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Prunol

NATURAL AND SYNTHETIC, POPULAR AND WEIRD  /  fruity · sweet · warm
Prunol
Prunol perfume ingredient
CategoryNATURAL AND SYNTHETIC, POPULAR AND WEIRD
Subcategoryfruity · sweet · warm
Origin
VolatilityHeart Note
BotanicalN/A — perfumery base (inspired by Prunus domestica fruit)
AppearanceColorless to pale yellow clear liquid
Odor StrengthMedium
PyramidHeart

Prunus-like, almond-cherry, faintly bitter. Prunol captures the benzaldehyde-driven character of stone fruits: cherry, almond, plum kernel.

  1. Scent
  2. The Full Story
  3. Fun Fact
  4. Extraction & Chemistry
  5. In Perfumery

Scent

Bitter almond, maraschino cherry, stone-fruit kernel. Less sweet than vanilla, less fruity than fresh cherry, more kernel-like than either.

Evolution over time

Immediately

Immediately

Bright bitter-almond cherry burst
After a few hours

After a few hours

Cherry-kernel warmth, faintly sweet
After a few days

After a few days

Soft almond-bitter persistence

The Full Story

Prunol references the olfactory character of Prunus genus materials. The dominant molecule is benzaldehyde (bitter-almond, maraschino-cherry). Related molecules include heliotropin and benzyl alcohol.

The name suggests a synthetic molecule or base capturing this bitter-kernel, fruity-almond character. It sits at the intersection of gourmand (cherry pie, marzipan) and slightly sinister (cyanide smells like bitter almonds for the same chemical reason).

In perfumery, this functions as a heart-to-base modifier adding faintly bitter, food-adjacent sweetness.

This note in Première Peau. Insuline Safrine. Sample all seven extraits in the Discovery Set.

Related: Acetyl Furan · Ambermax · Ambrofix · Egg · Ethyl Maltol · Flour · Furfural · Genepi

Did You Know?

Did you know?
Benzaldehyde and hydrogen cyanide are both produced when amygdalin in cherry pits breaks down enzymatically. Benzaldehyde itself is non-toxic; the danger comes from the co-produced HCN.

Extraction & Chemistry

Extraction method: Extraction data not independently verified. Benzaldehyde is produced synthetically or from natural sources.

Botanical NameN/A — perfumery base (inspired by Prunus domestica fruit)
IFRA StatusNo known restrictions
SynonymsPrunol SP, Prunol base, Prunol de Laire
Physical Properties
Odor StrengthMedium
AppearanceColorless to pale yellow clear liquid
Boiling Point~225 °C @ 760 mm Hg (est)
Flash Point> 200 °F TCC (est)
Specific Gravity0.830-0.850 @ 25 °C (est)

In Perfumery

Heart-to-base modifier for stone-fruit and almond compositions. Key molecule: benzaldehyde. Supported by heliotropin and benzyl alcohol. Must be dosed carefully to avoid medicinal overtones.

From the raw to the worn

This is what it becomes.