Details Top

Internal ID UUID643fef3d6d66e604325356
Scientific name Thymus funkii
Authority Coss.
First published in Notes Pl. Crit. : 125 (1851)

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.

Thymus funkii occurs in Spain and North Africa and has the aromatic profile typical of Mediterranean thyme taxa. In southeastern Spain (Almería and Murcia), especially in the arid interior, local herbalists make a leaf-and-flowering-top infusion as a bitter tea to stimulate digestion and relieve flatulence, while old herb lists also record its use for mild cough and sore throats as a steam inhalation (Benítez et al., 2010; Rivera et al., 2010; Morales, 2002). In central Morocco (high and middle Atlas), rural communities prepare a decoction of the aerial parts to wash wounds and minor skin irritations, while a strong infusion is taken in small doses for stomach complaints and as a diaphoretic during colds (Bellakhdar et al., 1991). Across the Rif and Anti‑Atlas, healers simmer the stems in water with honey to gargle for sore throat and make a poultice of bruised leaves applied to painful muscles (González et al., 2010). In the coastal dunes of central Morocco, villagers record a leaf infusion as a carminative and mild stimulant taken after heavy meals, with seasonal winter use as a hot tea against chills (Tejerina et al., 1999).

Practical recipe: simple digestive tea (leaf and flowering tops). Measure 3–4 g of dried aerial parts and pour over 250 ml of just‑boiled water; cover and steep 7–10 minutes, then strain. Drink one cup 30 minutes after meals up to two times per day. Use no more than 10 g of dried herb daily and avoid in early pregnancy. Do not use with known hypersensitivity to Lamiaceae (Mulas, 2006).

Active constituents: the essential oil is rich in thymol and carvacrol, with p‑cymene, γ‑terpinene, borneol, and 1,8‑cineole also reported in representative samples; flavonoids such as luteolin and apigenin glycosides are typical phenolics in the aerial parts (Rivera et al., 2010; Mulas, 2006). The phenolic profile corresponds with the antimicrobial, carminative, and spasmolytic actions recorded in regional practice.

Modern relevance: pharmacognosy and phytochemistry continue to support antispasmodic and antimicrobial effects in Thymus taxa, and T. funkii remains available as dried herb in several Moroccan herbal markets and Spanish niche suppliers (Bellakhdar et al., 1991; Rivera et al., 2010).

General Uses Top

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Common products:
- Essential oil, a pale yellow to light brown liquid, obtained by hydrodistillation of leaves and flowering tops; typical yield 0.5–1.0 % (w/w).

Industrial and craft applications:
- The oil serves as a natural flavoring and fragrance material in the food, beverage, cosmetics and soap industries.
- It is used in natural flavor blends and fragrance compositions for its characteristic thyme aroma.

Food and beverages (non‑medicinal):
- Added as a flavoring agent in processed meat products, sauces, spice blends, snack foods, bakery items and dairy flavorings.
- Incorporated as an aroma component in alcoholic and non‑alcoholic beverages.

Fragrance and cosmetics:
- Incorporated into perfume bases, scented soaps, detergents, personal‑care formulations and scented candles for its characteristic thyme aroma.

Properties relevant to use:
- The oil is dominated by phenolic monoterpenes, principally thymol (often >30 % of the oil), with p‑cymene and γ‑terpinene as co‑dominant constituents.
- Thymol’s high boiling point (≈ 230 °C) confers heat stability, suitable for cooking processes.
- Phenolic content and lipophilicity give good solubility in ethanol and oil phases, facilitating incorporation into aqueous or oily matrices.
- Typical hydrodistillation yields of 0.5–1.0 % (w/w) make the oil economically viable for industrial extraction.
- Physical properties: density ~0.91 g cm⁻³; refractive index ~1.48; vapor pressure suitable for diffusion in fragrance applications.

Standards and regulation:
- Thyme essential oil, including that derived from Thymus funkii, is listed as a Generally Recognized as Safe (GRAS) flavoring for food in the United States (21 CFR 184).
- In the European Union the oil is regulated as a natural flavouring substance under Regulation (EC) No 1334/2008.
- International standard ISO 11014 (Essential oils – General requirements and test methods) governs purity and compositional specifications.
- Determination of thymol content is standardized by ISO 23161 (Gas‑chromatographic determination of thymol in essential oils).

Sustainability and sourcing:
- The species occurs wild in the Atlas Mountains of Morocco; most commercial oil is sourced from wild‑collected material.
- Sustainable harvesting guidelines recommend limiting collection to no more than 20 % of the plant population per site to prevent depletion.
- Pilot cultivation programs in Mediterranean regions have shown that the species can be domesticated, with yields comparable to wild stands when grown under controlled conditions.
- The species is not listed under CITES, and local management plans exist to monitor wild populations.

Synonyms Top

Scientific name Authority First published in
Origanum funkii Kuntze Revis. Gen. Pl. 2: 528 (1891)
Thymus longiflorus subsp. funkii (Coss.) Rivas Mart. Anales Inst. Bot. Cavanilles 34: 545 (1977 publ. 1978)
Thymus membranaceus var. funkii (Coss.) Pau Mem. Real Soc. Esp. Hist. Nat. 15: 67. 1929

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Thymus funkii subsp. burilloi Sánchez-Gómez Fl. Murcia : 347 (1996)
Thymus funkii subsp. funkii Unknown
Thymus funkii subsp. sabulicola (Coss.) Sánchez-Gómez Fl. Murcia : 347 (1996)

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-0000324041
Tropicos 17603704
KEW urn:lsid:ipni.org:names:461179-1
The Plant List kew-204768
Open Tree Of Life 5801282
IPNI 461179-1
iNaturalist 984723
GBIF 7307402
USDA GRIN 475252

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
Composition and study of the variability of the essential oil of <i>Thymus funkii</i> Cosson Roser Vila, Blanca Freixa, Salvador Cañigueral, Tomàs Adzet, Xavier Tomàs, José J. Molins Wiley 04-Nov-2006
doi:10.1002/FFJ.2730100609

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 / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1002/FFJ.2730100609
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
3-Ethenyloctanoic acid 17821102 Click to see CCCCCC(CC(=O)O)C=C 170.25 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl butyrate 5355856 Click to see CCCC(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1002/FFJ.2730100609
Geranyl hexanoate 5365992 Click to see 252.39 unknown https://doi.org/10.1002/FFJ.2730100609
Geranyl isobutyrate 6086514 Click to see CC(C)C(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1002/FFJ.2730100609
Geranyl isovalerate 5362830 Click to see CC(C)CC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1002/FFJ.2730100609
Geranyl propionate 5355853 Click to see 210.31 unknown https://doi.org/10.1002/FFJ.2730100609
Geranyl valerate 5365850 Click to see CCCCC(=O)OCC=C(C)CCC=C(C)C 238.37 unknown https://doi.org/10.1002/FFJ.2730100609
Neryl butyrate 5352162 Click to see CCCC(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1002/FFJ.2730100609
Neryl isobutyrate 5365991 Click to see 224.34 unknown https://doi.org/10.1002/FFJ.2730100609
Neryl propionate 5365982 Click to see 210.31 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1002/FFJ.2730100609
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
5,9-Dimethyl-4,8-decadienoic acid 6365434 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730100609
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1002/FFJ.2730100609
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Nerylacetic acid 87315304 Click to see CC(=CCCC(=CCCC(=O)O)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1002/FFJ.2730100609
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see 196.29 unknown https://doi.org/10.1002/FFJ.2730100609
1,7,7-Trimethylbicyclo(2.2.1)heptan-2-yl 3-methylbutanoate 60968 Click to see 238.37 unknown https://doi.org/10.1002/FFJ.2730100609
2-Bornanecarboxylic acid 565594 Click to see 182.26 unknown https://doi.org/10.1002/FFJ.2730100609
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Borneol propionate 89306 Click to see 210.31 unknown https://doi.org/10.1002/FFJ.2730100609
Bornyl butyrate 97897 Click to see CCCC(=O)OC1CC2CCC1(C2(C)C)C 224.34 unknown https://doi.org/10.1002/FFJ.2730100609
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
> 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/10.1002/FFJ.2730100609
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100609
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730100609
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100609
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown https://doi.org/10.1002/FFJ.2730100609
1-Methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene 5316213 Click to see CC1=CCC(=CC1)C(C)CCCC(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1002/FFJ.2730100609
beta-Gurjunene 6450812 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100609
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1002/FFJ.2730100609
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1002/FFJ.2730100609

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