2-Cyclopentene-1-acetic acid, ethyl ester (CAS 15848-49-4) — Green Top to middle Note Fragrance Ingredient

Green · Floral

2-_Cyclopentene-_1-_acetic acid, ethyl ester

CAS 15848-49-4

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

What Is 2-_Cyclopentene-_1-_acetic acid, ethyl ester?

2-Cyclopentene-1-acetic acid, ethyl ester is a synthetic fragrance compound primarily used in perfumery. Consumers might encounter it as a subtle component in modern floral or fruity fragrances. This ingredient matters because it contributes unique green-fruity nuances that help perfumers create fresh, contemporary scent profiles.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns reported
Limited safety data available
CAS
15848-49-4
Formula
Mixture
MW
Variable
Odor Family
Green · Floral
Layer 1 · Enthusiast

What Does 2-_Cyclopentene-_1-_acetic acid, ethyl ester Smell Like?

This ester delivers a crisp, green-fruity character reminiscent of unripe apples and freshly cut stems. The initial burst carries a slightly tart, berry-like quality that evolves into a cleaner, more floral heart. As it dries down, it leaves a subtle woody-herbaceous trail that blends well with other green notes. The overall effect is like walking through an orchard after rain – dewy, slightly tart, and alive with vegetative energy.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Cyclopentene-1-acetic acid, ethyl ester belongs to the class of cyclic unsaturated esters. While not found in nature, it’s synthesized through esterification reactions of cyclopentene derivatives. The molecule features a cyclopentene ring with an acetic acid ethyl ester side chain, creating its distinctive green-fruity odor profile. Its reactivity is typical of unsaturated esters, making it useful for creating more complex fragrance molecules through additional chemical modifications.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Green-fruity modifier
Functional Fragrance0.1-1%Up to 3%Freshness booster

Classic Accords

Tip: Use as a bridge between citrus top notes and floral heart notes in fresh compositions.

Alternatives & Comparisons

1
Ethyl-2-methyl-2-pentenoate CAS 39255-32-8

Offers similar green-fruity character with more pronounced apple-like tones.

2
Hexyl acetate CAS 142-92-7

Provides a cleaner fruity note when less green character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions currently apply to this material.

RIFM Assessment

No RIFM safety assessment currently available for this material.

Sustainability

As a synthetic material, this ester has minimal environmental impact in production. Being petroleum-derived, its sustainability depends on the energy sources used in manufacturing. Future green chemistry approaches could improve its ecological profile through bio-based feedstocks or more efficient synthesis routes.

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References

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

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