Details Top

Internal ID UUID64400f25c9e6b998616844
Scientific name Canarium luzonicum
Authority (Blume) A.Gray
First published in U.S. Expl. Exped., Phan. 1: 374 1854

Ethnobotanical Use Top

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General Uses Top

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Industrial and craft applications:
Manila elemi, the oleoresin tapped from Canarium luzonicum, is a semi-liquid, pale amber resin used in spirit varnishes, oil varnishes, lacquers, printing inks, and as a plasticizer/tackifier in adhesives and natural resin systems. The resin is used both as a base and an additive. In lacquers, it improves leveling, gloss, and flexibility of spirit lacquers. In oil-bound systems, it is combined with drying oils to control rheology and gloss and is suitable for fine art varnishes and protective finishes. Historically, it was adopted as a substitute for copal in varnish making.

Colorants and tanning:
Elemi imparts a warm amber color in varnishes and lacquers, and, when combined with mordanted fibers, it can yield brown tones.

Fragrance and cosmetics:
The resin is a source of elemi oil, used in perfumery as a fixative and fresh-spicy note in fragrance compositions.

Properties relevant to use:
Elemi is a soft, low-melting, semi-liquid oleoresin with high solubility in ethanol and moderate solubility in ether. It comprises a mixture of sesquiterpenes (notably elemol), monoterpenes (e.g., phellandrene, limonene), and phenylpropene derivatives (e.g., elemicin). The resin is readily soluble in alcohol-based media and forms stable, film-forming blends with drying oils and film-forming polymers. It is typically non-drying as a resin but imparts tack when incorporated in adhesives. Volatile constituents confer a characteristic odor and aid in solvent release.

Standards and regulation:
Food contact or ingestible uses are not regulated for this oleoresin. Cosmetic and fragrance uses of elemi oil/oleoresin are subject to industry and regulatory guidelines for fragrance materials; relevant bodies include IFRA for fragrance practices and the EU Cosmetic Regulation for ingredients.

Sustainability and sourcing:
Commercial resin is collected from wild or cultivated trees in the Philippines through bark or stem tapping; tapping intervals and species distribution shape the supply. Sustainable resin harvesting focuses on maintaining tree health and avoiding girdling.

Synonyms Top

Scientific name Authority First published in
Pimela luzonica Blume Mus. Bot. 1: 220 (1850)
Canarium carapifolium Perkins Fragm. Fl. Philipp. 1: 91 (1904)
Canarium oliganthum Merr. Philipp. J. Sci., C 10: 23 (1915)
Canarium polyanthum Perkins Fragm. Fl. Philipp. 1: 95 (1904)
Canarium triandrum Engl. Monogr. Phan. 4: 145 (1883)
Canarium album Blanco Fl. Filip. [F.M. Blanco] 793 (1837)

Common names Top

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Language Common/alternative name
English elemi tree
German manilaelemi
German manilaelemibaum
German canarium carapifolium
German canarium oliganthum
German canarium polyanthum
German canarium triandrum
German pimela luzonica
Persian لامی
French élémi de manille
Japanese エレミ
Chinese 吕宋橄榄

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000583598
UNII 5BH1ESR432
Tropicos 100304623
KEW urn:lsid:ipni.org:names:127401-1
The Plant List kew-2695949
IUCN Red List 33352
IPNI 127401-1
iNaturalist 190244
GBIF 5636182
Freebase /m/054p46
EPPO CNBLU
EOL 5615746
USDA GRIN 8816
Wikipedia Canarium_luzonicum
Open Tree Of Life 146994

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
[Monoterpenes, sesquiterpenes and dimeric phellandrenes from manila-elemi]. Brieskorn CH, Krauss G Planta Med 01-Aug-1986
doi:10.1055/S-2007-969160
PMID:17345315

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969160
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-2007-969160
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2007-969160
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-2007-969160
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2007-969160
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1055/S-2007-969160
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1055/S-2007-969160
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2007-969160
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969160
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969160
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1055/S-2007-969160
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1055/S-2007-969160
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969160
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1055/S-2007-969160
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1055/S-2007-969160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2007-969160

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