Amylcyclohexyl acetate (mixed isomers) (CAS 67874-72-0) — Sweet Top to middle Note Fragrance Ingredient

Sweet · Floral

Amylcyclohexyl acetate (mixed isomers)

CAS 67874-72-0

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

What Is Amylcyclohexyl acetate (mixed isomers)?

Amylcyclohexyl acetate is a synthetic fragrance ingredient used in perfumes and scented products. It’s found in air fresheners, cleaning products, and some personal care items. This versatile material helps create fresh, fruity-floral notes that blend well with other fragrance components.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns at typical usage levels
Potential skin sensitizer at high concentrations
CAS
67874-72-0
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does Amylcyclohexyl acetate (mixed isomers) Smell Like?

Amylcyclohexyl acetate presents a bright, fruity opening reminiscent of ripe pears and apples with a subtle floral undertone. As it evolves, the scent reveals a clean, slightly woody character that adds depth without heaviness. The dry-down is soft and persistent, leaving a fresh impression that works particularly well in modern floral and fruity compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Dynamisante(Clarins, 1987)

Used here for its fresh fruity character that complements the citrus and herbal notes, adding brightness without overpowering the delicate balance.

Green Tea(Elizabeth Arden, 1999)

Provides subtle fruity-floral nuances that enhance the tea accord, creating a refreshing yet sophisticated effect.

Layer 2

2D Molecular Structure

2-(2-Methylbutan-2-yl)cyclohexyl acetate

SMILES: CCC(C)(C)C1CCCCC1OC(C)=O

Chemistry, Properties & Perfumer Guide

The Chemistry

Amylcyclohexyl acetate belongs to the ester class of fragrance compounds. While not found in nature, it’s synthesized through esterification reactions between cyclohexanol derivatives and acetic acid. The mixed isomers contribute to its complex olfactory profile. Its molecular structure allows for good volatility and diffusion properties.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
SolubilitySoluble in alcohol and oils

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 10%Fresh fruity-floral modifier
Functional Fragrance0.5-3%Up to 5%Air fresheners and cleaning products

Classic Accords

Tip: Use to brighten floral compositions without adding excessive sweetness.

Alternatives & Comparisons

1
Hexyl acetate CAS 142-92-7

For a simpler fruity note with less floral character and higher volatility.

2
Cyclohexyl acetate CAS 622-45-7

When a more pronounced woody-floral character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA standards.

RIFM Assessment

Considered safe for use in fragrance applications at current levels.

Sustainability

As a synthetic material, amylcyclohexyl acetate doesn’t rely on natural resources. Its production can be optimized for minimal environmental impact through green chemistry principles.

Explore Amylcyclohexyl acetate (mixed isomers)

Browse essential oils and aroma compounds.

Browse on iHerb →

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

References

  1. Bauer, K. et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH.

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

Report a data error

Ingredient Data Sheet

CAS 67874-72-0

Physical Properties

Molecular Weight212.33 g/mol🔬 PubChem
LogP (Octanol-Water)4.1🔬 PubChem
Boiling Point251.9 °C🔬 EPA CompTox
Vapor Pressure0.0318 mmHg @ 25°C📊 OPERA
Flash Point99 °C🔬 EPA CompTox
Involatility Index0.0024💻 Calculated
log Kp (skin permeability)-1.084💻 Calculated
SMILESCCC(C)(C)C1CCCCC1OC(=O)C🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score3.3 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfloralsweet• leffingwell
Functional Groupsesterether💻 RDKit
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: DTXSID0044573

Physical Properties

Molecular Weight 212.333 g/mol🔬 EPA CompTox
Density 0.946 g/cm^3🔬 EPA CTX
Boiling Point 251.9 °C🔬 EPA CTX
Melting Point 4.652 °C📊 OPERA
Flash Point 99 °C🔬 EPA CTX
Refractive Index 1.453 Dimensionless📊 OPERA
Molar Volume 229.5 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 5.4 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 4.729 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.729 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.97 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.032 mmHg🔬 EPA CTX
Viscosity 4.929 cP📊 OPERA
Surface Tension 29.792 dyn/cm📊 OPERA
Thermal Conductivity 126.304 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 3 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 62.011 cm^3/mol📊 OPERA
Polarizability 24.583 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.

Similar Posts