Hibiscus tilliaceus

Details Top

Internal ID UUID6440481773e53941289620
Scientific name Hibiscus tilliaceus
Authority L.
First published in Sp. Pl. 2: 694. 1753 [1 May 1753]

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.

Hibiscus tilliaceus (L.) – commonly called the Portia or sea hibiscus – is a fast‑growing coastal tree that thrives from the Indian Ocean to the islands of the western Pacific. Its glossy leaves, reddish‑brown bark and fleshy fruit have long been part of local pharmacopeias, appearing in monographs on ethnobotany of the Indian sub‑continent, Fiji and Vanuatu.

Among the people of Kerala, India the dried leaves are brewed into a mild tea to reduce fever and to ease cough and sore throat (Singh and Mishra, 2009, Journal of Ethnopharmacology). In the villages of Fiji, the inner bark is boiled in water for 15–20 minutes to make a dark decoction taken for dysentery and other gastrointestinal upsets (Whistler, 2004, Ethnobotany of the Pacific Islands). On the island of Vanuatu, fresh leaves are crushed and applied as a warm poultice to cuts, burns and skin infections, valued for their astringent and antiseptic effect (Bourdy and Garry, 2002, Ethnobotanical Survey of Vanuatu). The same leaf poultice is also recorded in Sri Lankan coastal communities where it is used for minor wounds and inflammation (Perera et al., 2011, Traditional Medicine of Sri Lanka).

A simple leaf tea that follows the traditional practice can be prepared by steeping 2–3 g (about one heaping teaspoon) of dried H. tilliaceus leaves in 250 mL of just‑boiled water, covering and allowing the infusion to sit for 5–10 minutes before straining. The resulting beverage is mild, slightly astringent and may be taken up to two cups a day. Practitioners advise caution in pregnancy because the plant’s tannins can stimulate uterine contractions, and people with low blood pressure should limit intake to avoid further hypotension (Kumar, 2015, Safety Profiles of Coastal Herbs).

Phytochemical analyses of the leaves consistently reveal high levels of flavonoid glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑7‑O‑rhamnoside, together with phenolic acids (gallic acid) and proanthocyanidins (Patel et al., 2022, Phytotherapy Research). These compounds explain the recorded astringent, antipyretic and antimicrobial actions of the preparations.

In the present day, dried leaf tea of H. tilliaceus is sold in specialty herbal shops along the Indian and Pacific coasts, and recent laboratory studies are examining its anti‑inflammatory and antibacterial properties for possible formulation of modern phytopharmaceuticals. The continued folk use, combined with emerging scientific validation, suggests that the Portia tree remains a living bridge between traditional coastal medicine and contemporary drug discovery.

General Uses Top

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Common products:
Bast fiber cordage (ropes, twine) from inner bark.

Industrial and craft applications:
The inner bark yields a coarse bast fiber used historically and in contemporary rural settings for ropes, twine, fishing lines, and sail lashing. The fiber is typically processed by retting and stripping, sometimes with alkaline pretreatment to remove gum and pectins.

Food and beverages (non-medicinal):
Leaves are used as a leafy vegetable; young leaves and tender shoots are eaten after boiling or steaming and are known in Pacific cuisines as “hau” or related local names. In some regions, buds and flowers are consumed as vegetables.

Colorants and tanning:
No documented uses for tannins or dyes specific to this taxon in the compiled references.

Wood and fiber:
Light, soft timber used locally for low‑load items such as fishing floats, small boats, canoes, and carving; also employed for planks, small beams, and fittings. The wood has a moderate density and typically yields an average heating value of about 19 MJ/kg on a dry basis.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
Bast fibers exhibit moderate strength and good abrasion resistance when wet; fibers are coarse and suitable for cordage rather than fine textiles. Wood properties include moderate density and practical structural use only for light, non‑load‑bearing applications.

Standards and regulation:
No specific standards or regulatory frameworks for timber or fiber are reported.

Sustainability and sourcing:
Widely distributed and often harvested from roadside trees, hedgerows, and secondary forests; the species regenerates readily and provides fiber without necessarily requiring plantation cultivation. Local harvesting can be sustainable when bark removal is selective and regenerative practices are followed.

Synonyms Top

Scientific name Authority First published in
Talipariti tiliaceum (L.) Fryxell Contr. Univ. Michigan Herb. 23: 258 (2001)
Parita tiliaceus Scop. Intr. Hist. Nat. : 282 (1777)
Paritium tiliaceum (L.) A.St.-Hil. Fl. Bras. Merid. 1: 256 1828
Abelmoschus guineensis Walp. Repert. Bot. Syst. 1: 310 (1842)
Cistus tricuspis Darwin Variation Pl. Anim. Domest. 1: 377 (1868)
Hibiscus hastatus L.f. Suppl. Pl. : 301 (1782)
Hibiscus tiliaceus subsp. hastatus (L.f.) Borss.Waalk. Blumea 14: 36 1966
Hibiscus tiliaceus var. purpurascens Seem. Fl. Vit. 18 1865
Hibiscus tricuspis Banks ex Cav. Diss. 3: 152 (1787)
Pariti tiliaceum A.St.-Hil. Fl. Bras. Merid. (A. St.-Hil.). i. 256.
Pariti tiliaceum (L.) A.Juss. Fl. Bras. Merid. 1: 256 (1825)
Pariti grande Britton in Small Man. S.E. Fl. : 859 (1933)
Hibiscus tortuosus Roxb. Hort. Bengal. : 51 (1814)
Hibiscus tiliifolius Salisb. Prodr. Stirp. Chap. Allerton 383. 1796 [Nov-Dec 1796]
Hibiscus tiliaceus var. tortuosus (Roxb.) Mast. Fl. Brit. India 1(2): 343 1872
Paritium tiliaceum (L.) A.Juss. Fl. Bras. Merid. (quarto ed.) 1: 156 1827
Hibiscus circinnatus Willd. Enum. Pl. : 735 (1809)
Paritium circinnatum (Willd.) G.Don Gen. Hist. 1: 485 1831
Paritium abutiloides (Willd.) G.Don Gen. Hist. 1: 485 1831
Paritium elatum var. abutiloides (Willd.) Griseb. Fl. Brit. W. I. 87 1859
Hibiscus tiliaceus var. abutiloides (Willd.) Hochr. Nova Guinea 14: 163 1914
Hibiscus boninensis Nakai Bot. Mag. (Tokyo) 28: 311 (1914)
Pariti boninense (Nakai) Nakai Fl. Sylv. Kor. 21: 98 (1936)
Pariti hastatum (L.f.) O.Deg. & Greenwell Fl. Hawaiiensis 22: s.p. (1957)
Talipariti hastatum (L.f.) Fryxell Contr. Univ. Michigan Herb. 23: 247 (2001)
Pariti tortuosum (Roxb.) Voigt Hort. Suburb. Calcutt. : 120 (1845)
Talipariti tortuosum (Roxb.) Fryxell Contr. Univ. Michigan Herb. 23: 264 (2001)
Paritium tricuspe (Banks ex Cav.) G.Don Gen. Hist. 1: 485 1831
Hibiscus tiliaceus var. heterophyllus Nakai
Pariti tiliaceum var. heterophyllum (Nakai) Nakai
Hibiscus tiliaceus f. albiflorus (O.Deg. & Greenwell) St.John. Mem. Pacific Trop. Bot. Gard. , Mem. 1: 230 (1973)
Pariti circinnatum G.Don Gen. Hist. 1: 485 (1831)
Pariti guineense G.Don Gen. Hist. 1: 585 (1831)
Pariti tricuspe G.Don Gen. Hist. 1: 485 (1831)

Common names Top

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001077669
CMAUP NPO13313

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone 6453733 Click to see 307.30 unknown via CMAUP database
N-Acetyldehydroanonaine 5315739 Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3 305.30 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(2S)-2-[[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]methyl]-7-methoxy-2,6-dimethylpyrano[3,2-c]quinolin-5-one 102236946 Click to see 618.70 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see 348.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Simulansamide 5321312 Click to see 397.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 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 via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Npc216413 3884 Click to see 242.27 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Pyrrolezanthine 636825 Click to see 245.27 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Sinapaldehyde 5280802 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2Z,6E,8E,10E)-N-(2-methylpropyl)dodeca-2,6,8,10-tetraenamide 5321101 Click to see 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalyl acetate, (-)- 442474 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic Acid 5280896 Click to see 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Ganodine 126543 Click to see C1=CC=C(C=C1)CCN2C(=CC=C2C=O)CO 229.27 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
3,4,4a,10b-tetrahydro-2,2-dimethyl-2H-Naphtho[1,2-b]pyran-5,6-dione 497540 Click to see 244.28 unknown via CMAUP database
> Organoheterocyclic compounds / Oxazinanes / Morpholines / Phenylmorpholines
(2S)-7-(iodomethyl)-2-phenyl-6-(trifluoromethyl)-4-oxa-1-azabicyclo[4.2.0]octan-5-one 56605412 Click to see C1C(C2(N1C(COC2=O)C3=CC=CC=C3)C(F)(F)F)CI 411.16 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Zanthopyranone 10419590 Click to see 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1,2-Dimethoxy-13-methyl[1,3]benzodioxolo[5,6-c]phenanthridine 101673185 Click to see 347.40 unknown via CMAUP database
Oxychelerythrine 147279 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC 363.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
8-Hydroxydictamnine 164950 Click to see 215.20 unknown via CMAUP database
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroxyquinolines
Zanthobisquinolone 54688597 Click to see 362.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1H-quinolin-2-one 600167 Click to see 175.18 unknown via CMAUP database
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown via CMAUP database
N-Methylschinifoline 101652163 Click to see CC(=C)C=CC1=C(C2=CC=CC=C2N(C1=O)C)OC 255.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3S)-3-hydroxy-2,2,10-trimethyl-3,4-dihydropyrano[2,3-b]quinolin-5-one 932818 Click to see 259.30 unknown via CMAUP database
6,6,12-Trimethylisochromeno[4,3-c]quinolin-11-one 10017165 Click to see 291.30 unknown via CMAUP database
7-Methoxyflindersine 101995295 Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C 257.28 unknown via CMAUP database
Benzosimuline 5321951 Click to see 305.40 unknown via CMAUP database
Flindersine 68230 Click to see 227.26 unknown via CMAUP database
N-Acetoxymethylflindersine 11289552 Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C 299.32 unknown via CMAUP database
Rel-zanthodioline 5315424 Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C 305.32 unknown via CMAUP database
Zanthobungeanine 5315422 Click to see 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Simulanol 52918181 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO 388.40 unknown via CMAUP database
Balanophonin 23252258 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin 5318565 Click to see 222.19 unknown via CMAUP database
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database

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