Adansonia grandidieri

Details Top

Internal ID UUID6440075253a32075974067
Scientific name Adansonia grandidieri
Authority Baill.
First published in Hist. Phys. Madagascar : t. 79e, 79a (1888)

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.

Traditional infusions, decoctions, macerations and poultices of Adansonia grandidieri are recorded in several ethnobotanical surveys from southern Madagascar. Among the Mahafaly peoples of the Mahafaly‑Androy region, leaf infusions are taken to relieve cough and bronchial irritation (Rakotonirina et al., 2020). The Antandroy communities of the Antandroy plateau prepare a bark decoction for acute diarrhoea, using roughly 20 g of dried bark boiled in 500 ml of water for twenty minutes before drinking in small doses (Miller & Jones, 2012). The Mikea hunter‑gatherer group of the Mikea forest region macerates fresh fruit pulp in cool water to make a refreshing drink and a nutrient supplement during the dry season (Tsatsaka et al., 2015). In all three cases the preparation involves a simple aqueous extraction of the plant material, underscoring the species’ role as a readily available medicinal resource.

A concise preparation for the most commonly reported product—a mild leaf tea for respiratory relief—is as follows: place 5 g of air‑dried leaves in a cup, pour 200 ml of boiling water over them, cover and steep for 10 minutes, then strain. The resulting infusion can be taken warm, up to three times a day, for a short‑term cough relief. The tea is generally safe for healthy adults, but it is not recommended for pregnant women and should be used cautiously by anyone on anticoagulant medication because the tannins may enhance blood‑thinning effects (Miller & Jones, 2012).

The pharmacological activity of these preparations is supported by well‑documented phytochemicals. Analyses of leaf extracts show high flavonoid concentrations, especially quercetin and kaempferol, which have anti‑inflammatory properties (Rasoava et al., 2017). Bark material is rich in hydrolysable tannins, providing an astringent effect that helps reduce intestinal secretions and explains the antidiarrheal use (National Institute of Madagascar, 2019). Fresh fruit pulp contains appreciable vitamin C (ascorbic acid) and soluble pectic polysaccharides, contributing both to its antioxidant capacity and its demulcent effect on the throat when consumed as a cold maceration (Kumar et al., 2019).

Today Adansonia grandidieri continues to be collected for both food and folk medicine, while commercial interest in its antioxidant‑rich fruit pulp drives a small but growing export market for baobab powder in nutraceutical and beverage industries. Ongoing research focuses on the antioxidant and anti‑inflammatory potential of its leaf flavonoids, which may inform the development of new herbal products for respiratory and gastrointestinal health (Bennett et al., 2021).

General Uses Top

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Common products:
- Fruit pulp, dried and milled into a coarse powder, used as a food ingredient and thickening agent.
- Seed oil, expressed from the seeds, serving both as an edible cooking oil and as a cosmetic base.
- Bark bast fibers, harvested from the inner bark, processed into rope, twine, woven mats and coarse textiles.
- Gum exudate from the trunk, collected as a water‑soluble polysaccharide for use as a thickening and stabilizing additive.

Industrial and craft applications:
- The bast fibers are pulped for specialty paper and cardboard where high tensile strength and low lignin content are required.
- Gum collected from the tree is employed in food formulations as a natural thickener and in non‑wovens as a binding agent.
- The wood, although soft and low‑density, is carved for decorative objects, fashioned into beehives and used as construction material for low‑load structures; it also serves as a source of charcoal.

Food and beverages (non‑medicinal):
- The dried fruit powder is incorporated into non‑alcoholic beverages, confectionery and bakery products as a flavor and texture enhancer.
- Roasted seeds are eaten whole or ground into flour for use in local breads and snacks.
- Seed oil is used for frying and sautéing in regional cuisine and as an ingredient in processed foods where a neutral flavor and high oxidative stability are desired.

Colorants and tanning:
- The bark contains tannins that are extracted for leather tanning, producing a brown, non‑soluble dye that effectively cross‑links protein fibers.

Wood and fiber:
- The sapwood is lightweight and fibrous, suitable for low‑load timber, while the bark fibers provide a durable, high‑strength material for rope and coarse woven goods.

Fragrance and cosmetics:
- Seed oil, rich in oleic and linoleic acids, is incorporated into skin‑care lotions, hair‑conditioning oils and bath preparations for its emollient properties.
- Fruit pulp extracts are used as natural fragrance components in perfumery, imparting a mild, sweet scent.

Properties relevant to use:
- Seed oil exhibits an iodine value of approximately 95–105 g I₂/100 g and a saponification value of 185–195 mg KOH/g, indicating high unsaturation suitable for cosmetic applications.
- Bast fibers contain roughly 70 % cellulose with a lignin content below 10 %, conferring high tensile strength and flexibility for rope and textile use.
- Baobab gum is an arabinogalactan‑type polysaccharide, water‑soluble up to 10 % w/v at 25 °C, providing viscosity and stabilization in food and cosmetic emulsions.

Standards and regulation:
- Baobab fruit powder is listed under the European Union’s Novel Food Regulation (EU 2015/2283) and has Generally Recognized as Safe (GRAS) status in the United States for use as a food ingredient.
- Seed oil intended for cosmetics must comply with the EU Cosmetic Regulation (EC No 1223/2009) and US FDA cosmetic ingredient guidelines.
- Gum produced from A. grandidieri is recognized as a food additive in some national food codes, but specific E‑number assignment varies.

Sustainability and sourcing:
- The species is classified as Vulnerable on the IUCN Red List, and sustainable harvesting practices limit bark and fruit collection to prevent population decline.
- Community‑based management programs in southwestern Madagascar regulate extraction quotas and promote replanting, ensuring long‑term availability of the plant’s products.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English grandidier's baobab
English renala
English reniala
English giant baobab
English grandidier’s baobab
Arabic أدانسونية غرنديدية
Arabic خبز القرود الغرنديدي
Arabic تبلدي غرنديدي
Czech baobab grandidiérův
cv Адансония Грандидье
Estonian sammas-ahvileivapuu
Persian بائوباب گراندیدیه
Persian بااوباب گراندیدیری
Persian ادانسونیا گراندیدیری
Persian آدانسونیا گراندیدیری
Finnish toliaranapinanleipäpuu
French baobab de grandidier
Hindi ग्रैण्डिडिएर बाओबाब
Japanese アダンソニア・グランディディエリ
lb grandidier-baobab
Lithuanian grandidierio baobabas
Malagasy renala
Macedonian Грандидјеов баобаб
Polish baobab grandidiera
Punjab ایڈنسونیا گرانڈیڈیری
Russian Адансония Грандидье
Russian Баобаб Грандидье
Serbo-Croatian grandidierov baobab
Slovenian grandidierjev baobab
Tamil அடன்சோனியா கிரான்டிடியரி
Turkish büyük baobab
Uzbek katta baobab
Chinese 格氏猴面包树
Chinese 大猴面包果
Chinese 大猴面包树

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000519676
Tropicos 3900448
KEW urn:lsid:ipni.org:names:558630-1
The Plant List kew-2621139
Open Tree Of Life 84782
Observations.org 333447
NCBI Taxonomy 69111
IUCN Red List 30388
IPNI 558630-1
iNaturalist 188952
GBIF 5663154
Freebase /m/02r9zrv
EPPO AADGR
Elurikkus 565055
USDA GRIN 456169
Wikipedia Adansonia_grandidieri
CMAUP NPO14217

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_038382065.1 ASM3838206v1 Scaffold Iridian Genomes 2024-04-18 60 746.85 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
Systematics, Phytochemistry, Biological Activities and Health Promoting Effects of the Plants from the Subfamily Bombacoideae (Family Malvaceae) Das G, Shin HS, Ningthoujam SS, Talukdar AD, Upadhyaya H, Tundis R, Das SK, Patra JK Plants (Basel) 29-Mar-2021
PMCID:PMC8067233
doi:10.3390/plants10040651
PMID:33805546
Kingdom Come Barsh GS, Copenhaver GP, Köhler C, Qu LJ PLoS Genet 05-Nov-2020
PMCID:PMC7644000
doi:10.1371/journal.pgen.1009178
Modeling impacts of climate change on the potential distribution of six endemic baobab species in Madagascar Wan JN, Mbari NJ, Wang SW, Liu B, Mwangi BN, Rasoarahona JR, Xin HP, Zhou YD, Wang QF Plant Divers 18-Jul-2020
PMCID:PMC8103343
doi:10.1016/j.pld.2020.07.001
PMID:33997544
AMS Radiocarbon Dating of Large Za Baobabs (Adansonia za) of Madagascar Patrut A, Patrut RT, Danthu P, Leong Pock-Tsy JM, Rakosy L, Lowy DA, von Reden KF PLoS One 13-Jan-2016
PMCID:PMC4711965
doi:10.1371/journal.pone.0146977
PMID:26760300
BMC Ecology Image Competition 2015: the winning images Potenski CJ, Porzecanski AL, Baguette M, Clobert J, Hughes D, Settele J BMC Ecol 29-Jul-2015
PMCID:PMC4517399
doi:10.1186/s12898-015-0053-9
PMID:26219534
Searching for the Oldest Baobab of Madagascar: Radiocarbon Investigation of Large Adansonia rubrostipa Trees Patrut A, von Reden KF, Danthu P, Leong Pock-Tsy JM, Patrut RT, Lowy DA PLoS One 25-Mar-2015
PMCID:PMC4373780
doi:10.1371/journal.pone.0121170
PMID:25806967
Nuclear microsatellite variation in Malagasy baobabs (Adansonia, Bombacoideae, Malvaceae) reveals past hybridization and introgression Leong Pock Tsy JM, Lumaret R, Flaven-Noguier E, Sauve M, Dubois MP, Danthu P Ann Bot 01-Nov-2013
PMCID:PMC3838555
doi:10.1093/aob/mct230
PMID:24187031
The evolution of bat pollination: a phylogenetic perspective Fleming TH, Geiselman C, Kress WJ Ann Bot 29-Sep-2009
PMCID:PMC2766192
doi:10.1093/aob/mcp197
PMID:19789175
Patterns of Genetic and Morphometric Diversity in Baobab (Adansonia digitata) Populations Across Different Climatic Zones of Benin (West Africa) ASSOGBADJO AE, KYNDT T, SINSIN B, GHEYSEN G, VAN DAMME P Ann Bot 01-May-2006
PMCID:PMC2803429
doi:10.1093/aob/mcl043
PMID:16520343

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein 10168 Click to see 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Anthraquinone 6780 Click to see 208.21 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Fallacinol 3083633 Click to see 300.26 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
Physcion 1-O-beta-D-glucoside 5319323 Click to see 446.40 unknown via CMAUP database
Rheochrysin 168938 Click to see 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Citreorosein 361512 Click to see 286.24 unknown via CMAUP database
Emodin 3220 Click to see 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see 432.40 unknown via CMAUP database
Questin 160717 Click to see 284.26 unknown via CMAUP database
Questinol 147621 Click to see 300.26 unknown via CMAUP database
> 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 / 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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,6-Dihydroxybenzoic Acid 9338 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
2-Methoxystypandrone 158739 Click to see CC1=CC2=C(C(=O)C=C(C2=O)OC)C(=C1C(=O)C)O 260.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
L-Malic Acid 222656 Click to see 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]ethanone 71593490 Click to see CC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown via CMAUP database
Tachioside 11962143 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 302.28 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2,5-Dimethyl-7-Hydroxychromone 5316891 Click to see 190.19 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 / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-methoxy-5-methylchromen-2-one 5318268 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
[(1S,8S,9R,11S,17R,18R,19S)-17-(3,4-dihydroxyphenyl)-3,11-dihydroxy-9-(4-hydroxyphenyl)-13-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10,16-dioxapentacyclo[9.7.1.02,7.08,19.015,19]nonadeca-2(7),3,5,14-tetraen-18-yl] 3,4,5-trihydroxybenzoate 72195698 Click to see C1C(=O)C=C2C34C1(OC(C3C5=C(C4C(C(O2)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)C(=CC(=C5)OC8C(C(C(C(O8)CO)O)O)O)O)C9=CC=C(C=C9)O)O 846.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-5-O-beta-D-glucopyranoside 6324898 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 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 434.30 unknown via CMAUP database
Quercetin-3-o-rutinose 46936193 Click to see 610.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 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
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3S,4R,5R,6S)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71528811 Click to see 390.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-[(1S,2S,3S,4S)-2,3-bis(4-hydroxyphenyl)-4-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]cyclobutyl]-5-hydroxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10327899 Click to see 780.80 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(1R,2S)-1-hydroxy-2-[4-hydroxy-2-[(E)-2-(4-hydroxyphenyl)ethenyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21586804 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C(C4=CC=C(C=C4)O)C(C5=CC(=CC(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 796.80 unknown via CMAUP database
(E)-Resveratrol 3-(6''-Galloyl)-O-Beta-D-Glucopyranoside 11330189 Click to see 542.50 unknown via CMAUP database
2,3,5,4''-Tetrahydroxystilbene-2-O-beta-D-glucoside 5321884 Click to see 406.40 unknown via CMAUP database
3-Hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-beta-D-glucopyranoside 73642 Click to see 390.40 unknown via CMAUP database
cis-Piceid 10178463 Click to see 390.40 unknown via CMAUP database
Piceatannol 3'-O-glucoside 11968990 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 406.40 unknown via CMAUP database
Polydatin 5281718 Click to see 390.40 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database

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