3-tert-Butylcyclohexyl acetate (CAS 31846-06-07) — Woody Top to Middle Note Fragrance Ingredient

Woody · Floral

3-tert-Butylcyclohexyl acetate

CAS 31846-06-07

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

What Is 3-tert-Butylcyclohexyl acetate?

3-tert-Butylcyclohexyl acetate is a synthetic fragrance ingredient used in modern perfumery. It’s found in many fresh, woody, and masculine fragrances. This molecule matters because it adds a crisp, clean woody character with excellent diffusion, making it popular in body care products and fine fragrances aiming for a contemporary vibe.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in current IFRA guidelines
Limited toxicology data available
CAS
31846-06-07
Formula
Mixture
MW
Variable
Odor Family
Woody · Floral
Layer 1 · Enthusiast

What Does 3-tert-Butylcyclohexyl acetate Smell Like?

3-tert-Butylcyclohexyl acetate delivers a crisp, woody aroma with distinct freshness. Imagine freshly planed cedarwood with a sparkling ozonic edge – like walking through a lumberyard after rain. The acetate group lends a clean, slightly fruity nuance that prevents the woodiness from becoming heavy. It maintains excellent linearity throughout evaporation, making it reliable for functional perfumery. In dilution, it reveals subtle floral undertones reminiscent of magnolia petals.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Bleu de Chanel(Chanel, 2010)

Used as a woody-modifier in the heart, adding crispness to the incense-amber accord while enhancing the fragrance’s modern masculinity.

Dior Homme Sport(Dior, 2012)

Provides the clean woody backbone that supports the citrus top notes, creating a sporty yet sophisticated effect.

Acqua di Giò Profumo(Giorgio Armani, 2015)

Contributes to the marine-woody character, blending with patchouli and incense for a contemporary aquatic depth.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3-tert-Butylcyclohexyl acetate is a synthetic monoterpenoid derivative featuring a bulky tert-butyl group at the 3-position of a cyclohexyl ring. The acetate ester enhances volatility while moderating the woody character. Industrially produced via Friedel-Crafts alkylation of cyclohexene followed by acetylation, this molecule demonstrates how strategic substitution patterns can dramatically alter olfactory properties. The tert-butyl group creates significant steric hindrance, influencing both odor character and molecular interactions with olfactory receptors.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point≈230-240 °C (estimated)
Density≈0.92-0.94 g/cm³ (estimated)

Perfumer Guide

Note Position
Top to Middle
Volatility
Moderate (2-4 hours)
Blending
Very Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Woody-modifier in masculine accords
Body Care0.5-1.5%Up to 2%Fresh woody character in deodorants
Functional Products0.1-0.5%Up to 1%Clean background note

Classic Accords

Tip: Use with citrus top notes to prevent the woody character from becoming too heavy in the opening.

Alternatives & Comparisons

1
Verdox CAS 88-41-5

For a sharper, more diffusive woody note with green apple facets.

2
Isobornyl acetate CAS 125-12-2

When a softer, more traditional woody character is desired.

3
Cedryl acetate CAS 77-54-3

For deeper, longer-lasting woody notes with amber undertones.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No current IFRA restrictions. Listed as safe under IFRA 49th Amendment.

RIFM Assessment

Under review by RIFM; preliminary data suggests low sensitization potential.

Sustainability

As a fully synthetic material, 3-tert-Butylcyclohexyl acetate has minimal environmental impact in production compared to natural wood extracts. Its efficient synthesis from petrochemical feedstocks makes it a sustainable choice for woody notes, reducing pressure on forest resources. The molecule’s potency allows for low usage levels in formulations.

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References

  1. Brenna et al. (2002). Structure-Odor Relationships. Chemical Reviews. DOI: 10.1021/cr000664p
  2. IFRA Standards Library. 49th Amendment. IFRA 49th

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

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