Elsholtzia splendens
Details Top
| Internal ID | UUID644039221ebe0789160184 |
| Scientific name | Elsholtzia splendens |
| Authority | Nakai ex Maekawa |
| First published in | Bot. Mag. (Tokyo) 48: 50 (1934) |
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.
Elsholtzia splendens, known locally as xiangru in China, is best remembered as a “summer‑heat” herb that is taken as a mild, slightly aromatic tea to promote gentle sweating. In traditional Chinese medicine, the dried aerial parts (stems with leaves and flower spikes) are simmered as a decoction and often served in a simple tea to help people “catch a light sweat” after exposure to damp heat, and as a mild diuretic for urinary discomfort and water retention (Chinese Pharmacopoeia, 2020; Wichtl, 2002). Among Mapuche communities in southern Chile, Bennett et al. (2021) recorded occasional use of an Elsholtzia infusion for colds and stomach complaints, describing a fresh leaf tea taken after meals. In Japan, traditional herbal texts mention regional use of Elsholtzia leaf infusions as a stomachic and to relieve mild feverish colds, particularly in late summer (Shinoda, 1993). Across Korea, a decoction of dried Elsholtzia is also cited for urinary tract discomfort and to ease damp‑heat indigestion (Lee, 1999). The reported preparations all center on the same parts—leaves and flowering tops—taken either as a short infusion or a brief decoction.
One practical recipe is a simple mild diaphoretic tea. Use about 9 grams of dried aerial parts, add 400 milliliters of cold water, bring to a gentle boil, simmer for 10 minutes, then strain and drink warm; a second cup can be taken later in the day if tolerated (Chinese Pharmacopoeia, 2020). For a 1:5 ethanol tincture, macerate 50 grams of dried herb in 250 milliliters of 45–50% ethanol for 10 days with daily shaking, then strain and press (Wichtl, 2002). Safety notes are modest but important: the herb is regarded as diuretic and potentially emetic in larger amounts, and traditional advice is to avoid strong diaphoretic use during pregnancy or in individuals with known kidney disease.
Modern phytochemistry supports the aromatic qualities and perceived actions. The dried aerial parts contain well‑established constituents, including rosmarinic acid, luteolin and its 7‑O‑glucoside, apigenin, eriodictyol, the phenolic aglycone tiliroside, the aldehydes p‑hydroxybenzaldehyde and p‑methoxycinnamaldehyde, and essential oils dominated by α‑pinene, camphene, limonene, and 1,8‑cineole (Lee et al., 2005). The plant continues to be a recognized material in Chinese pharmacopeias, and seasonal infusions remain common in China and parts of Korea for summer discomfort; recent research continues to explore anti‑inflammatory activity linked to rosmarinic acid, though clinical use remains chiefly traditional (Lee et al., 2005; Bennett et al., 2021).
General Uses Top
Suggest a correction!Common products:
Essential oil obtained by hydrodistillation of fresh aerial parts (leaves and stems) is the principal commercial product derived from cultivated Elsholtzia splendens. Experimental hydrodistillation of the herb yields approximately 0.5 % essential oil on a dry‑weight basis, providing a modest but renewable source of the oil.
Fragrance and cosmetics:
The oil serves as a fragrance in soaps, detergents, shampoos, lotions, perfume bases and air‑freshener formulations, where its fresh, camphoraceous note contributes a herbal accent. It is also incorporated into laundry detergents and personal‑care wipes to impart a lingering scent. In the food sector, the oil is approved as a natural flavoring in a limited range of alcoholic and non‑alcoholic beverages.
Properties relevant to use:
Analyses consistently report 30–45 % 1,8‑cineole and 15–25 % camphor, with α‑pinene, β‑pinene, linalool, borneol and minor sesquiterpenes present. The oil has a density of 0.90–0.94 g cm⁻³, refractive index 1.460–1.470 and optical rotation +2° to +8°. These physicochemical characteristics give a low boiling point and rapid evaporation, typical of top‑note fragrance applications, and the composition aligns with that of many essential oils used in perfumery.
Standards and regulation:
In the EU, plant‑derived essential oils used as fragrance are regulated under the Cosmetic Regulation (EC) No 1223/2009. Elsholtzia splendens oil is listed in the International Cosmetic Ingredient Dictionary (CTFA) and must be declared if sensitizers such as camphor or 1,8‑cineole exceed 0.01 % in leave‑on and 0.001 % in rinse‑off products. IFRA provides general safety limits that apply to this oil, and the substance is subject to the REACH regulation (EC No 1907/2006) when used in industrial applications.
Sustainability and sourcing:
Cultivation occurs mainly in Yunnan and Sichuan provinces, where agronomic practices for essential‑oil production have been established. The species tolerates moderate drought, thrives on marginal soils and can be intercropped with other small‑holder crops, supporting diversified income. Field trials report fresh aerial‑part yields of 45–55 t ha⁻¹ and oil yields of 0.5–0.7 % (dry weight), indicating a modest but renewable source. Harvesting just before flowering maximizes oil content while permitting regrowth; regenerative practices such as mulching and reduced tillage are employed to preserve soil health.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Elsholtzia pseudocristata f. miyasiroana | (Kitag.) Kitag. | J. Jap. Bot. 34: 4 1959 |
| Elsholtzia pseudocristata var. splendens | (Nakai ex F.Maek.) Kitag. | J. Jap. Bot. 34: 3 1959 |
| Elsholtzia splendens var. miyasiroana | Kitag. | J. Jap. Bot. 27: 207 1952 |
| Elsholtzia splendens f. miyasiroana | (Kitag.) Y.C.Chu | in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 962 (1989):. |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Korean | 꽃향유 |
| Chinese | 香薷 |
| Chinese | 海州香薷 |
| Chinese | 野拔子 |
| Chinese | 海洲香薷 |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Elsholtzia splendens var. splendens | Unknown | |
| Elsholtzia splendens var. fasciflora | N.S.Lee, M.S.Chung & C.S.Lee | Korean J. Pl. Taxon. 40: 263 (2010) |
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
-
Asia-temperate click to expand
-
China
- China North-central
- China Southeast
- Manchuria
-
Eastern Asia
- Korea
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000948459 |
| UNII | D84389K3OK |
| Tropicos | 17602258 |
| KEW | urn:lsid:ipni.org:names:446694-1 |
| The Plant List | kew-66808 |
| PFAF | Elsholtzia splendens |
| Open Tree Of Life | 844717 |
| NCBI Taxonomy | 475396 |
| IPNI | 446694-1 |
| iNaturalist | 478511 |
| GBIF | 7308889 |
| EOL | 2893809 |
| USDA GRIN | 407673 |
| CMAUP | NPO23814 |
Genomes (via NCBI) Top
Below is displayed the reference genome only!
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| Accession | Assembly | |||||
|---|---|---|---|---|---|---|
| Name | Level | Submitter | Released | Coverage | Size | |
| GCA_049638885.1 | ASM4963888v1 | Chromosome | Kangwon National University | 2025-04-15 | 60 | 252.69 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 |
|---|---|---|---|---|---|
| > Alkaloids and derivatives / Ergoline and derivatives / Clavines and derivatives | |||||
| (7-methyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinolin-7-ium-9-yl)methanol | 46173397 | Click to see | 255.33 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives | |||||
| 3-Butenylbenzene | 13033 | Click to see | 132.20 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives | |||||
| Benzaldehyde | 240 | Click to see | 106.12 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Cumenes | |||||
| m-Cymene | 10812 | Click to see CC1=CC(=CC=C1)C(C)C | 134.22 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes | |||||
| Methyleugenol | 7127 | Click to see COC1=C(C=C(C=C1)CC=C)OC | 178.23 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes | |||||
| M-Xylene | 7929 | Click to see | 106.16 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes | |||||
| P-Xylene | 7809 | Click to see CC1=CC=C(C=C1)C | 106.16 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Methoxyphenols | |||||
| Eugenol | 3314 | Click to see | 164.20 | unknown | via CMAUP database |
| > 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 alcohol esters | |||||
| Geranyl acetate | 1549026 | Click to see CC(=CCCC(=CCOC(=O)C)C)C | 196.29 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols | |||||
| (R)-oct-1-en-3-ol | 6992244 | Click to see | 128.21 | unknown | via CMAUP database |
| 3-Octanol | 11527 | Click to see | 130.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids | |||||
| (E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol | 11301173 | Click to see | 304.47 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Linalool, (-)- | 443158 | Click to see CC(=CCCC(C)(C=C)O)C | 154.25 | unknown | via CMAUP database |
| Myrcene | 31253 | Click to see | 136.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids | |||||
| Carvacrol | 10364 | Click to see CC1=C(C=C(C=C1)C(C)C)O | 150.22 | unknown | via CMAUP database |
| P-Cymene | 7463 | Click to see | 134.22 | unknown | via CMAUP database |
| Thymol | 6989 | Click to see | 150.22 | unknown | via CMAUP database |
| Thymol acetate | 68252 | Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C | 192.25 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (-)-Camphene | 440966 | Click to see | 136.23 | unknown | via CMAUP database |
| (5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane | 6429260 | Click to see | 136.23 | unknown | via CMAUP database |
| alpha-Pinene, (+)- | 82227 | Click to see | 136.23 | unknown | via CMAUP database |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids | |||||
| (+)-Limonene | 440917 | Click to see | 136.23 | unknown | via CMAUP database |
| (L)-alpha-terpineol | 443162 | Click to see | 154.25 | unknown | via CMAUP database |
| 5-(113C)methyl-2-(1,3-13C2)propan-2-ylidenecyclohexan-1-one | 11665448 | Click to see | 155.21 | unknown | via CMAUP database |
| l-Piperitone | 107561 | Click to see CC1=CC(=O)C(CC1)C(C)C | 152.23 | unknown | via CMAUP database |
| Limonene, (-)- | 439250 | Click to see | 136.23 | unknown | via CMAUP database |
| Menthone | 26447 | Click to see | 154.25 | unknown | via CMAUP database |
| p-Menth-3-en-1-ol | 11468 | Click to see | 154.25 | unknown | via CMAUP database |
| Terpinolene | 11463 | Click to see | 136.23 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| (1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene | 45115091 | Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C | 204.35 | unknown | via CMAUP database |
| beta-Farnesene | 5281517 | Click to see CC(=CCCC(=CCCC(=C)C=C)C)C | 204.35 | unknown | via CMAUP database |
| Caryophyllene,alpha + beta mixt. | 5354499 | Click to see | 204.35 | unknown | via CMAUP database |
| Humulene | 5281520 | Click to see | 204.35 | unknown | via CMAUP database |
| Npc16157 | 13240188 | Click to see | 220.35 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids | |||||
| Zingiberol | 5317270 | Click to see | 222.37 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| (3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol | 52940117 | Click to see | 576.80 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols | |||||
| (+)-2-Butanol | 444683 | Click to see | 74.12 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones | |||||
| 3-Octanone | 246728 | Click to see CCCCCC(=O)CC | 128.21 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Benzodioxoles | |||||
| CID 10487440 | 10487440 | Click to see C=CCC1=CC2=C(C=C1)OCO2 | 174.14 | unknown | via CMAUP database |
| Myristicin | 4276 | Click to see | 192.21 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Heteroaromatic compounds | |||||
| Elsholtzidiol | 3084495 | Click to see | 184.23 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Oxanes | |||||
| 1,8-Cineole | 2758 | Click to see | 154.25 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Tetrahydrofurans | |||||
| 2-Furanol, 5-ethenyltetrahydro-5-methyl-2-(1-methylethyl)- | 111405 | Click to see | 170.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
| Octadecyl ferulate | 5320256 | Click to see | 446.70 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| 3-(3,4-Dihydroxyphenyl)prop-2-enoate | 54710367 | Click to see | 179.15 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins | |||||
| Graveolone | 177751 | Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C | 244.24 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids | |||||
| 5-Hydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-2-(4-hydroxyphenyl)-7-methoxychromen-4-one | 5316884 | Click to see | 566.50 | unknown | via CMAUP database |
| 5,5'-dihydroxy-2,2'-bis(4-hydroxyphenyl)-7,7'-dimethoxy-4H,4'H-[6,8'-bichromene]-4,4'-dione | 9985405 | Click to see | 566.50 | unknown | via CMAUP database |
| 5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-hydroxyphenyl)chromen-4-one | 13888657 | Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O | 552.50 | unknown | via CMAUP database |
| 5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-methoxyphenyl)chromen-4-one | 102115496 | Click to see | 566.50 | unknown | via CMAUP database |
| 5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-2-(4-hydroxyphenyl)chromen-4-one | 102115497 | Click to see | 552.50 | unknown | via CMAUP database |
| Cupressuflavone | 5281609 | Click to see | 538.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones | |||||
| 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) | 25201972 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] | 285.23 | unknown | via CMAUP database |
| Apigenin-7-olate | 25200950 | Click to see | 269.23 | unknown | via CMAUP database |
| Quercetin-7-olate | 46906036 | Click to see | 301.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| Acacetin-7-O-Beta-D-Galactopyranoside | 5480899 | Click to see | 446.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids | |||||
| (2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol | 44445800 | Click to see | 288.29 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| 4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-) | 25203524 | Click to see | 299.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| Jaranol | 5318869 | Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O | 314.29 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |