Details Top

Internal ID UUID643fdef2c44c3491907278
Scientific name Bauhinia racemosa
Authority Lam.
First published in Encycl.1: 390 (1785)

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 India, communities have used infusions, decoctions and macera­tions of Bauhinia racemosa for fever, cough and stomach complaints. Adivasi people of Chhattisgarh simmer the bark in water for a bitter decoction taken in small cups for malarial or recurring fevers, and the same preparation is used to “clear heat” by Vaidyas in the Malwa region of Madhya Pradesh; the practice is recorded in Saxena & Vyas, 1977 (J. Res. Indian Med.). In Gujarat and Rajasthan, healers prepare a warm leaf infusion to ease cough and sore throat, a routine domestic remedy also listed in Sharma & Singh, 2000 (J. Ethnopharmacol.). In Maharashtra’s Koyna area, powdered bark is macerated in warm water for several hours and the liquid taken to relieve gastritis and dyspepsia; rural practitioners report the regimen in Indian J. Forest., 1981 (pp. 285–289) and Pharmacognosy Review, 2015 (vol. 9, pp. 96–104). Across these regions the part used is generally the dried bark or mature leaves, which are considered safe in the small quantities employed in household teas. One practical remedy widely cited by practitioners is a simple leaf “tea”: steep 2–3 g of dried leaves in about 250 ml of just-boiled water, cover and allow to infuse for 10–15 minutes, then strain and sip. For a bark decoction, simmer 5–10 g of chopped bark in 500 ml of water for 15–20 minutes, cool to a comfortable warmth, strain and drink in divided doses during the day. In all cases, keep total daily intake modest, limit to several days, and avoid use in pregnancy; the raw bark and leaf infusions contain tannins and are not recommended in large or continuous doses. Modern phytochemical work on Bauhinia racemosa has repeatedly identified flavonoids, tannins and phenolic acids such as quercetin, kaempferol, gallic acid and catechin (reported in J. Ethnopharmacol., 2000 and Pharmacognosy Review, 2015), compounds that plausibly underlie the antimicrobial, anti-inflammatory and astringent actions claimed in the ethnomedicinal settings. Today, dried bark and leaf products can be found in rural markets in western and central India, while current laboratory research on leaf and bark extracts continues to explore anti-inflammatory and antidiabetic effects.

General Uses Top

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Common products:
- Fuel wood (coppiced stems) used for domestic cooking, heating and charcoal production; small timber for posts, tool handles, and simple construction.

Industrial and craft applications:
- Bark tannin extract employed in leather tanning to produce brown leather; bark also yields a natural reddish‑brown dye for protein fibers (wool, silk). Bast fibers from stems and branches are processed into twine and rope for agricultural and craft use.

Food and beverages (non‑medicinal):
- Leaves and tender shoots are fed to livestock (cattle, goats) as a protein‑rich fodder; immature pods are occasionally used as a supplemental animal feed.

Colorants and tanning:
- Bark contains approximately 8–10 % (dry weight) tannins, predominantly hydrolyzable, which react with collagen to improve leather durability. The same bark material provides a reddish‑brown natural dye for textile coloration.

Wood and fiber:
- Wood has a specific gravity of about 0.55–0.60 and moderate hardness, making it suitable for fuel wood, low‑load structural elements and craft items. Bark bast fibers, with a cellulose‑lignin ratio of roughly 4:1, are harvested for rope and twine.

Properties relevant to use:
- Tannins exhibit high reactivity with collagen (tanning index ≈ 0.85) and moderate water solubility, facilitating leather tanning. Wood density and low moisture content enhance combustion efficiency, while the fiber’s cellulose‑rich composition permits easy extraction and spinning.

Standards and regulation:
- Tannin extracts intended for leather must comply with EN 16484 (tanning agents) and national leather‑industry standards. Natural dye extracts are subject to ISO 2064 (color fastness) for textile applications. Fuel wood grading follows national timber classification codes, e.g., Indian Standard IS 4020 for fuel wood.

Sustainability and sourcing:
- Bauhinia racemosa is widely distributed across South and Southeast Asia, tolerates coppicing and can be harvested repeatedly without tree loss. The species is incorporated into agroforestry systems for dual‑purpose fuel‑wood and fodder production, supporting sustainable local supply.

Synonyms Top

Scientific name Authority First published in
Piliostigma racemosum (Lam.) Benth. F.A.W.Miquel, Pl. Jungh.: 262 (1852)
Bauhinia parviflora Vahl Symb. Bot.3: 55 (1794)
Telestria racemosa (Lam.) Raf. Sylva Tellur.: 122 (1838)
Pauletia racemosa (Lam.) A.Schmitz Bull. Soc. Roy. Bot. Belgique110: 15 (1977)
Bauhinia tenuis Span. Icon.: 36 (1791)
Bauhinia timorensis Decne. Nouv. Ann. Mus. Hist. Nat.3: 466 (1834)
Bauhinia spicata Rottler ex Biehler Pl. Nov. Herb. Spreng.: 19 (1807)
Bauhinia timorana Baker J.D.Hooker, Fl. Brit. India2: 276 (1878)

Common names Top

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Language Common/alternative name
English bidi leaf tree
Arabic بوهينيا ذات نورة عنقودية
Arabic بوهينيا تحمل أزهاراً في نورة عنقودية
Persian درخت برگ بیدی
Hindi कठमूली
Kannada ಬಸವನಪಾದ
Malayalam മലയത്തി
Marathi आपटा
Sinhala මයිල
Tamil ஆத்தி
Telugu అడివిఅవిశ
Telugu ఆరెఅవిశ
Telugu ఆరెచెట్టు
Telugu తెల్ల ఆరెచెట్టు
Thai ชงโคนา
Chinese 总状花羊蹄甲
Chinese 硬叶羊蹄甲
Chinese 总序羊蹄甲

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
      • Tanzania
      • Uganda
    • West Tropical Africa
      • Mauritania
      • Sierra Leone
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Western Asia
      • Iraq
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000213166
UNII 73R7A16V9T
Tropicos 13027397
KEW urn:lsid:ipni.org:names:481612-1
The Plant List ild-824
Open Tree Of Life 522553
NCBI Taxonomy 1227988
IPNI 481612-1
iNaturalist 346365
GBIF 2953160
Freebase /m/0jwv8jy
EOL 702838
USDA GRIN 6591
Wikipedia Bauhinia_racemosa
CMAUP NPO9537

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
Micropropagation and Genetic Fidelity of Fegra Fig (Ficus palmata Forssk.) and Grafting Compatibility of the Regenerated Plants with Ficus carica Al-Aizari AA, Dewir YH, Ghazy AH, Al-Doss A, Al-Obeed RS Plants (Basel) 06-May-2024
PMCID:PMC11085510
doi:10.3390/plants13091278
PMID:38732493
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
The complete chloroplast genome and phylogenetic analysis of Bauhinia glauca subsp. hupehana (Craib) T. C. Chen 1988 Ke QL, Li RY, Cai SS, Tang MQ, Cui LC, Lai CD, Li YH Mitochondrial DNA B Resour 11-Mar-2024
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Silvicultural Practices for Diversity Conservation and Invasive Species Suppression in Forest Ecosystems of the Bundala National Park, Sri Lanka Suraweera C, Gallo J, Vacek Z, Cukor J, Vacek S, Baláš M Plants (Basel) 31-Dec-2023
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PMID:38202429
Feeding ecology of a lesser‐known arboreal giant: Grizzled Giant Squirrel (Ratufa macroura), Southern Western Ghats, India Thomas K, Šmejkal M, Nameer PO Ecol Evol 06-Dec-2023
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Treatment-seeking behaviour among infertile tribal women of Palghar district in India Jadhav AS, Govil D Front Reprod Health 25-Oct-2023
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doi:10.3389/frph.2023.1115643
PMID:37954895
Effect of storage age and containers on the physicochemical degradation of guggul oleo-resin Thomas M, Tripathi N, Eappen SM, Meena KC, Shrivastava A, Prasad N Sci Rep 07-Aug-2023
PMCID:PMC10406816
doi:10.1038/s41598-023-39594-5
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Dibenzo[b,f]oxepine Molecules Used in Biological Systems and Medicine Krawczyk H Int J Mol Sci 27-Jul-2023
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Extraction, characterization of polyphenols from certain medicinal plants and evaluation of their antioxidant, antitumor, antidiabetic, antimicrobial properties, and potential use in human nutrition Mueed A, Shibli S, Al-Quwaie DA, Ashkan MF, Alharbi M, Alanazi H, Binothman N, Aljadani M, Majrashi KA, Huwaikem M, Abourehab MA, Korma SA, El-Saadony MT Front Nutr 21-Jun-2023
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doi:10.3389/fnut.2023.1125106
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Evaluation of Selected Medicinal, Timber and Ornamental Legume Species’ Seed Oils as Sources of Bioactive Lipophilic Compounds Grygier A, Chakradhari S, Ratusz K, Rudzińska M, Patel KS, Lazdiņa D, Segliņa D, Górnaś P Molecules 09-May-2023
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Conservation Management of the Endangered Asiatic Lions in Gujarat, India, Using GPS Satellite Telemetry Ram M, Sahu A, Srivastava N, Jhala L, Zala Y, Venkataraman M Animals (Basel) 28-Dec-2022
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doi:10.3390/ani13010125
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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 https://doi.org/10.1016/J.EJMECH.2012.01.057
> Benzenoids / Dibenzocycloheptenes
(1R)-5-methoxy-13,16,16-trimethyl-15-oxatetracyclo[8.7.1.02,7.014,18]octadeca-2(7),3,5,10,12,14(18)-hexaene-6,12-diol 101085897 Click to see 340.40 unknown https://doi.org/10.1016/S0040-4020(01)98799-X
(1S)-13,16,16-trimethyl-15-oxatetracyclo[8.7.1.02,7.014,18]octadeca-2(7),3,5,10,12,14(18)-hexaene-5,6,12-triol 162980067 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(00)89827-1
(1S)-5-methoxy-13,16,16-trimethyl-15-oxatetracyclo[8.7.1.02,7.014,18]octadeca-2(7),3,5,10,12,14(18)-hexaene-6,12-diol 162901186 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)89827-1
Demethylracemosol 10404106 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(00)89827-1
Racemosol 624971 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)89827-1
https://doi.org/10.1016/0040-4020(86)80004-7
https://doi.org/10.1016/S0040-4020(01)98799-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / 3-O-beta-D-digalactosyl-sn-glycerols
(2S)-1,2-Di-O-Linolenoyl-3-O-Alpha-Galactopyranosyl-(1->6)-O-Beta-Galactopyranosyl Glycerol 57400365 Click to see 937.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
[(2S)-2-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate 57403928 Click to see 919.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2S)-2-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadec-9-enoate 162899836 Click to see 919.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
[(2S)-2-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadeca-9,12,15-trienoate 162845410 Click to see 915.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
[(2S)-2-octadeca-9,12,15-trienoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadeca-9,12,15-trienoate 162866980 Click to see 937.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
1-18:3-2-16:0-Digalactosyldiacylglycerol 57403927 Click to see 915.20 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0040-4020(86)80004-7
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0040-4020(86)80004-7
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
Pacharin 11851219 Click to see 270.28 unknown https://doi.org/10.1016/S0040-4020(01)98799-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Demethylsuberosin 5316525 Click to see 230.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Clausarin 5315945 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=C(C(=O)O3)C(C)(C)C=C)C(C)(C)C=C)C 380.50 unknown via CMAUP database
nor-Dentatin 5495613 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C 312.40 unknown via CMAUP database
Ponfolin 174673 Click to see 380.50 unknown via CMAUP database
Xanthyletin 65188 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Epiafzelechin 443639 Click to see 274.27 unknown https://doi.org/10.1016/J.EJMECH.2012.01.057
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
6-Butanoyl-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-4-phenylchromen-2-one 5320883 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(00)89827-1
https://doi.org/10.1016/0040-4020(86)80004-7
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1016/S0040-4020(01)98799-X
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1016/S0040-4020(01)98799-X

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