4′-Hydroxy-3′-methoxyacetophenone (CAS 0498-02-02) — Woody Middle Note Fragrance Ingredient

Woody · Spicy

4'-Hydroxy-3'-methoxyacetophenone

CAS 0498-02-02

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

What Is 4'-Hydroxy-3'-methoxyacetophenone?

4′-Hydroxy-3′-methoxyacetophenone is a synthetic fragrance ingredient used in perfumery. It’s not commonly encountered in everyday products but appears in niche fragrances. This molecule contributes to complex scent profiles, often adding depth to woody or spicy compositions.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
No major restrictions
Limited safety data available
CAS
0498-02-02
Formula
Mixture
MW
Variable
Odor Family
Woody · Spicy
Layer 1 · Enthusiast

What Does 4'-Hydroxy-3'-methoxyacetophenone Smell Like?

This synthetic molecule presents a warm, slightly phenolic character with subtle vanilla undertones. The initial impression is medicinal-aromatic, evolving into a dry woody-spicy heart. In drydown, it reveals faint smoky facets reminiscent of guaiacol derivatives. The overall profile is moderately tenacious with a clean, modern edge that works well in contemporary woody compositions.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

4′-Hydroxy-3′-methoxyacetophenone belongs to the acetophenone class, specifically a methoxy-substituted derivative. It’s synthesized through Friedel-Crafts acylation of guaiacol derivatives. The molecule features a phenolic hydroxyl group and methoxy substitution pattern that influences its polarity and odor characteristics. While not chiral itself, its synthesis may involve chiral intermediates in some routes.

Physical & Chemical Properties

Boiling PointNot available
Melting PointNot available

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used as woody-spicy modifier
Functional Fragrance0.1-1%Up to 3%For masculine accords

Classic Accords

Tip: Use in trace amounts to add phenolic complexity without overwhelming the composition.

Alternatives & Comparisons

1
Acetovanillone CAS 498-02-2

Similar structure with slightly softer profile, better solubility in alcohol bases.

2
Guaiacol CAS 90-05-1

More phenolic and medicinal, for stronger smoky effects.

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

Limited safety assessment available. Considered safe at current usage levels.

Sustainability

As a synthetic material, this compound is produced through controlled chemical processes with minimal environmental impact. Being petroleum-derived, its sustainability depends on the manufacturer’s energy sources and waste management practices. No known ecological concerns at typical usage levels.

Explore 4'-Hydroxy-3'-methoxyacetophenone

Browse essential oils and aroma compounds.

Browse on iHerb →

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

References

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

    Report a data error

    Similar Posts