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Tamanu Oil in Perfumery | Première Peau

FRUITS, VEGETABLES AND NUTS  /  nutty · rich · musky
Tamanu
Tamanu perfume ingredient
CategoryFRUITS, VEGETABLES AND NUTS
Subcategorynutty · rich · musky
Origin
VolatilityBase Note
BotanicalCalophyllum inophyllum
AppearanceDark green to greenish-brown viscous oil
Odor StrengthMedium
Producing CountriesFrench Polynesia, Madagascar, Southeast Asia
PyramidBase

Thick, dark, and vegetal. A heavy green oil that smells like crushed walnuts left on warm earth — nutty, bitter, faintly resinous, with a curry-leaf undertone that no other carrier oil shares.

  1. Scent
  2. Terroir & Origins
  3. The Full Story
  4. Fun Fact
  5. Extraction & Chemistry
  6. In Perfumery
  7. See Also

Scent

Dense, dark, lipidic. The immediate impression is of crushed walnut — not the refined walnut oil used in cooking, but the raw shell and bitter green skin. Heavier and more bitter than sweet almond oil, with none of coconut's lactonic sweetness. A vegetal spiciness recalls curry leaf or fenugreek. As the oil warms on skin, the bitterness lifts and a praline-like resinous warmth takes its place — roasted, slightly smoky, with a faint caramel undertone. Moderate sillage; strong tenacity on fabric and skin.

Evolution over time

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Terroir & Post-Harvest Process

Indicative 2025 wholesale prices.

The Full Story

Tamanu oil is cold-pressed from the dried kernels of Calophyllum inophyllum, a coastal evergreen native to Southeast Asia, Polynesia, and East Africa. The tree belongs to the Calophyllaceae family — its genus name, from the Greek kalos (beautiful) and phullon (leaf), refers to the glossy, lacquered foliage, not the oil. The French Polynesian name tamanu is the one that stuck in global trade; in Madagascar it is foraha, in Hawaii kamani, in Fiji dilo.

Scent Profile

The oil is dark green to brown, viscous, and strongly aromatic. The smell opens nutty and vegetal — walnut shells, raw peanut skin — with a pronounced bitter-green undercurrent that separates it from lighter nut oils like sweet almond or macadamia. A faint curry-leaf spiciness runs through the mid-register. On dry-down, the bitterness recedes and a warm, resinous sweetness emerges — closer to aged praline than to any floral. The overall impression is dense, lipidic, and earthy. Headspace analysis of the oil reveals a range of aldehydes, ketones, and heterocyclic compounds contributing to the characteristic walnut-like olfactive signature.

Origin and Extraction

The extraction follows a slow, traditional process that cannot be mechanically accelerated. Ripe fruits fall naturally from the tree and are collected. The pale, odourless kernels are then sun-dried for one to two months — a critical curing phase during which enzymatic and oxidative reactions generate the oil's colour, aroma, and bioactive compounds. The kernels turn dark brown and sticky. Only then are they cold-pressed at low temperature (26–32°C), yielding a viscous oil at 40–60% by weight. Approximately 90 kg of dried drupes produces 4–5 litres of finished oil.

Chemistry

The fatty acid backbone is oleic (30–55%), linoleic (15–45%), palmitic (5–20%), and stearic (5–25%). What distinguishes tamanu from other seed oils chemically is its resinous fraction (10–30% of total composition), containing neoflavonoids and pyranocoumarins found nowhere else in nature: calophyllolide (CAS 548-27-6, C₂₆H₂₄O₅ — the first neoflavone ever isolated from a natural source, in 1951), inophyllums B, C, D, E, P, calanolides, and tamanolides. These compounds are responsible for the oil's documented anti-inflammatory and antimicrobial activity, and contribute to its unusually heavy, resinous odour profile.

Did You Know?

Did you know?
Calophyllolide, the signature neoflavonoid in tamanu oil, was the first neoflavone ever isolated from a natural source — extracted from C. inophyllum seeds by Gruenwald, Ormancy-Potier, Buzas, and Lederer in 1951. Its discovery established an entirely new class of plant compounds. The same molecule was later found to have anticoagulant properties comparable to warfarin.

Extraction & Chemistry

Extraction method: Cold-pressed from sun-cured kernels of Calophyllum inophyllum. The process is slow and cannot be industrially accelerated. Ripe fruits are collected after falling naturally from the tree. Kernels are separated from the outer shell and spread to sun-dry for 4–8 weeks. During this curing phase, enzymatic and oxidative reactions transform the pale, odourless kernels into dark brown, sticky, oil-rich masses — this step generates the oil's characteristic colour, aroma, and bioactive resinous compounds (calophyllolide, inophyllums). The cured kernels are then mechanically cold-pressed at 26–32°C. Yield: 40–60% oil by weight from dried kernel. Approximately 90 kg of raw drupes yields 4–5 litres of finished oil. No solvent, no heat beyond ambient sun. Major production regions: French Polynesia (Tahiti), Madagascar, Vanuatu, Fiji, and Southeast Asia.

↑ See Terroir & Origins for origin-specific methods.

Molecular FormulaComplex mixture. Key bioactives: calophyllolide (C₂₆H₂₄O₅, CAS 548-27-6), inophyllum B (C₂₅H₂₂O₅), oleic acid (C₁₈H₃₄O₂), linoleic acid (C₁₈H₃₂O₂)
CAS Number241148-25-4 (seed oil)
Botanical NameCalophyllum inophyllum
IFRA StatusNo specific IFRA restriction on tamanu seed oil as of the 51st Amendment. Individual constituents present in trace amounts may carry their own limits.
SynonymsFORAHA · KAMANI
Physical Properties
Odor StrengthMedium
AppearanceDark green to greenish-brown viscous oil
Flash Point> 200.00 °F. TCC ( > 93.33 °C. ) (est)
Specific Gravity0.930 to 0.960 @ 25.00 °C.

In Perfumery

Tamanu oil functions primarily as a carrier and base-note modifier rather than a conventional fragrance ingredient. Its role in perfumery is structural, not melodic: it provides lipidic body, anchors volatile top notes, and introduces a nutty-resinous undertone that synthetic carriers cannot replicate. In practice, tamanu operates at the boundary between perfumery and cosmetics. Its resinous fraction — calophyllolide, inophyllums, calanolides — acts as a natural fixative, slowing evaporation of lighter molecules. The oil's high viscosity and substantivity make it useful in oil-based perfume formats (attars, body oils, solid perfumes) where alcohol-free delivery is the goal. It complements earthy, woody, and gourmand accords. Structurally, it sits well alongside patchouli, vetiver, sandalwood, and labdanum. Its nutty character can reinforce gourmand bases built on tonka bean, praline, or coffee. No Première Peau fragrance currently lists tamanu as a named note, but its earthy-gourmand character occupies similar olfactive territory to the truffle and ink accord in ALBATRE SEPIA (/products/albatre-sepia-white-truffle-ink-perfume).

See Also

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