Nopyl acetate (CAS 128-51-8) — Woody Middle Note Fragrance Ingredient

Woody · Green

Nopyl acetate

CAS 128-51-8

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

What Is Nopyl acetate?

Nopyl acetate is a synthetic fragrance ingredient used in perfumes and scented products. It contributes a fresh, woody aroma often found in masculine fragrances. This ester compound matters because it provides longevity and blending versatility, making it valuable for creating complex scent profiles that evolve beautifully on skin.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
Safe in regulated products
Check for individual sensitivity
CAS
128-51-8
Formula
Mixture
MW
Variable
Odor Family
Woody · Green
Layer 1 · Enthusiast

What Does Nopyl acetate Smell Like?

Nopyl acetate opens with a crisp, pine-like freshness reminiscent of crushed evergreen needles. The heart reveals subtle floral undertones wrapped in clean linen warmth. Dry-down showcases its true strength – a polished woody base with faintly sweet, almost vanillic whispers that linger close to skin. Imagine walking through a sunlit conifer forest where the air carries traces of blooming heather.

Scent Profile
Layer 2

2D Molecular Structure

2-(6,6-Dimethylbicyclo[3.1.1]hept-2-en-3-yl)ethyl acetate

SMILES: CC(=O)OCCC1=CC2CC(C1)C2(C)C

Chemistry, Properties & Perfumer Guide

The Chemistry

Nopyl acetate is a synthetic ester derived from nopol (a terpene alcohol) and acetic acid. Its molecular structure features a bicyclic framework that contributes to excellent stability and diffusion properties. Industrial synthesis typically involves acid-catalyzed esterification under controlled conditions. The compound lacks chirality but demonstrates stereospecific odor reception.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance2-5%Up to 10%Adds woody freshness
Functional Fragrance0.5-2%Up to 5%Fabric softeners, detergents

Classic Accords

Tip: Use with citrus top notes to prevent excessive sharpness in dry-down.

Alternatives & Comparisons

1
Isobornyl acetate CAS 125-12-2

Similar woody character but with more pronounced pine notes. Preferred for cleaner, more transparent effects.

2
Cedryl acetate CAS 77-54-3

Deeper woody profile with excellent fixation. Used when more substantial base support is needed.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions. Compliant under all current standards.

RIFM Assessment

RIFM assessment complete – no safety concerns at current usage levels.

Sustainability

As a synthetic material, nopyl acetate production avoids natural resource depletion. Modern manufacturing processes achieve high atom efficiency with minimal waste streams. The compound’s stability reduces environmental persistence compared to some natural terpenes.

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References

  1. PubChem Compound Summary for Nopyl acetate CID Not available

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

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Physicochemical Properties

DTXSID: DTXSID6051645

Physical Properties

Molecular Weight 208.301 g/mol🔬 EPA CompTox
Density 1.006 g/cm^3📊 OPERA
Boiling Point 253.476 °C📊 OPERA
Melting Point 56.786 °C📊 OPERA
Flash Point 96.378 °C📊 OPERA
Refractive Index 1.482 Dimensionless📊 OPERA
Molar Volume 208.981 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.062 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.062 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.062 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.56 Log10 unitless📊 OPERA
Water Solubility 0.001 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.012 mmHg📊 OPERA
Viscosity 5.98 cP📊 OPERA
Surface Tension 30.683 dyn/cm📊 OPERA
Thermal Conductivity 128.69 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 59.623 cm^3/mol📊 OPERA
Polarizability 23.636 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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