Cyclohexene, 3-methylene- (CAS 1888-90-0) — Green Top Note Fragrance Ingredient

Green · Woody

Cyclohexene, 3-methylene-

CAS 1888-90-0

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

What Is Cyclohexene, 3-methylene-?

Cyclohexene, 3-methylene- is a synthetic fragrance ingredient used in modern perfumery to create fresh, green, and slightly woody accords. You might encounter it in air fresheners and functional fragrances. While not as widely known as natural ingredients, it plays a crucial role in creating crisp, clean scent profiles that mimic outdoorsy freshness without relying on plant extracts.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns in current use
Limited toxicology data available
CAS
1888-90-0
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does Cyclohexene, 3-methylene- Smell Like?

This synthetic molecule delivers a sharp, piercing greenness reminiscent of snapped twigs and crushed leaves, with a subtle metallic edge. The initial burst evolves into a cleaner, more transparent woody character – like the scent left on hands after gardening with freshly oiled tools. Unlike natural materials, it maintains linearity without sweetening over time, making it ideal for functional fragrances requiring stability.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Vent Vert(Balmain, 1947)

Used in reformulations to replace galbanum, contributing to the iconic crushed-leaf effect without relying on natural variability. Provides the razor-sharp green top note that defines this classic.

Eau Dynamisante(Clarins, 1987)

Enhances the aromatic freshness in this functional fragrance, pairing with synthetic musks to create an invigorating, long-lasting green accord that survives frequent product use.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

As a simple cyclohexene derivative, 3-methylenecyclohexene belongs to the class of unsaturated alicyclic hydrocarbons. The molecule features a reactive exocyclic double bond that contributes to its sharp olfactory character. Industrially produced through acid-catalyzed reactions of cyclohexanol derivatives, its synthesis avoids the sustainability challenges of harvesting natural green materials like galbanum or violet leaf absolute.

Physical & Chemical Properties

AppearanceColorless liquid
Boiling PointApprox. 130-140°C (estimated)

Perfumer Guide

Note Position
Top
Volatility
High (30-90 min)
Blending
Good with synthetics
ApplicationTypical %RangeNotes
Functional Fragrances0.5-2%Up to 5%Provides clean green effects
Fine Fragrance0.1-0.5%Up to 1%Used as green modifier

Classic Accords

Tip: Stabilize with antioxidants if using in products containing bleach or other oxidizers.

Alternatives & Comparisons

1
Verdox CAS 88-41-5

More diffusive and less harsh green note with apple-like facets, suitable when a softer effect is desired without losing projection.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. No specific use limits established.

RIFM Assessment

Not currently evaluated by RIFM due to limited commercial use history.

Sustainability

As a purely synthetic material, production avoids agricultural land use and seasonal variability. However, as a petrochemical derivative, its environmental impact depends on manufacturing energy sources. Some producers are exploring bio-based routes using renewable feedstocks.

Explore Cyclohexene, 3-methylene-

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

  1. Arctander, S. (1969). Perfume and Flavor Chemicals. Montclair, NJ.

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

Report a data error

Similar Posts