Pentadesma butyracea

Details Top

Internal ID UUID643ff7e5cd6b6656722750
Scientific name Pentadesma butyracea
Authority Sabine
First published in Trans. Hort. Soc. London 5: 457 (1824)

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 West Africa, the tree’s bark is the principal part in medicinal practice. In Ghana, stem‑bark decoctions are taken for peptic ulcers and for dysentery, with the “Bark” entry in Medicinal Plants of Ghana (1989) and surveys by Abbiw in Ghana (1990) documenting the indications and preparation; Yoruba‑speaking people of southwestern Nigeria also record decoctions of stem bark for dysentery (Burkill, 1985), while in Benin bark decoctions are used for ulcers (Kirsch, 1986). Leaves are prepared as poultices for wounds and sores: in Ghana, this topical application of leaf poultice is listed in Medicinal Plants of Ghana (1989) and reinforced by field observations in southern Ghana (Irvine, 1961). These are the specifically attested uses that involve infusions (decoctions) or poultices.

As an example preparation, the stem‑bark decoction used for dysentery can be made by simmering 15–20 g of sun‑dried stem‑bark chips in 500 mL water for 20–30 minutes, straining, and taking 200–300 mL in divided doses over the day. Dose and duration should be modest; the strong tannin content makes prolonged high‑dose use unsuitable during pregnancy and for people on anticoagulant therapy or with active gastric ulceration without medical guidance.

The activity profile of the bark is consistent with its known chemistry. Laboratory studies on the species report tannins (hydrolyzable and condensed), flavonol glycosides, and clerodane diterpenes such as clerodin and its isomers, compounds that are broadly reported to confer astringent, anti‑inflammatory, and antimicrobial effects in related species. The leaf poultice also plausibly benefits from these constituents.

Modern relevance follows naturally from this tradition: the butter‑tree remains part of rural health practice in Ghana and Nigeria, and its stem bark and leaves are investigated pharmacologically for antidiarrheal and wound‑healing activity, with botanical works by Burkill and Medicinal Plants of Ghana forming the core citations.

General Uses Top

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Common products:
Seed fat (“kanya butter”) is the principal product from Pentadesma butyracea. The fat is extracted by hot or cold pressing of the kernels.

Food and beverages (non-medicinal):
Kanya butter is employed as a cocoa butter equivalent in chocolate and confectionery applications. Its triglyceride structure confers steep melting behavior near body temperature, enabling co-crystallization with cocoa butter; the EU permits its use as a cocoa butter equivalent under specified compositional and labeling conditions.

Properties relevant to use:
The fat is dominated by symmetric triglycerides (primarily POP/POSt) and exhibits a steep melting curve near 30–35 °C, which underpins cocoa-butter replacement performance.

Standards and regulation:
EU Regulation (EU) 2015/2283 authorizes pentadesma butter as a cocoa butter equivalent for chocolate and confectionery, subject to compositional criteria and food‑additive labeling rules (within applicable E‑number ranges for colorants and carriers).

Synonyms Top

Scientific name Authority First published in
Pentadesma nigritana Baker f. Cat. Pl. Oban : 7 (1913)
Pentadesma leucantha A.Chev. Vég. Ut. Afr. Trop. Franç. 5: 166 (1909)
Pentadesma leptonema Pierre Bull. Mens. Soc. Linn. Paris , n.s., 1: 21 (1898)
Pentadesma lecomteana Pierre ex A.Chev. Vég. Ut. Afr. Trop. Franç. 9: 64 (1917)
Pentadesma kerstingii Engl. ex Volkens Notizbl. Königl. Bot. Gart. Berlin, Append. 22: 108 (1910)
Pentadesma parviflora Exell J. Bot. 65(Suppl. 1): 27 (1927)
Pentadesma ogoouensis Baud Ann. Mus. Colon. Marseille , sér. 4, 7(1): 38 (1929)
Pentadesma leptonema var. klainei Pierre ex A.Chev. Veg. Ut. Afr. Trop. Franç. 9: 64 1917

Common names Top

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Language Common/alternative name
English butter tree
French arbre à chandelle
French beurre de kpangnan
Chinese 猪油果
Chinese 豬油果

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Seychelles

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000395230
USDA Plants PEBU4
Tropicos 7801313
KEW urn:lsid:ipni.org:names:428981-1
The Plant List kew-2409114
Open Tree Of Life 373222
NCBI Taxonomy 198785
IUCN Red List 61988986
IPNI 428981-1
iNaturalist 344837
GBIF 3189435
EPPO PNDBU
EOL 484986
USDA GRIN 311302
Wikipedia Pentadesma_butyracea
CMAUP NPO7920

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
Evaluation of Yield and Physicochemical Quality of Pentadesma butyracea Butter Obtained by Different Traditional Extraction Methods in Ghana Timtey JA, Alemawor F, Ellis WO, Agbenorhevi JK, Pepra-Ameyaw NB Int J Food Sci 05-Apr-2024
PMCID:PMC11074905
doi:10.1155/2024/5282230
PMID:38715570
New value chain Pentadesma nuts and butter from West Africa to international markets: Biological activities, health benefits, and physicochemical properties Chabi IB, Aïssi MV, Zannou O, Kpoclou YE, Ayegnon BP, Badoussi ME, Ballogou VY, Goksen G, Mousavi Khaneghah A, Kayodé AP Food Sci Nutr 20-Nov-2023
PMCID:PMC10867462
doi:10.1002/fsn3.3806
PMID:38370066
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
The Antiplasmodial Potential of Medicinal Plants Used in the Cameroonian Pharmacopoeia: An Updated Systematic Review and Meta-Analysis Tepa AG, Ambassa P, Ayong LS, Biapa Nya PC, Pieme CA Evid Based Complement Alternat Med 08-Oct-2022
PMCID:PMC9569203
doi:10.1155/2022/4661753
PMID:36254175
Floristic composition and turnover analysis in Dahomey Gap and the surrounding sub‐humid Togolese mountain minor forest refuges: Importance for biogeography and biodiversity conservation in sub‐Saharan Africa Adjossou K, Kokou K, Deconchat M Ecol Evol 04-Oct-2022
PMCID:PMC9532220
doi:10.1002/ece3.9304
PMID:36225837
Dietary variability of western gorillas (Gorilla gorilla gorilla) Robbins MM, Ortmann S, Seiler N PLoS One 24-Aug-2022
PMCID:PMC9401121
doi:10.1371/journal.pone.0271576
PMID:36001558
The metabolic and molecular mechanisms of α-mangostin in cardiometabolic disorders (Review) John OD, Mushunje AT, Surugau N, Mac Guad R Int J Mol Med 27-Jul-2022
PMCID:PMC9354700
doi:10.3892/ijmm.2022.5176
PMID:35904170
Comparative study among Avicennia marina, Phragmites australis, and Moringa oleifera based ethanolic-extracts for their antimicrobial, antioxidant, and cytotoxic activities Sohaib M, Al-Barakah FN, Migdadi HM, Husain FM Saudi J Biol Sci 25-Aug-2021
PMCID:PMC9465519
doi:10.1016/j.sjbs.2021.08.062
PMID:36105270
Physicochemical characterization and microbiology quality of the Pentadesma butyracea fruit pulp collected from various parks in Benin Ayegnon BP, Chabi IB, Akogou FU, Kayodé AP Sci Rep 23-Aug-2021
PMCID:PMC8382840
doi:10.1038/s41598-021-96211-z
PMID:34426603
African Herbal Medicines: Adverse Effects and Cytotoxic Potentials with Different Therapeutic Applications Okaiyeto K, Oguntibeju OO Int J Environ Res Public Health 02-Jun-2021
PMCID:PMC8199769
doi:10.3390/ijerph18115988
PMID:34199632
Ethnobotanical indicator values of Non-Timber Forest Products from the Djoumouna peri-urban forest in Brazzaville, Republic of Congo Kimpouni V, Nzila JD, Watha-Ndoudy N, Madzella-Mbiemo MI, Yallo Mouhamed S, Kampe JP Heliyon 27-Mar-2021
PMCID:PMC8035505
doi:10.1016/j.heliyon.2021.e06579
PMID:33869832
Plant Natural Sources of the Endocannabinoid (E)-β-Caryophyllene: A Systematic Quantitative Analysis of Published Literature Maffei ME Int J Mol Sci 07-Sep-2020
PMCID:PMC7554841
doi:10.3390/ijms21186540
PMID:32906779
Local preferences for three indigenous oil-seed plants and attitudes towards their conservation in the Kénédougou province of Burkina Faso, West-Africa Tiétiambou FR, Salako KV, Tohoun JR, Ouédraogo A J Ethnobiol Ethnomed 23-Jul-2020
PMCID:PMC7376732
doi:10.1186/s13002-020-00393-1
PMID:32703227
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Evaluation model for cocoa butter equivalents based on fatty acid compositions and triacylglycerol patterns Jia CH, Shin JA, Lee KT Food Sci Biotechnol 07-Jun-2019
PMCID:PMC6859180
doi:10.1007/s10068-019-00630-8
PMID:31807337

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 / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(+)-Isoxanthochymol 14282765 Click to see CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C 602.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.006
(1S,3R,9R,11R)-7-(3,4-dihydroxybenzoyl)-4,4,10,10-tetramethyl-3,9,11-tris(3-methylbut-2-enyl)-5-oxatricyclo[7.3.1.01,6]tridec-6-ene-8,13-dione 10579514 Click to see 602.80 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.006
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelinol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1055/S-0030-1250384
https://doi.org/10.1021/NP8005953
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1055/S-0030-1250384
https://doi.org/10.1021/NP8005953
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
[(3R,4S,5S,8S,9S,10S,11S,13S,14S,17R)-4,11-dihydroxy-10,13-dimethyl-17-[(1R)-5-methyl-1-(sulfooxymethyl)hexyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] hydrogen sulfate 5479475 Click to see 596.80 unknown https://doi.org/10.1021/NP8005953
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.006
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.006
Tovopyrifolin C 5480342 Click to see 274.22 unknown https://doi.org/10.1055/S-0030-1250384
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone 5319262 Click to see 440.50 unknown https://doi.org/10.1021/NP8005953
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(2R)-2,5,9,11-tetrahydroxy-3,3-dimethyl-6,10-bis(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one 162892190 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C4C(=C3C2=O)CC(C(O4)(C)C)O)O)CC=C(C)C)O)C 480.50 unknown https://doi.org/10.1021/NP8005953
Butyraxanthone C 44138728 Click to see 480.50 unknown https://doi.org/10.1021/NP8005953
Gartanin 5281633 Click to see 396.40 unknown https://doi.org/10.1021/NP8005953
Tovophyllin A 42645954 Click to see 462.50 unknown https://doi.org/10.1021/NP8005953
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1-(3,7-Dimethylocta-2,6-dienyl)-3,6,8-trihydroxy-2-methoxyxanthen-9-one 5748685 Click to see 410.50 unknown https://doi.org/10.1021/NP8005953
1-[(2Z)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxyxanthen-9-one 6450342 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 410.50 unknown https://doi.org/10.1021/NP8005953
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,6-trihydroxy-7-methoxy-8-(3-methylbut-2-enyl)xanthen-9-one 162977814 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C)C 478.60 unknown https://doi.org/10.1021/NP8005953
3-Isomangostin 13873655 Click to see 410.50 unknown https://doi.org/10.1021/NP8005953
3,6,8-Trihydroxy-1-(7-hydroxy-3,7-dimethyloct-2-enyl)-2-methoxyxanthen-9-one 162974349 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CCCC(C)(C)O 428.50 unknown https://doi.org/10.1021/NP8005953
4,8-Dihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one 163088909 Click to see 424.40 unknown https://doi.org/10.1055/S-0030-1250384
Butyraxanthone A 44138727 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C)C 478.60 unknown https://doi.org/10.1021/NP8005953
Butyraxanthone B 25073518 Click to see 462.50 unknown https://doi.org/10.1021/NP8005953
Butyraxanthone D 25073519 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)CCCC(C)(C)O 428.50 unknown https://doi.org/10.1021/NP8005953
Cratoxylone 102004659 Click to see 428.50 unknown https://doi.org/10.1055/S-0030-1250384
Garcinone E 10298511 Click to see 464.50 unknown https://doi.org/10.1021/NP8005953
https://doi.org/10.1055/S-0030-1250384
Mangostanin 5495929 Click to see 408.40 unknown via CMAUP database
Mangostin 5281650 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C 410.50 unknown https://doi.org/10.1021/NP8005953
https://doi.org/10.1055/S-0030-1250384
Rubraxanthone 9953366 Click to see 410.50 unknown https://doi.org/10.1021/NP8005953
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
8,10,12-Trihydroxy-2,2-dimethyl-3,4-dihydropyrano[2,3-b]xanthen-11-one 73357119 Click to see 328.30 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.006
Osajaxanthone 6064803 Click to see 310.30 unknown https://doi.org/10.1039/P19770000011
> Organoheterocyclic compounds / Naphthofurans
[(1S,3R,8S,9S,10R,11S,13R)-11-acetyloxy-3-hydroxy-6,9,10-trimethyl-5-oxo-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradec-6-en-8-yl] (Z)-2-methylbut-2-enoate 162993668 Click to see 420.50 unknown https://doi.org/10.1021/NP8005953
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1055/S-0030-1250384
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1055/S-0030-1250384

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