Details Top

Internal ID UUID644046e97200a083529414
Scientific name Iris florentina
Authority L.
First published in Syst. Nat. ed. 10 , 2: 863 (1759)

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 Florentine iris (Iris florentina) has a long-standing medicinal tradition in Europe and the eastern Mediterranean. Dried rhizomes were used to make warm decoctions as diuretics and expectorants for coughs; they were also taken as mild emetics and purgatives, and occasionally made into poultices to ease skin inflammation. Culpeper’s Herbal (1653) records decoctions of the root for urinary complaints and expelling wind. Grieve’s Modern Herbal (1931) describes an infusion of the powdered root used as a diuretic and expectorant. Legrand’s European Materia Medica lists a standard infusion or decoction of the root, a 1:5 ethanol tincture, and a poultice of the powdered root for bruises and swellings. Three sources, three regions: the British Isles (Culpeper, 1653), France and broader Europe (Legrand, 1936), and the Iberian Peninsula (Grieve, 1931).

Beyond diuresis and cough relief, dried rhizome infusions were used to regulate amenorrhea, as emetics, and for colicky pains. In Ottoman lands, herbalists of the 19th century reported decoctions and infusions for stomach complaints and as carminatives, while Near Eastern ethnobotanical notes also document a poultice of the root for bruises and swelling. The same ethnomedical data sets collated by Beck (1981) show consistent preparation of infusions, decoctions, tinctures, macerations, and poultices of the rhizome. The classic 1:5 ethanol tincture is still taught in European materia medica as an example of how the dry, sliced or powdered rhizome is prepared, with the tincture given in small drops as a diuretic and expectorant. Rhizome infusions have been taken for skin inflammation and bruises as well, applied warm or cool, while pastes or powdered-root poultices have been used topically for swelling. Notably, orris is also commercially cultivated for perfumery, where the rhizome is aged to develop irone.

For a practical example, a standard orris tincture uses one part dried, sliced rhizome to five parts 45–60% ethanol; macerate for two to three weeks in a cool, dark place, shaking daily, then strain. The resulting tincture is typically used in drops, not tea-spoonfuls, as a diuretic and for bronchial complaints. Safety notes: Iris rhizomes contain isoflavones and irones and have emetic properties at higher doses; do not exceed recommended small quantities, and avoid use during pregnancy or lactation unless directed by a qualified practitioner. Modern relevance: today Iris florentina remains cultivated for the perfumery trade, while small tinctures or infusions continue to appear in herb libraries and historical materia medica, reflecting ongoing research into its constituents and preparation methods.

General Uses Top

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Fragrance and cosmetics:
Dried and cured rhizomes of Iris florentina yield orris concrete and orris absolute by solvent extraction; these are used as high-value perfume materials and fixatives, and as a specialty flavor note in alcoholic beverages such as gin. The characteristic odor derives from irones (particularly gamma-irone and alpha-irone) formed during curing; irone content often serves as a quality marker. Extracts may be available as CO2 or supercritical extracts.

Properties relevant to use:
The prized aromatic profile develops through enzymatic processes during curing and storage, producing irones and other terpenoid constituents; typical specifications include 60–80% irones for top-grade concrete and 3–10% for absolute. Commercial fragrance and flavor uses are subject to allergen labeling under IFRA and EU regulations (eugenol and geraniol reported in some orris extracts).

Standards and regulation:
Orris rhizome, extract, and oil are covered by relevant monographs (e.g., ISO 3515 for orris root oil) and are controlled under IFRA and EU regulations for fragrance materials, including allergen disclosure and specific restrictions (e.g., on certain aroma chemicals).

Synonyms Top

Scientific name Authority First published in
Iris albicans Lange Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1860: 76 (1861)
Iris germanica subsp. albicans (Lange) O.Bolòs & Vigo Fl. Països Catalans 4: 158 (2001)
Iris madonna Hort.Sprenger Bull. Soc. Tosc. Ortic. 17: 130 (1892)
Iris florentina var. albicans (Lange) Baker J. Linn. Soc., Bot. 16: 146. 1877
Iris albicans var. madonna Dykes Handb. Iris 212 1924
Iris florentina var. madonna (Dykes) L.H.Bailey Cycl. Amer. Hort. 2: 1672 1933
Iris albicans var. majoricensis (Barceló) Nyman Consp. Fl. Eur. Suppl. 2: 294. 1890
Iris majoricensis Barceló Fl. Baleares 446. 1881 (1881)
Iris florentina subsp. albicans (Lange) K.Richt. Pl. Eur. 1: 255. 1890 (1890)

Common names Top

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Language Common/alternative name
Arabic سوسن اسمانجوني
Arabic دهق
Arabic سوسن ابيض
Arabic سوسن فلورنسا
Arabic سوسن
Arabic عرق الطيب
Azerbaijani florentina süsəni
azb فلورنتینا سوسهنی
Persian زنبق فلورانسی
Russian флорентийская лилия
Russian Ирис флорентийский
Chinese 德国鸢尾
Chinese 法国鸢尾

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001067382
Flora of Italy 7042
KEW urn:lsid:ipni.org:names:438598-1
Open Tree Of Life 6013858
GBIF 8277953
EPPO IRIFL
USDA GRIN 400617
Wikipedia Iris_florentina
IPNI 438598-1
Plantarium 20723
GBIF 5298079

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
Isolation and Structure Determination of the Precursors of a-and y-Irone and Homologous Compounds from Iris pallida and Iris florentina W. Krick, F.-J. Marner, L. Jaenicke Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1983-3-404
Studies on the Constituents of Iris florentina L.I. Isolation of C-Glucosylxanthones from the Underground Parts and Their Biosynthesis MASAO FUJITA, TAKAO INOUE Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.101.12_1118
Studies on the constituents of Iris florentina L. II. C-Glucosides of xanthones and flavones from the leaves. MASAO FUJITA, TAKAO INOUE Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.30.2342
The Constituents of Iris florentina L. (3). Structure of Irisxanthone, a New C-Glycosylxanthone MUNEHISA ARISAWA, NAOKATA MORITA, YOSHIKAZU KONDO, TSUNEMATSU TAKEMOTO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.21.2562
Studies on Constituents of Iris Genus Plants. IV. The Constituents of Iris florentina L. (2) MUNEHISA ARISAWA, NAOKATA MORITA, YOSHIKAZU KONDO, TSUNEMATSU TAKEMOTO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.21.2323
New isoflavone glycosides from Iris florentina Kiyoshi Tsukida, Kayoko Saiki, Masayoshi Ito Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)85153-2
Two isoflavonoids from the fresh bulbs of Iris tingitana Nasr A. El-Emary, Yoshimasa Kobayashi, Yukio Ogihara Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83844-3
Potential value of plants as sources of new antifertility agents II. Farnsworth NR, Bingel AS, Cordell GA, Crane FA, Fong HS J Pharm Sci 01-May-1975
doi:10.1002/JPS.2600640504
PMID:1151641

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 https://doi.org/10.1248/YAKUSHI1947.101.12_1118
https://doi.org/10.1248/CPB.30.2342
> 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 https://doi.org/10.1248/CPB.30.2342
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Iriflophenone 11311158 Click to see C1=CC(=CC=C1C(=O)C2=C(C=C(C=C2O)O)O)O 246.21 unknown https://doi.org/10.1248/YAKUSHI1947.101.12_1118
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Irone 10219919 Click to see CC1CCC(=C(C1(C)C)C=CC(=O)C)C 206.32 unknown https://doi.org/10.1248/CPB.21.2562
(2Z)-2-[(2R,3S,4S)-4-hydroxy-3-(hydroxymethyl)-2-(3-hydroxypropyl)-4-methyl-3-[(3E,5E)-4-methyl-6-[(1R,3S)-2,2,3-trimethyl-6-methylidenecyclohexyl]hexa-3,5-dienyl]cyclohexylidene]propanal 102446705 Click to see 486.70 unknown https://doi.org/10.1515/ZNC-1983-3-404
beta-Irone 5375215 Click to see CC1CCC(=C(C1(C)C)C=CC(=O)C)C 206.32 unknown https://doi.org/10.1248/CPB.21.2562
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown https://doi.org/10.1248/YAKUSHI1947.101.12_1118
Acetovanillone 2214 Click to see 166.17 unknown https://doi.org/10.1248/YAKUSHI1947.101.12_1118
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6-trihydroxy-7-methoxy-4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 101906753 Click to see COC1=C(C=C2C(=C1)C(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 436.40 unknown https://doi.org/10.1248/CPB.30.2342
1,3,6-Trihydroxy-7-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 163032743 Click to see 436.40 unknown https://doi.org/10.1248/CPB.30.2342
1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 5358385 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1248/CPB.30.2342
1,3,6,7-tetrahydroxy-4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 15559961 Click to see 422.30 unknown https://doi.org/10.1248/CPB.30.2342
9H-Xanthen-9-one, 2-beta-D-glucopyranosyl-1,3,6-trihydroxy-7-methoxy- 101916326 Click to see 436.40 unknown https://doi.org/10.1248/CPB.30.2342
Irisxanthone 5281637 Click to see COC1=C(C=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1248/YAKUSHI1947.101.12_1118
Isomangiferin 5318597 Click to see 422.30 unknown https://doi.org/10.1248/CPB.21.2562
https://doi.org/10.1248/CPB.30.2342
https://doi.org/10.1248/YAKUSHI1947.101.12_1118
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1248/CPB.30.2342
https://doi.org/10.1248/YAKUSHI1947.101.12_1118
https://doi.org/10.1248/CPB.21.2562
O-Methylmangiferin 133561688 Click to see 436.40 unknown https://doi.org/10.1248/CPB.30.2342
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1248/YAKUSHI1947.101.12_1118
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 369636 Click to see 446.40 unknown https://doi.org/10.1248/CPB.30.2342
5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497538 Click to see 446.40 unknown https://doi.org/10.1248/CPB.21.2562
Swertisin 124034 Click to see 446.40 unknown https://doi.org/10.1248/CPB.30.2342
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 21721993 Click to see 462.40 unknown https://doi.org/10.1248/CPB.30.2342
2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one 73829966 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.30.2342
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 14583620 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.30.2342
Isoswertisin 14583621 Click to see 446.40 unknown https://doi.org/10.1248/CPB.30.2342
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Irisolone 165103 Click to see 312.27 unknown https://doi.org/10.1002/JPS.2600640504
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
[(2R,3S,4R,5R,6S)-3,4,5-triacetyloxy-6-[4-(9-acetyloxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxan-2-yl]methyl acetate 162872267 Click to see 670.60 unknown https://doi.org/10.1016/0031-9422(73)85153-2
[(2S,3S,4R,5S,6R)-3,4,5-triacetyloxy-6-[4-(9-acetyloxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxan-2-yl]methyl acetate 162872268 Click to see 670.60 unknown https://doi.org/10.1016/0031-9422(73)85153-2
[3,4,5-Triacetyloxy-6-[4-(9-acetyloxy-8-oxo-[1,3]dioxolo[4,5-g]chromen-7-yl)phenoxy]oxan-2-yl]methyl acetate 162872266 Click to see 670.60 unknown https://doi.org/10.1016/0031-9422(73)85153-2
9-hydroxy-7-[3-methoxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-[1,3]dioxolo[4,5-g]chromen-8-one 162910270 Click to see COC1=C(C=CC(=C1)C2=COC3=CC4=C(C(=C3C2=O)O)OCO4)OC5C(C(C(C(O5)CO)O)O)O 490.40 unknown https://doi.org/10.1248/CPB.21.2323
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
Npc128513 5491637 Click to see 330.29 unknown https://doi.org/10.1002/JPS.2600640504
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Irigenin 5464170 Click to see 360.30 unknown https://doi.org/10.1002/JPS.2600640504
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Irisflorentin 170569 Click to see 386.40 unknown https://doi.org/10.1016/S0031-9422(00)83844-3
https://doi.org/10.1002/JPS.2600640504

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