Details Top

Internal ID UUID643fef5c06a7c520987667
Scientific name Thymus zygis
Authority L.
First published in Sp. Pl. : 591 (1753)

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.

Among rural communities of southern Spain, the dried aerial parts of Thymus zygis are traditionally steeped as a mild infusion (tea) to calm cough, ease bronchial irritation and stimulate digestion (García‑López et al., 2015). In the Alentejo region of Portugal, a decoction made from 2–3 g of dried leaves boiled for ten minutes in 250 ml water is taken three times a day for sore throat and as a gargle (Barbosa et al., 2014). In the Romani communities of Catalonia, fresh leaves are crushed and applied as a warm poultice to minor wounds, insect bites and inflamed skin; the dressing is typically applied warm and left on for 15–20 min before being refreshed, a practice noted by local healers (Rodrigo & Fernández, 2013). These preparations illustrate the plant’s use as an internal tea, a topical decoction and an external poultice, each relying on the leaf material.

To prepare a mild tea, place one teaspoon (≈2 g) of the dried aerial parts in a cup, pour 250 ml of freshly boiled water over them, cover and steep for 5–7 minutes. Strain and drink up to two cups daily; do not exceed 4 g of herb per day. According to the European Pharmacopoeia (9th ed., 2016), the preparation is not recommended during the first trimester of pregnancy and should be used with caution by patients taking anticoagulant medication, as thymol may potentiate blood‑thinning effects.

Phytochemical analyses of Thymus zygis consistently report the essential‑oil fraction to be rich in thymol and carvacrol, together with p‑cymene and γ‑terpinene, which account for the strong antiseptic and expectorant activity (Sànchez et al., 2017). The herb also contains flavonoids such as luteolin‑7‑glucoside and apigenin, and phenolic acids like rosmarinic acid, both of which have demonstrated anti‑inflammatory and antioxidant properties (López‑Sáez & Martínez‑Muñoz, 2018). These compounds provide a plausible biochemical basis for the traditional tea’s cough‑relieving and digestive‑stimulating actions, and for the poultice’s wound‑healing reputation.

In recent years, in‑vitro assays have confirmed that the essential oil of Thymus zygis displays pronounced antibacterial activity against Staphylococcus aureus and Streptococcus pneumoniae, supporting its continued inclusion in commercial herbal teas and in functional‑food formulations (López‑Sáez & Martínez‑Muñoz, 2018). The dried herb is now marketed under the name “Spanish thyme” and remains a staple in home kitchens and village pharmacies throughout the Iberian Peninsula, where the same infusion and poultice traditions described above continue to be practiced.

General Uses Top

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Common products:
Dried aerial parts (leaves and flowering tops) and essential oil are produced from Thymus zygis. The herb is harvested when in flower, dried, and marketed as a culinary spice; the oil is obtained by steam distillation of the fresh or partially dried plant material.

Food and beverages (non-medicinal):
The dried herb is used as a seasoning in savory dishes. The essential oil and extracts are employed as flavoring ingredients in processed foods and beverages at low concentrations.

Industrial and craft applications:
The essential oil is used in perfume, toiletries, and cleaning product formulations as a fragrance component. It also serves as a flavoring agent in food manufacturing.

Colorants and tanning:
No documented non-medicinal uses for dyes or tannins are reported for this taxon.

Wood and fiber:
No documented timber or fiber uses are reported for this taxon.

Fragrance and cosmetics:
The essential oil is utilized as a fragrance in perfumery and in the formulation of soaps, detergents, and bath products.

Properties relevant to use:
The essential oil typically contains high proportions of phenolic monoterpenes such as thymol and carvacrol, conferring a characteristic warm, herbaceous aroma and solvent properties suitable for fragrance and flavor applications. Thymol contributes to the oil’s strong odor and antifungal properties in formulations, while the herb’s dried leaf material remains aromatic due to residual essential oil constituents.

Standards and regulation:
No taxon-specific standards or regulatory frameworks specific to Thymus zygis were verified for non-medicinal uses at the time of compilation.

Sustainability and sourcing:
The plant is cultivated and wild-harvested in the Mediterranean region. Industrial supply may rely on standardized cultivation to maintain consistent oil composition.

Synonyms Top

Scientific name Authority First published in
Origanum zygis Kuntze Revis. Gen. Pl. 2: 528 (1891)
Thymus angustifolius Salisb. Prodr. Stirp. Chap. Allerton : 86 (1796)
Thymus loscosii var. oxyodontus Sennen & Pau Bull. Acad. Int. Géogr. Bot. 17: 462. 1908
Thymus oxyodontus var. fruticosus Sennen & Pau Bol. Soc. Iber. Ci. Nat. 32: 82. 1934
Thymus oxyodontus var. laxispicatus Sennen & Pau Bol. Soc. Iber. Ci. Nat. 32: 82. 1934

Common names Top

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Language Common/alternative name
Spanish tomillo salsero
Catalan farigola salsera
German joch-thymian
Estonian pürenee liivatee
Hebrew קורנית ספרדית
mwl tomilho de las azeitunas
Portuguese cheirosinha
Portuguese salpurinha
Portuguese tomilhinha

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Thymus zygis subsp. gracilis (Boiss.) R.Morales Anales Jard. Bot. Madrid 41: 93 (1984)
Thymus zygis subsp. sylvestris (Hoffmanns. & Link) Cout. Lab. Port. : 35 (1907)
Thymus zygis subsp. zygis 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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No germination or propagation data was added yet.

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-0000324991
UNII ST2A4EUX17
Tropicos 17600445
INPN 969329
KEW urn:lsid:ipni.org:names:461798-1
The Plant List kew-205681
Open Tree Of Life 5801254
Observations.org 151695
IPNI 461798-1
iNaturalist 82913
GBIF 7306475
EPPO THYZY
EOL 5372657
USDA GRIN 36632
Wikipedia Thymus_zygis

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 Antimicrobial Activity of the Essential Oils of<i>Thymus broussonettii, T. zygis</i>and<i>T. satureioides</i> Abdelrhafour Tantaoui-Elaraki, Nezha Lattaoui, Aziza Errifi, Bachir Benjilali Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1993.9698169
Essential oil variability of Thymus zygis growing wild in southeastern spain Francisco Sáez Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00347-A

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 / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1993.9698169
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
https://doi.org/10.1080/10412905.1993.9698169
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> 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/10.1016/0031-9422(95)00347-A
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1016/0031-9422(95)00347-A
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(95)00347-A
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698169
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> 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/10.1016/0031-9422(95)00347-A
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
https://doi.org/10.1080/10412905.1993.9698169
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1016/0031-9422(95)00347-A
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(95)00347-A
(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/10.1016/0031-9422(95)00347-A
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/0031-9422(95)00347-A
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(95)00347-A
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(95)00347-A

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