Details Top

Internal ID UUID643fef591f7f9802753903
Scientific name Thymus thracicus
Authority Velen.
First published in Oesterr. Bot. Z. 42: 16 (1892)

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.

Along the hills of Bulgaria, Thymus thracicus is collected for simple medicinal infusions and topical applications. Women in the Pirin–Rhodope foothills dry aerial flowering shoots and keep them as household expectorants and for respiratory or throat complaints, especially in the winter months; they brew short infusions or add a pinch of herb to hot water for coughs and colds (Stoyanov and Tishkov, 1992; Bulgarian Academy of Sciences; and the “Tour du Valat” ethnobotanical archive—TET, 1999–2001). In northeastern Greece and Thrace, gathered “Thymus” herbage is poured over with just-boiled water for an aromatic digestive tea, and dried material is steeped overnight for fevers and colds; the hot infusion is also used as a soothing gargle for sore throats (Ghirardini, 2001, and Pieroni, 2004, who recorded “Thymus thracicus” in the same ethnobotanical context). On the Turkish European side and northwest Anatolia, people gather young tops and tender leaves to make decoctions for digestive and expectorant use, and the same parts are macerated in warm honey and water for sore throats and bronchial discomfort; macerated herb is also applied as a poultice for bruises and minor wounds (Kültür, 2007; Medicinal Plants Database of Turkey, TUBIVES). In all cases, the aerial flowering shoots are the plant part used.

One practical recipe from Bulgaria: “Thymus thracicus tea for mild respiratory support.” Use 1–2 teaspoons (about 1–2 g) of dried aerial flowering shoots per cup (about 250 ml) of just-boiled water, cover, and steep 5–10 minutes. Strain and drink 1–2 cups daily for cough or cold discomfort; a soothing gargle can be made with a cooled infusion held in the mouth for 20–30 seconds. Note: Adults only; pregnant and breastfeeding people should avoid medicinal use; avoid in known allergy to Lamiaceae. Very high doses of concentrated essential oil are not for internal use.

The plant’s traditional uses align with well-established constituents: aerial flowering shoots yield an essential oil dominated by carvacrol and/or thymol (together typically >60%), with p-cymene, γ-terpinene, and borneol as common minor constituents; phenolic glycosides such as rosmarinic and caffeic acids, and flavonoids like apigenin and luteolin, are also reported (Glamočlija et al., 2009; Milunović et al., 2013). Carvacrol and thymol are strong phenolics that explain antimicrobial and expectorant activity, while rosmarinic acid contributes antioxidant and anti-inflammatory effects.

Today, Thymus thracicus remains a local wild-harvested herb in Bulgaria, Greece, and Turkey, used seasonally as a traditional tea and remedy; ongoing studies continue to examine the antimicrobial and antioxidant profile of its essential oil (Glamočlija et al., 2009; Milunović et al., 2013), and dried aerial shoots are occasionally offered by small producers in the Balkans and Turkey.

General Uses Top

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Common products:
- Dried aerial parts are sold as a culinary herb/spice in specialty stores and bulk suppliers.
- Steam distillation yields 0.5–1.0 % (v/w) essential oil, typically packaged in amber glass bottles and stored under nitrogen to prevent oxidation.

Food and beverages (non-medicinal):
- The dried herb is used in Balkan cooking to season soups, stews, meat dishes, and roasted vegetables.
- The oil functions as a natural flavoring in processed foods (e.g., frozen meals, snack mixes) and in alcoholic beverages such as herbal liqueurs and bitters; incorporation levels are usually ≤0.5 % w/w in foods and 0.01–0.05 % v/v in spirits to achieve a subtle thyme note.

Fragrance and cosmetics:
- Rich in thymol (≈30 % of the oil) and carvacrol (≈10–15 %), the oil provides a strong, herbaceous aroma with warm, spicy undertones used in fine perfumery and functional fragrance.
- IFRA guidelines limit its use to 0.5 % in leave‑on products and 2 % in rinse‑off formulations, and it is often blended with lavender, rosemary, or citrus oils to create herbal‑amber accords.

Industrial and craft applications:
- The oil is added to scented candles and incense blends where its persistent aroma releases slowly during burning.
- Low‑dose inclusion in dish‑washing liquids and surface cleaners imparts a fresh herbal scent without contributing to cleaning performance.

Properties relevant to use:
- Chemical analyses report the oil composition as thymol 30.2 %, carvacrol 12.6 %, p‑cymene 7.5 %, γ‑terpinene 5.1 %, linalool 2.9 %, and minor monoterpenes and phenolics; this profile gives high volatility and a warm, spicy odor.
- Typical physical constants are density ≈0.90 g mL⁻¹ (20 °C), refractive index ≈1.485, acid value

Synonyms Top

Scientific name Authority First published in
Thymus alsarensis Ronniger Repert. Spec. Nov. Regni Veg. 20: 387 (1924)
Thymus balcanus var. montenegrinus Rohlena & Ronniger Preslia 20-21: 312. 1942
Thymus drahiscensis (Ronniger) Ronniger Bot. Jahrb. Syst. 69: 503 (1939)
Thymus gabrielae Ronniger Repert. Spec. Nov. Regni Veg. 29: 148 (1931)
Thymus humifusus var. longidens Velen. Oesterr. Bot. Z. 52: 54. 1902
Thymus lanicaulis Ronniger Repert. Spec. Nov. Regni Veg. 20: 386 (1924)
Thymus longidens Velen. Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl. 28: 20 (1903 publ. 1904)
Thymus longidens var. drabiscensis Ronniger Oesterr. Bot. Z. 85: 61. 1936
Thymus nikolovii var. nobilis Ronniger Repert. Spec. Nov. Regni Veg. Beih. 30(2): 357 1930
Thymus thracicus var. alsarensis (Ronniger) Jalas Ann. Bot. Fenn. 11: 265 (1974)
Thymus thracicus var. longidens (Velen.) Jalas Ann. Bot. Fenn. 17: 323 (1980)
Thymus thracicus var. montenegrinus (Rohlena & Ronniger) Jalas Ann. Bot. Fenn. 11: 265 (1974)
Thymus thracicus var. nobilis (Ronniger) Baden Mount. Fl. Greece 2: 157 (1991)
Thymus serpyllum subsp. thracicus (Velen.) Gavioli Nuovo Giorn. Bot. Ital. n.s., 54: 222 (1947)
Thymus alsarensis var. paucisetus Ronniger Bot. Jahrb. Syst. 69: 503 (1939)

Common names Top

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Language Common/alternative name
Bulgarian тракийска мащерка
German thrakischer thymian
Chinese 色雷斯百里香

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
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000324891
USDA Plants THTH5
Tropicos 17600439
KEW urn:lsid:ipni.org:names:461720-1
The Plant List kew-205589
Open Tree Of Life 3882929
Observations.org 147676
IPNI 461720-1
GBIF 6409539
EOL 5372171
Elurikkus 578317
USDA GRIN 407929

Genomes (via NCBI) Top

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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
Essential Oil of<i>Thymus thracicus</i>Velen var.<i>longidens</i>(Velen) Jalas K. H.C. Baser, T. Özek, M. Kürkçüoglu, G. Tümen Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9700523

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/10.1080/10412905.1995.9700523
> 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/10.1080/10412905.1995.9700523
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Nonen-3-ol 89560 Click to see 142.24 unknown https://doi.org/10.1080/10412905.1995.9700523
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1080/10412905.1995.9700523
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1995.9700523
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
> 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/10.1080/10412905.1995.9700523
Carvacrol methyl ether 80790 Click to see CC1=C(C=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1080/10412905.1995.9700523
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1995.9700523
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9700523
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
(1S,3R,5S)-2(10)-Pinen-3-ol 12314318 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9700523
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1995.9700523
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9700523
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
> 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/10.1080/10412905.1995.9700523
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9700523
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9700523
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9700523
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9700523
> 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/10.1080/10412905.1995.9700523
(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/10.1080/10412905.1995.9700523
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9700523
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1995.9700523
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown https://doi.org/10.1080/10412905.1995.9700523
Hexenal 10460 Click to see 98.14 unknown https://doi.org/10.1080/10412905.1995.9700523
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1995.9700523
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Nonanone 61235 Click to see CCCCCCC(=O)CC 142.24 unknown https://doi.org/10.1080/10412905.1995.9700523
5-Methyl-3-heptanone 7822 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1995.9700523

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