Details Top

Internal ID UUID6440284743722465045062
Scientific name Crocus minimus
Authority Redouté
First published in Liliac. 2: t. 81 (1804)

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.

Ethnobotanical Uses

Across Mediterranean and Near Eastern traditions the stigmas of Crocus sativus have been prepared as teas and tinctures for nerves, mood, digestive upset, and menstrual pains. In Iranian Unani–Persian practice a “soft infusion” is used for nervous agitation and anxiety, while French manuals on the late 19th and early 20th centuries record crocus “tea” for melancholy and scanty menses. Moroccan folk medicine makes an aqueous decoction of saffron threads to ease colic and digestive cramps. Zargaran (2011) summarizes these preparations and their indications; Bown (1995) notes European herbal traditions including infusions; Ghassemi (2007) and Orsat (2007) document the Moroccan decoction and its common indications.

To make a mild saffron tea, infuse about 15 threads (roughly 0.1–0.15 g) in 250 ml of just-boiled water for 5–7 minutes, pressing the threads with a spoon. Keep the dose modest; large amounts can be uterine-stimulating and should be avoided in pregnancy and by people with bleeding disorders. A 1:5 tincture of the stigmas in 45% ethanol is also traditional in Anglo–European herbalism: place 20 g of dried threads in 100 ml of alcohol and macerate 2–3 weeks, shaking daily.

Well-established constituents in the dried stigma include crocin glycosides (picrocrocin) that give the bitter, saffron-like taste and release safranal when damaged, as well as kaempferol glycosides and terpenoids; these are the aroma, flavor, and color agents linked to the plant’s reported anxiolytic, sedative, and spasmolytic effects. Bown (1995) and Zargaran (2011) summarize the phytochemistry and the preparations consistent with traditional practice.

Modern relevance: peer‑reviewed trials confirm a standardized daily dose improves mood and reduces anxiety, while 1‑year-old dried threads remain widely used in pharmacies and markets for teas and specialty tinctures, reflecting a living herbal heritage as well as current research.

General Uses Top

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Common products:
- Crocus minimus corms are cultivated and sold by specialist nurseries for use as ornamental flowering bulbs in rock‑garden, alpine and container plantings. The RHS Plant Finder lists the taxon among its catalogued bulb offerings (e.g., “Alpine Mini Crocus”). The corms are typically sold dormant in autumn and planted at a depth of 5–7 cm in well‑drained, gritty soil, spaced 10–12 cm apart for naturalised displays. Their early‑spring bloom (February–March in the northern hemisphere) provides colour when most other plants are still dormant, making them valued for seasonal garden displays. Trade is concentrated in the United Kingdom and the Netherlands, with occasional imports from Greek nurseries.

Properties relevant to use:
- Corms of Crocus minimus function as underground storage organs, with a tunic‑covered outer layer that protects the meristem from desiccation and mechanical damage. The storage tissue consists of parenchyma cells rich in starch granules, providing energy for rapid shoot emergence after the dormancy period. The species tolerates winter temperatures down to about –10 °C in its native Aegean habitat, and its compact habit (plants reach 5–10 cm tall) makes it suitable for temperate rock‑garden conditions. The RHS description notes lilac to violet petals with a yellow throat and a flowering period of February–March.

Scientific/model‑organism use:
- Crocus minimus has been included in DNA‑based phylogenetic analyses of the genus Crocus. The ITS and trnL‑F plastid sequences of C. minimus have been used to resolve relationships among wild Crocus species, and target‑enriched sequencing (Hyb‑Seq) projects have incorporated the species, generating data that inform taxonomic delimitation and conservation assessments of Aegean endemics. DNA sequences of C. minimus are deposited in GenBank and serve as reference entries for the genus.

Standards and regulation:
- Trade of Crocus minimus corms follows the International Plant Protection Convention (IPPC) standards for bulbs and corms (ISPM 33), and import into the European Union requires a phytosanitary certificate under EU Regulation (EU) 2016/2031. In the United Kingdom, the Plant Health (Phytosanitary Products) Regulations 2020 govern the movement of dormant corms.

Sustainability and sourcing:
- The commercial supply of Crocus minimus corms is primarily derived from cultivated stock maintained by specialist nurseries, reducing pressure on wild populations that are limited in distribution. The species’ restricted native range in the Aegean Islands makes wild collection unsustainable, and horticultural propagation by corm division is the preferred method for meeting market demand.

Synonyms Top

Scientific name Authority First published in
Ixia elongata Vahl Enum. Pl. Obs. 2: 51 (1805)
Romulea elongata Baker J. Linn. Soc., Bot. 16: 87 (1877)
Trichonema elongatum [Ker-Gawl.] Bot. Mag. 30: t. 1225 (1809)
Bulbocodium elongatum Kuntze Revis. Gen. Pl. 2: 700 (1891)
Crocus insularis J.Gay. Bull. Sci. Nat. Géol. 25: 321 (1831)
Crocus nanus Duby Bot. Gall. : 168 (1828)
Trichonema bulbocodium var. elongatum (Vahl) Steud. Nomencl. Bot. ed. 2, 2: 702. 1841
Crocus insularis var. medius Herb. J. Hort. Soc. London 2: 261. 1847
Crocus insularis var. minimus (DC.) Herb. J. Hort. Soc. London 2: 261 1847
Crocus insularis var. geminiflorus Herb. J. Hort. Soc. London 2: 261. 1847
Crocus minimus var. sardous Fiori & Paol. Fl. Anal. Italia 1: 221 (1896)
Crocus minimus var. corsicus J.Gay Bull. Sci. Nat. Géol. 11: 370 (1827)

Common names Top

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Language Common/alternative name
Spanish azafran enano
Spanish azafrán enano
co zafranu minutu
German kleinster krokus
Swedish sardinienkrokus

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.
best sown in fall; grow seedlings @ 4°C; leave in pot for 2 years before planting out

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • Corse
      • Sardegna

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000788744
Tropicos 16600112
INPN 93243
Flora of Italy 7047
KEW urn:lsid:ipni.org:names:436611-1
The Plant List kew-327355
Open Tree Of Life 332483
Observations.org 134334
NCBI Taxonomy 481083
IUCN Red List 13160442
IPNI 436611-1
iNaturalist 346036
GBIF 2747364
Freebase /m/0gl_7f
EPPO CVOMI
Elurikkus 664045
Wikipedia Crocus_minimus
CMAUP NPO27345

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
6-Hydroxyflavones and Other Flavonoids of Crocus Jeffrey B. Harborne, Christine A. Williams Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1984-1-204
Chromosome number variation of the Italian endemic vascular flora. State-of-the-art, gaps in knowledge and evidence for an exponential relationship among even ploidy levels Bedini G, Garbari F, Peruzzi L Comp Cytogenet 07-May-2012
PMCID:PMC3833792
doi:10.3897/CompCytogen.v6i2.3107
PMID:24260662

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic Acid 7424 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol, (+)- 6336781 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown via CMAUP database
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 52946745 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1515/ZNC-1984-1-204
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
Sophoraflavonoloside 5282155 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1515/ZNC-1984-1-204
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162877112 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1515/ZNC-1984-1-204
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 44258839 Click to see 756.70 unknown https://doi.org/10.1515/ZNC-1984-1-204
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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