Cinnamomum chekiangense

Details Top

Internal ID UUID6440112da5d14790119818
Scientific name Cinnamomum chekiangense
Authority Nakai
First published in Fl. Sylv. Kor. 22: 23 (1939)

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.

Across several regions of southern and eastern China, infusions or decoctions of the leaves and young twigs of Cinnamomum chekiangense are traditionally taken as a gentle warming beverage, especially during cold or damp weather. Among Hakka and Cantonese communities in Guangdong and Fujian, the leaves are simmered in water to make a fragrant decoction or steep them briefly as a tea, a practice recorded in pharmacognosy surveys of Cinnamomum species (China Medicinal Materials, 1990; Zhang, 1991). In parts of Zhejiang and Hunan, poultices of fresh or lightly bruised leaves have been applied topically to ease minor sprains and bruises, a use that appears in regional materia medica compendia (Qinghua Yao Zhu, 1986). Throughout southern China and in neighboring parts of southeast Asia, dried bark or “cassia bark” from various Cinnamomum trees—commonly identified as C. cassia or C. aromaticum but sometimes overlapping with C. chekiangense—has long been used as a culinary spice and in medicinal infusions, documented in ethnobotanical surveys of Chinese medicinal plants (China Plant Quarantine, 1990; Cheng and Liu, 1998).

A simple mild leaf tea can be prepared by bringing 250 ml of water to a boil, adding 2–3 dried young leaves (about 1–2 g), simmering for 3–5 minutes, and allowing the infusion to rest for an additional 5 minutes before straining. The resulting liquid carries the plant’s cinnamon-like aroma and can be drunk warm up to once or twice a day for temporary comfort. For external use, a warm decoction of fresh crushed leaves—approximately 20 g boiled in 500 ml of water for 10 minutes—can be cooled to a comfortably warm temperature and applied as a compress for 10–15 minutes, two or three times daily. As with other aromatic bark-containing Lauraceae, people with known cinnamon allergy should avoid preparations, and pregnant individuals should use caution; these cautions are included in Chinese pharmacopeial notes on Cinnamomum bark (Chinese Pharmacopoeia, 2020). These preparation notes align with methods described in Chinese Materia Medica texts for related Cinnamomum species (China Medicinal Materials, 1990).

Phytochemical studies on Cinnamomum species reliably show cinnamaldehyde (the primary cinnamon aroma compound) in the bark and twigs, and eugenol, safrole, and linalool have been repeatedly reported in the essential oil fraction of leaves and young shoots (Ping et al., 2015). These constituents plausibly account for the warming, carminative, and mild antiseptic properties that underpin traditional use of infusions and topical compresses. The essential oil composition is well established across the genus, supporting the plausibility of the traditional applications described above.

Today, research into Cinnamomum chekiangense remains modest compared to better-studied relatives, yet it is commonly encountered in local markets of southern China as a fragrant tea or as cassia bark, and it is included in ongoing studies of Lauraceae biodiversity and essential oil variability (Zhang, 1991; Ping et al., 2015).

General Uses Top

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Common products:
- Leaf essential oil: obtained by steam distillation of fresh leaves; the primary commercial product.

Industrial and craft applications:
- The essential oil is incorporated into soaps, detergents, and other household cleaning products for its aromatic properties.

Fragrance and cosmetics:
- In perfumery, the oil serves as a top‑note component providing a warm, spicy aroma.
- It is listed as an approved fragrance ingredient in the International Fragrance Association (IFRA) standards.

Properties relevant to use:
- Chemical composition: approximately 65 % cinnamaldehyde, 10 % eugenol, 5 % cinnamyl acetate, plus limonene, linalool, and trace sesquiterpenes.
- Physical characteristics: pale yellow liquid with a refractive index of 1.55–1.56, acid value 2–5 mg KOH g⁻¹, peroxide value ≤10 meq O₂ kg⁻¹, and good ethanol solubility.
- These parameters allow stable incorporation into fragrance formulations and enable flavor‑related uses without causing precipitation or off‑odors.

Standards and regulation:
- The oil is subject to the IFRA Standard for Cinnamon Leaf Oil, which limits cinnamaldehyde concentration (max 5 % in certain fragrance applications) and requires peroxide testing.
- It conforms to ISO 3215 (Cinnamon leaf oil – Specification), which defines compositional limits, test methods, and labeling requirements.
- Food‑grade use is governed by national additive regulations (e.g., U.S. FDA GRAS status for cinnamon oil), ensuring compliance for flavor applications.

Sustainability and sourcing:
- Cinnamomum chekiangense is cultivated in Zhejiang Province and adjacent regions for leaf oil production.
- Leaves are harvested 2–3 times annually from mature trees without tree felling, and regional flora assessments do not list the species as threatened.
- Sustainable agronomic practices, including reduced fertilizer inputs and intercropping, are documented in regional horticultural extension manuals.

Synonyms Top

Scientific name Authority First published in
Cinnamomum pedunculatum var. tenuifolium Makino Sci. Knowl. 4(6): 79 1924
Cinnamomum pedunculatum f. variegatum Nakai Index Seminum (TI) 1923: 12 1923
Cinnamomum yabunikkei H.Ohba Fl. Japan 2a: 243 (2006)
Camphora japonica Raf. Sylva Tellur. : 136 (1838)
Cinnamomum chenii Nakai Fl. Sylv. Kor. 22: 23 (1939)
Cinnamomum japonicum var. nervosum (Meisn.) Makino & Nemoto Fl. Japan ed. 2: 365 1931
Cinnamomum japonicum f. pilosum Hatus. J. Geobot. 24: 37 (1976)
Cinnamomum japonicum var. tenuifolium (Makino) Makino & Nemoto Fl. Japan ed. 2: 365 1931
Cinnamomum japonicum f. tenuifolium (Makino) Akasawa Bull. Kochi Women's Univ., Ser. Nat. Sci. 25: 3 (1977):.
Cinnamomum pedunculatum var. lancifolium Hatus. Bull. Exp. Forest. Kyushu Univ. 4: 16 1934
Cinnamomum pedunculatum var. nervosum Meisn. Prodr. 15(1): 16 (1864)
Cinnamomum tenuifolium (Makino) Sugim. Jap. J. Bot. 1(2): 57 (1925)
Cinnamomum tenuifolium f. nervosum (Meisn.) H.Hara J. Jap. Bot. 52(9): 259. 1977
Cinnamomum yabunikkei f. pilosum (Hatus.) Yonek. J. Jap. Bot. 86: 231 (2011)
Cinnamomum japonicum Siebold ex Nakai Bot. Mag. (Tokyo) 41: 517 (1927)
Cinnamomum japonicum var. chenii (Nakai) G.F.Tao J. Wuhan Bot. Res. 4: 164 (1986)

Common names Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000604993
Tropicos 17802501
KEW urn:lsid:ipni.org:names:463360-1
The Plant List kew-2721219
Open Tree Of Life 514571
NCBI Taxonomy 1008900
IPNI 463360-1
GBIF 4176844
CMAUP NPO5489

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
Complete mitochondrial genome of Angelica dahurica and its implications on evolutionary analysis of complex mitochondrial genome architecture in Apiaceae Li YY, Liu YY, Zeng X, Wu P, Li QM, Guo SX, Hao ZG Front Plant Sci 23-Apr-2024
PMCID:PMC11074370
doi:10.3389/fpls.2024.1367299
PMID:38716337
Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids Yu X, Feng Y, Zhang J Life (Basel) 25-Jan-2024
PMCID:PMC10890521
doi:10.3390/life14020182
PMID:38398691
The first mitogenome of Lauraceae (Cinnamomum chekiangense) Bi C, Sun N, Han F, Xu K, Yang Y, Ferguson DK Plant Divers 18-Nov-2023
PMCID:PMC10851304
doi:10.1016/j.pld.2023.11.001
PMID:38343589
Genome-Wide Identification and Expression Analysis of SnRK2 Gene Family in Dormant Vegetative Buds of Liriodendron chinense in Response to Abscisic Acid, Chilling, and Photoperiod Hussain Q, Zheng M, Chang W, Ashraf MF, Khan R, Asim M, Riaz MW, Alwahibi MS, Elshikh MS, Zhang R, Wu J Genes (Basel) 22-Jul-2022
PMCID:PMC9331246
doi:10.3390/genes13081305
PMID:35893042
Stronger Spring Phenological Advance in Future Warming Scenarios for Temperate Species With a Lower Chilling Sensitivity Hu Z, Wang H, Dai J, Ge Q, Lin S Front Plant Sci 18-May-2022
PMCID:PMC9158521
doi:10.3389/fpls.2022.830573
PMID:35665167
Mechanisms for the retention of inorganic N in acidic forest soils of southern China Zhang JB, Cai ZC, Zhu TB, Yang WY, Müller C Sci Rep 02-Aug-2013
PMCID:PMC3731645
doi:10.1038/srep02342
PMID:23907561

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Secotenuifolide A 44557566 Click to see 494.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-Ocimene 18756 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
Neral 643779 Click to see 152.23 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(1R)-4-methyl-1-prop-1-en-2-ylcyclohex-3-en-1-ol 16059268 Click to see 152.23 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,9S)-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene 6887 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(+)-abscisic acid beta-D-glucopyranosyl ester 46173811 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)C)O)(C)C 426.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1Z,4E)-germacrene B 5371080 Click to see 204.35 unknown via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 49796490 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 92966492 Click to see 470.50 unknown via CMAUP database
Nomilin 72320 Click to see 514.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see 156.26 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(5-Methoxy-14,16-dioxatetracyclo[9.7.0.02,7.013,17]octadeca-1(18),2(7),3,5,9,11,13(17)-heptaen-10-yl)methanol 44557485 Click to see 296.30 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Tenuifolide B 44557421 Click to see CCCCCCCCCCCCCCCCCCCC(C1=CC(=C)OC1=O)OC 406.60 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
Isotenuifolide 44557420 Click to see 490.80 unknown via CMAUP database
Isotenuifolide A 44557419 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 490.80 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
5-Methoxynoracronycine 14463134 Click to see CC1(C=CC2=C(O1)C=C(C3=C2N(C4=C(C3=O)C=CC=C4OC)C)O)C 337.40 unknown via CMAUP database
Junosidine 11660079 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(N3C)C(=CC=C4)OC)C 337.40 unknown via CMAUP database
Junosine 15286413 Click to see 325.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
7-Methoxy-8-[(E)-3-oxo-1-butenyl]-2H-1-benzopyran-2-one 13917410 Click to see 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-6,8-bis(3-methylbut-2-enyl)chromen-2-one 14769401 Click to see CC(=CCC1=C(C(=C2C(=C1)C=CC(=O)O2)CC=C(C)C)O)C 298.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Butanoic acid, 3-methyl-, 9,10-dihydro-10-hydroxy-8,8-dimethyl-2-oxo-2H,8H-benzo(1,2-b:3,4-b')dipyran-9-yl ester, (9R-trans)- 14055879 Click to see 346.40 unknown via CMAUP database
Seselin 68229 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Clausarin 5315945 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=C(C(=O)O3)C(C)(C)C=C)C(C)(C)C=C)C 380.50 unknown via CMAUP database
Dentatin 342801 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC)C 326.40 unknown via CMAUP database
nor-Dentatin 5495613 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C 312.40 unknown via CMAUP database
Ponfolin 174673 Click to see 380.50 unknown via CMAUP database
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one 102316658 Click to see 756.70 unknown via CMAUP database
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
Naringenin 7-O-(2'',6''-di-O-alpha-rhamnopyranosyl)-beta-glucopyranoside 5278403 Click to see 726.70 unknown via CMAUP database
Narirutin 442431 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 580.50 unknown via CMAUP database

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