Ethyl p-tolyl carbonate (CAS 22719-81-9) — Floral Top to middle Note Fragrance Ingredient

Floral · Sweet

Ethyl p-tolyl carbonate

CAS 22719-81-9

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

What Is Ethyl p-tolyl carbonate?

Ethyl p-tolyl carbonate is a synthetic fragrance ingredient used to add subtle floral and fruity nuances to perfumes. It’s found in various personal care products and fine fragrances. This molecule matters because it helps create light, airy top notes that blend well with citrus and floral compositions, offering perfumers a versatile building block for modern accords.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns reported
Limited toxicity data available
CAS
22719-81-9
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Ethyl p-tolyl carbonate Smell Like?

Ethyl p-tolyl carbonate presents a delicate interplay of fruity-floral character with crisp green undertones. The initial impression suggests pear drops dipped in white flowers, evolving into a clean, slightly powdery heart reminiscent of fresh linen. The dry-down reveals a subtle musky warmth that lingers close to the skin. Its transparent quality makes it ideal for modern floral compositions where a lightweight, diffusive effect is desired.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Modern Muse(Estée Lauder, 2013)

Used as a brightening agent in the floral bouquet, adding lift to the jasmine and lily notes while preventing heaviness.

Light Blue(Dolce & Gabbana, 2001)

Contributes to the sparkling citrus-floral accord, enhancing the freshness without competing with the dominant lemon note.

Layer 2

2D Molecular Structure

Ethyl 4-Methylphenyl carbonate

SMILES: CCOC(=O)OC1=CC=C(C)C=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl p-tolyl carbonate belongs to the aromatic carbonate ester class, synthesized through the reaction of p-cresol with ethyl chloroformate. The p-tolyl group provides aromatic character while the carbonate linkage contributes stability. Its molecular structure allows for both hydrogen bonding and hydrophobic interactions, making it useful in fragrance longevity enhancement.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used as floral modifier
Personal Care0.1-1%Up to 2%Adds freshness to floral compositions

Classic Accords

Tip: Use as a bridge between citrus top notes and floral heart notes to enhance diffusion.

Alternatives & Comparisons

1
Phenethyl carbonate CAS 102-08-9

Offers similar floral effects with slightly more rosy character and better substantivity.

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

No RIFM assessment currently available for this material.

Sustainability

As a synthetic material, ethyl p-tolyl carbonate has minimal environmental impact during production. Its efficient synthesis from readily available precursors makes it a sustainable choice compared to some natural alternatives requiring extensive agricultural inputs.

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References

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

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

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Ingredient Data Sheet

CAS 22719-81-9

Physical Properties

Molecular Weight180.2 g/mol🔬 PubChem
LogP (Octanol-Water)2.9🔬 PubChem
Boiling Point234 °C🔬 EPA CompTox
Vapor Pressure0.0056 mmHg @ 25°C📊 OPERA
Flash Point102.3 °C🔬 EPA CompTox
Involatility Index0.0005💻 Calculated
log Kp (skin permeability)-1.74💻 Calculated
SMILESCCOC(=O)OC1=CC=C(C=C1)C🔬 PubChem

Volatility & Performance

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

Odor & Flavor

Primary Descriptorsfloralsweet• leffingwell
Functional Groupsetheraromatic💻 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: DTXSID9051878

Physical Properties

Molecular Weight 180.203 g/mol🔬 EPA CompTox
Density 1.09 g/cm^3📊 OPERA
Boiling Point 243.795 °C📊 OPERA
Melting Point 17.333 °C📊 OPERA
Flash Point 103.632 °C📊 OPERA
Refractive Index 1.499 Dimensionless📊 OPERA
Molar Volume 166.207 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.278 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.278 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.278 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.19 Log10 unitless📊 OPERA
Water Solubility 0.003 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.008 mmHg📊 OPERA
Viscosity 5.574 cP📊 OPERA
Surface Tension 33.655 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 35.53 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 2 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 48.797 cm^3/mol📊 OPERA
Polarizability 19.345 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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