3-Hexenyl phenylacetate (CAS 42436-07-07) — Green Top to middle Note Fragrance Ingredient

Green · Sweet

3-Hexenyl phenylacetate

CAS 42436-07-07

Origin
synthetic
Note
Top to middle
IFRA
Generally safe
Data as of: Apr 2026

What Is 3-Hexenyl phenylacetate?

3-Hexenyl phenylacetate is a synthetic fragrance ingredient that mimics the fresh, green aroma of crushed leaves and stems. You’ll encounter it in modern perfumes, especially those aiming for a crisp, vegetal character. This molecule matters because it provides perfumers with a stable, consistent green note that doesn’t fade quickly like natural leaf absolutes, allowing for longer-lasting fresh accords in fragrances.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Not classified as an allergen
CAS
42436-07-07
Formula
Mixture
MW
Variable
Odor Family
Green · Sweet
Layer 1 · Enthusiast

What Does 3-Hexenyl phenylacetate Smell Like?

3-Hexenyl phenylacetate bursts with an intensely green, sappy aroma reminiscent of freshly cut grass stems and broken tomato leaves. The initial sharpness evolves into a smoother, honeyed green character with subtle floral undertones. Unlike more volatile leaf alcohols, this ester maintains its vegetal personality throughout the dry-down, blending particularly well with citrus and white florals to create modern, dewy-green compositions. The phenylacetate moiety adds a faint sweet-powdery nuance that prevents the greenness from becoming harsh or metallic.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Used to create the illusion of rain-drenched vegetation, contributing to the fragrance’s aquatic-green signature alongside calone and ginger.

Green Irish Tweed(Creed, 1985)

Provides a crisp, living green counterpoint to the violet leaf and sandalwood, enhancing the fragrance’s aristocratic freshness.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3-Hexenyl phenylacetate is an ester formed from phenylacetic acid and leaf alcohol (3-hexen-1-ol). As a synthetic material, it’s typically produced via esterification under acidic conditions. The molecule combines the green volatility of the hexenyl group with the stability and tenacity of the phenylacetate moiety. While not found in nature, its components occur widely in plants, making it a biomimetic fragrance material.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~280 °C (estimated)
Density~1.0 g/cm³ (estimated)

Perfumer Guide

Note Position
Top to middle
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Green note modifier
Functional Fragrance0.1-0.5%Up to 1%Freshness booster

Classic Accords

Tip: Use to extend the longevity of natural green notes like galbanum or stemone.

Alternatives & Comparisons

1
Leaf alcohol CAS 928-96-1

For a more volatile, natural green effect but with less tenacity.

2
Stemone CAS 67634-15-5

When a more intense, metallic-green character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

No restrictions under current IFRA standards.

RIFM Assessment

Considered safe for use in fragrance based on RIFM’s assessment of structurally similar materials.

Sustainability

As a synthetic material, 3-Hexenyl phenylacetate offers consistent quality without agricultural variability. Its production avoids the land-use issues associated with harvesting natural green materials. However, like all synthetic esters, it relies on petrochemical feedstocks, though the quantities used in fragrance are minimal.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.

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