petitianum A.Rich. Tent. Fl. Abyss. 2: 176 (1850)
Ocimum pilosum Willd. Enum. Pl. : 629 (1809)
Ocimum basilicum var. pilosum (Willd.) Benth. Pl. Asiat. Rar. 2: 13. 1830
Ocimum pilosum Roxb. Asiat. Res. 11: 173 (1810)

Common names Top

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Language Common/alternative name
Arabic حبق أفريقي
gor balakama
Indonesian kemangi
Japanese レモンバジル
Korean 레몬바질
Dutch citroenbasilicum
Chinese 柠檬罗勒
Chinese 疏柔毛罗勒

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Northern Provinces
    • West-central Tropical Africa
      • Cameroon
      • Zaïre
    • Western Indian Ocean
      • Madagascar
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Netherlands Antilles
    • Central America
      • Guatemala

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000253206
UNII ZFS0SU4466
Tropicos 17607556
KEW urn:lsid:ipni.org:names:452853-1
The Plant List kew-136798
IPNI 452853-1
iNaturalist 360190
GBIF 3898584
Freebase /m/094qqc
EPPO OCICI
USDA GRIN 463843
Wikipedia Lemon_basil
CMAUP NPO11046
Open Tree Of Life 5144688

Genomes (via NCBI) Top

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Scientific Literature Top

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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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Ndelta-acetylornithine 90658764 Click to see 174.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-p-Coumaroylquinic acid 9945785 Click to see 338.31 unknown via CMAUP database
3-p-Coumaroylquinic acid, (Z)- 92135690 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
5-p-Coumaroylquinic acid, (Z)- 90478782 Click to see 338.31 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see 326.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
Caffeic acid 4-O-glucoside 11382279 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 342.30 unknown via CMAUP database
cis-Ferulic acid 4-O-beta-D-glucopyranoside 9820054 Click to see 356.32 unknown via CMAUP database
Trans-4-O-Beta-D-Glucopyranosylferulic Acid 13916049 Click to see 356.32 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2-Hydroxy-4-methoxyphenyl)-6-methoxy-5-benzofuranol 185034 Click to see 286.28 unknown via CMAUP database
Methylsainfuran 44260111 Click to see 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxybutanedioic acid 26176222 Click to see C1=CC(=CC=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O 280.23 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15048037 Click to see 340.32 unknown via CMAUP database
2-[(1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexyl]acetic acid 10569992 Click to see 352.30 unknown via CMAUP database
Methyl 6-O-[(Z)-3-(4-hydroxyphenyl)propenoyl]-beta-D-glucopyranoside 102371158 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 102371159 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)O)O 504.40 unknown via CMAUP database
5,7-dihydroxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 14406834 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6S)-2-[[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781229 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 916.80 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781227 Click to see 962.90 unknown via CMAUP database
[(2S,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781228 Click to see 916.80 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781232 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 786.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781230 Click to see 816.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781231 Click to see 770.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101781233 Click to see 800.70 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-[4-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781226 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O)O 932.80 unknown via CMAUP database
Amurenoside A 10653411 Click to see 932.80 unknown via CMAUP database
Amurenoside B 11803929 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 932.80 unknown via CMAUP database
Clitorin 11592917 Click to see 740.70 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Manghaslin 11498684 Click to see 756.70 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see 772.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-vestitone 44446897 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

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