4-Penten-1-one, 1-spiro[4.5]dec-6-en-7-yl- (CAS 224031-71-4) — Green Middle Note Fragrance Ingredient

Green · Woody

4-Penten-1-one, 1-spiro[4.5]dec-6-en-7-yl-

CAS 224031-71-4

Origin
synthetic
Note
Middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is 4-Penten-1-one, 1-spiro[4.5]dec-6-en-7-yl-?

4-Penten-1-one, 1-spiro[4.5]dec-6-en-7-yl- is a synthetic fragrance ingredient used in niche perfumery. It contributes unique woody-green notes with subtle fruity undertones. Encountered in avant-garde fragrances seeking unconventional aroma profiles. This molecule matters because it exemplifies modern perfumery’s ability to create entirely novel scent experiences through synthetic chemistry, expanding the perfumer’s palette beyond natural extracts.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Not currently IFRA restricted
Limited safety data available
CAS
224031-71-4
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 4-Penten-1-one, 1-spiro[4.5]dec-6-en-7-yl- Smell Like?

Opens with a sharp, almost metallic greenness reminiscent of crushed vine leaves, quickly revealing a paradoxical fruity-waxy character like unripe banana peel. The heart develops into a damp woody accord with hints of mushroom cellar and freshly cut pine. Dry-down leaves a faintly animalic muskiness that lingers close to skin.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

A spirocyclic ketone with complex stereochemistry. The spiro junction between cyclopentene and cyclohexenone rings creates constrained molecular geometry that influences odor perception. Synthesized through Robinson annulation variations, often starting from cyclopentanone derivatives. The pentenone side chain introduces additional reactivity sites for further functionalization.

Physical & Chemical Properties

Molecular Weight192.25 g/mol
XLogP2.8 (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Challenging
ApplicationTypical %RangeNotes
Conceptual Fragrances0.1-0.5%Up to 1%Used for avant-garde effects
Functional FragrancesNot usedN/AToo unconventional for mass market

Classic Accords

Tip: Use micro-doses with powerful fixatives to tame the green sharpness.

Alternatives & Comparisons

1
Spirogalbanone CAS 15501-74-3

More refined woody-spicy alternative when smoother profile needed.

2
Dihydroionone beta CAS 79-77-6

Fruitier alternative with better blending properties in floral compositions.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No current IFRA restrictions. Monitoring status due to limited toxicological data.

RIFM Assessment

Not yet evaluated by RIFM. Recommended for professional use only until full assessment.

Sustainability

Synthesized from petrochemical precursors using energy-intensive processes. No known natural sources. Being a novel synthetic, its environmental fate is poorly characterized. Recommended for minimal use until full lifecycle assessment available.

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References

  1. PubChem Compound Summary CID 22403171-4 PubChem

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

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