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
Suggest a correction!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) |
Subspecies (abbr. subsp./ssp.) Top
Add a new one! Suggest a correction!| 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 |
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
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Africa click to expand
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Northern Africa
- Algeria
- Morocco
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Northern Africa
Links to other databases Top
Suggest others/fix!| 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)!
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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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |