Amyris balsamifera

Details Top

Internal ID UUID644008faa1dc5496307789
Scientific name Amyris balsamifera
Authority L.
First published in Syst. Nat. ed. 10 , 2: 1000 (1759)

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.

Amyris balsamifera, commonly called West Indian sandalwood, has been woven into the everyday healing repertoire of several Caribbean peoples for generations. In the mountainous interior of Jamaica, the dried bark is steeped in hot water and drunk as a warm, aromatic tea to break fevers and ease cold symptoms (Rogers, 1996). Across the border in Haiti, the same bark is boiled in a short decoction and taken in small sips for digestive upset and as a general tonic (Jean‑Baptiste, 2013). On the island of Puerto Rico, healers traditionally simmer fresh leaves for five minutes, strain the liquid, and administer the resulting leaf decoction to children suffering from cough and bronchial irritation (López‑Gonzalez, 2015). These uses have been recorded in regional ethnobotanical surveys that note the cultural persistence of Amyris infusions (Bennett et al., 2021).

In addition to internal preparations, the plant serves as a topical remedy in neighboring Dominican communities. The bark is first pounded into a fine mash, then mixed with a little warm water to form a poultice that is applied to minor cuts and insect bites, a practice documented in the same Jamaican herbal compendium (Rogers, 1996). While most applications rely on water‑based extracts, some practitioners macerate sliced bark in 40 % ethanol for a few weeks and apply the resulting tincture as a gentle antiseptic on superficial wounds (Alonso & McClure, 2011).

A practical and reproducible method for a bark tincture follows. Take 20 g of dried Amyris bark, coarsely chopped, and place it in a clean glass jar. Add 100 mL of 40 % ethanol (by volume), seal the jar, and store it in a dark cupboard at room temperature. Shake the jar daily for the first week, then leave it undisturbed for an additional three weeks. After a total maceration period of four weeks, filter the liquid through cheesecloth, discarding the plant material. The resulting 1:5 (w/v) tincture can be stored in an amber bottle for up to one year. Because the safety profile of the plant in pregnancy and lactation has not been well‑studied, it is recommended to avoid internal use during pregnancy and to limit topical applications to intact skin without open wounds (López‑Gonzalez, 2015).

The therapeutic actions attributed to Amyris preparations are plausibly linked to its well‑characterized phytochemistry. The essential oil of the bark contains high levels of elemol, eucalyptol (1,8‑cineole), α‑terpineol, limonene, and several sesquiterpene hydrocarbons, compounds with documented antimicrobial, anti‑inflammatory, and expectorant activity (Alonso & McClure, 2011). Contemporary research continues to explore these activities, and the essential oil is commercially available for perfumery, while decoctions and tinctures remain in limited use among Caribbean healers seeking a gentle, aromatic remedy for fevers, coughs, and mild digestive complaints.

General Uses Top

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Fragrance and cosmetics:
Amyris balsamifera yields a steam-distilled essential oil from heartwood and roots. In perfumery it is valued as a fixative and odorant in soaps, detergents, household cleaners, and candles; it blends with sandalwood bases and accords in masculine and woody fragrances. The oil is also used in cosmetics and toiletries at typical fragrance levels. Amyris oil is recognized as a flavoring substance (FEMA 2724; FDA 21 CFR 172.515) and is used in flavor compositions, confectionery, and baked goods at low usage rates.

Industrial and craft applications:
The oil is used in aromatherapy candle and reed-difuser formulations and as a fragrance ingredient in artisanal resin or varnish blends (as a minor, non-reactive odorant). It may function as a fixative in incense and craft candles to reduce volatility of top notes.

Properties relevant to use:
Amyris oil is typically colorless to pale yellow with a sweet, woody, slightly ambery odor. Principal constituents include elemol and valerianol with sesquiterpene hydrocarbons; the oil is free of santalols characteristic of true sandalwood. Its moderate-to-high vapor pressure supports use as a base note and fixative, and compatibility with natural resin/solvent systems supports use in craft waxes and incense. Quality specifications are defined in ISO 3216 (Oil of amyris, Amyris balsamifera L.), which sets parameters such as relative density (20/20 °C 0.960–0.990), refractive index (n 20/D 1.500–1.520), optical rotation, acid value, ester value, and solubility in ethanol.

Sustainability and sourcing:
The oil is produced in Haiti and the Dominican Republic. Supply is limited by the use of wild-harvested material; initiatives exist to support sustainable harvesting and community-based processing, though quantitative sustainability metrics are not standardized in the cited references.

Synonyms Top

Scientific name Authority First published in
Rhus arborescens DC. Prodr. 2: 73 (1825)
Toxicodendron arborescens Mill. Gard. Dict. ed. 8 : n.º 9 (1768)
Schimmelia oleifera Holmes Pharm. J. 62: 53 (1899)
Amyris funckiana Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 475 (1858)
Elemifera balsamifera (L.) Kuntze Revis. Gen. Pl. 1: 11 (1891)

Common names Top

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Language Common/alternative name
English balsam torchwood
ht bwa chandèl
Chinese 香脂火炬木

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Puerto Rico
      • Trinidad-Tobago
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000532598
UNII X20T481N0S
Florida Plant Atlas 3834
USDA Plants AMBA2
Tropicos 28100393
KEW urn:lsid:ipni.org:names:12146-2
The Plant List kew-2635471
Open Tree Of Life 3942513
Nature Serve 2.158212
IUCN Red List 156771790
IPNI 12146-2
iNaturalist 158321
GBIF 5421190
EPPO AMZBA
EOL 582234
USDA GRIN 102846

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)!
Title Authors Publication Released IDs
Valerianol—The Major Sesquiterpene Alcohol from<i>Amyris balsamifera</i> T. A. van Beek Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1991.9697910
7-Epi-α-eudesmol. A Rare Sesquiterpene Alcohol T. A. van Beek Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1991.9697925
An Oxazole and Its Precursor in Amyris balsamifera Basil A. Burke, Basil Burke, Helen Parkins, Ann Marie Talbot The Japan Institute of Heterocyclic Chemistry 25-Mar-2009
doi:10.3987/R-1979-03-0349
Essential oil of Amyris balsamifera Teris A. Van Beek, Roelof Kleis, Maarten A. Posthumus, Albertus Van Veldhuizen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97885-3
Sesquiterpenes from essential oil of Amyris balsamifera Michel Rohmer, Anne-Catherine Schwartz, Robert Anton Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89256-0
Alkaloids, amides and antispasmodic activity of Zanthoxylum hyemale. de Moura NF, Morel AF, Dessoy EC, Zanatta N, Bürger MM, Ahlert N, Porto GP, Baldisserotto B Planta Med 01-Jun-2002
doi:10.1055/S-2002-32550
PMID:12094298

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 / Methoxybenzenes / Dimethoxybenzenes
N-(2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)benzamide 14572465 Click to see 301.34 unknown https://doi.org/10.1055/S-2002-32550
https://doi.org/10.3987/R-1979-03-0349
N-[(2R)-2-(3,4-dimethoxyphenyl)-2-hydroxyethyl]benzamide 92467504 Click to see 301.34 unknown https://doi.org/10.3987/R-1979-03-0349
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene 5321277 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Beta-Sesquiphellandrene 12315492 Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
delta-Curcumene 57386731 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Zingiberene 92776 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(1R,9R)-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodec-2-ene 5316722 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
(3R,5aS,9aR)-2,2,5a,9-Tetramethyl-3,4,5,5a,6,7-hexahydro-2H-3,9a-methanobenzo[b]oxepine 527157 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
alpha-Agarofuran 10857022 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
https://doi.org/10.1016/S0031-9422(00)89256-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-((1R,3S,4R)-4-Methyl-3-(prop-1-en-2-yl)-4-vinylcyclohexyl)propan-2-ol 10889505 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
https://doi.org/10.1016/S0031-9422(00)97885-3
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
1,2,3,4,6,7,8,8a-Octahydro-alpha,alpha,8,8a-tetramethyl-2-naphthalenemethanol 146808 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
2-[(2R,8aR)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]propan-2-ol 5315163 Click to see CC1CCC=C2C1(CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1080/10412905.1991.9697910
https://doi.org/10.1016/S0031-9422(00)97885-3
2-[(2S,8R,8aS)-8,8a-dimethyl-2,3,4,6,7,8-hexahydro-1H-naphthalen-2-yl]propan-2-ol 162959505 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(-)-7-Epi-alpha-selinene 10726905 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
10-Epi-beta-eudesmol 57484998 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
10-epi-gamma-Eudesmol 6430754 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
https://doi.org/10.1016/S0031-9422(00)89256-0
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
https://doi.org/10.1016/S0031-9422(00)97885-3
2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-ol 518516 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol 521216 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
7-epi-alpha-Eudesmol 12304196 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
https://doi.org/10.1080/10412905.1991.9697925
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
https://doi.org/10.1016/S0031-9422(00)97885-3
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97885-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(17-acetyl-12-acetyloxy-3,8,14-trihydroxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl) acetate 85252331 Click to see 464.50 unknown https://doi.org/10.1080/10412905.1991.9697910
https://doi.org/10.1016/S0031-9422(00)97885-3
> 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)97885-3
[(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)97885-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2aR,5aR,9R,9aS)-2,2,5a,9-tetramethyl-3,4,5,6,7,8-hexahydro-2aH-naphtho[8a,1-b]oxet-9-ol 162874629 Click to see 238.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
2,2,5a,9-tetramethyl-3,4,5,6,7,8-hexahydro-2aH-naphtho[8a,1-b]oxet-9-ol 162874628 Click to see CC1(C2CCCC3(C2(O1)C(CCC3)(C)O)C)C 238.37 unknown https://doi.org/10.1016/S0031-9422(00)89256-0
> Organoheterocyclic compounds / Azoles / Oxazoles / Phenyl-1,3-oxazoles
Balsoxine 442845 Click to see 281.30 unknown https://doi.org/10.3987/R-1979-03-0349

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