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

Suggest a correction!
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

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

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
    • China
      • China North-central
      • China South-central
      • China Southeast

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.
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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Preparation, Characterization and Application of Active Food Packaging Films Based on Sodium Alginate and Twelve Varieties of Mandarin Peel Powder Yun D, Liu J Foods 12-Apr-2024
PMCID:PMC11048805
doi:10.3390/foods13081174
PMID:38672846
The lemon genome and DNA methylome unveil epigenetic regulation of citric acid biosynthesis during fruit development Yu H, Zhang C, Lu C, Wang Y, Ge C, Huang G, Wang H Hortic Res 05-Jan-2024
PMCID:PMC10923643
doi:10.1093/hr/uhae005
PMID:38464476
Transposable elements cause the loss of self‐incompatibility in citrus Hu J, Liu C, Du Z, Guo F, Song D, Wang N, Wei Z, Jiang J, Cao Z, Shi C, Zhang S, Zhu C, Chen P, Larkin RM, Lin Z, Xu Q, Ye J, Deng X, Bosch M, Franklin‐Tong VE, Chai L Plant Biotechnol J 01-Dec-2023
PMCID:PMC11022811
doi:10.1111/pbi.14250
PMID:38038155
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Bayesian phylodynamic analysis reveals the evolutionary history and the dispersal patterns of citrus tristeza virus in China based on the p25 gene Wang C, Chen C, Chen Y, Zhong K, Yi L Virol J 03-Oct-2023
PMCID:PMC10548698
doi:10.1186/s12985-023-02190-0
PMID:37789347
Comprehensive analyses of the citrus WRKY gene family involved in the metabolism of fruit sugars and organic acids Zhang M, Lu W, Yang X, Li Q, Lin X, Liu K, Yin C, Xiong B, Liao L, Sun G, He S, He J, Wang X, Wang Z Front Plant Sci 15-Sep-2023
PMCID:PMC10540311
doi:10.3389/fpls.2023.1264283
PMID:37780491
Evolutionary assessment of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE genes in citrus relatives with a specific focus on flowering Li Y, Wang S, Adhikari PB, Liu B, Liu S, Huang Y, Hu G, Notaguchi M, Xu Q Mol Hortic 20-Jul-2023
PMCID:PMC10515035
doi:10.1186/s43897-023-00061-4
PMID:37789480
Evolution‐guided multiomics provide insights into the strengthening of bioactive flavone biosynthesis in medicinal pummelo Zheng W, Zhang W, Liu D, Yin M, Wang X, Wang S, Shen S, Liu S, Huang Y, Li X, Zhao Q, Yan L, Xu Y, Yu S, Hu B, Yuan T, Mei Z, Guo L, Luo J, Deng X, Xu Q, Huang L, Ma Z Plant Biotechnol J 28-Apr-2023
PMCID:PMC10363765
doi:10.1111/pbi.14058
PMID:37115171
Citrus genomic resources unravel putative genetic determinants of Huanglongbing pathogenicity Gao Y, Xu J, Li Z, Zhang Y, Riera N, Xiong Z, Ouyang Z, Liu X, Lu Z, Seymour D, Zhong B, Wang N iScience 23-Jan-2023
PMCID:PMC9941208
doi:10.1016/j.isci.2023.106024
PMID:36824272
Nanopore long-read RNAseq reveals transcriptional variations in citrus species Hu XL, You C, Zhu K, Li X, Gong J, Ma H, Sun X Front Plant Sci 04-Jan-2023
PMCID:PMC9845879
doi:10.3389/fpls.2022.1077797
PMID:36684788
A chromosome-level phased genome enabling allele-level studies in sweet orange: a case study on citrus Huanglongbing tolerance Wu B, Yu Q, Deng Z, Duan Y, Luo F, Gmitter Jr F Hortic Res 03-Nov-2022
PMCID:PMC9832951
doi:10.1093/hr/uhac247
PMID:36643761
Insights into the mechanism of Huanglongbing tolerance in the Australian finger lime (Citrus australasica) Weber KC, Mahmoud LM, Stanton D, Welker S, Qiu W, Grosser JW, Levy A, Dutt M Front Plant Sci 21-Oct-2022
PMCID:PMC9634478
doi:10.3389/fpls.2022.1019295
PMID:36340410
Pan-mitogenomics reveals the genetic basis of cytonuclear conflicts in citrus hybridization, domestication, and diversification Wang N, Li C, Kuang L, Wu X, Xie K, Zhu A, Xu Q, Larkin RM, Zhou Y, Deng X, Guo W Proc Natl Acad Sci U S A 19-Oct-2022
PMCID:PMC9618123
doi:10.1073/pnas.2206076119
PMID:36260744
The complex genome and adaptive evolution of polyploid Chinese pepper (Zanthoxylum armatum and Zanthoxylum bungeanum) Hu L, Xu Z, Fan R, Wang G, Wang F, Qin X, Yan L, Ji X, Meng M, Sim S, Chen W, Hao C, Wang Q, Zhu H, Zhu S, Xu P, Zhao H, Lindsey K, Daniell H, Wendel JF, Jin S Plant Biotechnol J 07-Oct-2022
PMCID:PMC9829393
doi:10.1111/pbi.13926
PMID:36117410
Transcriptome analysis of the pulp of citrus fruitlets suggests that domestication enhanced growth processes and reduced chemical defenses increasing palatability Perez-Roman E, Borredá C, Tadeo FR, Talon M Front Plant Sci 02-Sep-2022
PMCID:PMC9478336
doi:10.3389/fpls.2022.982683
PMID:36119632

Phytochemical Profile Top

Add a new one!
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
> 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

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.