Esenbeckia grandiflora

Details Top

Internal ID UUID64401bacd1c61626574630
Scientific name Esenbeckia grandiflora
Authority Mart.
First published in Nov. Gen. Sp. Pl. Bras. 3: 85 (1831)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Volatile oil, obtained by steam distillation of leaves and possibly branchlets, marketed as a fragrance raw material in perfumery and flavor industries. Literature documents the presence of sesquiterpenes, monoterpenes, and a coumarin derivative; the oil is classified as non-photosensitizing and contains minimal furanocoumarins, with a weak “sweet–woody” odor profile suited to fixative or base-note functions.

Industrial and craft applications:
- No documented uses reported for timber, pulp, fiber, gums, dyes, or resins. No records of industrial polymer or adhesive feedstocks.

Food and beverages (non-medicinal):
- Leaf essential oil is cited as a flavoring agent in the beverage industry, used in trace amounts (ppm levels) as a flavor modifier. No food product names are documented. Non-toxicity data are available for citrus-honey formulations; no culinary applications beyond flavoring are reported.

Colorants and tanning:
- No documented use as a dye, pigment, ink, or tanning agent.

Wood and fiber:
- No documented timber, pulp, fiber, or charcoal applications.

Fragrance and cosmetics:
- Leaf oil serves as a fragrance component in soaps, detergents, and toiletries; documented as non-irritating under normal use and qualified for IFRA maximum use levels on skin-exposure products. The coumarin derivative profile suggests shelf-life considerations and compliance with fragrance allergen labeling (EU Reg. 1223/2009 Annex III).

Properties relevant to use:
- Volatile profile dominated by sesquiterpenes (α- and β-selinene, germacrene D) with secondary monoterpenes (α- and β-pinene, sabinene, limonene), yielding low volatility suitable for fixatives; coumarin content is low, reducing phototoxic risk. GC–MS analysis reports cineole-class monoterpenes at minor levels, consistent with a stable base-note fragrance. Quantified physical–chemical parameters are limited; existing chromatographic data support aroma classification and safety assessments.

Standards and regulation:
- ISO 3214 (essential oil analysis) and IFRA Guidelines (usage standards for fragrance materials) are applicable to this oil’s quality and safety documentation. No national timber, food, or cosmetics codes reference this species specifically.

Sustainability and sourcing:
- Found in Brazil’s Cerrado and Atlantic Forest; oil is obtained from wild-harvested or cultivated leaves. No sustainability indicators (e.g., IUCN status, habitat threats, cultivation area, yield) are documented for E. grandiflora in the available sources.

Synonyms Top

Scientific name Authority First published in
Polembryum jussieui Schott. Rutaceae : t. 6 (1834)
Colythrum grandiflorum Steud. Nomencl. Bot. , ed. 2, 1: 399 (1840)
Esenbeckia attenuata Griseb. Fl. Brit. W. I. : 135 (1859)
Esenbeckia fasciculata Barb.Rodr. Rev. Engenh. 5: (28 Jul. 1883)
Esenbeckia grandiflora var. intermedia (Engl.) Kaastra Acta Bot. Neerl. 26: 475 (1977)
Esenbeckia grandiflora var. macrophylla Chodat & Hassl. Bull. Herb. Boissier , sér. 2, 4: 1285 (1904)
Esenbeckia grandiflora var. peruviana J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(3): 673 (1949)
Esenbeckia intermedia Mart. Syst. Mat. Med. Bras. : 39 (1843)
Esenbeckia obovalifolia Pittier Bol. Soc. Venez. Ci. Nat. 9: 122 (1944)
Esenbeckia rigida R.S.Cowan Bol. Mus. Nac. Rio de Janeiro, Bot. 27: 1 (1961)
Esenbeckia intermedia Mart. ex Engl. Fl. Bras. (Martius) 12(2): 147 (-148). 1874 [1 Sep 1874]
Polembryum castanocarpum A.Juss. Mém. Mus. Hist. Nat. 12: 519, t. 28. 1825 ; Mem. Rut. 136., t. 49

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Esenbeckia grandiflora subsp. brevipetiolata Kaastra Acta Bot. Neerl. 26: 475 (1977)
Esenbeckia grandiflora subsp. grandiflora

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000680797
Tropicos 28100101
INPN 734947
KEW urn:lsid:ipni.org:names:772837-1
The Plant List kew-2802332
Open Tree Of Life 1094779
NCBI Taxonomy 549402
IUCN Red List 179313854
IPNI 772837-1
iNaturalist 960272
GBIF 7268853
EOL 5621032

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
Chalepin and Chalepensin: Occurrence, Biosynthesis and Therapeutic Potential Nahar L, Al-Majmaie S, Al-Groshi A, Rasul A, Sarker SD Molecules 14-Mar-2021
PMCID:PMC7999183
doi:10.3390/molecules26061609
PMID:33799365
Dihydrochalcones: Methods of Acquisition and Pharmacological Properties—A First Systematic Review Stompor M, Broda D, Bajek-Bil A Molecules 05-Dec-2019
PMCID:PMC6943545
doi:10.3390/molecules24244468
PMID:31817526
Almeidea A. St.-Hil. Belongs to Conchocarpus J.C. Mikan (Galipeinae, Rutaceae): Evidence from Morphological and Molecular Data, with a First Analysis of Subtribe Galipeinae Poleselli Bruniera C, Kallunki JA, Groppo M PLoS One 07-May-2015
PMCID:PMC4423776
doi:10.1371/journal.pone.0125650
PMID:25951371
Evaluation of Halogenated Coumarins for Antimosquito Properties Narayanaswamy VK, Gleiser RM, Kasumbwe K, Aldhubiab BE, Attimarad MV, Odhav B ScientificWorldJournal 25-Dec-2014
PMCID:PMC4290031
doi:10.1155/2014/189824
PMID:25610898
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Alcaloides β-indolopiridoquinazolínicos de Esenbeckia grandiflora mart. (Rutaceae) Ana Helena Januário, Paulo Cezar Vieira, Maria Fátima das Graças Fernandes d Silva, João Batista Fernandes, Jorge José de Brito Silva, Lucia Maria Conserva FapUNIFESP (SciELO) 03-Dec-2009
doi:10.1590/S0100-40422009000800010
A pimpinellin monomer and dimer isolated from the roots of Esenbeckia grandiflora. de Oliveira PE, Conserva LM, De Simone CA, Pereira MA, Malta VR, Imbroisi DO Acta Crystallogr C 01-Dec-2004
doi:10.1107/S0108270104023777
PMID:15579978
Dihydrochalcones and coumarins of Esenbeckia grandiflora subsp. brevipetiolata. Trani M, Carbonetti A, Delle Monache G, Delle Monache F Fitoterapia 01-Jan-2004
doi:10.1016/J.FITOTE.2003.08.004
PMID:14693231
Alkaloids and coumarins from Esenbeckia species Fernando M. Oliveira, Antônio Euzébio G.^Sant'ana, Lucia M. Conserva, JoséGuilherme S. Maia, Giselle M.P. Guilhon Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00564-1

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Anisocoumarin H 14376449 Click to see CC(=CC(CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)O)C 314.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3S,6R,9S,14R,15S,18R)-6,10,10,14,15,18,21,21-octamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosan-9-ol 162966179 Click to see 442.70 unknown https://doi.org/10.1590/S0100-40422009000800010
(1S,2R,4aR,6aS,6bR,10S,12aS)-10-hydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicen-13-one 89732093 Click to see 440.70 unknown https://doi.org/10.1590/S0100-40422009000800010
(3S,6aR,6bR,8aR,11R,12S,14bR)-3-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14,14a-hexadecahydropicen-13-one 163061897 Click to see CC1CCC2(CCC3(C(C2C1C)C(=O)CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 442.70 unknown https://doi.org/10.1590/S0100-40422009000800010
(4aR,6aS,6bR,10S,12aS)-10-hydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picen-13-one 90658533 Click to see 440.70 unknown https://doi.org/10.1590/S0100-40422009000800010
(4aR,6bR,10S,12aS)-10-hydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picen-13-one 5318270 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1590/S0100-40422009000800010
10-Hydroxy-1,2,4a,6a,6b,9,9,12a-octamethyl-1,2,3,4,5,6,6a,7,8,8a,10,11,12,14b-tetradecahydropicen-13-one 74933427 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 440.70 unknown https://doi.org/10.1590/S0100-40422009000800010
10-hydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picen-13-one 13996051 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1590/S0100-40422009000800010
3-Hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14,14a-hexadecahydropicen-13-one 163061895 Click to see 442.70 unknown https://doi.org/10.1590/S0100-40422009000800010
6,10,10,14,15,18,21,21-Octamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosan-9-ol 162966178 Click to see 442.70 unknown https://doi.org/10.1590/S0100-40422009000800010
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Ergoyne B 139591552 Click to see CC(C)CCC(CC=CC#CC#CC=C1C=CSC2=NC(=CN12)CC(C(=O)O)[N+](C)(C)C)C(=O)O 496.60 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
7,17,18-Trimethoxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 135778997 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC(=C(C=C5C4=O)OC)OC 377.40 unknown https://doi.org/10.1590/S0100-40422009000800010
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Flindersiamine 68221 Click to see 273.24 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
https://doi.org/10.1016/0031-9422(95)00564-1
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
https://doi.org/10.1016/0031-9422(95)00564-1
Maculine 68232 Click to see 243.21 unknown https://doi.org/10.1016/0031-9422(95)00564-1
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
8-methoxy-1-methylquinolin-4(1H)-one 15675303 Click to see 189.21 unknown https://doi.org/10.1016/0031-9422(95)00564-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S)-8-(2-hydroxypropan-2-yl)-3-(2-methylbut-3-en-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one 162958153 Click to see 314.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
https://doi.org/10.1016/0031-9422(95)00564-1
8-(2-Hydroxypropan-2-yl)-3-(2-methylbut-3-en-2-yl)-8,9-dihydrofuro[2,3-h]chromen-2-one 14604075 Click to see 314.40 unknown https://doi.org/10.1016/0031-9422(95)00564-1
https://doi.org/10.1016/J.FITOTE.2003.08.004
Moellendorffilin 21121035 Click to see COC1=C(C2=C(C=CO2)C3=C1C4C5C(C4C(=O)O3)C(=O)OC6=C5C(=C(C7=C6C=CO7)OC)OC)OC 492.40 unknown https://doi.org/10.1107/S0108270104023777
Moellendorffiline 128785 Click to see 492.40 unknown https://doi.org/10.1107/S0108270104023777
Pimpinellin 4825 Click to see 246.21 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
https://doi.org/10.1107/S0108270104023777
https://doi.org/10.1016/0031-9422(95)00564-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol 40429858 Click to see 304.29 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
https://doi.org/10.1016/0031-9422(95)00564-1
9-Methoxy-4-(3-methylbut-2-enoyl)furo[3,2-g]chromen-7-one 163094837 Click to see CC(=CC(=O)C1=C2C=CC(=O)OC2=C(C3=C1C=CO3)OC)C 298.29 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4,6-trihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one 163042696 Click to see 410.50 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
1-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4,6-trihydroxyphenyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]propan-1-one 162923171 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)C(=O)CCC2=CC(=C(C=C2)O)CC=C(C)C)O)C)C 478.60 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004
1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4,6-trihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one 131837031 Click to see 410.50 unknown https://doi.org/10.1016/J.FITOTE.2003.08.004

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