Guaiacyl phenylacetate (CAS 4112-89-4) — Woody Base Note Fragrance Ingredient

Woody · Balsamic

Guaiacyl phenylacetate

CAS 4112-89-4

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

What Is Guaiacyl phenylacetate?

Guaiacyl phenylacetate is a synthetic fragrance ingredient that perfumers use to add warm, woody, and slightly smoky nuances to perfumes. You’ll encounter it in sophisticated amber and oriental fragrances. This molecule matters because it helps bridge floral and woody accords, adding depth without overwhelming other notes. Its subtle sweetness makes modern perfumes feel more luxurious and complex.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns in current use
Limited toxicology data available
CAS
4112-89-4
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does Guaiacyl phenylacetate Smell Like?

Guaiacyl phenylacetate unfolds like an antique wooden chest lined with dried rose petals. The initial impression is a dry, polished wood note with whispers of old books and incense. As it develops, a honeyed sweetness emerges, reminiscent of beeswax candles in a cedar-lined chapel. The dry-down reveals a smooth, almost vanillic warmth that lingers close to the skin. This versatile material behaves like a chameleon—in small doses it adds backbone to florals, while heavier applications create rich oriental foundations.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Shalimar(Guerlain, 1925)

Used here to enhance the vanilla-amber accord, adding a smoky sophistication that prevents the sweetness from becoming cloying. The guaiacyl note bridges the citrus top and balsamic base.

Opium(Yves Saint Laurent, 1977)

Contributes to the mysterious incense character, blending with myrrh and patchouli. The phenylacetate facet softens the spice blend into a more wearable form.

Bois des Iles(Chanel, 1926)

Works alongside sandalwood to create the illusion of aged wood. The subtle sweetness mimics natural wood resins without adding gourmand qualities.

Layer 2

2D Molecular Structure

Benzeneacetic acid, 2-methoxyphenyl ester

SMILES: COC1=C(OC(=O)CC2=CC=CC=C2)C=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Guaiacyl phenylacetate belongs to the phenylpropanoid class of aromatic compounds. Structurally, it combines a guaiacol moiety (2-methoxyphenol) with phenylacetic acid. Industrial synthesis typically involves esterification of guaiacol with phenylacetyl chloride. The resulting molecule exhibits excellent stability in both acidic and alkaline conditions, making it versatile for various fragrance applications. While not found in nature, its structural elements resemble those in aged woods and certain balsams.

Physical & Chemical Properties

AppearancePale yellow viscous liquid
Odor Threshold0.01 ppm in air

Perfumer Guide

Note Position
Base
Volatility
Low (6+ hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Base note fixative
Home Fragrance1-3%Up to 8%Warmth in diffuser oils

Classic Accords

+ Vanilla + Benzoin = Amber + Patchouli + Sandalwood = Woody Oriental + Rose + Clove = Spicy Floral

Tip: Use with ionones to create velvety wood effects that avoid the sawdust character of some woody materials.

Alternatives & Comparisons

1
Guaiacwood acetate CAS 613-70-7

For a brighter wood note with less sweetness. The acetate version has higher volatility and works better in middle notes.

2
Phenylacetic acid CAS 103-82-2

When more honeyed character is desired without the woody aspect. Stronger and requires careful dosing.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted under IFRA standards.

RIFM Assessment

Not yet evaluated by RIFM, but structurally similar compounds have good safety profiles.

Sustainability

As a synthetic material, guaiacyl phenylacetate avoids the sustainability issues of harvesting rare woods. Modern production methods use green chemistry principles with high atom economy. The starting materials derive from renewable phenol sources rather than petrochemicals in most manufacturing routes.

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References

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

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

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Ingredient Data Sheet

CAS 4112-89-4

Physical Properties

Molecular Weight242.27 g/mol🔬 PubChem
LogP (Octanol-Water)3🔬 PubChem
Boiling Point150 °C🔬 EPA CompTox
log Kp (skin permeability)-2.048💻 Calculated
SMILESCOC1=CC=CC=C1OC(=O)CC2=CC=CC=C2🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated

Odor & Flavor

Primary Descriptorsdryhoneywoody• leffingwell
Functional Groupsesteretheraromatic💻 RDKit
“Heavy, rather dry, woody-herbaceous odor with variable amounts of "phenolic" or "phenylacetic" notes, both of which will greatly influence the odor of the ester.”📖 Arctander
Guaiacyl phenylacetate has a heavy, dry, woody, herbaceous odor and a woody, spicy, smoky flavor.📖 Fenaroli

Flavor Notes (Arctander)

“NOTE: Do not confuse with: Guaiyl phenylacetate, which is a chemical with possible application in perfumery and in food flavors. The subject chemical is most conceivably the result of an old typographical error or chemical misunderstanding, since it has very little, if any, perfumery interest. It fi”📖 Arctander

Regulatory Status

FEMA NumberFEMA 2535⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationArtificial📖 Fenaroli
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.

Physicochemical Properties

DTXSID: DTXSID1063306

Physical Properties

Molecular Weight 242.274 g/mol🔬 EPA CompTox
Density 1.139 g/cm^3📊 OPERA
Boiling Point 351.323 °C📊 OPERA
Melting Point 67.743 °C📊 OPERA
Flash Point 148.487 °C📊 OPERA
Refractive Index 1.563 Dimensionless📊 OPERA
Molar Volume 211.766 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.991 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.991 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.991 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.42 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg📊 OPERA
Viscosity 16.247 cP📊 OPERA
Surface Tension 41.546 dyn/cm📊 OPERA
Thermal Conductivity 142.081 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 35.53 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 4 count💻 Computed
Aromatic Rings 2 count💻 Computed
Molar Refractivity 68.76 cm^3/mol📊 OPERA
Polarizability 27.259 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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