Details Top

Internal ID UUID64401d219c04b224885913
Scientific name Muscari botryoides
Authority (L.) Mill.
First published in Gard. Dict., ed. 8. n. 1. 1768 [16 Apr 1768]

Ethnobotanical Use Top

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General Uses Top

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Common products:
Muscari botryoides is cultivated primarily as an ornamental spring‑flowering bulb. Commercial nurseries supply bulbs for garden planting, naturalisation in lawns and woodland margins, container displays, and for mass planting in public parks and landscapes. The species is also marketed as a cut‑flower crop for early‑season floral arrangements (Royal Horticultural Society Plant Finder, 2022; International Bulb Society, 2021).

Industrial and craft applications:
The principal industrial use lies in the horticultural trade. Large‑scale bulb production in the Netherlands, Germany and the United States provides the planting material that feeds the ornamental‑plant market. The plant’s early bloom and compact habit make it valuable for the cut‑flower sector, where stems are harvested for indoor vase displays during late winter and early spring (Horticultural Trade Association, 2020).

Properties relevant to use:
M. botryoides exhibits a low growth habit (10–30 cm), cold‑hardiness to USDA zones 4–8, and an early spring flowering period (March–April in temperate regions). The bulbs store starch, a typical carbohydrate reserve in Liliaceae, which supports rapid leaf and flower emergence after the winter dormant phase. Inflorescences are dense racemes of bell‑shaped, violet‑blue flowers, providing vivid colour and a mild fragrance that are prized for ornamental appeal (Flora Europaea, 1993). The species naturalises readily in well‑drained soils and tolerates light shade, attributes that reduce maintenance requirements in landscape design (RHS Award of Garden Merit, 2015).

Standards and regulation:
No dedicated industry standard exists for M. botryoides; trade follows general plant‑trade regulations such as the EU Plant Variety Protection Regulation and national phytosanitary requirements for bulb imports and exports (EU Plant Health Directive 2000/29/EC).

Sustainability and sourcing:
The plant is predominantly sourced from cultivated stock, which diminishes pressure on wild populations. Commercial growers employ bulblet propagation, disease‑free seed production, and controlled‑environment forcing to meet market demand while maintaining genetic integrity. Wild collection is discouraged, as the species is listed as regionally rare in parts of its Mediterranean range (IUCN Red List, assessed 2021). Sustainable practices include rotating bulb fields, using integrated pest management, and limiting harvest to cultivated plots rather than natural habitats.

Synonyms Top

Scientific name Authority First published in
Czekelia transsylvanica (Schur) Schur Oesterr. Bot. Wochenbl. 6: 237 (1856)
Hyacinthus botryoides L. Sp. Pl. : 318 (1753)
Muscari botryoides subsp. motelayi (Foucaud) Kerguélen Lejeunia , n.s., 120: 130 (1987)
Muscari botryoides subsp. lelievrii (Boreau) Garbari Webbia 38: 142. 1984
Muscari carpaticum Racib. Fl. Polska 1: 137 (1919)
Muscari botryoides subsp. hungaricum Priszter Bot. Közlem. 59: 46 (1972)
Muscari botryoides subsp. longifolium (Rigo) Garbari Inform. Bot. Ital. 28: 59 (1996)
Muscari polyphyllum Schur Enum. Pl. Transsilv. : 676 (1866)
Muscari pocuticum Zapal. Consp. Fl. Gallic. Crit. 1: 164 (1906)
Muscari transsilvanicum Schur Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 76 (1853)
Muscari longifolium Rigo Nuovo Giorn. Bot. Ital. , n.s., 12: 152 (1905)
Muscari motelayi Foucaud Bull. Soc. Sci. Nat. Char. Infer. 1891: 60 (1891)
Muscari inodorum Friche-Joset & Montandon Syn. Fl. Jura 313. 1856
Botryanthus kerneri Marches. Boll. Soc. Adriat. Sci. Nat. Trieste 7: 266 (1882)
Muscari hymenophorum Heldr. ex Boiss. Diagn. Pl. Orient. , ser. 2, 4: 109 (1859)
Muscari lelievrii Boreau Notes Pl. Franç. 2: 29 (1846)
Scilla inflata Salisb. Prodr. Stirp. Chap. Allerton : 243 (1796)
Botryanthus alpestris Jord. & Fourr. Icon. Fl. Eur. 2: 23 (1870)
Botryanthus boraeanus Jord. & Fourr. Icon. Fl. Eur. 2: 22 (1870)
Botryanthus candidus Jord. & Fourr. Icon. Fl. Eur. 2: 23 (1870)
Botryanthus compactus Jord. & Fourr. Icon. Fl. Eur. 2: 24 (1870)
Botryanthus conicus Jord. & Fourr. Icon. Fl. Eur. 2: 24 (1870)
Botryanthus festinus Jord. & Fourr. Icon. Fl. Eur. 2: 23 (1870)
Botryanthus heldreichii Jord. & Fourr. Icon. Fl. Eur. 2: 24 (1870)
Botryanthus lelievrii (Boreau) Jord. & Fourr. Icon. Fl. Eur. 2: 23 (1870)
Botryanthus vulgaris Kunth Enum. Pl. 4: 311 (1843)
Botryphile botryoides (L.) Salisb. Gen. Pl. : 25 (1866)
Eubotrys arvensis Raf. Autik. Bot. : 124 (1840)
Muscari botryoides f. candicum Voss Vilm. Blumengärtn. ed. 3 1: 1125 1896
Muscari kerneri var. lacteiflorum Borbás Term. Közl. 1896: 277.
Muscari botryoides var. lelievrii (Boreau) Baker J. Linn. Soc., Bot. 11: 418 1870
Botryanthus vulgaris var. transsilvanicus (Schur) Nyman Consp. Fl. Eur. 734. 1882
Botryanthus odorus var. compactus (Jord. & Fourr.) Nyman Consp. Fl. Eur. 734. 1882
Muscari botryoides subsp. kerneri (Marches.) K.Richt. Pl. Eur. 1: 227. 1890 (1890)
Muscari botryoides subsp. transsilvanicum (Schur) Soó Acta Bot. Acad. Sci. Hung. 10: 376. 1964 (1964)
Botryanthus vulgaris var. kerneri (Marches.) Nyman Consp. Fl. Eur. Suppl. 2: 307. 1890
Muscari kerneri (Marches.) Soldano Annot. Checkl. Italian Vasc. Fl. : 20 (2005)
Muscari alpinum Szafer ex Racib. Kosmos (Lvov) 35: 739 (1910)
Muscari botryoides var. lacteiflorum (Borbás) Soó Acta Bot. Acad. Sci. Hung. 16(3-4): 365. 1971 [1970 publ. 1971]

Common names Top

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Language Common/alternative name
English common grape hyacinth
Spanish jacinto ramoso
Spanish jacinto de la uva
Arabic حلحل جميل
Arabic قيسامه
Arabic بصل الزير
Belarusian гадзючая цыбуля гронкападобная
Bulgarian горско кукувиче грозде
Czech modřenec širolistý
Welsh clychau dulas cryno
Danish almindelig perlehyacint
German kleines träubel
German kleine traubenhyazinthe
Estonian harilik kobarhüatsint
Finnish hentohelmililja
Croatian razgranjena presličica
Upper Sorbian mała kitelnička
Hungarian epergyöngyike
Japanese ルリムスカリ
Lithuanian smulkiažiedė žydrė
Latvian mazā muskare
Dutch blauwe druifjes
Norwegian Nynorsk perleblom
Polish szafirek drobnokwiatowy
Slovak modrica širokolistá
Serbian Пресличица
Swedish pärlhyacint
Ukrainian Гадюча цибулька гроноподібна
Chinese 葡萄風信子
Chinese 蓝壶花
Chinese 葡萄风信子
Chinese 串铃花

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
grow seedlings at cool temperature - best achieved by sowing in open ground

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000694229
Flora of Alabama 4459
Canadensys 2743
USDA Plants MUBO
Tropicos 18401237
INPN 108869
Flora of Italy 6861
KEW urn:lsid:ipni.org:names:1027825-2
The Plant List kew-281677
Open Tree Of Life 498453
NCBI Taxonomy 81769
NBN Atlas NHMSYS0000460801
Nature Serve 2.131141
IPNI 538454-1
iNaturalist 56134
GBIF 2772094
Freebase /m/026g_4g
WisFlora 4297
EPPO MUSBO
EOL 1004033
Elurikkus 5815
Calflora (Californian flora) 5719
USDA GRIN 24751
Wikipedia Muscari_botryoides
CMAUP NPO15502

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
Identification and Validation of Reference Genes for qRT-PCR Analysis of Petal-Color-Related Genes in Rosa praelucens Jian H, Wang H, Qiu X, Yan H, Ma L Genes (Basel) 23-Feb-2024
PMCID:PMC10970342
doi:10.3390/genes15030277
PMID:38540336
Metabolome and Transcriptome Analyses Reveal Flower Color Differentiation Mechanisms in Various Sophora japonica L. Petal Types Guan L, Liu J, Wang R, Mu Y, Sun T, Wang L, Zhao Y, Zhu N, Ji X, Lu Y, Wang Y Biology (Basel) 25-Nov-2023
PMCID:PMC10740404
doi:10.3390/biology12121466
PMID:38132292
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
DoMYB5 and DobHLH24, Transcription Factors Involved in Regulating Anthocyanin Accumulation in Dendrobium officinale Yang K, Hou Y, Wu M, Pan Q, Xie Y, Zhang Y, Sun F, Zhang Z, Wu J Int J Mol Sci 20-Apr-2023
PMCID:PMC10142772
doi:10.3390/ijms24087552
PMID:37108715
Integrated Transcriptome and Metabolome Analyses Reveal the Anthocyanin Biosynthesis Pathway in AmRosea1 Overexpression 84K Poplar Yan H, Zhang X, Li X, Wang X, Li H, Zhao Q, Yin P, Guo R, Pei X, Hu X, Han R, Zhao X Front Bioeng Biotechnol 06-Jun-2022
PMCID:PMC9207281
doi:10.3389/fbioe.2022.911701
PMID:35733524
Fusarium and allied genera from China: species diversity and distribution Wang MM, Crous PW, Sandoval-Denis M, Han SL, Liu F, Liang JM, Duan WJ, Cai L Persoonia 21-Feb-2022
PMCID:PMC10792286
doi:10.3767/persoonia.2023.48.01
PMID:38234691
High honeybee abundances reduce wild bee abundances on flowers in the city of Munich Renner SS, Graf MS, Hentschel Z, Krause H, Fleischmann A Oecologia 07-Feb-2021
PMCID:PMC7940282
doi:10.1007/s00442-021-04862-6
PMID:33550468
Transcriptomic and chemical analyses to identify candidate genes involved in color variation of sainfoin flowers Qiao Y, Cheng Q, Zhang Y, Yan W, Yi F, Shi F BMC Plant Biol 22-Jan-2021
PMCID:PMC7825240
doi:10.1186/s12870-021-02827-8
PMID:33482728
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Generalized host‐plant feeding can hide sterol‐specialized foraging behaviors in bee–plant interactions Vanderplanck M, Zerck P, Lognay G, Michez D Ecol Evol 14-Dec-2019
PMCID:PMC6972837
doi:10.1002/ece3.5868
PMID:31993117
A survey of wild plant species for food use in Sicily (Italy) – results of a 3-year study in four Regional Parks Licata M, Tuttolomondo T, Leto C, Virga G, Bonsangue G, Cammalleri I, Gennaro MC, La Bella S J Ethnobiol Ethnomed 09-Feb-2016
PMCID:PMC4748641
doi:10.1186/s13002-015-0074-7
PMID:26860327
Factors affecting efficient in vitro micropropagation of Muscari muscarimi Medikus using twin bulb scale Ozel CA, Khawar KM, Unal F Saudi J Biol Sci 19-Sep-2014
PMCID:PMC4336438
doi:10.1016/j.sjbs.2014.09.007
PMID:25737643
Cryptic diversity in the Antherospora vaillantii complex on Muscari species Piątek M, Lutz M, Chater AO IMA Fungus 04-Apr-2013
PMCID:PMC3719206
doi:10.5598/imafungus.2013.04.01.02
PMID:23898408
Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies) Ali SS, Yu Y, Pfosser M, Wetschnig W Ann Bot 27-Oct-2011
PMCID:PMC3241591
doi:10.1093/aob/mcr274
PMID:22039008
Glycosides from <i>Muscari</i> <i>armeniacum</i> and <i>Muscari</i> <i>botryoides</i>. Isolation and structure of Muscarosides G–N Matteo Adinolfi, Gaspare Barone, Maria Michela Corsaro, Lorenzo Mangoni, Rosa Lanzetta, Michelangelo Parrilli Canadian Science Publishing 08-May-2006
doi:10.1139/V88-430

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(+)-Rhododendrol 919204 Click to see 166.22 unknown via CMAUP database
4-(4'-Hydroxyphenyl)-2-butanone 21648 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 162966578 Click to see CCC(=O)C1CC(C2(O1)CC(=O)C3(C2(CCC4=C3CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC1C(C(C(C(O1)C)O)O)O)O)O)O)C)C)C)C 1207.30 unknown https://doi.org/10.1139/V88-430
1-[(2'S,3S,4'R,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 162872884 Click to see 1357.40 unknown https://doi.org/10.1139/V88-430
1-[(2'S,3S,4'R,5R,10S,13S,14S,17S)-3-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 101215403 Click to see CCC(=O)C1CC(C2(O1)CCC3(C2(CCC4=C3CCC5C4(CCC(C5(CO)CO)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)C)O)O)O)O)O)O)C)C)C)C 1077.20 unknown https://doi.org/10.1139/V88-430
1-[3-[6-[[3-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-[3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 162872883 Click to see 1357.40 unknown https://doi.org/10.1139/V88-430
1-[3-[6-[[3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,4-bis(hydroxymethyl)-4',10,13,14-tetramethylspiro[1,2,3,5,6,7,11,12,15,16-decahydrocyclopenta[a]phenanthrene-17,5'-oxolane]-2'-yl]propan-1-one 14263469 Click to see 1077.20 unknown https://doi.org/10.1139/V88-430
3-[6-[[4,5-dihydroxy-3-[5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propanoylspiro[2,3,5,6,7,11,12,16-octahydro-1H-cyclopenta[a]phenanthrene-17,2'-oxolane]-15-one 14263450 Click to see 1207.30 unknown https://doi.org/10.1139/V88-430
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Hydroxydaidzein 5466139 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
6''-O-Acetylononin 102463148 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)OC)O)O)O 472.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(+)-Vestitol 177149 Click to see 272.29 unknown via CMAUP database
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin 5281704 Click to see 298.29 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database

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