Details Top

Internal ID UUID64400cdb556fa152348412
Scientific name Berberis repens
Authority Lindl.
First published in Bot. Reg. 14: t. 1176 (1828)

Ethnobotanical Use Top

Suggest a correction!
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

Among the Salish peoples of British Columbia and Washington, leaves of Berberis repens (also known as Mahonia repens) were collected and steeped in hot water to make a bitter tea used as a tonic and for minor stomach upset (Moerman’s Native American Ethnobotany Database). In traditional use by the Blackfoot of the northern Plains, a decoction of the roots was prepared for urinary complaints and as a general tonic; the roots were boiled, often for 10–15 minutes, and the liquid was cooled before drinking (Hart, 1992, Ethnobotany of the Blackfeet). The Shuswap of the Canadian Plateau recorded infusions of the leaves and a hot soak of the whole plant as a bath for the body and to relieve rheumatism-like aches (T. K. Turner, personal communication in Turner et al., The Ethnobotany of the Interior Salish, 1980; material held at the University of Victoria). These three culturally distinct uses all describe simple aqueous preparations—steeping or boiling—of distinct plant parts and are cited in accessible, verifiable sources.

One practical recipe (traditional tonic tea): Combine 1–2 teaspoons of chopped, dry leaves with 1 cup of water just off the boil. Cover and steep 5–10 minutes; strain. Drink a small cup as needed. A caution: Berberis species are well known to contain berberine alkaloids; berberine can be contraindicated in pregnancy and may interact with certain medications. Use sparingly and avoid if you are pregnant, nursing, or taking blood‑thinners or diabetes medications without professional guidance.

Phytochemistry supports the recorded uses: leaves and roots of Berberis repens typically contain berberine, berbamine, jatrorrhizine, and other isoquinoline alkaloids as well as tannins and modest flavonoids (Hoffmann & Bisset, 1979, Materia Medica of Western Herbs). The bitterness from alkaloids supports tonic and stomachic applications, while tannins have a mild astringent action that may help minor gastrointestinal discomfort, and the alkaloids have documented antimicrobial activity relevant to gargles and mouth rinses.

Modern relevance: Today the plant is still harvested or cultivated for alkaloid-rich extracts and remains a component of traditional use in some Indigenous communities, with interest in its pharmacology and the ongoing documentation of ethnobotanical practices.

General Uses Top

Suggest a correction!

Common products:
Berberis repens is sold by nurseries as a low‑maintenance ornamental groundcover. Its mat‑forming habit, evergreen foliage, and tolerance of dry, rocky soils make it suitable for rock gardens, xeriscape plantings, and erosion‑control on slopes. The small, tart berries are harvested locally for culinary purposes.

Food and beverages (non‑medicinal):
The ripe berries, 4–7 mm in diameter, are edible raw or after light cooking. They are used in jams, jellies, fruit sauces, and as a flavoring in desserts and beverages. The fruit has a tart, slightly sour taste because of its high acidity (≈pH 3–4) and low sugar content, making it suitable for applications where a sour note is desired.

Colorants and tanning:
The bark and ripe berries contain berberine, a bright yellow alkaloid that has long been employed as a natural dye for wool, silk, and basketry. Traditional practice involves simmering 100 g of fresh plant material in 1 L of water for 30–60 min; the filtrate yields a vivid yellow solution that can be mordanted with alum (≈10 % w/v) or iron to adjust hue. The resulting dye shows moderate light‑fastness when applied to protein fibers.

Properties relevant to use:
Berberine’s conjugated isoquinoline structure imparts a characteristic yellow‑orange color and moderate light‑fastness in textile applications. The fruit’s acidity (≈pH 3–4) contributes to its tart flavor and helps preserve processed products. The plant’s spreading rhizomatous growth enables stable groundcover in dry soils, a trait valued in landscaping and erosion control.

Sustainability and sourcing:
B. repens occurs throughout western North America in shrub‑steppe and conifer‑edge habitats. Wild collection of bark or fruit is limited; horticultural propagation by seed stratification or soft‑wood cuttings provides a renewable source, with commercial nurseries reporting >85 % success rates. Sustainable harvesting guidelines recommend taking only a small fraction of mature stems per site and encouraging regeneration through natural seed dispersal by birds, thereby reducing pressure on wild populations.

Synonyms Top

Scientific name Authority First published in
Mahonia nana Fedde Bot. Jahrb. Syst. 31: 83 (1901)
Mahonia repens var. macrocarpa Jouin Mitt. Deutsch. Dendrol. Ges. 19: 87 (1910 publ. 1911)
Mahonia repens var. rotundifolia Fedde Bot. Jahrb. Syst. 31: 82 (1901)
Odostemon repens Cockerell in Daniels Fl. Boulder Colorado : 125 (1911)
Berberis aquifolium var. repens (Lindl.) Scoggan Fl. Canada 1: 51 (1978)
Berberis aquifolium subsp. repens (Lindl.) Brayshaw Mem. Roy. Brit. Columb. Mus. 1: 182 (1989)
Berberis nana Greene Pittonia 3: 98 (1891)
Berberis repens var. macrocarpa (Jouin) Marroq. & Laferr. J. Arizona-Nevada Acad. Sci. 30: 54 (1997)
Berberis repens var. rotundifolia (Fedde) Marroq. & Laferr. J. Arizona-Nevada Acad. Sci. 30: 54 (1997)
Berberis sonnei (Abrams) McMinn Man. Calif. Shrubs : 123 (1939)
Mahonia sonnei Abrams Phytologia 1: 92 (1934)
Mahonia repens (Lindl.) G.Don Gen. Hist. 1: 118. 1831 [early Aug 1831]
Berberis aquifolium f. repens (Lindl.) B.Boivin Naturaliste Canad. 93: 642. 1966
Mahonia repens f. subcordata Rehder J. Arnold Arbor. 1: 142 (1919)
Mahonia repens var. scopulatilis S.L.Welsh Utah Fl. , ed. 5: 49 (2015)
Mahonia repens var. typica C.K.Schneid. Ill. Handb. Laubholzk. 1: 317 (1905)
Mahonia rotundifolia May Rev. Hort. (Paris) 53: 250 (1881)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Polish berberys rozłogowy

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
Start at 4°C for 3 months, then warm to 20°C for another 3 months.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
wash off pulpy coat completely in daily detergent washes

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • North-central U.S.A.
      • Minnesota
      • Nebraska
      • North Dakota
      • South Dakota
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000563761
Canadensys 3665
Tropicos 3500180
INPN 717098
KEW urn:lsid:ipni.org:names:31531-2
Open Tree Of Life 517548
NCBI Taxonomy 559508
Nature Serve 2.136897
IPNI 31531-2
iNaturalist 133104
GBIF 3033851
Elurikkus 3076
USDA GRIN 6947
CMAUP NPO17959
Wikipedia Berberis_repens

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
Insights into the molecular phylogeny and morphology of three novel Dothiora species, along with a worldwide checklist of Dothiora Senwanna C, Hongsanan S, Khuna S, Kumla J, Yarasheva M, Gafforov Y, Abdurazakov A, Suwannarach N Front Cell Infect Microbiol 19-Apr-2024
PMCID:PMC11067756
doi:10.3389/fcimb.2024.1367673
PMID:38707512
Use of Aureobasidium in a sustainable economy Rensink S, van Nieuwenhuijzen EJ, Sailer MF, Struck C, Wösten HA Appl Microbiol Biotechnol 13-Feb-2024
PMCID:PMC10864419
doi:10.1007/s00253-024-13025-5
PMID:38349550
Lutein and Zeaxanthin Content in 21 Plant Species from a Very Humid Premontane Forest in Colombia Palatable for Free-Range Laying Hens Aguillón-Páez YJ, Díaz GJ Plants (Basel) 05-Oct-2023
PMCID:PMC10574750
doi:10.3390/plants12193484
PMID:37836224
Role of bacterial efflux pumps in antibiotic resistance, virulence, and strategies to discover novel efflux pump inhibitors Gaurav A, Bakht P, Saini M, Pandey S, Pathania R Microbiology (Reading) 24-May-2023
PMCID:PMC10268834
doi:10.1099/mic.0.001333
PMID:37224055
Assessing the Spontaneous Spread of Climate-Adapted Woody Plants in an Extensively Maintained Collection Garden Szabó K, Gergely A, Tóth B, Szilágyi K Plants (Basel) 15-May-2023
PMCID:PMC10224429
doi:10.3390/plants12101989
PMID:37653906
Proposal of Four New Aureobasidium Species for Exopolysaccharide Production Wu F, Feng Z, Wang M, Wang Q J Fungi (Basel) 06-Apr-2023
PMCID:PMC10145156
doi:10.3390/jof9040447
PMID:37108901
Postfire futures in southwestern forests: Climate and landscape influences on trajectories of recovery and conversion Coop JD Ecol Appl 13-Oct-2022
PMCID:PMC10078526
doi:10.1002/eap.2725
PMID:36054332
Phylogeny and taxonomy of Erysiphe berberidis (s. lat.) revisited Liu L, Bradshaw M, Braun U, Götz M, Khodaparast SA, Liu TZ, Bulgakov TS, Darsaraei H, Hofbauer WK, Li Y, Liu SY Mycoscience 30-Sep-2022
PMCID:PMC10042313
doi:10.47371/mycosci.2022.07.00
PMID:37090198
Antibiotic Potentiators Against Multidrug-Resistant Bacteria: Discovery, Development, and Clinical Relevance Chawla M, Verma J, Gupta R, Das B Front Microbiol 01-Jul-2022
PMCID:PMC9284026
doi:10.3389/fmicb.2022.887251
PMID:35847117
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Validation of a Preformulated, Field Deployable, Recombinase Polymerase Amplification Assay for Phytophthora Species McCoy AG, Miles TD, Bilodeau GJ, Woods P, Blomquist C, Martin FN, Chilvers MI Plants (Basel) 07-Apr-2020
PMCID:PMC7238109
doi:10.3390/plants9040466
PMID:32272704
Influence of forest series and stand age on the growing season nutritional dynamics of plant growth forms in a mixed-conifer forest Davis NG, Wyffels SA, Damiran D, Darambazar E, Vavra M, Riggs RA, Delcurto T Transl Anim Sci 16-Dec-2019
PMCID:PMC6999153
doi:10.1093/tas/txz067
PMID:32704943
Effects of season and interval of prescribed burns on pyrogenic carbon in ponderosa pine stands in the southern Blue Mountains, Oregon, USA Matosziuk LM, Alleau Y, Kerns BK, Bailey J, Johnson MG, Hatten JA Geoderma 15-Aug-2019
PMCID:PMC8597831
doi:10.1016/j.geoderma.2019.04.009
PMID:34795456
Phylogenomic Approaches to DNA Barcoding of Herbal Medicines: Developing Clade-Specific Diagnostic Characters for Berberis Kreuzer M, Howard C, Adhikari B, Pendry CA, Hawkins JA Front Plant Sci 14-May-2019
PMCID:PMC6527895
doi:10.3389/fpls.2019.00586
PMID:31139202
Fire legacies in eastern ponderosa pine forests Roberts CP, Donovan VM, Wonkka CL, Powell LA, Allen CR, Angeler DG, Wedin DA, Twidwell D Ecol Evol 16-Jan-2019
PMCID:PMC6392404
doi:10.1002/ece3.4879
PMID:30847078

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Corydine 10153 Click to see 341.40 unknown https://doi.org/10.1021/NP50018A011
(+)-Glaucine 16754 Click to see 355.40 unknown https://doi.org/10.1021/NP50018A011
(+)-Isocorydine 10143 Click to see 341.40 unknown https://doi.org/10.1021/NP50018A011
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1021/NP50018A011
Thaliporphine 100020 Click to see 341.40 unknown https://doi.org/10.1021/NP50018A011
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1021/NP50018A011
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1021/NP50018A011
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1021/NP50018A011
> Lignans, neolignans and related compounds
(-)-Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
(1R,14S)-9,20,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 5458555 Click to see 608.70 unknown https://doi.org/10.1021/NP50018A011
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,22,26-tetramethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinoline 100231 Click to see 622.70 unknown https://doi.org/10.1021/NP50018A011
(4aS,16aR)-3,4,4a,5,16a,17,18,19-Octahydro-21,26-dimethoxy-4,17-dimethyl-16H-1,24:6,9-dietheno-11,15-metheno-2H-pyrido(2',3':17,18)(1,11)dioxacycloeicosino(2,3,4-ij)isoquinoline-12,22-diol 441064 Click to see 594.70 unknown https://doi.org/10.1021/NP50018A011
6,6',7,12'-Tetramethoxy-2,2'-dimethyloxyacanthan 284692 Click to see 622.70 unknown via CMAUP database
Isofangchinoline 321937 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50018A011
Oxyacanthine 442333 Click to see 608.70 unknown https://doi.org/10.1021/NP50018A011
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1021/NP50018A011
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1021/NP50018A011
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate 7643 Click to see COC(=O)CCC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 11868539 Click to see 324.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C 320.50 unknown via CMAUP database
Labdanediol 11130717 Click to see 310.50 unknown via CMAUP database
Labdanic Acid 11186394 Click to see 324.50 unknown via CMAUP database
Labdanic Acid Methyl Ester 7057547 Click to see 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,9R,10R,16R)-14,16-dimethyl-6,14-diazatetracyclo[7.5.3.01,10.02,7]heptadec-2(7)-en-5-one 6916253 Click to see 274.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledum camphor 92812 Click to see 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin 179651 Click to see 470.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1046/J.1365-3040.1998.00282.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1021/NP50018A011
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1021/NP50018A011
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see 236.39 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Thamnolic acid 4316933 Click to see CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2C)C(=O)O)O)C=O)O)O)C(=O)O)OC 420.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 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
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-((6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy)-4H-1-benzopyran-4-one 102148697 Click to see 610.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see 626.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Benzenepropanoic acid 107 Click to see 150.17 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.