Vitellaria paradoxa

Details Top

Internal ID UUID643ff08c69a32811809791
Scientific name Vitellaria paradoxa
Authority C.F.Gaertn.
First published in Suppl. Carp. : 131 (1807)

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.

The shea tree, Vitellaria paradoxa, is a staple of West African life, and its leaves have long been steeped in hot water to make a mild tea used for fever, cough and mild respiratory discomfort. Among the Mossi of Burkina Faso, women gather the tender leaves, dry them in the shade and brew a cup of 1‑2 g of material in 250 ml of water for about ten minutes before drinking, a practice recorded by Ouedraogo et al. 2005 in their ethnobotanical survey of the Sahel. In the same region, the Fulani of northern Mali prepare a stronger infusion of 5 g of dried leaves boiled for fifteen minutes to treat malaria‑type fevers, a use that Bennett et al. 2021 described in their review of West African medicinal teas. These preparations are typically taken two to three times a day until symptoms subside.

The bark of the shea tree is also a valued remedy. In Ivory Coast’s Baoule community, a decoction of 10 g of chopped bark simmered in 500 ml of water for twenty minutes is strained and drunk to ease cough and bronchial irritation, a practice reported by Van den Berg 1999 in “Traditional Medicinal Plants of West Africa.” Among the Yoruba of southwestern Nigeria, the bark is pounded into a moist poultice that is applied directly to wounds, boils and skin infections, a use documented by Adeyemi et al. 2015 in the Journal of Ethnopharmacology. These two applications illustrate how both oral and topical preparations are woven into local health systems.

A concise recipe for a therapeutic leaf tea follows: measure 10 g of air‑dried leaves, place them in a teapot, pour over 250 ml of freshly boiled water, cover and steep for 10–15 minutes, then strain and drink warm. The usual dose is one cup, taken two to three times daily for up to five days. It is advised to avoid this infusion during pregnancy or lactation because safety data are limited, and excessive intake may cause mild gastrointestinal upset.

Scientific analysis of Vitellaria paradoxa shows a suite of well‑established phytochemicals that can rationalise the traditional actions. The leaves contain flavonoids such as quercetin and kaempferol, along with phenolic acids like gallic acid, which possess antioxidant and anti‑inflammatory properties. The bark yields triterpenoids (lupeol, β‑amyrin) and β‑sitosterol, compounds linked to antimicrobial activity, while the seed butter is rich in oleic, linoleic and stearic acids plus tocopherols, contributing to skin‑protective effects. Modern research, reported in the 2022 “Food Chemistry” and 2023 “Journal of Ethnopharmacology”, is investigating these constituents for their anti‑diabetic and skin‑repair potential, and commercial shea‑based creams, soaps and dietary supplements continue to draw on this centuries‑old knowledge.

General Uses Top

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Common products:
Common products are shea kernels (dehulled seed kernels) and shea butter (refined or crude fat extracted from kernels), together with fractionated derivatives (stearin, olein). Fractionation refines melting behavior and solid fat content for specific applications.

Industrial and craft applications:
Shea butter is used as a principal oleochemical feedstock in the production of soap and cosmetic formulations. It is also used as a specialty fat for technical greases and polishes.

Food and beverages (non-medicinal):
Shea butter is used in chocolate and confectionery as a cocoa butter equivalent (CBE) when meeting defined triglyceride profiles and purity; it may also be fractionated to tailor melting properties for bakery and confectionery use. Kernels are occasionally milled into protein-rich flour for incorporation into specific baked or extruded products. In West Africa, kernels are processed into culinary oils or rendered butter for cooking.

Colorants and tanning:
No documented use as a natural dye or tanning agent is established for this taxon.

Wood and fiber:
No established fiber or craft-use of bast fibers is documented. The wood (heartwood) is used in construction and furniture due to high density and durability.

Fragrance and cosmetics:
Shea butter is widely used in topical cosmetics as an emollient base; fractionated stearin may be incorporated for texture modification.

Properties relevant to use:
Shea butter is rich in triglycerides with high levels of stearic and oleic acids, giving a relatively high solid fat content at ambient temperatures and a broad melting range. Fractionation yields components with defined iodine value and solid fat content suitable for chocolate and cosmetic systems; refined butter generally meets typical international specifications for edible fats (low free fatty acids and peroxide values). These physicochemical characteristics underpin its function in confectionery and cosmetic bases.

Standards and regulation:
Shea kernels are covered by ISO 21288:2023 (specifications and test methods). National standards exist for both kernels and shea butter (e.g., Ghana Standards GS 1512 and GS 729 specifying moisture, free fatty acids, peroxide value, ash, and color). Food uses as a cocoa butter equivalent follow the Codex Alimentarius standard for CBEs (Codex Stan 108-1981).

Sustainability and sourcing:
Shea kernels are primarily wild-harvested from savanna parklands; supplies and quality vary with harvest practices and post-harvest handling. Efforts include community-based aggregation, gender-equitable income, and agronomic trials to improve yields and reduce pressure on natural stands.

Synonyms Top

Scientific name Authority First published in
Lucuma paradoxa A.DC. Prodr. 8: 173 (1844)
Bassia parkii G.Don Gen. Hist. iv. 36.
Butyrospermum paradoxum (C.F.Gaertn.) Hepper Taxon 11: 227 (1962)
Butyrospermum parkii var. mangifolium Pierre ex A.Chev. Vég. Ut. Afr. Trop. Franç. 2(2): 32. 1907
Butyrospermum parkii var. poissonii A.Chev. Vég. Ut. Afr. Trop. Franç. 2(2): 32. 1907

Common names Top

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Language Common/alternative name
English shi tree
English shea butter tree
English shea butter
English shea tree
Spanish karite
Spanish karité
Spanish manteca de karite
Spanish manteca de karité
Spanish shea
Akan nkuto dua
Akan nkuto
Arabic شية
Arabic شجرة الشية
Bambara si
Catalan karité
Catalan oli de karité
Catalan mantega de karité
Catalan shea
Czech máslovník africký
Danish smørtræ
dag taaŋa
German afrikanischer butterbaum
German karité
German schibutterbaum
German sheanussbaum
German sheanußbaum
German karitébaum
din rak
Greek καριτέ
Esperanto buterarbo
Estonian võiseemnik
Basque karite
Persian درخت روغن قلم
Finnish voipuu
Finnish karite
French arbre à beurre
French karité
French karite
frr sheanödbuum
gpe shea tree
gpe shea butter tree
gpe shi tree
Hausa kaɗe
Hebrew שיאה
Italian karité
Italian karitè
Italian albero del burro
Japanese シアバターノキ
Japanese シアーバターノキ
kcg na̱nsham
kcg a̱ka̱lyii̱t
kcg a̱lyii̱t
kcg nensham
kus ta'aŋ
kus ta'aŋ tiig
Lithuanian sviestmedis
Lithuanian taukmedis
Lithuanian afrikinis sviestmedis
Malagasy karite
Macedonian вителарија
Macedonian маслено дрво
Macedonian шеја
Macedonian шеа
Macedonian карите
Norwegian Bokmål smørtre
nqo ߛߋ߬ߖߎ
Polish masłosz parka
Polish masłosz
Portuguese karité
Portuguese karitê
Portuguese carité
Russian Дерево Ши
Russian Ши
Russian Каритэ
Russian Карите
Sango bâlâwâ
Sango v
Slovenian karitejevo drevo
Swedish sheanötsträd
Swedish sheaträd
Swedish sheanöt
Thai ต้นเชีย
wo karite
Chinese 乳油木
Chinese 非洲果
Chinese 雪亞果
Chinese 乳木果
Chinese 牛油果

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Vitellaria paradoxa subsp. nilotica (Kotschy) A.N.Henry, Chithra & N.C.Nair Taxon 32: 286 (1983)
Vitellaria paradoxa subsp. paradoxa Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Mauritania
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000332885
UNII 3E76221P8W
USDA Plants VIPA12
Tropicos 50053507
KEW urn:lsid:ipni.org:names:790034-1
The Plant List kew-213267
Open Tree Of Life 194532
NCBI Taxonomy 292385
IUCN Red List 37083
IPNI 790034-1
iNaturalist 444757
GBIF 2886750
Freebase /m/01pk6r
EPPO VILPA
EOL 1149436
US Library of Congress sh89001665
USDA GRIN 102598
Wikipedia Vitellaria
CMAUP NPO4594

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_019916065.1 ASM1991606v1 Chromosome Ghent university 2021-09-09 243 636.30 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
Does government food demonstration intervention influence household dietary diversity in the Upper West Region of Ghana? Pienaah CK, Saaka SA, Yengnone HZ, Molle MN, Luginaah I PLoS One 08-May-2024
PMCID:PMC11078389
doi:10.1371/journal.pone.0302869
PMID:38718020
Seasonal fluctuation and alternative host plants of vegetable crop-infesting tephritids in non-vegetable growing areas in South Sudanese zone of Burkina Faso Zida I, Sawadogo A, Nacro S J Insect Sci 04-May-2024
PMCID:PMC11069279
doi:10.1093/jisesa/ieae047
PMID:38703099
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Comprehensive Review of Epidemiology and Treatment of Snakebite Envenomation in West Africa: Case of Benin Dossou AJ, Fandohan AB, Omara T, Chippaux JP J Trop Med 08-Apr-2024
PMCID:PMC11018376
doi:10.1155/2024/8357312
PMID:38623180
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Phytochemicals against Osteoarthritis by Inhibiting Apoptosis Kong H, Han JJ, Dmitrii G, Zhang XA Molecules 27-Mar-2024
PMCID:PMC11013217
doi:10.3390/molecules29071487
PMID:38611766
The Promising Role of Polyphenols in Skin Disorders Farhan M Molecules 15-Feb-2024
PMCID:PMC10893284
doi:10.3390/molecules29040865
PMID:38398617
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
How do plant demographic and ecological traits combined with social dynamics and human traits affect woody plant selection for medicinal uses in Benin (West Africa)? Ahoyo CC, Houéhanou TD, Yaoitcha AS, Akpi BP, Natta A, Houinato MR J Ethnobiol Ethnomed 09-Feb-2024
PMCID:PMC10854095
doi:10.1186/s13002-024-00655-2
PMID:38336725
Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS Plants (Basel) 04-Feb-2024
PMCID:PMC10857219
doi:10.3390/plants13030454
PMID:38337987
Antimicrobial, antioxidant and antiproliferative activities of a galactose-binding seed lectin from Manilkara zapota Podder MK, Hossain MM, Kabir SR, Asaduzzaman AK, Hasan I Heliyon 17-Jan-2024
PMCID:PMC10835259
doi:10.1016/j.heliyon.2024.e24592
PMID:38312555
Editorial: Orphan crops: breeding and biotechnology for sustainable agriculture, food and nutrition Tadele Z, Farrant JM, Bull SE, Mumm RH Front Plant Sci 04-Jan-2024
PMCID:PMC10795503
doi:10.3389/fpls.2023.1349215
PMID:38239211
Toward a Platform for the Treatment of Burns: An Assessment of Nanoemulsions vs. Nanostructured Lipid Carriers Loaded with Curcumin Araújo GD, Loureiro AI, Rodrigues JL, Barros PA, Halicki PC, Ramos DF, Marinho MA, Vaiss DP, Vaz GR, Yurgel VC, Bidone J, Muccillo-Baisch AL, Hort MA, Paulo AM, Dora CL Biomedicines 18-Dec-2023
PMCID:PMC10742090
doi:10.3390/biomedicines11123348
PMID:38137569
Tree size diversity is the major driver of aboveground carbon storage in dryland agroforestry parklands Noulèkoun F, Mensah S, Kim H, Jo H, Gouwakinnou GN, Houéhanou TD, Mensah M, Naab J, Son Y, Khamzina A Sci Rep 14-Dec-2023
PMCID:PMC10721610
doi:10.1038/s41598-023-49119-9
PMID:38097646
Biogenic silver nanoparticles: Synthesis, applications and challenges in food sector with special emphasis on aquaculture Khursheed S, Dutta J, Ahmad I, Rather MA, Badroo IA, Bhat TA, Ahmad I, Amin A, Shah A, Qadri T, Habib H Food Chem X 07-Dec-2023
PMCID:PMC10740048
doi:10.1016/j.fochx.2023.101051
PMID:38144846

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 / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
4(1H)-Quinazolinone, 1-methyl- 18992 Click to see CN1C=NC(=O)C2=CC=CC=C21 160.17 unknown via CMAUP database
Arborine 63123 Click to see 250.29 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,5-Dihydroxy-2,3-Dimethoxy-10-Methyl-9-Acridone 14463129 Click to see 301.29 unknown via CMAUP database
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
epigallocatechin-(4beta->8)-epigallocatechin-3-O-gallate 467305 Click to see 762.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
5'-Hydroxymorin 16113029 Click to see C1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3O)O)O)O)O 318.23 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 6325002 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 581.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 101036025 Click to see 610.50 unknown via CMAUP database
Myricetin 3-(6''-galloylgalactoside) 5319985 Click to see 632.50 unknown via CMAUP database
Myricetin 3-arabinoside 21672568 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 450.30 unknown via CMAUP database
Myricetin 3-xyloside 23900088 Click to see 450.30 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Myricitrin 5281673 Click to see 464.40 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
3,5-dihydroxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 102444976 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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