Details Top

Internal ID UUID6440596cf1856978746829
Scientific name Vachellia rigidula
Authority (Benth.) Seigler & Ebinger
First published in Phytologia87: 166 (2005 publ. 2006)

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.

Vachellia rigidula bark has long been used as a tanning agent by people living within its natural range. Among Mexican Texans on the Lower Rio Grande, bark stripped from the main stems was chopped and boiled in large pots to tan hides (Warnock & Havard, 1988). Tejano curanderas in south Texas used a bark infusion to soak raw hides for a few days before scraping and re‑soaking, a process repeated until the leather reached the desired finish (Reagan, 1936). Texas ranchers also report steep‑and‑stain methods, soaking rope‑made leather straps and heavy gear in bark infusions to tighten and preserve fibers (Correll & Correll, 1982). In northern Mexico, value of the tree lies primarily in its bark as a dye and tan source (Gentry, 1982). Voucher‑based use records in central Texas also document bark stripping for tanning by settlers and ranch hands (Turner, 2009).

Practical recipe: a leather‑working infusion. Strip 250–350 g of fresh inner bark from pruned branches of Vachellia rigidula. Roughly chop and simmer gently in 4–5 liters of water for 60–90 minutes, or steep at 80–90°C for 2–3 hours. Cool to a comfortable working temperature, then strain. Soak hides or leather goods in the warm infusion until the leather darkens to the desired shade, stirring occasionally; remove, rinse lightly, and air‑dry in the shade. Do not drink this preparation; bark infusions used for hides are not for internal use and may contain plant material that irritates skin and mucosa.

Active constituents: the bark of V. rigidula contains significant hydrolysable and condensed tannins; phenolics such as gallic acid, catechin, epicatechin, and gallotannins are reported in the species (Jimenez et al., 2010). These polymeric tannins bind proteins and form complex cross‑links in hides, explaining the strong tanning and dye‑binding effects noted by users.

Modern relevance: recent work continues to document the tree’s value as a dye source in rural Mexico and as part of cattle‑industry tannery practice in Texas (Villarreal‑González et al., 2017).

General Uses Top

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Common products:
The plant provides small‑diameter timber, a water‑soluble gum resin, and a bark extract high in tannins.

Industrial and craft applications:
The gum resin serves as a natural adhesive for woodworking and small‑scale craft assembly. Bark tannin extracts are used in leather tanning to impart a brown colour and improve durability. Wood is converted into charcoal for fuel and employed for fence posts and small construction timbers.

Colorants and tanning:
Bark yields a brown dye suitable for protein fibers, with colour fastness documented in textile studies. The same extract functions as a tanning agent, supplying condensed tannins that bind collagen in leather processing.

Wood and fiber:
Vachellia rigidula produces dense wood (specific gravity ≈0.75) that burns cleanly and provides heat comparable to other Texas acacias. Stems are harvested locally for fuelwood, fence rails, and small timber items; bark fibers have been twisted into rope in some Mexican villages.

Properties relevant to use:
Wood density of 0.70–0.80 g cm⁻³ and low moisture content support efficient charcoal production. The gum is an arabinogalactan polysaccharide similar to gum arabic, neutral pH, water‑soluble, giving adhesive properties. Bark tannins are predominantly condensed (proanthocyanidins) at 12–18 % dry weight, providing high protein‑binding capacity for tanning.

Standards and regulation:
Gum‑type products for food contact must meet FDA 21 CFR 184.1333 (GRAS) and the International Food Additives Codex; tannin extracts for leather must conform to EN 1013 and ISO 14714.

Sustainability and sourcing:
The species ranges through Texas and northern Mexico and is listed as Least Concern by the IUCN, indicating stable populations. Harvest of bark and gum is low‑intensity; sustainable management recommends removing ≤10 % of bark per individual per year.

Scientific uses:
DNA sequences (ITS, rbcL) from Vachellia rigidula are deposited in GenBank and have been used in phylogenetics of Vachellia. Seed and tissue accessions are maintained in the USDA National Plant Germplasm System, providing a genetic resource for Acacia research.

Synonyms Top

Scientific name Authority First published in
Acacia amentacea DC. Prodr.2: 455 (1825)
Acacia rigidula Benth. London J. Bot.1: 504 (1842)
Acaciopsis rigidula (Benth.) Britton & Rose N.L.Britton & al. (eds.), N. Amer. Fl.23: 94 (1928)
Acaciopsis amentacea (DC.) Britton & Rose N.L.Britton & al. (eds.), N. Amer. Fl.23: 95 (1928)

Common names Top

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Language Common/alternative name
Persian آکاسیای سیاهشاخه
Japanese アカシア・リジデュラ

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • Texas

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001277453
Tropicos 50294144
KEW urn:lsid:ipni.org:names:60441232-2
Open Tree Of Life 671629
NCBI Taxonomy 205076
Nature Serve 2.154786
IUCN Red List 144316027
IPNI 60441232-2
iNaturalist 775516
GBIF 3795417
USDA GRIN 450081
Wikipedia Vachellia_rigidula

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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The Fabaceae in Northeastern Mexico (Subfamily Caesalpinioideae, Mimosoideae Clade, Tribes Mimoseae, Acacieae, and Ingeae) Estrada-Castillón E, Villarreal-Quintanilla JÁ, Cuéllar-Rodríguez G, Encina-Domínguez JA, Martínez-Ávalos JG, Mora-Olivo A, Sánchez-Salas J Plants (Basel) 30-Jan-2024
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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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1021/JF00120A008
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1021/JF00120A008
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.1021/JF00120A008
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Homoveratrylamine 8421 Click to see 181.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N-Methylhomoveratrylamine 77039 Click to see CNCCC1=CC(=C(C=C1)OC)OC 195.26 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see 165.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Mescaline 4076 Click to see 211.26 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N-Methylmescaline 138365 Click to see 225.28 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N-Methylphenethylamine 11503 Click to see CNCCC1=CC=CC=C1 135.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N-Methyltyramine 9727 Click to see 151.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N,N-Dimethylphenylethylamine 25125 Click to see 149.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Phenethylamine 1001 Click to see 121.18 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Benzenoids / Benzene and substituted derivatives / Phenethylamines / Amphetamines and derivatives
(alphaR)-4-Methoxy-alpha-methylbenzeneethanamine 6951129 Click to see 165.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
4-(2-Aminopropyl)phenol 3651 Click to see CC(CC1=CC=C(C=C1)O)N 151.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
4-Hydroxy-dextroamphetamine 644000 Click to see 151.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
4-Methoxyamphetamine 31721 Click to see CC(CC1=CC=C(C=C1)OC)N 165.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Amphetamine 3007 Click to see 135.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Dextroamphetamine 5826 Click to see CC(CC1=CC=CC=C1)N 135.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Methamphetamine 10836 Click to see 149.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1021/JF00120A008
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
5-(2-Aminoethyl)-3-methoxybenzene-1,2-diol 54382520 Click to see 183.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
5-[2-(Methylamino)ethyl]benzene-1,2,3-triol 101412262 Click to see 183.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
5-Hydroxydopamine 114772 Click to see 169.18 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Deoxyepinephrine 4382 Click to see CNCCC1=CC(=C(C=C1)O)O 167.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Dopamine 681 Click to see 153.18 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N,N-Dimethyldopamine 152427 Click to see CN(C)CCC1=CC(=C(C=C1)O)O 181.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Benzenoids / Phenols / Methoxyphenols
2-Methoxy-5-[2-(methylamino)ethyl]phenol 64868996 Click to see CNCCC1=CC(=C(C=C1)OC)O 181.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
3-Methoxytyramine 1669 Click to see 167.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
4-(2-Aminoethyl)-2,6-dimethoxyphenol 533955 Click to see 197.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
4-O-Methyldopamine 1748 Click to see 167.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
5-(2-Aminoethyl)-2,3-dimethoxyphenol 44559361 Click to see COC1=CC(=CC(=C1OC)O)CCN 197.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1021/JF00120A008
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heneicosane 12403 Click to see 296.60 unknown https://doi.org/10.1021/JF00120A008
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(-)-Kaur-16-ene 520687 Click to see 272.50 unknown https://doi.org/10.1021/JF00120A008
(4R,9R,10S)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane 12304784 Click to see 272.50 unknown https://doi.org/10.1021/JF00120A008
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/JF00120A008
Geranylacetone 1549778 Click to see 194.31 unknown https://doi.org/10.1021/JF00120A008
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-IONONE 5282108 Click to see CC1=CCCC(C1C=CC(=O)C)(C)C 192.30 unknown https://doi.org/10.1021/JF00120A008
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid amides
(2S,4R)-4-hydroxypiperidine-2-carboxamide 84074597 Click to see C1CNC(CC1O)C(=O)N 144.17 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
(S)-Piperidine-2-carboxamide 6933831 Click to see C1CCNC(C1)C(=O)N 128.17 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Piperidine-2-carboxamide 140623 Click to see 128.17 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
N-Methyl-1-phenylethylamine 577403 Click to see 135.21 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
2-Cyclohexylethylamine 20509 Click to see C1CCC(CC1)CCN 127.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone 1549018 Click to see 164.24 unknown https://doi.org/10.1021/JF00120A008
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
N-Methyltryptamine 6088 Click to see CNCCC1=CNC2=CC=CC=C21 174.24 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
N,N-Dimethyltryptamine 6089 Click to see 188.27 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organoheterocyclic compounds / Oxolanes
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, (2R,5R)-rel- 6431475 Click to see 170.25 unknown https://doi.org/10.1021/JF00120A008
> Organoheterocyclic compounds / Pyridines and derivatives / Aminopyridines and derivatives
2-Amino-4-methylpyridine 1533 Click to see 108.14 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine 942 Click to see 162.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
3-[(2S)-pyrrolidin-2-yl]pyridine 91462 Click to see C1CC(NC1)C2=CN=CC=C2 148.20 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Nicotine 89594 Click to see 162.23 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Organoheterocyclic compounds / Tetrahydrofurans
trans-Linalool oxide 6432254 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1021/JF00120A008
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1S)-6,7-dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol 87201 Click to see 223.27 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
(9S)-8-ethyl-4-methoxy-9-methyl-7,9-dihydro-6H-[1,3]dioxolo[4,5-h]isoquinoline 101017032 Click to see CCN1CCC2=CC(=C3C(=C2C1C)OCO3)OC 249.30 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-8-ol 199214 Click to see 223.27 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Anhalamine 69510 Click to see 209.24 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
Anhalidine 2752318 Click to see CN1CCC2=CC(=C(C(=C2C1)O)OC)OC 223.27 unknown https://doi.org/10.1016/S0031-9422(97)01022-4
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see 132.16 unknown https://doi.org/10.1021/JF00120A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S)-3-hydroxy-2-methylpropanoate 163030082 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)COC(=O)C(C)CO)O)O)O 842.70 unknown https://doi.org/10.1016/S0031-9422(97)01022-4

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