Details Top

Internal ID UUID6440247c5b196658718906
Scientific name Allium ascalonicum
Authority L.
First published in Fl. Palaest. : 117 (1756)

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.

In Mediterranean folk medicine a decoction of shallot bulbs is taken as a mild diuretic and to soothe coughs (Duke, 1997). In the Turkish tradition an infusion of shallot leaves is drunk to relieve fever and cold symptoms (Davis, 1975). The Mapuche people of southern Chile apply a fresh bulb poultice to infected skin lesions (Bennett et al., 2021). In Indian Ayurvedic practice a macerated bulb mixture is sometimes used to treat stomach cramps (Wichtl, 2004). In Ethiopia, an infusion of dried shallot leaves is taken to relieve dyspepsia and gastritis (Wegayehu et al., 2020). In traditional Chinese medicine a decoction of whole bulbs is prescribed for bronchial congestion and cough (Li et al., 2012). Each preparation uses a specific part of the plant—bulb for decoction, leaves for infusion, or fresh bulb for poultice—demonstrating how different communities have adapted the same taxon to local therapeutic needs.

To prepare a mild tea, place one tablespoon (≈2 g) of dried shallot leaves in a cup, pour 250 ml of freshly boiled water, cover, and steep for 10 minutes. Strain and drink up to two cups a day. The tea is most effective when consumed warm, and the dried leaves can be stored in a dark airtight container for up to a year. Safety notes: this dose is safe for most adults but should be limited in pregnancy; individuals with severe heartburn, peptic ulcer disease, or those taking anticoagulant drugs (such as warfarin) because of the plant’s blood‑thinning organosulfur compounds should avoid regular consumption or consult a health professional.

The bulb and leaf tissues of Allium ascalonicum contain the characteristic organosulfur compounds that give Allium species their pungent aroma—allicin, diallyl disulfide and S‑allyl‑cysteine (Alam et al., 2014). These sulfur volatiles are produced when the tissue is disrupted and have demonstrated antimicrobial activity against common pathogens. The plant also houses flavonoids such as quercetin and its glycosides (Mao et al., 2015) and phenolic acids including caffeic and ferulic acid, both of which are potent antioxidants. In vitro studies show that extracts inhibit bacterial growth and reduce oxidative markers, providing a plausible mechanistic basis for the cough‑relieving, diuretic and wound‑healing uses documented in ethnobotanical records.

Contemporary research continues to explore shallot extracts for functional‑food applications and nutraceutical development, and commercial products ranging from dried leaf capsules to standardized bulb tinctures are now marketed in Europe, North America and Asia (García et al., 2022). Ongoing clinical trials are investigating its anti‑inflammatory and metabolic effects, while the plant remains a staple in many home gardens and rural kitchens, preserving its traditional role alongside scientific validation.

General Uses Top

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Food and beverages (non-medicinal):
Shallots are primarily cultivated as a culinary vegetable. The primary edible products are:
* **Fresh Bulbs:** Utilized raw or cooked across global cuisines, particularly in sauces (e.g., French vinaigrette, Southeast Asian sambals), dressings, and as a flavoring base.
* **Dried/Dehydrated Products:** Sliced or chopped shallots are dehydrated and sold as a shelf-stable ingredient. This includes shallot flakes and powders used in spice blends, rubs, soups, sauces, and processed foods.
* **Processed Forms:** Common processed forms include pickled shallots and various forms of pre-prepared chopped or sliced fresh shallots for retail consumers and foodservice.

Scientific uses:
* **Model Organism/Genetic Research:** *Allium cepa* var. *aggregatum* (syn. *A. ascalonicum*) is frequently used in cytogenetics and plant genetics research. Its large chromosomes and low chromosome number (2n=16) make it a standard subject for studying mitosis, chromosome structure, mutagensis, and polyploidy. It serves as an important reference plant in these scientific disciplines.

Properties relevant to use:
* **Culinary Value:** The primary non-medicinal value lies in its distinct culinary properties – flavor and aroma profile characterized by complex sulfur-containing compounds. Texture and size differences compared to common onions contribute to its specific culinary applications. The dried forms retain these flavor characteristics and offer convenience. Dehydration allows for significant shelf-life extension. The known chemical composition (e.g., fructose, glucose, sucrose, fructooligosaccharides) relates to flavor but does not by itself constitute a verified non-culinary industrial use.

Standards and regulation:
* Shallots traded internationally for food follow standard agricultural commodity specifications and food safety regulations applicable to Allium vegetables (e.g., Codex Alimentarius standards for fresh fruits and vegetables, national food laws).

Sustainability and sourcing:
* Shallots are cultivated widely in temperate and subtropical regions globally. Sustainability considerations mirror those of other Allium vegetable crops, relating to land use, water requirements, soil management, pest control, and waste generation during processing (e.g., dehydration and flake production).

Synonyms Top

Scientific name Authority First published in
Cepa ascalonica (L.) Garsault Fig. Pl. Méd. : t. 208 (1764)
Porrum ascalonicum (L.) Rchb. Fl. Germ. Excurs. : 110 (1830)
Allium carneum Willd. Enum. Pl. : 359 (1809)
Allium fissile Gray Nat. Arr. Brit. Pl. 2: 183 (1821 publ. 1822)
Allium hierochuntinum Boiss. Fl. Orient. 5: 244 (1882)

Common names Top

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Language Common/alternative name
English wild onion
English shallot
Spanish cebolla ascalonica
Spanish cebolla ascalónica
Spanish cebolla de ascalon
Spanish cebolla de ascalón
Spanish cebolla escaloena
Spanish cebolla escaloeña
Spanish cebolla macho
Spanish cebolleta ascalonica
Spanish cebolleta ascalónica
Spanish chalota
Spanish echalote
Spanish escalluna
Spanish escaluna
Spanish escaluña
Spanish chalote
Spanish allium fissile
Spanish cepa ascalonica
Spanish porrum ascalonicum
Afrikaans sjalot
Amharic ቀይ ሽንኩርት
Arabic كراث أندلسي
Arabic ثوم عسقلاني
bjn bawang habang
br chalotez
Catalan escalunyes
Catalan escalunya
Czech Šalotka
Czech cibule šalotka
Danish skalotteløg
German schalotten
German askalonzwiebel
German echalotte
German echalotten
German edelzwiebel
German eschalotte
German eschlauch
German zwiebel von askalon
German schalotte
Greek ασκαλώνιο
Greek εσαλότ
Esperanto askalono
Esperanto ŝaloto
Estonian jeeriku lauk
Basque tipulatx
Persian موسیر
Finnish salottisipuli
French echalote
French Échalotes
French Échalotte
French échalote
Galician chalota
Hebrew בצלצול
Hebrew אשלוט
Hebrew בצל אשקלון
Hebrew בצל הסריס
Hebrew בצל פנינה
Hebrew שאלוט
Hebrew שלוט
Hebrew בצלצל
ht echalot
Hungarian salottahagyma
Hungarian mogyoróhagyma
Indonesian brambang
Indonesian bawang merah
io shaloto
Icelandic skalottlaukur
Italian scalogno
Japanese シャロット
Japanese エシャロット
jv brambang
kge bawang siyaw
Korean 셜롯
lb schalott
Lithuanian askaloniniai česnakai
Latvian šalotes sīpoli
mad bhâbâng mèra
mad bâng mèra
mad bhâbâng bungkol
mai छ्यापी
Malagasy tongolomadinika
min bawang merah
Macedonian скалунка
Macedonian шалот
Macedonian козји лук
Malayalam shallot
Malayalam ചുകന്നുള്ളി
Malayalam ചെറിയ ഉള്ളി
Malayalam ചെറിയഉള്ളി
Malayalam പാലണ്ഡു
Malayalam ചുവന്നുള്ളി
Malay bawang merah
Burmese ကြက်သွန်နီကလေး
nan Âng-chhang-thaû
nan âng-chhang-thâu
Norwegian Bokmål sjalott
Norwegian Bokmål sjalottløk
Nepali छ्यापी
Dutch sjalot
Norwegian Nynorsk sjalottlauk
oc escaluènha
Polish szalotka
Polish czosnek askaloński
Polish allium hierochuntinum
Portuguese echalota
Portuguese chalota
Romanian ceapă franţuzească
Romanian ceapă franțuzească
Romanian eşalot
Romanian eșalot
Romanian haşmă
Romanian hașmă
Russian Шалот
Russian Лук ашкелонский
Russian Шалот-лук
Russian Лук-шалот
sco shallot
Slovenian šalotka
Serbian Šalot
su bawang beureum
Swedish schalottenlök
Tamil சின்ன வெங்காயம்
tg Картошкапиёз
Thai หัวหอมแดง
Thai หอมแดง
Turkish arpacık soğanı
Ukrainian Цибуля шалот
Urdu eschallot
Urdu shallot
Urdu کراث اندلسی
Urdu موسیر
Urdu قفلوط
vec scałogni
vec scalogno
vec scarlogna
yi שעלאט
Chinese 分蔥
Chinese 火葱
Chinese 香葱
Chinese 细香葱
Chinese 火葱(细香葱)
Chinese 西亚火葱
Chinese 火蔥
Chinese 紅蔥頭
Chinese 紅蔥

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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No germination or propagation data was added yet.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000755698
USDA Plants ALAS2
Tropicos 18400404
INPN 456844
Flora of Italy 6949
KEW urn:lsid:ipni.org:names:30185627-2
The Plant List kew-295055
Open Tree Of Life 5511448
Observations.org 114225
NCBI Taxonomy 1476995
IPNI 527632-1
iNaturalist 739210
GBIF 2856558
Freebase /m/0c2qc
EOL 1084258
Elurikkus 231170
USDA GRIN 2221
Wikipedia Shallot
PFAF Allium cepa aggregatum

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
Performance Evaluation of a Commercial Real-Time PCR Method for the Detection of Lupin Traces in Food Tramuta C, Decastelli L, Ingravalle F, Barcucci E, Fragassi S, Bianchi DM Foods 17-Feb-2024
PMCID:PMC10888417
doi:10.3390/foods13040609
PMID:38397586
Phytochemical Profiling and Antioxidant Activities of the Most Favored Ready-to-Use Thai Curries, Pad-Ka-Proa (Spicy Basil Leaves) and Massaman Siripongvutikorn S, Pumethakul K, Yupanqui CT, Seechamnanturakit V, Detarun P, Utaipan T, Sirinupong N, Chansuwan W, Wittaya T, Samakradhamrongthai RS Foods 14-Feb-2024
PMCID:PMC10887624
doi:10.3390/foods13040582
PMID:38397559
Antioxidant and Nitric Oxide Inhibitory Activity of the Six Most Popular Instant Thai Curries Siripongvutikorn S, Pumethakul K, Yupanqui CT, Seechamnanturakit V, Detarun P, Utaipan T, Sirinupong N, Chansuwan W, Wittaya T, Samakradhamrongthai RS Foods 05-Jan-2024
PMCID:PMC10814089
doi:10.3390/foods13020178
PMID:38254479
Ethnomedicinal plants in Champadevi rural municipality, Okhaldhunga district, Nepal Karki D, Khadka D, Kunwar RM, Aryal PC, Paudel HR, Bhatta S, Shi S J Ethnobiol Ethnomed 11-Dec-2023
PMCID:PMC10712033
doi:10.1186/s13002-023-00627-y
PMID:38072922
Natural Chalcones for the Management of Obesity Disease Maisto M, Marzocchi A, Keivani N, Piccolo V, Summa V, Tenore GC Int J Mol Sci 03-Nov-2023
PMCID:PMC10648025
doi:10.3390/ijms242115929
PMID:37958912
Conservation and Global Distribution of Onion (Allium cepa L.) Germplasm for Agricultural Sustainability Ochar K, Kim SH Plants (Basel) 18-Sep-2023
PMCID:PMC10535454
doi:10.3390/plants12183294
PMID:37765458
Assessment of Antioxidant Stability of Meat Pâté with Allium cepa Husk Extract Chernukha I, Kupaeva N, Khvostov D, Bogdanova Y, Smirnova J, Kotenkova E Antioxidants (Basel) 16-May-2023
PMCID:PMC10215231
doi:10.3390/antiox12051103
PMID:37237969
Structures, Sources, Identification/Quantification Methods, Health Benefits, Bioaccessibility, and Products of Isorhamnetin Glycosides as Phytonutrients Wang H, Chen L, Yang B, Du J, Chen L, Li Y, Guo F Nutrients 18-Apr-2023
PMCID:PMC10143801
doi:10.3390/nu15081947
PMID:37111165
Gelatin/carboxymethyl cellulose edible films: modification of physical properties by different hydrocolloids and application in beef preservation in combination with shallot waste powder Tran TT, Nguyen NN, Nguyen QD, Nguyen TP, Lien TN RSC Adv 29-Mar-2023
PMCID:PMC10052562
doi:10.1039/d3ra00430a
PMID:37006365
Plant ingredients in Thai food: a well-rounded diet for natural bioactive associated with medicinal properties Buathong R, Duangsrisai S PeerJ 01-Mar-2023
PMCID:PMC9985418
doi:10.7717/peerj.14568
PMID:36879911
Role and Mechanisms of Phytochemicals in Hair Growth and Health Kesika P, Sivamaruthi BS, Thangaleela S, Bharathi M, Chaiyasut C Pharmaceuticals (Basel) 30-Jan-2023
PMCID:PMC9963650
doi:10.3390/ph16020206
PMID:37259355
Topical Delivery of Atraric Acid Derived from Stereocaulon japonicum with Enhanced Skin Permeation and Hair Regrowth Activity for Androgenic Alopecia Pulat S, Subedi L, Pandey P, Bhosle SR, Hur JS, Shim JH, Cho SS, Kim KT, Ha HH, Kim H, Park JW Pharmaceutics 19-Jan-2023
PMCID:PMC9960134
doi:10.3390/pharmaceutics15020340
PMID:36839662
New Insights into the Research of Bioactive Compounds from Plant Origins with Nutraceutical and Pharmaceutical Potential Dincheva I, Badjakov I, Galunska B Plants (Basel) 05-Jan-2023
PMCID:PMC9860645
doi:10.3390/plants12020258
PMID:36678971
Optimization of a Microwave Assisted Extraction Method for Maximum Flavonols and Antioxidant Activity of Onion Extracts V. González-de-Peredo A, Vázquez-Espinosa M, Espada-Bellido E, Ferreiro-González M, F. Barbero G, Palma M, Carrera C Antioxidants (Basel) 02-Dec-2022
PMCID:PMC9774159
doi:10.3390/antiox11122393
PMID:36552601
The Molecular Mechanism of Natural Products Activating Wnt/β-Catenin Signaling Pathway for Improving Hair Loss Shin DW Life (Basel) 11-Nov-2022
PMCID:PMC9693075
doi:10.3390/life12111856
PMID:36430990

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102206753 Click to see 919.10 unknown https://doi.org/10.1021/JF020396T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-6,16-dihydroxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102206754 Click to see 919.10 unknown https://doi.org/10.1021/JF020396T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[(2R)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-6-methoxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163085298 Click to see 933.10 unknown https://doi.org/10.1021/JF020396T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[(2R)-4-[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-6-methoxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163085299 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)OC 933.10 unknown https://doi.org/10.1021/JF020396T
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2R)-4-[(1S,2S,4S,8S,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-14-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-6-yl]-2-methylbutoxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102206755 Click to see 901.00 unknown https://doi.org/10.1021/JF020396T
2-[4,5-Dihydroxy-2-[4-[16-hydroxy-6-methoxy-7,9,13-trimethyl-14-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163085297 Click to see 933.10 unknown https://doi.org/10.1021/JF020396T
Furostane base-1H2O-2H + 1O, O-Hex, O-Hex-dHex 139291953 Click to see 901.00 unknown https://doi.org/10.1021/JF020396T
Furostane base-2H + 1O, O-Hex, O-Hex-dHex 76448345 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)OC1(CCC(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)O 919.10 unknown https://doi.org/10.1021/JF020396T
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1021/JF020396T
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1021/JF020396T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Alliumoside A 73157059 Click to see 478.40 unknown https://doi.org/10.1021/JF020396T
isorhamnetin 4'-O-beta-D-glucopyranoside 11968470 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 478.40 unknown https://doi.org/10.1021/JF020396T
Quercetin-4'-o-glucoside 12442954 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1021/JF020396T
Spiraeoside 5320844 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1021/JF020396T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(3-hydroxy-4-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyphenyl)-3-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 22630387 Click to see 626.50 unknown https://doi.org/10.1021/JF020396T
Quercetin 3,4'-diglucoside 5320835 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)OC5C(C(C(C(O5)CO)O)O)O 626.50 unknown https://doi.org/10.1021/JF020396T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-4-oxo-4H-1-benzopyran-7-yl hexopyranoside 5381351 Click to see 464.40 unknown https://doi.org/10.1021/JF020396T
Quercimeritrin 5282160 Click to see 464.40 unknown https://doi.org/10.1021/JF020396T

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