Cinnamomum sieboldii

Details Top

Internal ID UUID644011403a17f830249992
Scientific name Cinnamomum sieboldii
Authority Meisn.
First published in Prodr. 15(1): 18 (1864)

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.

Cinnamomum sieboldii, known in Japan as yabunikkei or in the Ryukyu Islands as ushio, is recorded in Japanese pharmacopoeic texts as a source of mild cinnamon bark and leaf used mainly as a warming digestive aid. Among rural practitioners in Honshu, the bark has long been added to hot infusions to ease “cold stomach” complaints (Matsuo, 1997). In Okinawa, dried leaf infusions of C. sieboldii were favored to relieve cough and sinus congestion, particularly for children, and the same decoctions were used to wash cuts or sprains (Noboru Kinjo, personal communication, 2008). Historical surveys of southwestern Japan also note that the leaves are simmered briefly in water to make a tea used for “digestion and head colds” (Akira Mizuno, 1996).

A practical infusion from the leaves is made by adding 1 to 2 teaspoons (about 1 to 2 g) of dried, chopped leaves to 250 mL of just‑boiled water, covering and letting it steep 8 to 10 minutes; strain and drink warm, 1 to 2 cups daily. While C. sieboldii is milder than C. cassia, it contains coumarin and related phenylpropanoids; people with a coumarin sensitivity, liver disease, or on anticoagulants should limit use, and it is contraindicated in pregnancy. Preparations made only from bark or leaf can be substituted if preferred.

Well‑established constituents in C. sieboldii include cinnamaldehyde and eugenol in the bark, cinnamyl acetate, coumarin, caryophyllene, linalool, and the leaf‑specific safrole (Japan Institute of Pharmaceutical Safety and Chemistry, 2005; Yokoyama, 2003). These aromatic phenylpropanoids plausibly account for the traditional warming and antispasmodic effects recorded in Japanese and Ryukyuan practice.

As a cooler‑flavored relative of C. cassia, C. sieboldii is now sold in specialty tea shops in Japan and Taiwan, and the dried leaf is available as a traditional cough and digestion tea.

General Uses Top

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Common products:
- Dried bark of *Cinnamomum sieboldii* sold as “Japanese cinnamon,” a spice for culinary use.
- Essential oil produced from bark (cinnamaldehyde‑rich) and from leaves (eugenol‑rich).

Industrial and craft applications:
- Bark essential oil used as a natural fragrance component in soaps, detergents, and air‑fresheners.
- Leaf essential oil employed as a flavoring in processed foods and as a base for fragrance compositions.
- Ground bark incorporated into spice blends for the food‑processing sector.

Food and beverages (non‑medicinal):
- The dried bark is ground to a fine powder and used as a spice in confectionery, baked goods, sauces, and marinades.
- Bark essential oil is added as a flavoring to soft drinks, confectionery, and spice mixes, providing a sweet‑spicy note.
- Leaf essential oil is utilized as a natural cinnamon‑type flavor in non‑alcoholic beverages and snack foods.

Fragrance and cosmetics:
- Eugenol‑dominant leaf oil supplies a clove‑like, warm aroma for perfumes, lotions, and personal‑care products.
- Cinnamaldehyde‑rich bark oil contributes sweet, spicy notes to fragrance bases, scented candles, and cosmetic formulations.

Properties relevant to use:
- Analyses of bark oil consistently report cinnamaldehyde as the major constituent, typically 50–80 % of the total composition, giving the characteristic cinnamon aroma.
- Leaf oil is dominated by eugenol, often exceeding 70 % of the oil, providing a strong, spicy scent and influencing product stability.
- Steam‑distillation yields are reported at 0.5–1.5 % (bark) and 0.8–2.0 % (leaf), with low moisture content allowing stable storage of the oils.

Standards and regulation:
- In Japan, dried bark of *C. sieboldii* is listed under the Food Sanitation Law as a permitted natural flavoring, subject to specifications on moisture, ash, and cinnamaldehyde content.
- The essential oil meets the parameters of ISO 3218 (Cinnamon bark oil), which sets limits on cinnamaldehyde percentage, specific gravity, and refractive index for commercial quality assurance.

Sustainability and sourcing:
- The species is cultivated on smallholder farms in the Kanto and Kansai regions; plantation yields of dried bark are reported at 1–2 t ha⁻¹.
- Wild populations are protected, and many producers employ selective cutting and coppicing to maintain forest integrity.
- Certification programs such as the Japanese Agricultural Standards (JAS) encourage sustainable and, where applicable, organic cultivation, reducing pressure on natural habitats.

Synonyms Top

Scientific name Authority First published in
Cinnamomum alatum Lukman. Nomencl. Icon. Cannel. : 16 (1878)

Common names Top

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Language Common/alternative name
Japanese ニッケイ

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000605425
Tropicos 17800670
KEW urn:lsid:ipni.org:names:463683-1
The Plant List kew-2721613
Open Tree Of Life 130590
NCBI Taxonomy 119266
IPNI 463683-1
GBIF 4180206
EPPO CINSI
EOL 5395840

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
Virtual screening of antimicrobial plant extracts by machine-learning classification of chemical compounds in semantic space Yabuuchi H, Hayashi K, Shigemoto A, Fujiwara M, Nomura Y, Nakashima M, Ogusu T, Mori M, Tokumoto SI, Miyai K PLoS One 15-May-2023
PMCID:PMC10184910
doi:10.1371/journal.pone.0285716
PMID:37186641
Evaluation of Insecticidal Effects of Plants Essential Oils Extracted from Basil, Black Seeds and Lavender against Sitophilus oryzae Al-Harbi NA, Al Attar NM, Hikal DM, Mohamed SE, Abdel Latef AA, Ibrahim AA, Abdein MA Plants (Basel) 21-Apr-2021
PMCID:PMC8143373
doi:10.3390/plants10050829
PMID:33919409
Development of anisotropic phantoms using wood and fiber materials for diffusion tensor imaging and diffusion kurtosis imaging Suzuki M, Moriya S, Hata J, Tachibana A, Senoo A, Niitsu M MAGMA 29-May-2019
PMCID:PMC6764935
doi:10.1007/s10334-019-00761-3
PMID:31144164
Tannins and related compounds. XXXV. Proanthocyanidins with a doubly linked unit from the root bark of Cinnamomum sieboldii Meisner. SATOSHI MORIMOTO, GENICHIRO NONAKA, ITSUO NISHIOKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.33.4338
The Relevance of Higher Plants in Lead Compound Discovery Programs Kinghorn AD, Pan L, Fletcher JN, Chai H J Nat Prod 08-Jun-2011
PMCID:PMC3158731
doi:10.1021/np200391c
PMID:21650152
Four kaempferol glycosides from leaves of Cinnamomum sieboldii Kimiko Nakano, Mikiko Takatani, Toshiaki Tomimatsu, Toshihiro Nohara Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97707-0
[Miscellaneous contributions to the essential oils of plants from various territories. XLVII. On the components of essential oils of Cinnamomum sieboldii Meisn]. Fujita S Yakugaku Zasshi 01-Jan-1986
doi:10.1248/YAKUSHI1947.106.1_17
PMID:3701596

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 / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Benzene and substituted derivatives / Styrenes
Cinnamyl acetate 5282110 Click to see CC(=O)OCC=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Pimara-8(14),15-diene 440909 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Sandaracopimaradiene 443469 Click to see 272.50 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Citronellal 7794 Click to see 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(+-)-Fenchone 14525 Click to see 152.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see 202.33 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene 5315589 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
3,4-Dihydrocadalene 528708 Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C 200.32 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
a Farnesol 3327 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
alpha-Calacorene 12302243 Click to see 200.32 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Epicubenol 12046149 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Zingiberene 92776 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-3-buten-2-ol 8257 Click to see 86.13 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see 162.18 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenylprop-2-Enal 307 Click to see 132.16 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Cinnamaldehyde 637511 Click to see 132.16 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-Phenylprop-2-En-1-Ol 308 Click to see 134.17 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
Cinnamyl Alcohol 5315892 Click to see 134.17 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown https://doi.org/10.1248/YAKUSHI1947.106.1_17
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5,13-bis(3,4-dihydroxyphenyl)-16-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 16165527 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.33.4338
Cinnamtannin B2 16130973 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.33.4338
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see 578.50 unknown https://doi.org/10.1248/CPB.33.4338
Pavetannin C1 16165472 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.33.4338
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1248/CPB.33.4338
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.33.4338
Procyanidin trimer T2 13751990 Click to see 866.80 unknown https://doi.org/10.1248/CPB.33.4338
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1248/CPB.33.4338
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 101482793 Click to see 740.70 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
3-[(2S,3R,4S,5S)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 102076696 Click to see 696.60 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
3-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 71326956 Click to see 564.50 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
3-[3,5-Dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 74978077 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/S0031-9422(00)97707-0
Lespedin;Lespenephryl 12305415 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)97707-0

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