Details Top

Internal ID UUID64401874e9a1d607547029
Scientific name Drimys winteri
Authority J.R.Forst. & G.Forst.
First published in Char. Gen. Pl. 42. 1775 [29 Nov 1775]

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Bark-derived essential oil, known as “winter’s bark oil”, obtained by steam distillation of dried bark.
- Bark-derived natural brown dye, prepared by aqueous extraction and used as a textile colorant.
- Tanning extracts containing tannins, also derived from the bark.
- Timber from mature trees, used in furniture and small construction.

Industrial and craft applications:
- The essential oil serves as a fragrance raw material in soaps, detergents, candles, and fine perfumery.
- The brown dye, extracted from the bark, is employed to color protein fibers (wool, silk) and can be combined with mordants for leather tanning.
- Bark extracts are used in natural craft dye processes for hand‑loom textiles.

Colorants and tanning:
- The bark contains approximately 15 % (dry weight) of hydrolysable tannins, mainly gallotannins and ellagitannins, which provide a reddish‑brown pigment.
- The dye yields a brown hue on wool and silk and is suitable for vegetable‑tanned leather.

Wood and fiber:
- The wood is light yellow to pale brown, relatively soft (density ~0.5 g cm⁻³) and easily machined.
- It is used for interior furniture, small structural elements, and as firewood.

Fragrance and cosmetics:
- The essential oil is rich in eugenol (>30 % of total), β‑caryophyllene, and α‑humulene, giving a warm, spicy aroma that is incorporated into cosmetic formulations, skin‑care products, and perfume bases.

Properties relevant to use:
- Oil composition: eugenol, β‑caryophyllene, α‑humulene; typical specific gravity 0.95–0.98 at 20 °C; refractive index 1.508–1.513; these properties support its role as a stable fragrance material.
- Tannin profile: gallotannins and ellagitannins give high protein‑binding capacity, enabling effective tanning and coloration of protein fibers.

Standards and regulation:
- The essential oil is subject to IFRA (International Fragrance Association) standards for fragrance materials and to the European Cosmetic Regulation (EC No 1223/2009) for cosmetic safety assessments.
- Natural dye and tanning extracts must comply with textile colorfastness standards (ISO 20787).
- Timber extraction in Chile is governed by the National Forest Code and, because the species is listed as Vulnerable, requires official permits and adherence to sustainable harvest quotas.

Sustainability and sourcing:
- Drimys winteri is classified as Vulnerable on the IUCN Red List; over‑harvesting of bark and timber threatens wild populations.
- Sustainable strategies include limited bark extraction, propagation of seedlings for plantation, and compliance with Chilean forestry regulations to ensure long‑term availability.

Synonyms Top

Scientific name Authority First published in
Michelia acris Ruiz & Pav. ex Lopez Anales Inst. Bot. Cavanilles 17(1): 415. 1959
Wintera aromatica Murray Syst. Veg. ed. 14 : 507 (1784)
Drimys aromatica Descourt. Fl. Méd. Antilles 1: 188 (1821)
Drimys polumorpha Spach ex Baill. Hist. Pl. 1: 157 1868
Drimys punctata Lam. Encycl. 2: 330 (1786)
Drimys winteriana Thell. Bull. Herb. Boissier , sér. 2, 8: 781 (1908)
Drimys winteri f. magellanica Eichler Fl. Bras. 13(1): 134 (1864)
Drimys winteri var. morenonis Kuntze Revis. Gen. Pl. 3(2): 2 (1898)
Drimys winteri var. punctata (Lam.) DC. Syst. Nat. 1: 443 (1817)
Drimys winteri var. semiglobulosa Dusén Arq. Mus. Nac. Rio de Janeiro 13: 62 (1903)

Common names Top

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Language Common/alternative name
English winter's bark
Spanish canelo
Spanish canelo de magallanes
Arabic دريمس مجلان
Catalan canelo
Czech rozpylec lékařský
Finnish canelo
Finnish kanelo
Croatian zimska kora
Portuguese casca-de-anta
Quechua chili kanila
Russian Дримис Винтера
Ukrainian Канело
Chinese 林仙
Chinese 冬木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Drimys winteri var. chilensis (DC.) A.Gray U.S. Expl. Exped., Phan. 1: 24 (1854)
Drimys winteri var. winteri Unknown

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000656761
USDA Plants DRWI
Tropicos 34200002
KEW urn:lsid:ipni.org:names:330748-2
The Plant List kew-2777998
PaleoBotany 52680
Open Tree Of Life 777325
NCBI Taxonomy 3419
IUCN Red List 61968097
IPNI 871218-1
iNaturalist 278781
GBIF 4020527
Freebase /m/028411x
EPPO DRIWI
EOL 392723
USDA GRIN 400792
Wikipedia Drimys_winteri

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
White-crested elaenias (Elaenia albiceps chilensis) breeding across Patagonia exhibit similar spatial and temporal movement patterns throughout the year Jara RF, Jiménez JE, Rozzi R PLoS One 18-Apr-2024
PMCID:PMC11025734
doi:10.1371/journal.pone.0299954
PMID:38635514
Biological activity of the essential oil of Drimys winteri Navarro M, Urrejola F, Espinoza M, Silva S, González S, Utreras D, Fernandez K, Bravo J Front Chem 11-Apr-2024
PMCID:PMC11043559
doi:10.3389/fchem.2024.1321300
PMID:38666047
Humid and cold forest connections in South America between the eastern Andes and the southern Atlantic coast during the LGM Pinaya JL, Pitman NC, Cruz FW, Akabane TK, Lopez MD, Pereira-Filho AJ, Grohman CH, Reis LS, Rodrigues ES, Ceccantini GC, De Oliveira PE Sci Rep 24-Jan-2024
PMCID:PMC10808232
doi:10.1038/s41598-024-51763-8
PMID:38267489
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
Deep learning for Chilean native flora classification: a comparative analysis Figueroa-Flores C, San-Martin P Front Plant Sci 11-Sep-2023
PMCID:PMC10520280
doi:10.3389/fpls.2023.1211490
PMID:37767291
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
Chemical Fingerprinting, Aorta Endothelium Relaxation Effect, and Enzymatic Inhibition of Canelo (Drimys winteri J. R. Forst. & G. Forst, (D.C) A. Gray, Family Winteraceae) Fruits Barrientos RE, Romero-Parra J, Cifuentes F, Palacios J, Romero-Jola NJ, Paredes A, Vargas-Arana G, Simirgiotis MJ Foods 01-Jul-2023
PMCID:PMC10340587
doi:10.3390/foods12132580
PMID:37444318
Marine Puupehenone and Puupehedione: Synthesis and Future Perspectives Rosales Martínez A, Rodríguez-García I Mar Drugs 26-May-2023
PMCID:PMC10301801
doi:10.3390/md21060322
PMID:37367647
Comparative Physiological and Transcriptome Analysis Reveals Potential Pathways and Specific Genes Involved in Waterlogging Tolerance in Apple Rootstocks Zhang K, Chen X, Yuan P, Song C, Song S, Jiao J, Wang M, Hao P, Zheng X, Bai T Int J Mol Sci 26-May-2023
PMCID:PMC10253570
doi:10.3390/ijms24119298
PMID:37298249
Argentatin C Analogues with Potential Antinociceptive Activity and Other Triterpenoid Constituents from the Aerial Parts of Parthenium incanum Xu YM, Wijeratne EM, Calderon-Rivera A, Loya-López S, Perez-Miller S, Khanna R, Gunatilaka AA ACS Omega 25-May-2023
PMCID:PMC10249386
doi:10.1021/acsomega.3c02302
PMID:37305315
Cytotoxic Activity, Topoisomerase I Inhibition and In Silico Studies of New Sesquiterpene-aryl Ester Derivatives of (-) Drimenol Araque I, Ramírez J, Vergara R, Mella J, Aránguiz P, Espinoza L, Vera W, Montenegro I, Salas CO, Villena J, Cuellar MA Molecules 08-May-2023
PMCID:PMC10179937
doi:10.3390/molecules28093959
PMID:37175368
Insight into the phytochemical profile and antimicrobial activities of Amomum subulatum and Amomum xanthioides: an in vitro and in silico study Alruhaili MH, Almuhayawi MS, Gattan HS, Alharbi MT, Nagshabandi MK, Jaouni SK, Selim S, AbdElgawad H Front Plant Sci 20-Apr-2023
PMCID:PMC10157186
doi:10.3389/fpls.2023.1136961
PMID:37152127

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
> Organic oxygen compounds / Organic oxides
5,5,8a-Trimethyl-1,4,4a,6,7,8-hexahydronaphthalene-1,2-dicarbaldehyde 5080908 Click to see 234.33 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
https://doi.org/10.1016/S0031-9422(00)00515-X
Polygodial 72503 Click to see 234.33 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
https://doi.org/10.1080/10412905.1995.9700538
https://doi.org/10.1016/S0378-8741(98)00069-5
https://doi.org/10.1016/S0031-9422(00)94542-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(2,5,5,8a-Tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)methanol 298071 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
[(4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]methanol 138113874 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
Drimendiol 11064467 Click to see 238.37 unknown https://doi.org/10.1016/S0031-9422(00)90650-2
https://doi.org/10.1080/10412905.1995.9700538
Drimenol 3080551 Click to see CC1=CCC2C(CCCC2(C1CO)C)(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,4R,4aS,8aS)-1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 14313008 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
1,4-dihydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalene-1,2-dicarbaldehyde 3504627 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
Mukaadial 159088 Click to see CC1(CCCC2(C1C(C=C(C2(C=O)O)C=O)O)C)C 266.33 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see 162.18 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
> Organoheterocyclic compounds / Naphthofurans
(6,6,9a-trimethyl-1-oxo-5,5a,7,8,9,9b-hexahydro-3H-benzo[e][2]benzofuran-7-yl) acetate 45782981 Click to see 292.40 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
[(5aR,7S,9aS,9bR)-6,6,9a-trimethyl-1-oxo-5,5a,7,8,9,9b-hexahydro-3H-benzo[e][2]benzofuran-7-yl] acetate 11483206 Click to see CC(=O)OC1CCC2(C(C1(C)C)CC=C3C2C(=O)OC3)C 292.40 unknown https://doi.org/10.1016/S0031-9422(00)94542-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
(7,8-Diformyl-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl) 3-(4-methoxyphenyl)prop-2-enoate 75028052 Click to see 410.50 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
(7,8-diformyl-4a-hydroxy-4,4,8a-trimethyl-2,3,5,8-tetrahydro-1H-naphthalen-1-yl) 3-(4-methoxyphenyl)prop-2-enoate 73880652 Click to see 426.50 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
[(1R,4aS,8R,8aS)-7,8-diformyl-4,4,8a-trimethyl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 12043873 Click to see CC1(CCC(C2(C1CC=C(C2C=O)C=O)C)OC(=O)C=CC3=CC=C(C=C3)OC)C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
Drimanial 636975 Click to see 426.50 unknown https://doi.org/10.1016/S0031-9422(00)00515-X
> 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 https://doi.org/10.1016/S0378-8741(98)00069-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one 316844 Click to see 450.40 unknown https://doi.org/10.1016/S0378-8741(98)00069-5
Astilbin 119258 Click to see 450.40 unknown https://doi.org/10.1016/S0378-8741(98)00069-5

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