2-Phenoxyethyl propionate (CAS 23495-12-7) — Floral Middle Note Fragrance Ingredient

Floral · Sweet

2-Phenoxyethyl propionate

CAS 23495-12-7

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

What Is 2-Phenoxyethyl propionate?

2-Phenoxyethyl propionate is a synthetic fragrance ingredient used in perfumes and personal care products. It contributes fresh, floral, and slightly fruity nuances to compositions. You’ll encounter it in fine fragrances, body lotions, and air fresheners where it adds brightness and lift. This ester compound matters because it offers perfumers a versatile building block that blends well with other ingredients while providing good stability in formulations.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Stable in formulations
CAS
23495-12-7
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does 2-Phenoxyethyl propionate Smell Like?

2-Phenoxyethyl propionate opens with a crisp, slightly green floral character reminiscent of crushed rose stems with a hint of pear skin. The heart develops into a soft, powdery floralcy akin to violet petals dusted with icing sugar. As it dries down, it reveals a clean muskiness with whispers of fresh linen. The overall effect is airy and transparent – like sunlight filtering through a floral bouquet wrapped in tissue paper.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Clean Reserve Skin(Clean, 2017)

Used here for its soft musky-floral character that enhances the fragrance’s ‘your skin but better’ concept. Provides subtle lift without overpowering the warm amber base.

Glossier You(Glossier, 2017)

Contributes to the fragrance’s signature ‘amorphous’ floral quality, blending seamlessly with iris and ambroxan to create an intimate skin scent.

Layer 2

2D Molecular Structure

2-Phenoxyethyl propanoate

SMILES: CCC(=O)OCCOC1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Phenoxyethyl propionate is an ester formed from phenoxyethanol and propionic acid. As a synthetic molecule, it doesn’t occur naturally. Industrial synthesis typically involves direct esterification of phenoxyethanol with propionic acid under acidic conditions. The ester linkage gives the molecule moderate polarity while the aromatic ring contributes stability. Its balanced structure allows both hydrophilic and hydrophobic interactions in fragrance systems.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~250 °C (estimated)
Density~1.05 g/cm³ (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Very good
ApplicationTypical %RangeNotes
Fine Fragrance1-5%Up to 8%Floral-musk modifier
Body Care0.5-3%Up to 5%Softening agent
Home Fragrance2-7%Up to 10%Diffusive floral note

Classic Accords

Tip: Use to soften harsh floral notes and add diffusion to musky compositions.

Alternatives & Comparisons

1
Phenoxyethyl isobutyrate CAS 103-60-6

Offers similar floral character with more fruity nuances. Slightly more diffusive but less tenacious.

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

Considered safe for current usage levels based on RIFM data.

Sustainability

As a synthetic material, 2-Phenoxyethyl propionate has minimal environmental impact from sourcing. Production typically uses green chemistry principles with high atom economy. Offers consistent quality without natural variation or agricultural resource demands.

Explore 2-Phenoxyethyl propionate

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

Physicochemical Properties

DTXSID: DTXSID9047203

Physical Properties

Molecular Weight 194.23 g/mol🔬 EPA CompTox
Density 1.059 g/cm^3📊 OPERA
Boiling Point 260.719 °C📊 OPERA
Melting Point 51.145 °C📊 OPERA
Flash Point 109.104 °C📊 OPERA
Refractive Index 1.494 Dimensionless📊 OPERA
Molar Volume 182.945 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.302 Log10 unitless📊 OPERA
LogD (pH 5.5) 2.302 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.302 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.08 Log10 unitless📊 OPERA
Water Solubility 0.006 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.005 mmHg📊 OPERA
Viscosity 3.918 cP📊 OPERA
Surface Tension 35.818 dyn/cm📊 OPERA
Thermal Conductivity 149.628 mW/(m*K)📊 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 5 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 53.238 cm^3/mol📊 OPERA
Polarizability 21.105 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