3(or 4)-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde (CAS 130066-44-3) — Floral Middle Note Fragrance Ingredient

Floral · Woody

3(or 4)-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde

CAS 130066-44-3

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

What Is 3(or 4)-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde?

3(or 4)-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde is a synthetic fragrance ingredient used in modern perfumery. It’s found in various personal care products and fine fragrances, contributing to complex scent profiles. This aldehyde is valued for its ability to enhance floral and woody accords while adding diffusion and longevity to fragrance compositions.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA approved for use
Potential sensitizer – requires careful dosing
CAS
130066-44-3
Formula
Mixture
MW
Variable
Odor Family
Floral · Woody
Layer 1 · Enthusiast

What Does 3(or 4)-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde Smell Like?

This aldehyde presents a sophisticated bouquet that evolves intriguingly on the skin. Initially, it offers a fresh, slightly citrus-tinged greenness reminiscent of crushed leaves, which quickly melds into a floral heart with lily-of-the-valley nuances. The dry-down reveals its true character – a warm, woody-ambery base with subtle musk undertones that provide excellent tenacity. The overall effect is clean yet complex, with a radiant quality that lifts compositions without overpowering them.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

This synthetic aldehyde belongs to the cyclohexene carboxaldehyde class, specifically designed for perfumery applications. The molecule features both aldehyde and hydroxyl functional groups attached to a cyclohexene ring system, creating unique odor properties. Industrial synthesis typically involves multi-step processes including Diels-Alder reactions and selective hydrogenation. The 4-hydroxy-4-methylpentyl side chain contributes significantly to the molecule’s diffusion and substantivity.

Physical & Chemical Properties

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used as floral-woody modifier
Personal Care0.1-0.5%Up to 1%Provides clean, fresh character

Classic Accords

Tip: Use in conjunction with ionones to enhance floralcy without excessive sweetness.

Alternatives & Comparisons

1
Lyral CAS 31906-04-4

Similar floral-lily character but with greater diffusion and slightly sweeter profile.

2
Hydroxycitronellal CAS 107-75-5

Classic floral aldehyde with more pronounced citrus-lily aspects.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions under current IFRA standards (Amendment 49).

RIFM Assessment

RIFM safety assessment completed – approved for use at recommended levels.

Sustainability

As a synthetic material, this ingredient avoids natural resource depletion concerns. Modern manufacturing processes aim to minimize environmental impact through efficient catalysis and waste reduction. The molecule’s substantivity helps reduce overall fragrance load in products.

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References

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

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    Ingredient Data Sheet

    CAS 130066-44-3
    Data Sources & Attribution
    Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

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