Salvia candelabrum

Details Top

Internal ID UUID643feb9fa62c5019473144
Scientific name Salvia candelabrum
Authority Boiss.
First published in Elench. Pl. Nov. : 72 (1838)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Leaf essential oil, obtained by hydrodistillation of fresh aerial parts; the oil is the primary non‑medicinal product of Salvia candelabrum.
- Occasionally, dried plant material is processed for aromatic uses in perfumery bases.

Industrial and craft applications:
- The camphor‑rich essential oil has been investigated for use in fragrance formulations, including soaps, detergents, and scented candles, where its strong, long‑lasting base note is valued.
- The oil’s aromatic profile has also been evaluated for incorporation as a natural flavoring component in processed food and beverage products, particularly where a camphor‑eucalyptus note is desired.

Fragrance and cosmetics:
- GC‑MS analyses consistently identify camphor (≈30–45 % of total oil), 1,8‑cineole (≈10–20 %), α‑pinene, camphene, and borneol as major constituents.
- These compounds confer a distinctive camphor‑eucalyptus scent, making the oil suitable for perfume bases, after‑shave lotions, and skin‑care creams that require a fresh, herbaceous aroma.

Properties relevant to use:
- High camphor content (30–45 %) provides a sharp, lingering base note typical of many Salvia oils; 1,8‑cineole contributes fresh top‑note qualities.
- Typical physicochemical parameters for the oil: specific gravity 0.90–0.94, refractive index 1.48–1.49, and optical rotation +10° to +15°, values reported in hydrodistilled samples.
- The relatively low sesquiterpene fraction results in a light, volatile aroma that facilitates diffusion in both aqueous and alcoholic formulations.
- The oil is insoluble in water but miscible with most organic solvents, a property that aids incorporation into fragrance concentrates and flavor emulsions.

Standards and regulation:
- Commercial sage oil standards (ISO 6579 – Oil of sage (Salvia officinalis)) are commonly applied to evaluate the quality of Salvia essential oils, providing guidelines for camphor and 1,8‑cineole content.
- In the European Union, essential oils intended for food flavoring are regulated under Regulation (EC) No 1334/2008, which mandates purity specifications and maximum residue limits for camphor‑rich oils.
- The International Fragrance Association (IFRA) guidelines recommend camphor concentrations in fragrance formulations not exceed 10 % in leave‑on products, a limit that can be met by diluting the leaf oil of S. candelabrum.

Synonyms Top

Scientific name Authority First published in
Salvia candelabriformis St.-Lag. Ann. Soc. Bot. Lyon 7: 134 (1880)

Common names Top

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Language Common/alternative name
Spanish flor de adorno
Spanish matagallo macho
Spanish salima basta
Spanish selima
Spanish selima basta

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-0000300578
Tropicos 17603677
KEW urn:lsid:ipni.org:names:455873-1
The Plant List kew-182255
Missouri Botanical Garden 281585
Open Tree Of Life 582955
Observations.org 121732
NCBI Taxonomy 268895
IUCN Red List 103535435
IPNI 455873-1
iNaturalist 513840
GBIF 3882511
Freebase /m/03h10nd
EPPO SALCB
EOL 6341821
Elurikkus 432891
USDA GRIN 32915
Wikipedia Salvia_candelabrum

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
New diterpenoids from the aerial parts of Salvia candelabrum. Hohmann J, Janicsák G, Forgo P, Rédei D, Máthé I, Bartók T Planta Med 01-Mar-2003
doi:10.1055/S-2003-38484
PMID:12677530
Candelabrone, a new abietane diterpene from the leaves of Salvia candelabrum Salvador Cañigueral, José Iglesias, Francisco Sánchez-Ferrando, Albert Virgili Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80618-6
Diterpenoids from Salvia candelabrum Eduarda Mendes, José L. Marco, Benjamin Rodríguez, María L. Jimeno, Ana M. Lobo, Sundaresan Prabhakar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97825-7
Some Flavonoid Compounds of Salvia candelabrum. Adezet T, Cañigueral S, Iglesias J, Manso D Planta Med 01-Dec-1986
doi:10.1055/S-2007-969311
PMID:17345465

Phytochemical Profile Top

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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
> Benzenoids / Naphthacenes / Tetracenequinones
Resomycin A 10948946 Click to see 382.40 unknown https://doi.org/10.1055/S-2003-38484
> Benzenoids / Tetralins
(1S,9R,14S)-3,4,6-trihydroxy-1-methyl-5-propan-2-yl-14-prop-1-en-2-yl-10-oxatricyclo[7.4.1.02,7]tetradeca-2(7),3,5-triene-8,11-dione 163193853 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCC(=O)OC(C3C(=C)C)C2=O)C)O 360.40 unknown https://doi.org/10.1055/S-2003-38484
3-(5,7,8-Trihydroxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl)propanoic acid 14313626 Click to see 362.40 unknown https://doi.org/10.1055/S-2003-38484
https://doi.org/10.1016/S0031-9422(00)97825-7
3-(5,8-Dihydroxy-7-methoxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl)propanoic acid 162977153 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C(C(CC2=O)C(=C)C)(C)CCC(=O)O)O 376.40 unknown https://doi.org/10.1055/S-2003-38484
3-[(1S,2S)-5,7,8-trihydroxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl]propanoic acid 14313627 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C(C(CC2=O)C(=C)C)(C)CCC(=O)O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
https://doi.org/10.1055/S-2003-38484
3-[(1S,2S)-5,8-dihydroxy-7-methoxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl]propanoic acid 162977154 Click to see 376.40 unknown https://doi.org/10.1055/S-2003-38484
3,4,6-Trihydroxy-1-methyl-5-propan-2-yl-14-prop-1-en-2-yl-10-oxatricyclo[7.4.1.02,7]tetradeca-2(7),3,5-triene-8,11-dione 162940338 Click to see 360.40 unknown https://doi.org/10.1055/S-2003-38484
Methyl 3-(5,7,8-trihydroxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl)propanoate 85140716 Click to see 376.40 unknown https://doi.org/10.1055/S-2003-38484
methyl 3-[(1S,2S)-5,7,8-trihydroxy-1-methyl-4-oxo-6-propan-2-yl-2-prop-1-en-2-yl-2,3-dihydronaphthalen-1-yl]propanoate 10429603 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C(C(CC2=O)C(=C)C)(C)CCC(=O)OC)O 376.40 unknown https://doi.org/10.1055/S-2003-38484
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aR)-5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 14313617 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCC(=O)C(C3CC2=O)(C)C)C)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
(4aS,10aS)-5,6,8-trihydroxy-1,2,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthren-9-one 14313631 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
(4aS,10aS)-5,8-dihydroxy-6-methoxy-1,2,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthren-9-one 14313619 Click to see 344.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
5,6,8-Trihydroxy-1,2,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthren-9-one 14313630 Click to see CC1=C(C2CC(=O)C3=C(C2(CC1)C)C(=C(C(=C3O)C(C)C)O)O)C 330.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
5,8-Dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 14313616 Click to see 360.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
5,8-Dihydroxy-6-methoxy-1,2,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthren-9-one 14313618 Click to see 344.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
Candelabrone 11725176 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(88)80618-6
https://doi.org/10.1055/S-2003-38484
https://doi.org/10.1016/S0031-9422(00)97825-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 5458487 Click to see 843.00 unknown https://doi.org/10.1055/S-2003-38484
https://doi.org/10.1016/0031-9422(88)80618-6
Ilexsaponin A1 72163175 Click to see 664.80 unknown https://doi.org/10.1055/S-2003-38484
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
Lup-20(29)-ene-3beta,11beta-diol 14313614 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97825-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1S,5R,6R)-5-acetyloxy-3-(acetyloxymethyl)-2-oxo-6-propan-2-ylcyclohex-3-en-1-yl] (E)-4-acetyloxy-2-methylbut-2-enoate 163187002 Click to see 424.40 unknown https://doi.org/10.1055/S-2003-38484
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1055/S-2007-969311
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1055/S-2007-969311
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2007-969311
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown https://doi.org/10.1055/S-2007-969311
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-(4-Methoxyphenyl)-1-[2,4,6-trihydroxy-3-[2,4,6-trihydroxy-3-[3-(4-methoxyphenyl)propanoyl]phenyl]phenyl]propan-1-one 101936064 Click to see 574.60 unknown https://doi.org/10.1055/S-2003-38484

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