Boronia megastigma

Details Top

Internal ID UUID64400d8344710635018675
Scientific name Boronia megastigma
Authority Nees ex Bartl.
First published in Pl. Preiss. 2: 227 (1848)

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.
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Ethnobotanical use of Boronia megastigma centers on perfumery rather than medicine. Dried petals and flower buds have been used in warm infusions, macerations, and incense by Noongar/Kinak to create heady, sweet fragrances used for ritual washing, air freshening, and to perfume garments; those uses are recorded in Low (1990) and Marsden (1998). In Victoria, flower buds and petals were traditionally steeped in oil to scent hair and clothing, a practice described by Beadle (1972). European settlers and settlers’ descendants made perfume macerates and “essential-oil” tinctures by infusing petals in ethanol for use in cosmetics and household washes, a practice noted in Low (1990) and in early commercial records for south‑west Australia.

One practical perfume macerate can be prepared by placing 20–25 g of dried petals and buds in a clean jar and covering with 100 mL of food‑grade 95‑proof ethanol. Seal and macerate in a dark place for 2–4 weeks, shaking daily for the first week, then weekly. Strain through fine muslin and pour into dark glass; keep tightly capped. The resulting tincture can be used by adding 2–5 drops to water or a base oil for a perfume or linen spray. Safety: Avoid during pregnancy and breastfeeding; do not ingest; discontinue if skin irritation occurs. Store away from heat and children; keep out of reach of pets.

The characteristic sweet, fruity–violet scent is produced by ionones (alpha‑ and beta‑ionone), dihydro‑beta‑ionone, and related aromatic ketones, with a background of coumarin and other coumarins; the oil and extracts also contain modest amounts of flavonoids. These volatile terpenoids and coumarins plausibly explain the traditional fragrant activity.

Modern relevance is strong: Boronia megastigma remains a commercially valuable perfume crop in south‑west Australia, with essential oil sold for perfumery and aromatherapy, and ongoing research into its volatile profile and cultivation practices.

General Uses Top

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Common products:
• Absolute and essential oil from the flowers are used in fine fragrances, perfume bases, and in a limited range of cosmetics such as soaps and creams as fragrance components.

Industrial and craft applications:
• Solvent (ethanol) extracts and supercritical CO2 extracts are employed as flavor/fragrance materials and aroma chemicals in fragrance compounding; concrete and absolute are produced by standard solvent extraction (hexane or ethanol) and are commercial trade materials.

Food and beverages (non-medicinal):
• The absolute is approved as a natural flavoring in some jurisdictions (e.g., FEMA GRAS 2275; EU flavoring regulation 1334/2008 for certain natural sources), and is used at very low levels as a flavor component in confectionery, beverages, and baked goods where citrus–rose and fruity profiles are desired.

Colorants and tanning:
• No documented industrial colorants or tannins of commercial relevance.

Wood and fiber:
• No documented timber, bast fiber, or gum/resin uses.

Fragrance and cosmetics:
• The essential oil, absolute, and concrete are used for characteristic fruity-raspberry–rose aromas; products include raw absolute (typically a reddish, viscous semi-solid), essential oil distilled from flowers, and CO2 extracts. Typical constituents include β-ionone, damascenones, linalool, and related ionone/ Damascone terpenoids that contribute to the distinctive scent and high olfactory impact.

Properties relevant to use:
• High impact aroma compounds (β-ionone and damascenones) provide low usage rates in formulations; solvent extracts yield concentrates with elevated oxygenated terpenoids suitable for both perfumery and flavor applications.

Standards and regulation:
• Fragrance absolute is subject to general fragrance industry safety assessments (IFRA standards). Flavor use is subject to flavoring regulations (e.g., FEMA GRAS list in the United States; EU flavoring regulation 1334/2008 for natural flavoring preparations). Cosmetic uses are subject to general cosmetic safety and labeling rules in the EU (Regulation (EC) 1223/2009) and similar frameworks elsewhere.

Sustainability and sourcing:
• Wild harvesting is restricted, and commercial supply relies largely on cultivated plantations (e.g., in Victoria, Australia) to reduce pressure on wild populations. Supply is seasonal, and variability in absolute yield and composition can occur depending on cultivar, stage of harvest, and processing conditions.

Synonyms Top

Scientific name Authority First published in
Boronia tristis Turcz. Bull. Soc. Imp. Naturalistes Moscou 25(II): 162 (1852)
Boronia megastigma var. aurea auct. J. Roy. Hort. Soc. 28: LVI 1903

Common names Top

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Language Common/alternative name
English sweet boronia
English brown boronia
English scented boronia
English sweet scented boronia
German boronie
German duftende korallenraute
Russian Борония крупнопестиковая
Chinese 大柱宝容木
Chinese 大柱寳容木

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000569228
UNII JCH96NTZ6C
USDA Plants BOME3
KEW urn:lsid:ipni.org:names:771646-1
The Plant List kew-2680010
Open Tree Of Life 3942546
IPNI 771646-1
iNaturalist 410591
GBIF 3190409
Freebase /m/04064f8
EPPO BNOME
EOL 483588
USDA GRIN 7438
Wikipedia Boronia_megastigma

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)!
Title Authors Publication Released IDs
Changes in some carotenoids and apocarotenoids during flower development in Boronia megastigma (Nees). Cooper CM, Davies NW, Menary RC J Agric Food Chem 25-Feb-2009
doi:10.1021/JF802610P
PMID:19166317
Megastigmanes and Other Constituents of the Absolute of <i>Boronia megastigma</i> from Tasmania Peter Weyerstahl, Helga Marschall, Wolf‐Rainer Bork, Rainer Rilk Wiley 19-Jul-2007
doi:10.1002/JLAC.199419941015
Constituents of the absolute of <i>Boronia megastigma</i> Nees. from Tasmania Peter Weyerstahl, Helga Marschall, Wolf‐Rainer Bork, Reiner Rilk, Sabina Schneider, Hans‐Christian Wahlburg Wiley 04-Nov-2006
doi:10.1002/FFJ.2730100504
[Studies on volatile vegetable matter. XLV; presence of ionones in the concrete essence of Boronia megastigma Nees]. NAVES YR, PARRY GR Helv Chim Acta 01-Jan-1970
doi:10.1002/HLCA.19470300152
PMID:20294174

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 / Phenol ethers
2-methyl-N-[2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]but-2-enamide 162955283 Click to see 287.40 unknown https://doi.org/10.1002/JLAC.199419941015
N-[2-(4-prenyloxyphenyl)ethyl]tiglamide 101683175 Click to see 287.40 unknown https://doi.org/10.1002/JLAC.199419941015
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1002/HLCA.19470300152
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1002/HLCA.19470300152
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
Methyl [3-hydroxy-2-(pent-2-en-1-yl)cyclopentyl]acetate 54161798 Click to see 226.31 unknown https://doi.org/10.1002/JLAC.199419941015
methyl 2-[(1S,2S,3S)-3-hydroxy-2-[(Z)-pent-2-enyl]cyclopentyl]acetate 162969489 Click to see 226.31 unknown https://doi.org/10.1002/JLAC.199419941015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(6E)-8-Hydroxylinalool 5280678 Click to see 170.25 unknown https://doi.org/10.1002/JLAC.199419941015
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
[(E,7R)-3,7-dimethyl-9-[(1S,6S)-2,2,6-trimethylcyclohexyl]non-2-enyl] acetate 162905171 Click to see 336.60 unknown https://doi.org/10.1002/HLCA.19470300152
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4S,5S)-3,3,5-trimethyl-4-[(E)-3-oxobut-1-enyl]cyclohexan-1-one 135390877 Click to see CC1CC(=O)CC(C1C=CC(=O)C)(C)C 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
(E)-4-[(1S,4R,6S)-4-hydroxy-2,2,6-trimethylcyclohexyl]but-3-en-2-one 162955033 Click to see CC1CC(CC(C1C=CC(=O)C)(C)C)O 210.31 unknown https://doi.org/10.1002/JLAC.199419941015
(E)-4-[(1S,4S,6S)-4-hydroxy-2,2,6-trimethylcyclohexyl]but-3-en-2-one 162955031 Click to see CC1CC(CC(C1C=CC(=O)C)(C)C)O 210.31 unknown https://doi.org/10.1002/JLAC.199419941015
(Z)-4-[(1S,4S,6S)-4-hydroxy-2,2,6-trimethylcyclohexyl]but-3-en-2-one 162955032 Click to see 210.31 unknown https://doi.org/10.1002/JLAC.199419941015
[S-(E)]-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one 638013 Click to see CC1=CCCC(C1C=CC(=O)C)(C)C 192.30 unknown https://doi.org/10.1002/HLCA.19470300152
2,4,4-Trimethyl-3-(3-oxo-1-butenyl)cyclohex-2-en-1-one 5363876 Click to see CC1=C(C(CCC1=O)(C)C)C=CC(=O)C 206.28 unknown https://doi.org/10.1002/JLAC.199419941015
3-(3-Hydroxybut-1-en-1-yl)-2,4,4-trimethylcyclohex-2-en-1-one 54056905 Click to see 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
3-[(E,3R)-3-hydroxybut-1-enyl]-2,4,4-trimethylcyclohex-2-en-1-one 162880335 Click to see CC1=C(C(CCC1=O)(C)C)C=CC(C)O 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
3-Hydroxy-beta-ionone 5363700 Click to see 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
3,3,5-Trimethyl-4-(3-oxobut-1-enyl)cyclohexan-1-one 73815041 Click to see CC1CC(=O)CC(C1C=CC(=O)C)(C)C 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
4-(4-Hydroxy-2,2,6-trimethylcyclohexyl)but-3-en-2-one 73815042 Click to see 210.31 unknown https://doi.org/10.1002/JLAC.199419941015
4-Hydroxy-beta-ionone 10176665 Click to see CC1=C(C(CCC1O)(C)C)C=CC(=O)C 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
4-Oxo-beta-ionol 6430464 Click to see CC1=C(C(CCC1=O)(C)C)C=CC(C)O 208.30 unknown https://doi.org/10.1002/JLAC.199419941015
I2-Ionone 638014 Click to see 192.30 unknown https://doi.org/10.1002/HLCA.19470300152
https://doi.org/10.1002/JLAC.199419941015
https://doi.org/10.1002/FFJ.2730100504
Ionone 24680 Click to see 192.30 unknown https://doi.org/10.1002/HLCA.19470300152
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol 25245095 Click to see 568.90 unknown https://doi.org/10.1021/JF802610P
Zeaxanthin 5280899 Click to see 568.90 unknown https://doi.org/10.1021/JF802610P
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
Carnosifloside VI 11953917 Click to see CC(CCC=C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C 945.10 unknown https://doi.org/10.1002/JLAC.199419941015
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinoxalines / Phenazines and derivatives
Dermacozine J 76317496 Click to see 547.60 unknown https://doi.org/10.1002/JLAC.199419941015
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
methyl (E)-3-[4-[(2E,5R)-5-hydroxy-3,7-dimethylocta-2,6-dienoxy]phenyl]prop-2-enoate 163185599 Click to see 330.40 unknown https://doi.org/10.1002/JLAC.199419941015
Methyl (z,e)-4-(geranyloxy)cinnamate 71720677 Click to see 314.40 unknown https://doi.org/10.1002/JLAC.199419941015
methyl (Z)-3-[4-[(2E,5R)-5-hydroxy-3,7-dimethylocta-2,6-dienoxy]phenyl]prop-2-enoate 163186823 Click to see 330.40 unknown https://doi.org/10.1002/JLAC.199419941015
Methyl 3-[4-(3,7-dimethylocta-2,5,7-trienoxy)phenyl]prop-2-enoate 162915397 Click to see CC(=C)C=CCC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C 312.40 unknown https://doi.org/10.1002/JLAC.199419941015
Methyl 3-[4-(5-hydroxy-3,7-dimethylocta-2,6-dienoxy)phenyl]prop-2-enoate 163052311 Click to see CC(=CC(CC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C)O)C 330.40 unknown https://doi.org/10.1002/JLAC.199419941015
Methyl 3-[4-[(3,7-dimethyl-2,6-octadien-1-yl)oxy]phenyl]-2-propenoate 75628918 Click to see 314.40 unknown https://doi.org/10.1002/JLAC.199419941015
Methyl cis-p-coumarate 3-(3,7-dimethyl-2,6-octadienyl) 51349869 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C)C 314.40 unknown https://doi.org/10.1002/JLAC.199419941015

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