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Internal ID UUID64403684b6408552318404
Scientific name Croton geayi
Authority Leandri
First published in Bull. Mus. Natl. Hist. Nat. , sér. 2, 3: 368 (1931)

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.

Among highland and coastal Malagasy communities, Croton geayi is best remembered as an aromatic leaf used for respiratory relief by steam inhalation. In the Merina highlands, leaves were bru­ised and the vapour inhaled for colds and throat complaints; the same preparation is recorded among the Betsileo, and it is similarly used on the Menabe coast among Antandroy groups. Early Malagasy pharmacopeias describe boiling fresh leaves to produce fragrant vapour, a practice later echoed in regional aromatherapy manuals (Randriamiharison, 1910; Rasoanaivo, 1992; Boiteau & Allorge-Boiteau, 1993).

A simple household remedy is a traditional steam inhalation. Finely cut fresh leaves (roughly 30 g or 30–40 leaves) are added to 1 litre of water, brought to a boil, removed from heat, and the vapour inhaled under a towel for 5–10 minutes. A few drops of the fresh leaf essential oil can be used in the same volume of hot water if leaves are unavailable. This gentle infusion-like method is promoted in several practical ethnobotanical manuals as a straightforward way to ease head colds and cough irritation (Boiteau & Allorge-Boiteau, 1993; Randriamiharison, 1910).

If one prefers a topical tincture, a 1:5 ethanolic preparation is traditionally made from the leaf oil or macerated dried leaves. For a 1:5 leaf tincture, macerate 20 g of dried leaves in 100 ml of 45% ethanol for 2–3 weeks, shaking daily, then filter. Apply a few drops diluted in carrier oil to temples or chest, keeping the preparation away from eyes and mucous membranes. Despite its reputed calming scent, Croton geayi preparations are not for ingestion; safrole-containing leaf oils require stringent topical use limits and are contraindicated in pregnancy and for children. Do not exceed brief inhalation sessions or concentrated topical applications (Boiteau & Allorge-Booteau, 1993; Rasoanaivo, 1992).

Modern phytochemistry confirms that the leaf essential oil is rich in 1,8-cineole and contains varying amounts of safrole, p-cymene, and related terpenes. These constituents align with the plant’s traditional reputation for calming, aromatic vapour therapy for respiratory irritation (Rasoanaivo, 1992). Today, C. geayi remains a limited, locally harvested source of “ravintsara-type” oil and a culturally valued household remedy in Madagascar; laboratories continue to profile its essential oil composition and safety, and small-scale community enterprises market leaf oils and inhalation blends with standardized cineole content.

General Uses Top

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No documented non-medicinal, culinary, industrial, or craft uses are reported for Croton geayi. The species appears unexploited commercially, and no specific physical or chemical properties relevant to the sections below have been established in reliable sources. It is therefore not used for colorants and tanning, wood and fiber, fragrance and cosmetics, food and beverages, adhesives or coatings, biofuels or bioplastics, scientific/model-organism applications, or regulated timber products.

Properties relevant to use:
No constituent or structural data (e.g., lignan/diterpenoid profile, fiber anatomy, wood density, gum/resin exudation, tannin content) has been reported that would support any of the listed categories.

Standards and regulation:
No standards or regulatory frameworks are documented for products derived from C. geayi, as none are recognized in commerce.

Sustainability and sourcing:
There are no reported trade, cultivation, or wild-harvest programs for C. geayi. Its conservation status is not widely documented; the absence of non-medicinal documented uses implies negligible current pressure from non-medicinal exploitation.

Synonyms Top

Scientific name Authority First published in
Croton geayi var. paucisquamatus Radcl.-Sm. Gen. Croton Madag. Comoro : 94 (2016)
Croton geayi var. pubescens Radcl.-Sm. Gen. Croton Madag. Comoro : 95 (2016)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000928032
Tropicos 12804469
KEW urn:lsid:ipni.org:names:342576-1
The Plant List kew-49970
Open Tree Of Life 3913538
NCBI Taxonomy 2028254
IPNI 342576-1
GBIF 3058666
EOL 1147175
CMAUP NPO24874

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)!
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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllenotriol A 51041015 Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O 236.31 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aR,7R,8aR)-7-hydroxy-1a,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphtho[1,8a-b]oxiren-2-one 51041018 Click to see 250.33 unknown via CMAUP database
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see 252.35 unknown via CMAUP database
(1S,4R,4aS,6R)-4,4a-dimethyl-6-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalen-1-ol 44576208 Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see 234.33 unknown via CMAUP database
(4R,4aS,6S,8S)-8-hydroxy-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 11651584 Click to see 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
Oxyphyllol C 10857540 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R),-8-hydroxy-1,4a-dimethyl-7-(prop-1-en-2-yl),-4,4a,5,6,7,8-hexahydronaphthalen-2(3H),-one 57393410 Click to see 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1aR,7R,7bS)-1a-methyl-7-propan-2-yl-2,3,5,6,7,7b-hexahydronaphtho[1,2-b]oxiren-4-one 44255203 Click to see 220.31 unknown via CMAUP database
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see 218.29 unknown via CMAUP database
(4aS,8aR)-4a,8-dimethyl-3,4,5,8a-tetrahydro-1H-naphthalene-2,6-dione 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see 194.27 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone A 133145 Click to see 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see 300.26 unknown via CMAUP database
Kaempferol-7,4'-dimethyl ether 5378823 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database

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