4-tert-Butylcyclohexyl acetate (CAS 32210-23-4) — Woody Top to middle Note Fragrance Ingredient

Woody · Floral

4-tert-Butylcyclohexyl acetate

CAS 32210-23-4

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

What Is 4-tert-Butylcyclohexyl acetate?

4-tert-Butylcyclohexyl acetate is a synthetic fragrance ingredient commonly found in perfumes, body sprays, and household products. It contributes a fresh, woody aroma that enhances many modern fragrance compositions. This versatile molecule is valued for its ability to add clean, crisp notes that blend well with both floral and woody accords, making it a popular choice for fresh and masculine scents.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Check for skin sensitivity
CAS
32210-23-4
Formula
Mixture
MW
Variable
Odor Family
Woody · Floral
Layer 1 · Enthusiast

What Does 4-tert-Butylcyclohexyl acetate Smell Like?

4-tert-Butylcyclohexyl acetate opens with a crisp, clean woody note reminiscent of freshly cut cedar planks. As it evolves, it reveals a subtle floral undertone, like a whisper of lily-of-the-valley in a forest clearing. The dry-down is smooth and slightly musky, leaving a lingering impression of well-worn leather and polished wood. Its character is both sophisticated and approachable, making it a versatile building block in modern perfumery.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cool Water(Davidoff, 1988)

Used to enhance the fresh, aquatic character with its clean woody notes, providing a modern alternative to traditional woody ingredients.

L'Eau d'Issey(Issey Miyake, 1992)

Contributes to the crisp, transparent quality of this iconic aquatic fragrance, blending seamlessly with floral and citrus notes.

Acqua di Giò(Giorgio Armani, 1996)

Adds a refined woody freshness that complements the marine and citrus elements in this bestselling masculine scent.

Light Blue(Dolce & Gabbana, 2001)

Provides clean woody support to the bright citrus and floral heart, enhancing the fragrance’s daytime wearability.

Bleu de Chanel(Chanel, 2010)

Used in the woody-ambery base to create a polished, contemporary masculine character.

Layer 2

2D Molecular Structure

4-tert-Butylcyclohexyl acetate

SMILES: CC(=O)OC1CCC(CC1)C(C)(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

4-tert-Butylcyclohexyl acetate is a synthetic ester derived from the acetylation of 4-tert-butylcyclohexanol. The molecule features a cyclohexane ring with a bulky tert-butyl group at the 4-position and an acetate ester at the 1-position. This structure creates a balance between volatility and substantivity, making it useful as a top-to-middle note. The tert-butyl group introduces steric hindrance that influences both the odor character and the molecule’s resistance to hydrolysis compared to simpler cyclohexyl esters.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointApprox. 250-260 °C
Density~0.92 g/cm³
Refractive Index~1.45
SolubilityInsoluble in water, soluble in alcohol and oils

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Fresh woody modifier
Body Care0.5-2%Up to 3%Clean, fresh notes
Household0.1-1%Up to 2%Laundry fresh effect
Functional0.05-0.5%Up to 1%Masking agent

Classic Accords

Tip: Use with citrus top notes to extend their freshness into the heart phase.

Alternatives & Comparisons

1
Vertenex CAS 32210-23-4

Similar woody character but with more pronounced floral aspects and better diffusion.

2
Isobornyl acetate CAS 125-12-2

More piney and less refined, suitable for more rustic woody compositions.

3
Cedryl acetate CAS 77-54-3

Deeper, more ambery woody note with longer persistence.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards (as of 49th Amendment).

RIFM Assessment

Considered safe for use in fragrance by RIFM based on current data.

Sustainability

As a synthetic material, 4-tert-Butylcyclohexyl acetate has minimal environmental impact in production compared to some natural alternatives. Its synthesis from petrochemical feedstocks is energy efficient, and it doesn’t require agricultural land or contribute to deforestation. The material’s stability contributes to fragrance longevity, potentially reducing the need for reapplication and overall product consumption.

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References

  1. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Allured.
  3. IFRA Standards Library IFRA 49th Amendment

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

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Ingredient Data Sheet

CAS 32210-23-4

Physical Properties

Molecular Weight198.3 g/mol🔬 PubChem
LogP (Octanol-Water)3.4🔬 PubChem
Boiling Point243 °C🔬 EPA CompTox
Vapor Pressure0.0075 mmHg @ 25°C📊 OPERA
Flash Point104 °C🔬 EPA CompTox
Involatility Index0.0006💻 Calculated
log Kp (skin permeability)-1.496💻 Calculated
SMILESCC(=O)OC1CCC(CC1)C(C)(C)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score4.2 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfloralorriswoody• leffingwell
Functional Groupsesterether💻 RDKit

Sensory Thresholds

Odor Detection Threshold0.0244 ppm (n=2)📖 van Gemert
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: DTXSID1027974

Physical Properties

Molecular Weight 198.306 g/mol🔬 EPA CompTox
Density 0.936 g/cm^3🔬 EPA CTX
Boiling Point 243 °C🔬 EPA CTX
Melting Point -50 °C🔬 EPA CTX
Flash Point 104 °C🔬 EPA CTX
Refractive Index 1.451 Dimensionless📊 OPERA
Molar Volume 213.127 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.8 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 4.629 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.629 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.84 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.008 mmHg🔬 EPA CTX
Viscosity 3.356 cP📊 OPERA
Surface Tension 29.597 dyn/cm📊 OPERA
Thermal Conductivity 123.356 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 26.3 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 2 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 57.38 cm^3/mol📊 OPERA
Polarizability 22.747 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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