Details Top

Internal ID UUID6440402eeb76e506965155
Scientific name Rosa indica
Authority L.
First published in Sp. Pl. : 492 (1753)

Ethnobotanical Use Top

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General Uses Top

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Fragrance and cosmetics:
Fresh petals are processed by solvent extraction to yield a concrete, which is further refined to an absolute, or by steam distillation to yield an essential oil. These materials are used in fine fragrance compositions, as trace notes in perfumery accords, and as an aromatic component in soaps, detergents, and skincare and haircare formulations. The absolute is preferred when a rich, warm profile is desired; the essential oil is constrained by ISO 9842:2018, which sets compositional and physicochemical specifications for oil of rose (Rosa spp.), limiting its use in cosmetic products that require regulatory alignment.

Scientific/model-organism use:
The species accepted as Rosa chinensis (syn. R. indica L.) has an available reference genome and associated transcriptomic resources in public genomic databases, supporting studies of flowering time, scent biosynthesis, and petal pigment pathways. The widely cultivated cultivar “Old Blush” (R. chinensis ‘Old Blush’) has been used in cytogenetic and molecular studies and as a model system in genetics.

Food and beverages (non-medicinal):
In culinary traditions across South and East Asia, the species is cultivated for its edible petals, which are used as flavoring and garnish in sweets, confections, and syrups. Rose hips (the fruit) are also processed into preserves, jams, and syrups.

Properties relevant to use:
Rose absolute and essential oil are rich in monoterpenoid alcohols—geraniol, citronellol, and nerol—together with phenylethyl alcohol; these constituents confer characteristic rosy scent and influence solubility and stability in cosmetic media. ISO 9842 defines ranges for density, optical rotation, acid value, ester value, solubility in ethanol, and refractive index to control quality and authenticity of steam-distilled rose oil.

Standards and regulation:
ISO 9842:2018 (Oil of rose—Rosa spp.) provides compositional and specification limits for rose essential oil used in flavor and fragrance applications. International flavor and fragrance regulations, including the IFRA Standards and EU Flavouring Regulation (EC No 1334/2008), govern the use of rose materials in consumer products. Cosmetic use is also subject to regional cosmetic laws and safety assessments.

Sustainability and sourcing:
Scented rose production is water- and labor-intensive; practice is dominated by manual harvesting and extraction steps. Sustainable sourcing is guided by certification and fair-labor schemes in producing regions.

Synonyms Top

Scientific name Authority First published in
Rosa banksiae var. microcarpa (Lindl.) Regel ; 1878 376 1878
Rosa amoyensis Hance J. Bot. 6: 297 (1868)
Rosa sorbiflora Focke Gard. Chron. , ser. 3, 37: 227 (1905)
Rosa patrum H.Lév. ex Rehder J. Arnold Arbor. 17: 339 (1936)
Rosa bodinieri H.Lév. & Vaniot Bull. Soc. Bot. France 55: 56 (1908)
Rosa cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 8: 61 (1910)
Rosa chaffonjoni H.Lév. & Vaniot Bull. Soc. Bot. France 55: 56 (1908)
Rosa esquirolii H.Lév. & Vaniot Bull. Soc. Bot. France 55: 56 (1908)
Rosa fragariifolia Steud. Nomencl. Bot. [Steudel], ed. 2. ii. 468, sphalm.
Rosa microcarpa Lindl. Ros. Monogr. : 130 (1820)
Rosa cymosa var. puberula T.T.Yu & T.C.Ku Bull. Bot. Res., Harbin 1(4): 17 (1981)
Rosa limprichtii Pax & K.Hoffm. Repert. Spec. Nov. Regni Veg. Beih. 12: 413 (1922)
Rosa borbonica Dippel Handb. Laubholzk. 3: 563 (1893)
Rosa fukienensis F.P.Metcalf J. Arnold Arbor. 21: 274 (1940)
Rosa subumbellata Schur Enum. Pl. Transsilv. : 203 (1866)
Rosa pannosa Link Handbuch 2: 83 (1831)
Rosa persicifolia Hoffmanns. Verz. Pfl.-Kult. , Nachtr. 1: 108 (1824)
Rosa cymosa Tratt. Rosac. Monogr. : 87 (1823)
Rosa cymosa f. plena Z.X.Yu & G.Z.Liu Bull. Bot. Res., Harbin 11(1): 53 (1991)
Rosa indica var. acuminata Thory Roses 1: 53 (1817)
Rosa indica unranked alba Andrews Roses 2: t. 85 (1826)
Rosa indica unranked caryophyllea Thory Roses 3: 69 (1823)
Rosa indica unranked creunta Thory Roses 1: 128 (1818)
Rosa indica var. formosana Hayata J. Coll. Sci. Imp. Univ. Tokyo 22: 127 (1906)
Rosa indica unranked incurva Andrews Roses 2: t. 70 (1817)
Rosa indica unranked lawrenciana Thory Roses 2: 38 (1819)
Rosa indica var. lutea Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 359 (1878)
Rosa indica unranked minor Andrews Roses 2: t. 68 (1805)
Rosa indica var. odoratissima Lindl. Ros. Monogr. : 106 (1820)
Rosa indica unranked pannosa Thory Roses 2: 37 (1819)
Rosa indica unranked purpurea Andrews Roses 2: t. 80 (1812)
Rosa indica unranked rubra Andrews Roses 2: t. 67 (1805-1828)
Rosa indica unranked salicifolia Andrews Roses 2: t. 81 (1815)
Rosa indica unranked simplex Andrews Roses 2: t. 69 (1816)
Rosa indica unranked sulphurea Andrews Roses 2: t. 86 (1826)
Rosa indica var. ternauxiana Ser. Prodr. 2: 600 (1825)
Rosa indica unranked variegata Andrews Roses 2: t. 79 (1812)
Rosa limprichtii var. subumbellata Pax & K.Hoffm. Repert. Spec. Nov. Regni Veg. Beih. 12: 413 (1922)
Rosa cymosa var. dapanshanensis F.G.Zhang Acta Bot. Yunnan. 28: 606 (2006)
Rosa fragariiflora Ser. Prodr. 2: 601 (1825)
Rosa indica unranked longifolia Thory Roses 2: 38 (1819)

Common names Top

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Language Common/alternative name
English jh
English r. indica
English cyme rose
Arabic ورد هندي
Arabic ورد سنمي
Persian رز سالخورده
Russian Роза полузонтичная
Chinese 小果蔷薇果
Chinese 小果蔷薇根
Chinese 小果蔷薇花
Chinese 小果蔷薇茎
Chinese 小果薔薇
Chinese 山木香
Chinese 野蔷薇
Chinese 倒钩竻
Chinese 红荆藤
Chinese 小果蔷薇叶
Chinese 小果蔷薇

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 South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
    • Indo-China
      • Laos
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001014404
UNII 9J9U8OKR8A
USDA Plants ROIN5
Tropicos 27801708
KEW urn:lsid:ipni.org:names:732892-1
The Plant List rjp-6039
Open Tree Of Life 3904955
NCBI Taxonomy 2056386
IPNI 732892-1
iNaturalist 1127917
GBIF 3002711
EOL 637808
USDA GRIN 70579
Tropicos 27803785
KEW urn:lsid:ipni.org:names:732228-1
The Plant List rjp-9092
Open Tree Of Life 868176
NCBI Taxonomy 117261
IPNI 732228-1
iNaturalist 639233
GBIF 3005661
Freebase /m/0clj9n
EPPO ROSCY
EOL 235184
USDA GRIN 5327
Wikipedia Rosa_cymosa

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
Determinants of taxonomic, functional, and phylogenetic beta diversity in breeding birds within urban remnant woodlots: Implications for conservation Liu Y, Zhu Y, Wu S, Wang Y, Xie J, Zhang K, Xu Y Ecol Evol 14-May-2024
PMCID:PMC11091548
doi:10.1002/ece3.11426
PMID:38746544
Study of medicinal plants used in ethnoveterinary medical system in riverine areas of Punjab, Pakistan Umair M, Altaf M, Ahsan T, Bussmann RW, Abbasi AM, Gatasheh MK, Elrobh M J Ethnobiol Ethnomed 07-May-2024
PMCID:PMC11077875
doi:10.1186/s13002-024-00686-9
PMID:38715115
Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China Li K, Tan B, Liao M, Ni J Front Plant Sci 20-Mar-2024
PMCID:PMC10987713
doi:10.3389/fpls.2024.1348182
PMID:38571712
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
The In Vitro Assessment of Antibacterial and Antioxidant Efficacy in Rosa damascena and Hypericum perforatum Extracts against Pathogenic Strains in the Interplay of Dental Caries, Oral Health, and Food Microbiota Antoniadou M, Rozos G, Vaiou N, Zaralis K, Ersanli C, Alexopoulos A, Tzora A, Varzakas T, Voidarou C( Microorganisms 28-Dec-2023
PMCID:PMC10819596
doi:10.3390/microorganisms12010060
PMID:38257885
The complete chloroplast genome sequence of Rosa ‘Limoncello’ (Rosales: Rosaceae) Wang J, Xie QL, Feng EY, Liu XF Mitochondrial DNA B Resour 18-Dec-2023
PMCID:PMC10768736
doi:10.1080/23802359.2023.2290854
PMID:38189025
Exploration of the Wild Edible Plants Used for Basic Health Care by Local People of Bahawalpur and Adjacent Regions, Pakistan Anwar T, Qureshi H, Naeem H, Shahzadi S, Sehar Z, Hassan R Foods 25-Sep-2023
PMCID:PMC10573077
doi:10.3390/foods12193557
PMID:37835210
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Companion Plants of Tea: From Ancient to Terrace to Forest Wu H, Long X, Geng Y Plants (Basel) 25-Aug-2023
PMCID:PMC10490072
doi:10.3390/plants12173061
PMID:37687308
Biogenic Silver Nanoparticles for Targeted Cancer Therapy and Enhancing Photodynamic Therapy Kah G, Chandran R, Abrahamse H Cells 07-Aug-2023
PMCID:PMC10417642
doi:10.3390/cells12152012
PMID:37566091
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
Nanoengineering TiO2 for evaluating performance in dye sensitized solar cells with natural dyes Khan MJ, Ahirwar A, Sirotiya V, Rai A, Varjani S, Vinayak V RSC Adv 26-Jul-2023
PMCID:PMC10369046
doi:10.1039/d3ra02927a
PMID:37501775
Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y Heliyon 13-Jul-2023
PMCID:PMC10368863
doi:10.1016/j.heliyon.2023.e18214
PMID:37501975
SMRT Sequencing Technology Was Used to Construct the Batocera horsfieldi (Hope) Transcriptome and Reveal Its Features Wei X, Xu D, Liu Z, Liu Q, Zhuo Z Insects 11-Jul-2023
PMCID:PMC10380457
doi:10.3390/insects14070625
PMID:37504630

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 9982058 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
[3,4,5-Trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 85082218 Click to see 468.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 10395827 Click to see 866.80 unknown https://doi.org/10.1016/0031-9422(93)85250-U
2-(3,4-dihydroxyphenyl)-6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 15593127 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C(=C(C(=C4)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(3S)-3-hydroxy-3-(4-hydroxyphenyl)-1-[4-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 162877886 Click to see C1=CC(=CC=C1C(CC(=O)C2=C(C=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Rocymosin B 42607726 Click to see 436.40 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Tannins / Complex tannins
[(10R,11R)-10-[(14R,15S,19S)-19-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101458433 Click to see 1208.90 unknown https://doi.org/10.1016/0031-9422(93)85250-U
[(10R,11R)-10-[(15S,19S)-19-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101651021 Click to see 1208.90 unknown https://doi.org/10.1016/0031-9422(93)85250-U
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(93)85250-U
Rugosin D 16129626 Click to see 1875.30 unknown https://doi.org/10.1016/0031-9422(93)85250-U

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