Details Top

Internal ID UUID643fff55acc6d303474641
Scientific name Rhamnus fallax
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 5: 73 (1856)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The primary documented non-medicinal use of *Rhamnus fallax* is as a source of natural yellow and orange dyes. Historically, the unripe fruits have been collected for this purpose. The dye compounds are anthraquinone derivatives, notably emodin and frangulin. These water-soluble dyes are used directly or can be processed into pigments for textiles, particularly on protein fibers like wool and silk. The dye intensity is influenced by mordanting, which allows for different color fastness and shade variations. Fruit harvesting for dye production is a localized activity.

Industrial and craft applications:
While primarily a dye source, there are no specific documented industrial or craft applications beyond dye usage for this species.

Food and beverages (non-medicinal):
No established culinary or beverage uses are documented.

Colorants and tanning:
The bark of *Rhamnus fallax* contains significant levels of condensed tannins. This tannin-rich bark has historically been used locally for tanning leather. The tannins act as binding agents, converting animal hide into leather by cross-linking collagen fibers. The intensity and suitability for specific leather types depend on the concentration and type of tannins present. This tanning application is a minor, traditional craft rather than a large-scale industrial practice. The fruit dyes are also applicable to leather coloration.

Wood and fiber:
No significant timber or fiber applications are documented.

Fragrance and cosmetics:
No documented uses in fragrance or cosmetics.

Properties relevant to use:
The key properties enabling the uses are: (1) The presence of anthraquinone pigments in the fruits, yielding yellow to orange shades on fibers; (2) The presence of high levels of condensed tannins in the bark, suitable for leather tanning through protein precipitation and cross-linking.

Standards and regulation:
No specific standards or regulatory frameworks are documented for this species or its derived products.

Sustainability and sourcing:
Sourcing involves wild harvesting of fruits and bark. Sustainability concerns relate to overharvesting individual plants. Sustainable practices include limiting collection frequency, using selective harvesting, and replanting or allowing natural regeneration. The small, localized scale of traditional use minimizes large-scale environmental impact.

Synonyms Top

Scientific name Authority First published in
Oreoherzogia fallax (Boiss.) W.Vent Feddes Repert. Spec. Nov. Regni Veg. 65: 52 (1962)
Rhamnus crini Orph. ex Boiss. Fl. Orient. 2: 20 (1872)
Atadinus fallax (Boiss.) Hauenschild Taxon 65: 926 (2016)

Common names Top

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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
  • Europe
    • Middle Europe
      • Austria
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000460195
Tropicos 100356806
KEW urn:lsid:ipni.org:names:718330-1
IPNI 718330-1
iNaturalist 955095
GBIF 3875346
USDA GRIN 311613
CMAUP NPO10163

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-(3-methylbut-2-enoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 101618866 Click to see 400.50 unknown via CMAUP database
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-(3-methylbutanoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 101618868 Click to see 402.60 unknown via CMAUP database
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-[(Z)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 13969122 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown via CMAUP database
(4R)-15alpha-(Tigloyloxy)-kaura-16-ene-19-oic acid 101618867 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-5,9,14-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 102239831 Click to see 348.50 unknown via CMAUP database
Ent-Kaurenal 443466 Click to see 286.50 unknown via CMAUP database
Grandifloric acid 159930 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown via CMAUP database
Kaurenoic Acid 73062 Click to see 302.50 unknown via CMAUP database
Kaurenol 443465 Click to see 288.50 unknown via CMAUP database
Methyl ent-16beta,17-dihydroxy-9(11)-kauren-19-oate 46233508 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(C4)(CO)O)(C)C(=O)OC 348.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Vicodiol 182938 Click to see 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see 204.35 unknown via CMAUP database
(1E,6Z)-gamma-humulene 24798696 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol 91457 Click to see 222.37 unknown via CMAUP database
Beta-Selinene 442393 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
[(2S,3R)-2-[(E)-non-1-en-3,5,7-triynyl]oxan-3-yl] acetate 11242289 Click to see CC#CC#CC#CC=CC1C(CCCO1)OC(=O)C 256.30 unknown via CMAUP database
Ichthyothereol acetate 73759958 Click to see CC#CC#CC#CC=CC1CCCOC1OC(=O)C 256.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 5320668 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database

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