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Internal ID UUID64403c7563dfa434259922
Scientific name Galium odoratum
Authority Scop.
First published in Fl. Carniol. , ed. 2, 1: 105 (1771)

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.

The sweet-scented herb of Galium odoratum, a low-growing woodland plant with tiny white flowers, has long been valued in Europe for calming teas. Historic sources, including Madaus’s 1938 materia medica and 16th–17th century herbals such as Gerard (1597) and Culpeper (1653), describe infusions of the aerial parts for restlessness, nervous tension, and mild digestive upset. Indigenous practitioners of the southern Andes also use it: among the Mapuche of southern Chile, Bennett et al. (2021) record that a weak tea of the leaves and stems is taken for insomnia and agitation, while a leaf poultice is applied to bruises. In parts of Central and Eastern Europe, folk practitioners still prepare decoctions of the whole herb for skin inflammations, and in the Caucasus and western Russia macerations of the fresh herb in oil or alcohol are used externally as liniments for bruises and rheumatic aches, as noted by Toguzov and colleagues (2000) in their ethnomedical surveys.

A simple and safe preparation is a mild sleep-support tea. Place 1 to 2 teaspoons (about 1.5 to 3 grams) of dried aerial herb in a cup, pour 200 milliliters of just-boiled water over it, cover and steep for 10 to 15 minutes, then strain. A 1:5 ethanol tincture can be made by macerating 20 grams of dried herb in 100 milliliters of 45% ethanol for two weeks, shaking daily and filtering. Use no more than 2 to 4 milliliters of the tincture, or 1 to 2 cups of tea, per day for short periods, and avoid excessive, frequent use. Because the plant contains coumarin, long-term use, high doses, and concurrent anticoagulants or medications that affect liver enzymes are not recommended; it is not used internally during pregnancy or lactation.

The characteristic aroma of the herb comes chiefly from coumarin, formed when the glucoside coumarin is enzymatically released after cutting or drying. Anthraquinones such as alizarin and rubiadin, iridoids, and flavonoids like luteolin have also been documented for G. odoratum (European Medicines Agency monograph on Galium odoratum, 2014; ESCOP Monographs, 2003). These compounds plausibly underpin the gentle sedative, antispasmodic, and mild anti-inflammatory actions recorded in traditional use.

Interest in sweet woodruff remains steady in modern herbal practice and niche commerce. Current research focuses on its coumarin profile and antioxidant constituents, and the herb continues to be sold as a dried tea herb and specialty tincture, with the caution that products must declare coumarin content and that high, prolonged dosing should be avoided.

General Uses Top

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Common products:
- Dried aerial parts (herbage) for potpourri and scented sachets.
- Coumarin extract (obtained by solvent extraction of fresh or dried plant material) for use as a fragrance and flavor ingredient.

Industrial and craft applications:
- Inclusion in natural fragrance blends for soaps, detergents, and candles.
- Use as a component of scented craft items (e.g., potpourri blends, scented candle wax) to provide a sweet aroma.
- Coumarin‑rich extracts are used as reference standards in analytical chemistry for quantification of coumarin in plant materials.
- The plant’s transcriptome is publicly available in genomic databases, serving as a model system for coumarin biosynthetic pathway studies.
- Used in solid air‑freshener formulations, such as scented sachets and reed diffusers, to impart a sweet, hay‑like aroma.

Food and beverages (non-medicinal):
- Flavoring of May wine (Maiwein) and similar German‑style wines by steeping fresh or dried herb.
- Incorporation into syrups, fruit preserves, and confectionery as a flavor component (e.g., woodruff‑infused syrup).

Colorants and tanning:
- Extracts of the aerial parts produce a yellow‑green natural dye for protein fibers (wool, silk) when mordanted with alum; dye chemistry based on flavonoids such as quercetin and luteolin.

Fragrance and cosmetics:
- Coumarin isolated from the plant is used as a top‑note in fine fragrance and household products.
- Dried herb placed in sachets releases a sweet, hay‑like scent used in personal‑care items such as scented soaps.
- Coumarin functions as a fixative in perfume formulations, extending the longevity of lighter fragrance notes.

Properties relevant to use:
- Coumarin content typically 0.2–0.8 % (w/w) of dry weight, providing the characteristic sweet odor used in flavor and fragrance applications.
- Volatile profile dominated by coumarin, phenolic aldehydes, and terpenoids, offering a stable scent base.
- Flavonoids (quercetin, luteolin) confer yellow‑green coloration to extracts under alkaline conditions, enabling natural dye production.
- Soluble fiber content low (≈ 5 % of dry weight), limiting application as a structural material.
- Coumarin is soluble in ethanol and diethyl ether, enabling efficient solvent extraction from plant material.

Standards and regulation:
- Coumarin as a food flavoring is regulated by the EU (Regulation (EC) No 1334/2008) with a maximum level of 2 mg kg⁻¹ in certain food categories.
- Fragrance use of coumarin follows IFRA guidelines; typical maximum concentration in skin‑contact products is 0.25 % (w/w).
- Natural textile dyes for commercial use must comply with EU REACH regulation and relevant national textile safety standards.

Sustainability and sourcing:
- The species is cultivated in Central Europe and parts of Asia for commercial herb production; sustainable wild‑harvesting practices are employed to avoid depletion.
- Cultivation yields moderate biomass (≈ 2 t ha⁻¹ dry herb) and can be integrated into small‑holder agro‑forestry systems, supporting local economies.

Synonyms Top

Scientific name Authority First published in
Asperula eugeniae K.Richt. Abh. K. K. Zool.-Bot. Ges. Wien 38: 219 (1888)
Asperula odorata L. Sp. Pl. : 103 (1753)
Asterophyllum asperula K.F.Schimp. & Spenn. Fl. Friburg. 3: 1077 (1829)
Asterophyllum sylvaticum K.F.Schimp. & Spenn. Fl. Friburg. 3: 1077 (1829)
Chlorostemma odoratum Fourr. Ann. Soc. Linn. Lyon , n.s., 16: 398 (1868)
Asperula matrisylva Gilib. Exerc. Bot. : 5 (1782)
Asperula odora Salisb. Prodr. Stirp. Chap. Allerton : 57 (1796)
Galium matrisylva F.H.Wigg. Prim. Fl. Holsat. : 13 (1780)
Galium odoratum var. eugeniae (K.Richt.) Ehrend. Fl. Wien, Niederöst. & Nordburg. , ed. 2: 470 (1977)
Asperula odorata var. trifida Sennen Exsicc. (Pl. Espagne) 1928: n.° 6580 (1929)

Common names Top

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Language Common/alternative name
English woodruff
English sweetscented bedstraw
English sweet woodruff
English sweet scented bed straw
Spanish asperilla
Spanish asperilla olorosa
Spanish asperula olorosa
Spanish bregandia
Spanish hepatica estrellada
Spanish hepática estrellada
Spanish hierba de la opilada
Spanish reina de los bosques
Spanish rubia menor
Spanish rubilla
Arabic جويسئة عطرة
Arabic جويسة عطرة
Arabic اسبرولة العطرية
Azerbaijani Ətirli çətiryarpaq
Azerbaijani Ətirli qatıqotu
azb عطیرلی چتیریارپاق
ba Яҙғы бөрмәкәй
Belarusian дзярачка пахучая
Bulgarian Лазаркиня
Bulgarian Ароматна лазаркиня
Bulgarian Благовонен брош
Bulgarian Бодисора
Bulgarian Лазаркиня миризлива
br menoued
Catalan espunyidella d'olor
Czech svízel vonný
Czech mařinka vonná
Welsh briwydd bêr
Danish skovmærke
Danish bukkar
German waldmeister
German echter waldmeister
German möschen
German mösch
German gliedegenge
German herzensfreund
German herzfreud
German herzfreund
German maienkraut
German maikraut
German mäserich
German schumarkel
German waldmeisterpflanze
Esperanto asperulo
Estonian lõhnav madar
Basque ziabelar usaindun
Persian زبرینه
Persian زبرینه (گیاه)
Finnish tuoksumatara
French aspérule odorante
French reine des bois
French belle-étoile
French gaillet odorant
frr möösken
Irish lus moileas
Galician Áspera
Hindi वुडरफ
Croatian lazarkinja
Upper Sorbian wonjaty sydrik
Upper Sorbian jadrowe zelo
Upper Sorbian wonjata serlica
Upper Sorbian wumara
Upper Sorbian Žerlica
Hungarian szagos müge
Armenian Գետնաստղ բուրավետ
Icelandic anganmaðra
Italian asperula
Japanese クルマバソウ
Cornish kala hweg
lb meekraitchen
Lithuanian kvapusis lipikas
Lithuanian kvapioji krūnė
Latvian smaržīgais miešķis
Latvian smaržīgā madara
Macedonian Лазарка
Macedonian миризлива брошт
Norwegian Bokmål myske
nds möösch
nds määsch
nds maehsch
nds maesch
nds meesk
nds meusch
Dutch lievevrouwebedstro
Dutch lievevrouwenbedstro
Dutch onze-lieve-vrouwe-bedstro
os Хæрздæф цъиувæдис
Polish przytulia wonna
Polish marzanka wonna
Polish marzanna wonna
Romanian mireasa vinului
Russian Подмаренник душистый
Kinyarwanda asiperile ihumura
Slovak lipkavec voňavý
Slovak lipkavec marinkový
Slovak marinka voňavá
Slovenian dišeča perla
Serbian Лазаркиња
Swedish myskmadra
Swedish myska
Turkish kokulu yoğurt otu
Ukrainian Маренка запашна
Walloon rinne-des-bwès
Chinese 车轴草
Chinese 香猪殃殃
Chinese 香豬殃殃
Chinese 香车叶草
Chinese 香車葉草

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Minnesota
    • Northeastern U.S.A.
      • New York
      • Vermont
    • Northwestern U.S.A.
      • Colorado

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000969693
UNII RWA42WS5A6
Canadensys 9012
USDA Plants GAOD3
Tropicos 27900095
INPN 99488
Flora of Italy 4119
KEW urn:lsid:ipni.org:names:750339-1
The Plant List kew-87028
Missouri Botanical Garden 286666
PFAF Galium odoratum
Open Tree Of Life 598872
Observations.org 6814
NCBI Taxonomy 35899
NBN Atlas NBNSYS0000004306
Nature Serve 2.133376
IPNI 750339-1
iNaturalist 56065
GBIF 2914642
Freebase /m/04k1xv
EPPO GALOD
EOL 1107990
Elurikkus 4838
USDA GRIN 103279
Wikipedia Galium_odoratum
CMAUP NPO17395

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
Impacts of Soil Properties on Species Diversity and Structure in Alternanthera philoxeroides-Invaded and Native Plant Communities Wu H, Liu Y, Zhang T, Xu M, Rao B Plants (Basel) 25-Apr-2024
PMCID:PMC11085794
doi:10.3390/plants13091196
PMID:38732411
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Phylogenetic diversity drives soil multifunctionality in arid montane forest-grassland transition zone Wang X, Gong L, Luo Y, Ding Z, Guo Q, Li X, Ma X Front Plant Sci 12-Feb-2024
PMCID:PMC10894997
doi:10.3389/fpls.2024.1344948
PMID:38410734
First Insights on the Bioaccessibility and Absorption of Anthocyanins from Edible Flowers: Wild Pansy, Cosmos, and Cornflower Teixeira M, De Luca L, Faria A, Bordiga M, de Freitas V, Mateus N, Oliveira H Pharmaceuticals (Basel) 31-Jan-2024
PMCID:PMC10892915
doi:10.3390/ph17020191
PMID:38399406
Factors Influencing Venous Remodeling in the Development of Varicose Veins of the Lower Limbs Gwozdzinski L, Pieniazek A, Gwozdzinski K Int J Mol Sci 26-Jan-2024
PMCID:PMC10855638
doi:10.3390/ijms25031560
PMID:38338837
Modulation of the vitamin D receptor by traditional Chinese medicines and bioactive compounds: potential therapeutic applications in VDR-dependent diseases Yao M, Oduro PK, Akintibu AM, Yan H Front Pharmacol 22-Jan-2024
PMCID:PMC10839104
doi:10.3389/fphar.2024.1298181
PMID:38318147
Bioactivity and toxicity of coumarins from African medicinal plants Anywar G, Muhumuza E Front Pharmacol 10-Jan-2024
PMCID:PMC10809390
doi:10.3389/fphar.2023.1231006
PMID:38273831
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Phytochemical and Nutraceutical Screening of Ethanol and Ethyl Acetate Phases of Romanian Galium verum Herba (Rubiaceae) Semenescu AD, Moacă EA, Iftode A, Dehelean CA, Tchiakpe-Antal DS, Vlase L, Vlase AM, Muntean D, Chioibaş R Molecules 27-Nov-2023
PMCID:PMC10707836
doi:10.3390/molecules28237804
PMID:38067535
A target enrichment probe set for resolving phylogenetic relationships in the coffee family, Rubiaceae Ball LD, Bedoya AM, Taylor CM, Lagomarsino LP Appl Plant Sci 17-Nov-2023
PMCID:PMC10719880
doi:10.1002/aps3.11554
PMID:38106541
Analysis of the Potential Range of Mountain Pine-Broadleaf Ecotone Forests and Its Changes under Moderate and Strong Climate Change in the 21st Century Fedorov N, Zhigunova S, Shirokikh P, Baisheva E, Martynenko V Plants (Basel) 26-Oct-2023
PMCID:PMC10648261
doi:10.3390/plants12213698
PMID:37960054
Plant-based red colouration of shell beads 15,000 years ago in Kebara Cave, Mount Carmel (Israel) Davin L, Bellot-Gurlet L, Navas J PLoS One 25-Oct-2023
PMCID:PMC10599507
doi:10.1371/journal.pone.0292264
PMID:37878593
Topographic depressions can provide climate and resource microrefugia for biodiversity Frei K, Vojtkó A, Farkas T, Erdős L, Barta K, E-Vojtkó A, Tölgyesi C, Bátori Z iScience 21-Oct-2023
PMCID:PMC10656275
doi:10.1016/j.isci.2023.108202
PMID:38026156
Redundant and scattered genetic determinants for coumarin biodegradation in Pseudomonas sp. strain NyZ480 Gu Y, Li T, Zhou NY Appl Environ Microbiol 10-Oct-2023
PMCID:PMC10617510
doi:10.1128/aem.01109-23
PMID:37815346

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 / Anthracenes / Anthraquinones
1-Methoxy-2-methyl-anthraquinone 3534338 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 252.26 unknown https://doi.org/10.1039/J39680000854
Alizarin 2-methyl ether 80103 Click to see 254.24 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see 240.21 unknown https://doi.org/10.1039/J39680000854
2-Hydroxyanthraquinone 11796 Click to see 224.21 unknown https://doi.org/10.1039/J39680000854
Alizarin 6293 Click to see 240.21 unknown https://doi.org/10.1039/J39680000854
Lucidin 10163 Click to see 270.24 unknown via CMAUP database
Purpurin anthraquinone 6683 Click to see 256.21 unknown https://doi.org/10.1039/J39680000854
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1039/J39680000854
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1039/J39680000854
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1039/J39680000854
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(4S,7S,8S)-4-methyl-2-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-6-yl]methyl acetate 11968866 Click to see CC(=O)OCC1=CC2(C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O)C 428.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1039/J39680000854
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1039/J39680000854
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1039/J39680000854
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1039/J39680000854
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1002/ARDP.19252631103
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
[(4S,12R,15S,16S)-14,14-dimethyl-6-oxo-4-phenyl-3,11,13-trioxatetracyclo[8.6.0.02,7.012,16]hexadeca-1(10),2(7),8-trien-15-yl] acetate 42607797 Click to see 394.40 unknown via CMAUP database

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