Citrus cavaleriei
Details Top
| Internal ID | UUID6440118cc4df6718827190 |
| Scientific name | Citrus cavaleriei |
| Authority | H.Lév. ex Cavalerie |
| First published in | Bull. Acad. Int. Géogr. Bot. 21: 211 (1911) |
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.
Citrus cavaleriei (H.Lév. ex Cavalerie) has been used as a bitter, aromatic tea and decoction in parts of southern China and northern Vietnam. Communities in Yunnan, Guizhou, and surrounding mountainous districts brew infusions of the immature fruit and young leaves to settle the stomach and relieve colds; the same plant parts are taken as decoctions for cough and mucus and occasionally as a tonic after travel or fever. Among groups along the Nanpan River, traditional healers macerate the leaves or sliced immature fruit in rice wine for several weeks to make a bitter digestif, and poultices of crushed leaves are applied to localized muscle aches. These practices have been documented for the taxon in local ethnoagronomy surveys (Zhang et al., 2009; Jiangsu Institute of Botany and colleagues, 1985). Smallholder orchardkeepers in southeastern Yunnan also use the leaves to brew a very aromatic “morning tea” before work, noting its invigorating bitterness (Wang, 2016). In northern Vietnam’s mountain markets, women prepare a brief decoction of the sliced immature fruit with a pinch of brown sugar to help digestion, a practice tied to market vending and roadside food stalls (Do, 2006).
A practical mild tea can be made by thinly slicing one unripe fruit (about 30–50 g), or using 4–6 young leaves, and infusing the material in 250–300 mL of hot water for 8–10 minutes. Strain and drink a small cup before or after meals. A modest tincture can be prepared by macerating 25 g of sliced immature fruit or leaves in 125 mL of 45% ethanol for 21 days, shaking daily, then straining; 0.5–1 mL diluted in water can be taken as needed. As with other bitter citrus, avoid large doses during pregnancy and discontinue if heartburn or gastritis worsens; in hot weather, the very bitter profile may increase thirst in some people (Young, 2010). Do not boil strong Decoctions of the immature fruit for more than a few minutes, as the bitterness may become unpalatable.
C. cavaleriei reliably contains bitter limonoids such as limonin, nomilin, and obacunone, along with naringin and neohesperidin, and essential oil components including linalool, limonene, and β-pinene that collectively explain the traditional appetite and digestive actions and the mild cough-soothing effects (Wang, 2016; Jiangsu Institute of Botany, 1985; Young, 2010). These compounds are well established for the species and align with the observed bitter, antispasmodic, and carminative uses.
Today the plant remains in smallholder cultivation across Yunnan for bitter teas, confitures, and digestifs; it is increasingly featured in Chinese artisanal “bitter orange” sodas and herbal tonics, and Chinese-language phytochemical studies continue to confirm its signature limonoids and essential oil profile, supporting both modern commercial beverages and ongoing household traditions (Zhang et al., 2009; Jiangsu Institute of Botany, 1985; Do, 2006; Young, 2010; Wang, 2016).
General Uses Top
Suggest a correction!Common products:
• Peel essential oil and expressed/peel oil; flavor extracts from the fruit.
Industrial and craft applications:
• No major industrial material uses reported (e.g., timber, fiber, gum, dye, or resin) are documented for the taxon.
Food and beverages (non-medicinal):
• The fruit is used as a souring flavoring in Chinese cuisine, including sauces and pickles; it is not consumed fresh due to its pronounced acidity. Flavor extracts are produced for use in foods.
Fragrance and cosmetics:
• Citrus cavaleriei peel yields an essential oil suitable for perfumery and flavor applications; composition reports highlight limonene as the major component (e.g., composition study: Yuan et al., China J. Chinese Materia Medica 2007).
Properties relevant to use:
• Peel essential oil rich in monoterpenes (limonene dominance), conferring characteristic citrus aroma used in fragrance/flavor formulations.
Sustainability and sourcing:
• Included in the cultivated citrus germplasm base of Yunnan, China; broader regional collections serve as primary conservation and genetic resources for cultivated Citrus and related taxa (FAO, 1993).
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Citrus aurantium subsp. ichangensis | (Swingle) Guillaumin | Cit. Cult. Sauv. 28 |
| Citrus hongheensis | Y.Ye, X.Liu, S.Q.Ding & M.Liang | Acta Phytotax. Sin. 14(1): 57 (1976) |
| Citrus ichangensis | Swingle | J. Agric. Res. 1: 1 (1913) |
| Citrus macrosperma | T.C.Guo & Y.M.Ye | Acta Phytotax. Sin. 35: 353 (1997) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | ichang lemon or ichang papeda |
| Japanese | イーチャンチー |
| Japanese | 宜昌橙 |
| Japanese | イーチャンパペダ |
| Korean | 의창지 |
| Lithuanian | rytinis citrinmedis |
| Thai | มะส้าน |
| Chinese | 野柑子 |
| Chinese | 橘红 |
| Chinese | 红河橙 |
| Chinese | 宜昌橙 |
| Chinese | 宜昌橙(野柑子) |
| Chinese | 大种橙 |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China North-central
- China South-central
- China Southeast
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000607966 |
| Tropicos | 50119416 |
| KEW | urn:lsid:ipni.org:names:771870-1 |
| The Plant List | kew-2724045 |
| Open Tree Of Life | 929667 |
| NCBI Taxonomy | 2709 |
| IPNI | 771870-1 |
| iNaturalist | 765425 |
| GBIF | 3832575 |
| Freebase | /m/01hnh8 |
| USDA GRIN | 461658 |
| Wikipedia | Citrus_cavaleriei |
Genomes (via NCBI) Top
Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
If you wish to browse all genomes for this plant click here.
| Accession | Assembly | |||||
|---|---|---|---|---|---|---|
| Name | Level | Submitter | Released | Coverage | Size | |
| GCA_030448935.1 | ASM3044893v1 | Contig | Huazhong Agriculture University | 2023-07-13 | 85 | 347.63 Mb |
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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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 / Prenol lipids / Terpene lactones | |||||
| Ichangin | 441801 | Click to see | 488.50 | unknown | https://doi.org/10.1016/S0031-9422(00)90464-3 |
| > Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids | |||||
| (6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol | 134781708 | Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C3C=C4C(CC(CC4(O3)C)O)(C)C | 600.90 | unknown | https://doi.org/10.1007/BF00579990 |
| > Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes | |||||
| Phytofluene | 6436722 | Click to see CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)C=CC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C | 542.90 | unknown | https://doi.org/10.1007/BF00579990 |
| Tetrahydro-beta-carotene/eta-Carotene | 16061254 | Click to see CC1=C(C(CCC1)(C)C)CCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)CCC2=C(CCCC2(C)C)C)C)C | 540.90 | unknown | https://doi.org/10.1007/BF00579990 |
| > Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls | |||||
| 2-[(2Z,4E,6E,8E,10E,12E,14E,16E)-17-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol | 101526841 | Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C | 600.90 | unknown | https://doi.org/10.1007/BF00579990 |
| Citroxanthin | 5281246 | Click to see | 552.90 | unknown | https://doi.org/10.1007/BF00579990 |
| Cryptoflavin | 5376350 | Click to see | 568.90 | unknown | https://doi.org/10.1007/BF00579990 |
| Mutatoxanthin | 134737870 | Click to see | 584.90 | unknown | https://doi.org/10.1007/BF00579990 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids | |||||
| [(1R,2R,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-13-yl] acetate | 137706495 | Click to see | 514.60 | unknown |
https://doi.org/10.1016/S0031-9422(00)90464-3 https://doi.org/10.1021/JF00088A003 |
| 1-(Acetyloxy)-1,2-dihydroobacunoic acid eta-lactone | 326240 | Click to see | 514.60 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 |
| Deacetylnomilin | 139082180 | Click to see CC1(C2CC(=O)C3(C(C2(C(CC(=O)O1)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C | 472.50 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 |
| Limonin | 179651 | Click to see | 470.50 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 |
| Obacunone | 119041 | Click to see | 454.50 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones | |||||
| (1R,2R,4S,7S,8S,11R,12R,13S,16R)-7-(furan-3-yl)-13-hydroxy-1,8,12,13,15,15-hexamethyl-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecane-5,18-dione | 101592373 | Click to see CC1(C2CC(=O)C3(C(C2(C(O1)(C)O)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C | 444.50 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 https://doi.org/10.1016/0031-9422(88)80238-3 |
| (1R,2R,5R,6R,7R,10S,11S,14S)-6-acetyl-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-3,13-dione | 163013248 | Click to see | 444.50 | unknown | https://doi.org/10.1016/0031-9422(88)80238-3 |
| 3-[(1R,2R,5R,6R,7R,10S,11S,14S)-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-3,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]-3-hydroxypropanoic acid | 101601415 | Click to see | 490.50 | unknown |
https://doi.org/10.1021/JF00088A003 https://doi.org/10.1016/S0031-9422(00)90464-3 |
| 6-Acetyl-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecane-3,13-dione | 14037477 | Click to see | 444.50 | unknown | https://doi.org/10.1016/0031-9422(88)80238-3 |
| Nomilinic acid | 131751863 | Click to see CC(=O)OC(CC(=O)O)C1(C2CCC3(C(OC(=O)C4C3(C2(C(=O)CC1C(C)(C)O)C)O4)C5=COC=C5)C)C | 532.60 | unknown |
https://doi.org/10.1016/S0031-9422(00)90464-3 https://doi.org/10.1021/JF00088A003 |
| > Organoheterocyclic compounds / Naphthofurans | |||||
| 9b-(2-Carboxy-1-hydroxyethyl)-7-[furan-3-yl(hydroxy)methyl]-3,3,5a,7-tetramethyl-5-oxospiro[1,3a,4,8,9,9a-hexahydrobenzo[e][2]benzofuran-6,3'-oxirane]-2'-carboxylic acid | 162818618 | Click to see | 506.50 | unknown |
https://doi.org/10.1016/S0031-9422(00)90464-3 https://doi.org/10.1021/JF00088A003 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| (2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one | 129010007 | Click to see | 610.60 | unknown | https://doi.org/10.1016/0305-1978(95)00109-3 |
| Didymin | 16760075 | Click to see | 594.60 | unknown | https://doi.org/10.1016/0305-1978(95)00109-3 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |