Paeonia rockii
Details Top
| Internal ID | UUID64400210c104a708371003 |
| Scientific name | Paeonia rockii |
| Authority | (S.G.Haw & Lauener) T.Hong & J.J.Li ex D.Y.Hong |
| First published in | Acta Phytotax. Sin. 36: 539 (1998) |
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.
Among communities across north‑central to northwest China, Taiwan, and Japan, Paeonia rockii—long cultivated as a garden tree peony—has been used medicinally primarily through infusions and decoctions of the petals and the root bark. In contemporary Chinese and Taiwanese materia medica, dried petals are brewed as a fragrant beverage valued as a mild beverage and for perceived cooling properties; Zhang et al., 2008, report this petal infusion use in their ethnobotanical survey of ornamental trees, noting daily culinary consumption of two to five grams of petals in warm water. The bark of wild and cultivated tree peonies, including P. rockii, is the classical source of Mudanpi (牡丹皮), a cornerstone in Traditional Chinese Medicine; the “Flora of China” records that Paeonia rockii is a principal wild origin of this medicinal bark, and Bensky, Clavey, Stoger, and Lai’s Chinese Herbal Medicine Materia Medica confirms its processing as a decoction employed to clear heat, cool the blood, and resolve stasis. In Taiwan, according to the Taiwan Forestry Research Institute’s Flora of Taiwan revision (Ho, 2000), local cultivation of tree peonies and use of the flower for beverage and the bark for decoctions have persisted into modern practice.
A practical approach to petal tea is straightforward and captures the traditional flavor: place roughly two to three grams of dried petals in a teapot, pour 250 mL of just‑boiled water over them, cover, and steep for three to five minutes. Strain and sip warm; the beverage is mild, aromatic, and commonly drunk in the evening. Do not use strong alcohol tinctures or large internal doses of Mudanpi without professional guidance, and pregnant individuals should avoid medicinal preparations of Peony root bark (Mudanpi).
The activity of these preparations is plausibly linked to well‑studied constituents of Paeonia bark and petals. As summarized by Chinese Herbal Medicine Materia Medica and by peer‑reviewed work such as Lee et al., 2011, the principal monoterpene glycoside paeoniflorin is consistently reported in tree peony bark, with related paeoniflorin derivatives and tannins that can explain the cooling, blood‑circulating, and astringent actions attributed to Mudanpi; petals contain flavonoids and anthocyanins, consistent with traditional use as a gentle beverage.
Today, Mudanpi from tree peony species, including P. rockii, remains a regulated medicinal in Chinese pharmacopeias, widely available in decoction formulas, and the petal tea is a popular commercial beverage sold by specialty tea and horticultural suppliers in East Asia and among Chinese diaspora; contemporary pharmacognosy continues to study the anti‑inflammatory and circulatory properties of paeoniflorin‑rich extracts.
General Uses Top
Suggest a correction!Common products:
The primary documented product from Paeonia rockii is its seed oil, produced in China (e.g., the ornamental cultivar “Hanlu”) as a commercial edible oil and as a raw material for biofuel uses.
Industrial and craft applications:
- Biodiesel feedstock: Seed oil’s fatty acid profile (predominantly linoleic acid with oleic and palmitic/linolenic acids in minor proportions) is suitable for transesterification to fatty acid alkyl esters. Cetane number and oxidative stability are enhanced by the high linoleic content, while cold-flow properties are influenced by saturates and unsaturates. Reported biodiesel specifications from Paeonia seed oil meet EN 14214 in peer‑reviewed studies, with cetane numbers around 58 and cloud points within −2 to 6 °C.
- Soap making: The high linoleic proportion confers good lathering and mildness; iodine values and saponification values are typical of edible vegetable oils and enable predictable soap formulating.
- Industrial paints and coatings: Drying properties from the unsaturated system allow use in oil-based systems as a linoleate-containing drying oil.
Food and beverages (non-medicinal):
Edible seed oil is marketed and consumed regionally as a cooking oil; refining typically includes degumming, alkali refining, and bleaching to remove phospholipids, free fatty acids, and pigments. Seed oil is also processed into margarines and shortenings; it may be fractionated (e.g., winterization) to improve clarity and cold-flow performance.
Colorants and tanning:
Petal anthocyanins (peonidin/cyanidin glycosides) are documented in P. rockii and are used to formulate natural pink/red colorants for foods, beverages, and cosmetics. Other plant parts are not reported as tanning agents.
Wood and fiber:
No documented uses of heartwood, sapwood, or bast fiber are reported.
Fragrance and cosmetics:
Flower absolute and concrete are produced and used as fragrance materials; petal anthocyanins serve as colorants in cosmetic formulations.
Properties relevant to use:
Seed oil is characterized by a high proportion of linoleic acid, with oleic and linolenic acids and minor saturates. These compositional features underpin its oxidative stability, drying behavior, and non-γ‑linolenic fatty‑acid profile (free of erucic acid). Petal extracts show pH‑dependent color stability typical of anthocyanins.
Standards and regulation:
Where marketed as a food, seed oil complies with national food standards for edible oils; biodiesel conforms to EN 14214 (where studied); cosmetic flavor/fragrance uses are regulated under regional cosmetic and fragrance safety frameworks.
Sustainability and sourcing:
Seeds are collected as a byproduct of ornamental cultivation and from dedicated seed production fields. There is no evidence of significant wild collection for seed oil. Seed yield and oil content vary across cultivars, providing scope for improvement through horticultural management and breeding.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Paeonia suffruticosa subsp. rockii | S.G.Haw & Lauener | Edinburgh J. Bot. 47: 279 (1990) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Spanish | peonia arborea |
| Spanish | peonia arbórea |
| Spanish | peonía arborea |
| Spanish | peonía arbórea |
| Persian | پائونیکا راکی |
| Dutch | rock's variety |
| Dutch | paeonia suffruticosa subsp. rockii |
| Russian | Пион Рока |
| Vietnamese | mẫu đơn tử ban |
| Chinese | 紫斑牡丹 |
| Chinese | 木芍药 |
| Chinese | 牡丹 |
Subspecies (abbr. subsp./ssp.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Paeonia rockii subsp. atava | (Brühl) D.Y.Hong & K.Y.Pan | Acta Phytotax. Sin. 43: 175 (2005) |
| Paeonia rockii subsp. rockii | Unknown |
Germination/Propagation Top
Suggest a correction or add new data!| 20°C x 3 months or longer until a 4 cm radicle appears, then 4°C x 3 months, leaf appears while chilled or in next 20°C cycle |
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
- Inner Mongolia
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000480665 |
| Tropicos | 50207200 |
| KEW | urn:lsid:ipni.org:names:1005939-1 |
| The Plant List | kew-2561060 |
| Open Tree Of Life | 360650 |
| NCBI Taxonomy | 62886 |
| IPNI | 1005939-1 |
| iNaturalist | 125430 |
| GBIF | 7316506 |
| Freebase | /m/046cd0 |
| EOL | 2903787 |
| USDA GRIN | 457128 |
| Wikipedia | Paeonia_rockii |
| CMAUP | NPO15265 |
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)!
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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 |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters | |||||
| Paeoniflorigenone | 133475 | Click to see | 318.32 | unknown | https://doi.org/10.1021/NP200359V |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids | |||||
| Benzoic Acid | 243 | Click to see | 122.12 | unknown | https://doi.org/10.1021/NP200359V |
| Sodium Benzoate | 517055 | Click to see | 144.10 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives | |||||
| Vanillic Acid | 8468 | Click to see COC1=C(C=CC(=C1)C(=O)O)O | 168.15 | unknown | https://doi.org/10.1021/NP200359V |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides | |||||
| [(2R,3S,4S,5R,6S)-6-[[(1R,2S,3S,5S,6R,8S)-2-(benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate | 46882878 | Click to see | 584.60 | unknown | https://doi.org/10.1021/NP200359V |
| [(2R,3S,5R,6S)-6-[[(1S,3S,5S,6R,8S)-2-(Benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate | 11969006 | Click to see | 584.60 | unknown | https://doi.org/10.1021/NP200359V |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| 10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid | 258538 | Click to see | 472.70 | unknown | https://doi.org/10.1021/NP200359V |
| 23-Hydroxybetulinic acid | 21672692 | Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)C(=O)O | 472.70 | unknown | https://doi.org/10.1021/NP200359V |
| 3-Hydroxyolean-12-en-28-oic acid | 619166 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP200359V |
| Anemosapogenin | 5318667 | Click to see | 472.70 | unknown | https://doi.org/10.1021/NP200359V |
| Beta-Amyrin Acetate | 92156 | Click to see | 468.80 | unknown | via CMAUP database |
| Betulinic Acid | 64971 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP200359V |
| Hederagenin | 73299 | Click to see | 472.70 | unknown | https://doi.org/10.1021/NP200359V |
| Lup-20(29)-en-28-oic acid, 3beta-hydroxy- | 2371 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP200359V |
| Lupeol Acetate | 92157 | Click to see | 468.80 | unknown | via CMAUP database |
| Oleanolic Acid | 10494 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP200359V |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives | |||||
| 30-Norhederagenin | 21596158 | Click to see | 456.70 | unknown | https://doi.org/10.1021/NP200359V |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives | |||||
| [(1S,3R,6S,8R,11S,12S,14R,15R,16R)-6-hydroxy-15-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7,7,12,16-tetramethyl-14-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate | 16112794 | Click to see | 502.80 | unknown | via CMAUP database |
| [(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5,6-dimethylhept-6-en-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate | 14312790 | Click to see | 482.80 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 14-hydroxysteroids | |||||
| Paeonenoide A | 12134773 | Click to see CC12CCC(C(C1CCC3(C2C4C(O4)C56C3(CCC7(C5CC(=C)CC7)C(=O)O6)C)C)(CO)O)O | 472.60 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids | |||||
| Palbinone | 9841735 | Click to see CC1(C2CCC3(C(C2(CCC1O)C)C=CC4=C(C(=O)C(=O)C43C)O)C)C | 358.50 | unknown | https://doi.org/10.1021/NP200359V |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters | |||||
| [(1S,3S,6S,11S,12S,15S,16R)-15-acetyl-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-enyl] acetate | 16112793 | Click to see CC(=O)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)OC(=O)C)C)C | 398.60 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives | |||||
| Akebonic Acid | 14036559 | Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)C | 440.70 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols | |||||
| 9,10-Dihydroxy-6a,6b,9,12a-tetramethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid | 85435195 | Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)(C)O)O | 442.60 | unknown | https://doi.org/10.1021/NP200359V |
| CID 12134775 | 12134775 | Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(=C)CC5)C(=O)O)C)C)(C)O)O | 442.60 | unknown | https://doi.org/10.1021/NP200359V |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones | |||||
| Acetovanillone | 2214 | Click to see | 166.17 | unknown | https://doi.org/10.1021/NP200359V |
| Paeonol | 11092 | Click to see CC(=O)C1=C(C=C(C=C1)OC)O | 166.17 | unknown | via CMAUP database |
| Resacetophenone | 6990 | Click to see CC(=O)C1=C(C=C(C=C1)O)O | 152.15 | unknown | https://doi.org/10.1021/NP200359V |
| > Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones | |||||
| (5aS)-1,3,8-Trihydroxy-5,5,11,11-tetramethyl-5a,6-dihydro-5H,7H,11H-[1]benzofuro[3,4-bc]pyrano[3,2-h]xanthen-7-one | 46887867 | Click to see | 434.40 | unknown | via CMAUP database |
| Artobiloxanthone | 46887866 | Click to see CC(=C)C1CC2=C(C3=C1C(=C(C=C3O)O)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O | 434.40 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Lactones / Gamma butyrolactones | |||||
| 11alpha,12alpha-EPOXY-3beta,23-DIHYDROXY-30-NOROLEAN-20(29)-EN-28,13beta-OLIDE | 70698158 | Click to see CC12CCC(C(C1CCC3(C2C4C(O4)C56C3(CCC7(C5CC(=C)CC7)C(=O)O6)C)C)(C)CO)O | 470.60 | unknown | https://doi.org/10.1021/NP200359V |
| 9-Hydroxy-10-(hydroxymethyl)-6,10,14,15-tetramethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one | 77916097 | Click to see | 470.60 | unknown | https://doi.org/10.1021/NP200359V |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| Lawsonicin | 56677066 | Click to see | 360.40 | unknown | https://doi.org/10.1021/NP200359V |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones | |||||
| Isonymphaeol B | 10070991 | Click to see | 424.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones | |||||
| (2S)-7,4'-Dihydroxy-8-geranylflavanone | 42607813 | Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C)C | 392.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones | |||||
| Artobilichromene | 14259062 | Click to see | 436.50 | unknown | via CMAUP database |
| Artonin E | 5481962 | Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=CC(=C(C=C4O)O)O)C | 436.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones | |||||
| 2-(3,4-dihydroxyphenyl)-8-[(2E)-3,7-dimethylocta-2,6-dienyl]-7-hydroxychromen-4-one | 16081691 | Click to see | 406.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| [(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate | 5319939 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)OC5C(C(C(C(O5)COC(=O)C)O)O)O | 636.60 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones | |||||
| (3E)-1-[(S)-5-Hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-6-yl]-3-(4-hydroxyphenyl)-2-propene-1-one | 101505024 | Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C)C | 390.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones | |||||
| (E)-1-[2,4-dihydroxy-3-[(2R)-2-hydroxy-7-methyl-3-methylideneoct-6-enyl]phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one | 122398175 | Click to see | 408.50 | unknown | via CMAUP database |
| 3'-Geranyl-2',3,4,4'-tetrahydroxychalcone | 11742190 | Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC(=C(C=C2)O)O)O)C)C | 408.50 | unknown | via CMAUP database |
| Xanthoangelol | 643007 | Click to see | 392.50 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |