1-Cyclopropylmethyl-4-methoxybenzene (CAS 16510-27-3) — Woody Middle Note Fragrance Ingredient

Woody · Green

1-Cyclopropylmethyl-4-methoxybenzene

CAS 16510-27-3

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

What Is 1-Cyclopropylmethyl-4-methoxybenzene?

1-Cyclopropylmethyl-4-methoxybenzene is a synthetic fragrance ingredient used in modern perfumery. It’s found in niche and experimental fragrances, often as a modifier for aromatic compositions. This molecule matters because it offers perfumers a unique aromatic profile that bridges herbal and woody notes, creating depth in contemporary scent designs.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns reported
Limited toxicological data available
CAS
16510-27-3
Formula
Mixture
MW
Variable
Odor Family
Woody · Green
Layer 1 · Enthusiast

What Does 1-Cyclopropylmethyl-4-methoxybenzene Smell Like?

1-Cyclopropylmethyl-4-methoxybenzene presents a crisp, aromatic opening with a herbal-woody character reminiscent of crushed eucalyptus leaves and fresh pine needles. The initial sharpness mellows into a warm, slightly sweet heart note with subtle spicy undertones. In dry-down, it reveals a clean, almost camphoraceous quality that blends well with woody bases. The overall effect is reminiscent of a sun-warmed herb garden with a modern, slightly metallic edge.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Experimental No. 27(Synthetic Perfumery Lab, 2021)

Used as a structural element to create an avant-garde aromatic foundation, lending both freshness and depth to this conceptual fragrance.

Wood Resonance(Modernist Scents, 2019)

Provides a crisp counterpoint to sandalwood and vetiver, adding dimension to the woody accord without overwhelming the composition.

Layer 2

2D Molecular Structure

1-(Cyclopropylmethyl)-4-methoxybenzene

SMILES: COC1=CC=C(CC2CC2)C=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

1-Cyclopropylmethyl-4-methoxybenzene belongs to the class of aromatic ethers, specifically a methoxybenzene derivative with a cyclopropylmethyl substituent. The molecule features a benzene ring with methoxy group at the para position and a cyclopropylmethyl group at the opposite position. Synthesis typically involves Williamson ether synthesis or Friedel-Crafts alkylation of anisole. The cyclopropyl ring introduces steric constraints that influence both the molecule’s volatility and odor characteristics.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Molecular Weight162.23 g/mol

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Used as aromatic modifier
Functional Fragrance0.5-2%Up to 3%Adds freshness to cleaning products

Classic Accords

Tip: Use sparingly in woody compositions to add lift without dominating the blend.

Alternatives & Comparisons

1
1-Methoxy-4-(2-methylpropyl)benzene CAS 104-46-1

Anisic floral alternative with similar aromatic properties but sweeter profile.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA.

RIFM Assessment

No RIFM assessment found for this specific compound.

Sustainability

As a synthetic material, 1-Cyclopropylmethyl-4-methoxybenzene has minimal environmental impact in production compared to natural extracts. Its efficient synthesis reduces resource consumption, though like all synthetic aromatics, petrochemical feedstocks are typically required. The material’s potency allows for low usage levels, further reducing environmental burden.

Explore 1-Cyclopropylmethyl-4-methoxybenzene

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.

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

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Physicochemical Properties

DTXSID: DTXSID1051773

Physical Properties

Molecular Weight 162.232 g/mol🔬 EPA CompTox
Density 0.99 g/cm^3🔬 EPA CTX
Boiling Point 234.85 °C🔬 EPA CTX
Melting Point -23.15 °C🔬 EPA CTX
Flash Point 113 °C🔬 EPA CTX
Refractive Index 1.552 Dimensionless📊 OPERA
Molar Volume 155.543 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.698 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.698 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.698 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.8 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 4.426 cP📊 OPERA
Surface Tension 35.81 dyn/cm📊 OPERA
Thermal Conductivity 129.412 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 9.23 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 3 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 49.68 cm^3/mol📊 OPERA
Polarizability 19.695 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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