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TRANS-2-HEXENAL

RESTRICTIONConflicted evidence
CAS
6728-26-3
EC
—
Material type
other
Canonical source
document derived
Formulation

Usage guidance

Suggested min
—
Suggested max
—
Cost
—
Stock
—
Compatibility tags
floralfruitygreentopnote
How it behaves

Olfactory profile

Family
green
Note tendency
Top
Descriptors
greenfruitypungentvegetablefresh

Intensely green, sharp leaf-aldehyde with a piercing crushed-grass and unripe apple character. Extremely powerful and diffusive at trace levels, with a slightly fatty, cut-stem facet that fades quickly to a softer green fruitiness.AI · claude-opus-4-7

Intensity
9 / 10
Tenacity
2 / 10
Volatility
9 / 10
Members

The rest of this material

Composition, IFRA restriction figures, allergen concentrations and where this material is bought are part of Perfume Foundry’s curated library and need an account. Create one or sign in.

chemicals · No. 1599

Arctander monograph

Perfume and Flavor Chemicals, page 661.

TOPG.R.A.S.FEMA 2560
greenfruitypungentvegetablefresh
MW
98.15
BP
—
MP
—
Sp.Gr.
—
Refractive n
—
Rotation
—
Appearance

Colorless liquid.

Solubility

Almost insoluble in water, soluble in alcohol, propylene glycol and most perfume and flavor oils.

Odor

Powerful green-fruity, pungent vegetable-like odor, pungent in high concentrations, almost acrylic-sharp, but pleasant fruity and fresh-green in dilutions below 0.1%.

Flavor

This aldehyde finds even more use in flavor compositions, particularly in Strawberry, Banana, Apple, Apricot, Plum, Pear and many berry or fruit complexes. In Orange flavors it may introduce a much wanted lift to the freshness of such sweet flavor.

Uses in perfumery

Used in perfume compositions as part of fresh-green, natural topnote complexes, often in delicately floral or fruity fragrance types, and in general as a fresh topnote in bases and artificial essential oils.

Uses in flavor

A special use is in Cucumber imitation flavor, also occasionally asked for in perfumes for hand-lotions, etc. It forms an important part of the natural aldehyde portion in the aroma of Cucumber.

Production

1) by reduction of Hexenoic acid with Formic acid vapors over Manganese dioxide at 350° C. 2) by oxidation of the corresponding Hexenol. 3) by condensation of Acetaldehyde with n-Butyraldehyde.

Identity
Aliases · 13
16635-54-42-Hexenal, (E)-2-Hexenal, (Z)-6728-26-3beta-Propyl acroleincis-2-HexenalHex-2-enalHexen-2-altrans-2-Hexenal2-Hexenalalpha-beta-Hexylenic aldehydecis-3-HexenalLeaf aldehyde
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).