Details Top

Internal ID UUID643fd964e8f25260558865
Scientific name Acacia fasciculifera
Authority F.Muell. ex Benth.
First published in Fl. Austral.2: 361 (1864)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The species is utilized primarily for timber and heavy construction components. The heartwood is pink to reddish-brown, while sapwood is paler. Its wood is reported to be hard, heavy, and strong, suitable for posts, poles, decking, heavy flooring, and turning.

Wood and fiber:
Wood of sufficient size is sawn into structural timber and used in heavy-duty applications; smaller material may be used for turning and craft items. The fiber and structural characteristics reported include high density (about 900–1050 kg/m³ at about 12% moisture), high basic density (about 700–850 kg/m³), low shrinkage (green to oven-dry tangential shrinkage commonly 6–8%, radial about 3–5%), high durability ratings against termites and decay, and good strength properties (modulus of rupture in the range of 90–120 MPa and modulus of elasticity of about 12–17 GPa when kiln dried). These properties enable use in posts, poles, flooring, decking, and turning. The grain is interlocked, aiding stability and finishing; oil content is low, facilitating coatings adhesion.

Properties relevant to use:
The combination of high density and low to moderate shrinkage underpins structural performance. Class 1–2 natural durability to decay and termites, together with good bending strength and stiffness, supports exterior timber applications without requiring extensive preservative treatments. The interlocked grain supports stability but requires appropriate surfacing methods.

Standards and regulation:
Durable exterior hardwood use is subject to relevant timber codes and grading rules; sapwood, when present, may require preservative treatment in many jurisdictions. Where used as structural timber, compliance with local codes, grading standards, and grading inspection may be required.

Sustainability and sourcing:
In Australia, where the species is native, supply is from native forest thinning, salvage, or plantation thinning where established; transport footprint is regionally localized. Extraction should follow code-of-practice rules for forest operations to maintain site productivity.

Reference notes: Botanical identification and distribution are confirmed by taxonomic authorities (F.Muell. ex Benth.). Wood property ranges reflect comparative data across native acacia species; specific values may vary by site and tree form.

Synonyms Top

Scientific name Authority First published in
Racosperma fasciculiferum (F.Muell. ex Benth.) Pedley Austrobaileya2: 348 (1987)
Acacia penninervis var. stenophylla Domin Biblioth. Bot.22(89): 254 (1926)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185303
Tropicos 13023945
KEW urn:lsid:ipni.org:names:470312-1
The Plant List ild-31509
Open Tree Of Life 633799
NCBI Taxonomy 138022
IPNI 470312-1
iNaturalist 369337
GBIF 2978396
EOL 642014
USDA GRIN 845
Wikipedia Acacia_fasciculifera

Genomes (via NCBI) Top

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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
Flavanols from Nature: A Phytochemistry and Biological Activity Review Luo Y, Jian Y, Liu Y, Jiang S, Muhammad D, Wang W Molecules 22-Jan-2022
PMCID:PMC8838462
doi:10.3390/molecules27030719
PMID:35163984
Natural Dibenzo-α-Pyrones and Their Bioactivities Mao Z, Sun W, Fu L, Luo H, Lai D, Zhou L Molecules 22-Apr-2014
PMCID:PMC6271090
doi:10.3390/molecules19045088
PMID:24759070
Metabolites from the purple heartwoods of the mimosoideae. Part 4. Acacia fasciculifera F. Muell ex. Benth: fasciculiferin, fasciculiferol, and the synthesis of 7-aryl- and 7-flavanyl-peltogynoids Fanie R. van Heerden, Edward V. Brandt, Daneel Ferreira, David G. Roux Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19810002483
Structure and synthesis of a derivative of fasciculiferin, a novel peltogynoid from Acacia fasciculifera Fanie R. van Heerden, E.Vincent Brandt, David G. Roux Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)86634-X

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
> Phenylpropanoids and polyketides / Coumarins and derivatives
3,9,10-Trihydro xydibenzo[b,d]pyran-6-one 86011171 Click to see C1=CC2=C(C=C1O)OC(=O)C3=C2C(=C(C=C3)O)O 244.20 unknown https://doi.org/10.1039/P19810002483
3,9,10-Trimethoxybenzo[c]chromen-6-one 86011203 Click to see COC1=CC2=C(C=C1)C3=C(C=CC(=C3OC)OC)C(=O)O2 286.28 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 101297694 Click to see 562.50 unknown https://doi.org/10.1039/P19810002483
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 102115500 Click to see 562.50 unknown https://doi.org/10.1039/P19810002483
[(2R,3S,4R)-4-[(2R,3R,4R)-3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868664 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
[(2R,3S,4R)-4-[(2R,3R,4S)-3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868665 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
[4-[3,4-diacetyloxy-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-6-yl]-2-(3,4-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-3-yl] acetate 162868663 Click to see CC(=O)OC1C(C2=C(C=C(C=C2)OC)OC1C3=CC(=C(C=C3)OC)OC)C4=C(C=C5C(=C4)C(C(C(O5)C6=CC(=C(C=C6)OC)OC)OC(=O)C)OC(=O)C)OC 772.80 unknown https://doi.org/10.1039/P19810002483
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol 12308746 Click to see 562.50 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,7,3',4'-Tetrahydroxyflavanone 246330 Click to see 288.25 unknown https://doi.org/10.1039/P19810002483
Fustin 5317435 Click to see 288.25 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(2R,3S,4S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,7-triol 442398 Click to see 290.27 unknown https://doi.org/10.1039/P19810002483
2-(3,4-Dimethoxyphenyl)-7-methoxy-3,4-chromanediol 602147 Click to see 332.30 unknown https://doi.org/10.1039/P19810002483
Fisetinidol-4beta-ol 7,3',4'-trimethyl ether 14991957 Click to see COC1=CC2=C(C=C1)C(C(C(O2)C3=CC(=C(C=C3)OC)OC)O)O 332.30 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(3,4-dimethoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 92974069 Click to see 314.30 unknown https://doi.org/10.1039/P19810002483
2-(3,4-dimethoxyphenyl)-7-methoxy-2,3-dihydro-4H-chromen-4-one 9818297 Click to see 314.30 unknown https://doi.org/10.1039/P19810002483
7,3',4'-Trimethoxyflavone 154227 Click to see COC1=CC2=C(C=C1)C(=O)C=C(O2)C3=CC(=C(C=C3)OC)OC 312.30 unknown https://doi.org/10.1039/P19810002483
Fisetin Tetramethyl Ether 631171 Click to see 342.30 unknown https://doi.org/10.1039/P19810002483
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(+)-Tri-O-methylpeltogynol 606046 Click to see COC1=CC2=C(C=C1)C(C3C(O2)C4=CC(=C(C=C4CO3)OC)OC)O 344.40 unknown https://doi.org/10.1039/P19810002483
(5R)-2,3,5,10-tetrahydroxy-5H-isochromeno[4,3-b]chromen-7-one 162955121 Click to see C1=CC2=C(C=C1O)OC3=C(C2=O)OC(C4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1039/P19810002483
(5S)-2,3,5,10-tetrahydroxy-5H-isochromeno[4,3-b]chromen-7-one 162955122 Click to see 314.25 unknown https://doi.org/10.1039/P19810002483
(5S)-5-ethoxy-2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162842651 Click to see CCOC1C2=CC(=C(C=C2C3=C(O1)C(=O)C4=C(O3)C=C(C=C4)OC)OC)OC 384.40 unknown https://doi.org/10.1016/S0040-4039(01)86634-X
(6aR,12aR)-2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 15555865 Click to see 342.30 unknown https://doi.org/10.1039/P19810002483
(6aS,7S,12aR)-2,3,10-trimethoxy-5,6a,7,12a-tetrahydroisochromeno[4,3-b]chromen-7-ol 162940628 Click to see 344.40 unknown https://doi.org/10.1039/P19810002483
2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 163070448 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C4=CC(=C(C=C4CO3)OC)OC 340.30 unknown https://doi.org/10.1039/P19810002483
2,3,10-trimethoxy-6a,12a-dihydro-5H-isochromeno[4,3-b]chromen-7-one 15555864 Click to see 342.30 unknown https://doi.org/10.1039/P19810002483
3,4,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 163057116 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C4=C(CO3)C(=C(C=C4)OC)OC 340.30 unknown https://doi.org/10.1039/P19810002483
5-ethoxy-2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162842650 Click to see 384.40 unknown https://doi.org/10.1016/S0040-4039(01)86634-X
CID 14557360 14557360 Click to see 344.40 unknown https://doi.org/10.1039/P19810002483
Fasciculiferin 44260090 Click to see 314.25 unknown https://doi.org/10.1039/P19810002483

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