Thymus saturejoides

Details Top

Internal ID UUID643fef533cba4640963796
Scientific name Thymus saturejoides
Authority Coss. & Balansa
First published in Bull. Soc. Bot. France 20: 253 (1873)

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.

Across North Africa Thymus saturejoides is collected wild and used as an everyday tonic, especially when colds or indigestion strike. In Algeria, various communities record infusions of the leaves for coughs and colds, leaf and stem decoctions as a mild diaphoretic during fever, and macerations in wine or water for gas and stomach ache (Le Floc’h, 1983; Dob & Doumandji, 2011). In Tunisia, folk healers prepare leaf infusions for bronchitis-like coughs and colds, and ground plant poultices or diluted macerations for local wounds and sore throats (Haddad et al., 2003; Ben Sassi et al., 2008). In Morocco, women frequently drink a mint-thyme tisane of the leaves and stems to ease digestion and freshen the mouth, and poultices of the herb are applied to bruises or painful joints (Bellakhdar, 1997). These practices stem from a long tradition of using T. saturejoides for respiratory relief and digestive comfort, and they persist in domestic and small-scale market use today.

One practical recipe is a mild leaf infusion suitable for adults. Measure about 2 teaspoons of dried aerial parts (roughly 2–3 g) per cup of freshly boiled water, cover, and steep 8–10 minutes. A second cup can be drunk later in the day if needed. Use the same proportions for a cold or cough tisane; many homes add a few mint leaves for flavor. A 1:5 ethanol tincture can be made with 1 part dried aerial parts by weight to 5 parts 45% ethanol, shaken daily for 10–14 days in a cool, dark place, then filtered. Typical adult use is 2–3 mL up to three times daily for short periods only. Do not exceed recommended doses; Thymus oils can irritate mucous membranes or provoke allergic reactions, and essential-oil–rich preparations are not suitable for young children, pregnant or nursing women, or people with severe sagebrush/mint family allergy.

Phytochemical work explains the traditional uses. Leaves and stems are rich in phenolics such as carvacrol and thymol, with variable amounts of p-cymene, γ-terpinene, borneol, and camphor, and the herb contains flavonoids like apigenin and luteolin that have been detected in other Thymus species (Hazzit et al., 2009; Ben Sassi et al., 2007). These compounds, especially the phenolics, possess antimicrobial and spasmolytic activities consistent with the herb’s respiratory and digestive applications, while the flavonoids contribute antioxidant effects.

Modern relevance follows the tradition. Pharmacological studies confirm antimicrobial, antispasmodic, and antioxidant activities (Ben Sassi et al., 2007; Bousmaha et al., 2012), and the plant continues to appear in Moroccan herbal markets and is used domestically for coughs, colds, and indigestion (Bellakhdar, 1997).

General Uses Top

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Common products:
The aerial parts of Thymus saturejoides are harvested for three commercial streams. Steam distillation of fresh or semi‑dry material yields an essential oil (typical yield 0.8–1.5 % w/w). The dried herb is marketed as a culinary spice, and whole or clipped plants are produced by nurseries for ornamental use in rock gardens and low‑maintenance landscaping.

Industrial and craft applications:
The essential oil is employed in the manufacture of soaps, liquid detergents, and surface cleaners as a fragrant component and as a natural odorant in scented candles and room fresheners. Its aromatic profile also finds use in the production of craft incense and potpourri blends.

Food and beverages (non‑medicinal):
The oil is incorporated as a flavoring ingredient in processed foods, snack seasonings, and beverage flavor bases where a warm, herbaceous note is desired. The dried herb is sold as a spice for regional dishes in North‑African and Mediterranean cuisines.

Fragrance and cosmetics:
In perfumery the oil contributes a fresh‑herbaceous, slightly balsamic nuance, and it is a constituent of men’s and women’s fragrance compositions. It is also added to cosmetic creams, lotions, and shampoos to impart aromatic character and to enhance product scent stability.

Properties relevant to use:
The oil’s composition is dominated by thymol (≈45–55 % of the oil) with p‑cymene (≈10–20 %) and carvacrol (≈5–10 %). The high phenolic content confers strong oxidative stability and excellent heat resistance, making it suitable for high‑temperature applications in food flavoring and for use in fragrance formulations that require resistance to oxidation.

Standards and regulation:
International trade of Thymus saturejoides essential oil follows ISO 11014, which specifies compositional limits, identification criteria, and labeling for essential‑oil products. In the European Union the oil is governed by Regulation (EC) No 1334/2008 for use as a flavoring substance in food, and its import/export is subject to REACH registration for chemical substances.

Sustainability and sourcing:
Wild harvesting occurs primarily in the Atlas Mountains of Morocco and Tunisia. The species has not been assessed by the IUCN, and recent initiatives have begun to develop field‑grown plantations in Spain and Portugal to reduce pressure on wild populations. Certification programs such as FairWild are recommended to ensure traceable and ecologically sound collection.

Synonyms Top

Scientific name Authority First published in
Origanum saturejodes Kuntze Revis. Gen. Pl. 2: 528 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Thymus saturejoides subsp. commutatus Batt. Bull. Soc. Bot. France 58: 436 (1911)
Thymus saturejoides subsp. pseudomastichina (Ball) Dobignard J. Bot. Soc. Bot. France 28: 23 (2004)
Thymus saturejoides subsp. saturejoides Unknown

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-0000324708
Tropicos 50194500
KEW urn:lsid:ipni.org:names:461627-1
The Plant List kew-205412
Open Tree Of Life 905407
NCBI Taxonomy 751874
IUCN Red List 139600868
IPNI 461627-1
iNaturalist 789307
GBIF 7306681

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
Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry Oliveira GD, McManus C, Vale IR, dos Santos VM Pathogens 18-Mar-2024
PMCID:PMC10974541
doi:10.3390/pathogens13030260
PMID:38535603
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Antibacterial Activity of Essential Oils Combinations based on Thymus broussonnetii, and Their Synergism with some Antibiotics Amassmoud O, Abbad I, Iriti M, Hassani L, Mezrioui N, Abbad A Curr Microbiol 01-Nov-2023
PMCID:PMC10620311
doi:10.1007/s00284-023-03510-x
PMID:37910319
Harnessing Plant’s Arsenal: Essential Oils as Promising Tools for Sustainable Management of Potato Late Blight Disease Caused by Phytophthora infestans—A Comprehensive Review Martini F, Jijakli MH, Gontier E, Muchembled J, Fauconnier ML Molecules 27-Oct-2023
PMCID:PMC10650712
doi:10.3390/molecules28217302
PMID:37959721
Chemical Characterization and Antifungal Activity of Blue Tansy (Tanacetum annuum) Essential Oil and Crude Extracts against Fusarium oxysporum f. sp. albedinis, an Agent Causing Bayoud Disease of Date Palm Ettakifi H, Abbassi K, Maouni S, Erbiai EH, Rahmouni A, Legssyer M, Saidi R, Lamrani Z, Esteves da Silva JC, Pinto E, Maouni A Antibiotics (Basel) 16-Sep-2023
PMCID:PMC10526058
doi:10.3390/antibiotics12091451
PMID:37760747
Identification of phytochemical, antioxidant, anticancer and antimicrobial potential of Calotropis procera leaf aqueous extract Ahmad Nejhad A, Alizadeh Behbahani B, Hojjati M, Vasiee A, Mehrnia MA Sci Rep 07-Sep-2023
PMCID:PMC10485245
doi:10.1038/s41598-023-42086-1
PMID:37679486
Evaluation of the constituent compounds, antioxidant, anticancer, and antimicrobial potential of Prangos ferulacea plant extract and its effect on Listeria monocytogenes virulence gene expression Jalil Sarghaleh S, Alizadeh Behbahani B, Hojjati M, Vasiee A, Noshad M Front Microbiol 10-Jul-2023
PMCID:PMC10364450
doi:10.3389/fmicb.2023.1202228
PMID:37492261
Thymus satureioides Coss.: Mineral Composition, Nutritional Value, Phytochemical Profiling, and Dermatological Properties Mahdi I, Fahsi N, Annaz H, Drissi B, Barakate M, Mahmoud MF, Sobeh M Molecules 08-Jun-2023
PMCID:PMC10301826
doi:10.3390/molecules28124636
PMID:37375191
In Vitro Propagation of Origanum scabrum (Boiss. & Heldr.): An Endemic Medicinal Plant of Greece Alexopoulos AA, Kartsonas E, Karras S, Mavrommati E, Petropoulos SA, Papafotiou M Plants (Basel) 26-May-2023
PMCID:PMC10255548
doi:10.3390/plants12112118
PMID:37299098
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
Six Spain Thymus essential oils composition analysis and their in vitro and in silico study against Streptococcus mutans Park SY, Raka RN, Hui XL, Song Y, Sun JL, Xiang J, Wang J, Jin JM, Li XK, Xiao JS, Wu H BMC Complement Med Ther 05-Apr-2023
PMCID:PMC10074788
doi:10.1186/s12906-023-03928-7
PMID:37020229
Essential oil of Cymbopogon martini, source of geraniol, as a potential antibacterial agent against Bacillus subtilis, a pathogen of the bakery industry Santamarta S, Aldavero AC, Rojo MA F1000Res 24-Mar-2023
PMCID:PMC9936101
doi:10.12688/f1000research.54196.1
PMID:36817513
Essential Oils as Nematicides in Plant Protection—A Review Catani L, Manachini B, Grassi E, Guidi L, Semprucci F Plants (Basel) 22-Mar-2023
PMCID:PMC10058003
doi:10.3390/plants12061418
PMID:36987106
Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview Motti R, Paura B, Cozzolino A, de Falco B Plants (Basel) 28-Nov-2022
PMCID:PMC9736219
doi:10.3390/plants11233272
PMID:36501312
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263

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/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1080/10412905.1993.9698169
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1021/JF60206A038
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2,6-Dimethyl-3-propan-2-ylphenol 21908410 Click to see CC1=C(C(=C(C=C1)C(C)C)C)O 164.24 unknown https://doi.org/10.1080/10412905.1993.9698169
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/JF60206A038
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1021/JF60206A038
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/JF60206A038
https://doi.org/10.1080/10412905.1993.9698169
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid 20327362 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1993.9698169
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
4,6,6-Trimethyl-3-[2,6,6-trimethyl-3-(2,6,6-trimethyl-3-bicyclo[3.1.1]hept-1-enyl)-3-bicyclo[3.1.1]hept-1-enyl]bicyclo[3.1.1]hept-4-en-2-ol 56924154 Click to see 420.70 unknown https://doi.org/10.1021/JF60206A038
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/JF60206A038
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/JF60206A038
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/JF60206A038
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
trans-4-Thujanol 12315149 Click to see 154.25 unknown https://doi.org/10.1021/JF60206A038
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1021/JF60206A038
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
1,6-Dihydrocarvone 24473 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1993.9698169
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1993.9698169
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1021/JF60206A038
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1021/JF60206A038
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
https://doi.org/10.1021/JF60206A038
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1993.9698169
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF60206A038
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsilineol 162464 Click to see 344.30 unknown https://doi.org/10.1055/S-2007-969583
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1055/S-2007-969583
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4',5-Dihydroxy-3',6,7,8-tetramethoxyflavone 181092 Click to see 374.30 unknown https://doi.org/10.1055/S-2007-969583
Thymonin 442662 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)O 360.30 unknown https://doi.org/10.1055/S-2007-969583
Xanthomicrol 73207 Click to see 344.30 unknown https://doi.org/10.1055/S-2007-969583

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