Methyl beta-phenylglycidate (CAS 37161-74-3) — Sweet Heart Note Fragrance Ingredient

Sweet · Balsamic

Methyl beta-phenylglycidate

CAS 37161-74-3

Origin
synthetic
Note
Heart
IFRA
Use with awareness
Data as of: Apr 2026

What Is Methyl beta-phenylglycidate?

Methyl beta-phenylglycidate is a synthetic fragrance ingredient that creates a sweet, fruity aroma reminiscent of strawberries. You’ll encounter it in berry-flavored candies, fruity perfumes, and some gourmand fragrances. This molecule matters because it delivers an intense, photorealistic strawberry note that’s more stable than natural extracts, allowing consistent performance in various products.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for food and fragrance use
Moderate skin sensitization potential
CAS
37161-74-3
Formula
Mixture
MW
Variable
Odor Family
Sweet · Balsamic
Layer 1 · Enthusiast

What Does Methyl beta-phenylglycidate Smell Like?

Methyl beta-phenylglycidate bursts with an ultra-concentrated strawberry jam aroma – think reduced berry syrup with caramelized sugar edges. The top note has a bright, almost effervescent quality like carbonated strawberry soda. As it evolves, the sweetness deepens into a velvety compote character with hints of vanilla and rosewater. The dry-down reveals a subtle green nuance, like strawberry leaves crushed between fingers, adding dimensionality to what could otherwise be a one-dimensional candy note.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

This photorealistic fragrance uses methyl beta-phenylglycidate as its core note to replicate sun-warmed strawberries with uncanny accuracy, boosted by trace gamma-decalactone for creaminess.

La Vie est Belle(Lancôme, 2012)

Used sparingly here to add jammy fruitiness to the vanilla-orchid heart, creating a gourmand floral effect without descending into candy-like sweetness.

Layer 2

2D Molecular Structure

Methyl 3-phenyloxirane-2-carboxylate

SMILES: COC(=O)C1OC1C1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Methyl beta-phenylglycidate belongs to the glycidate ester class, synthesized through epoxidation of methyl cinnamate followed by hydrolysis. The beta-phenyl substitution creates exceptional odor potency – detectable at 5 ppb. While chiral centers exist, commercial material is typically racemic. Its stability comes from the epoxide ring which resists hydrolysis better than simple esters, making it valuable for soap and detergent formulations where longevity matters.

Physical & Chemical Properties

Boiling Point285 °C (estimated)
Density1.12 g/cm³ (estimated)

Perfumer Guide

Note Position
Heart
Volatility
Medium (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Powerful modifier for fruity accords
Functional Fragrance0.1-0.5%Up to 1%Strawberry note in soaps/detergents

Classic Accords

Tip: Balance with green notes (stemone) to prevent cloying sweetness in high concentrations.

Alternatives & Comparisons

1
Ethyl Methylphenylglycidate CAS 77-83-8

The ethyl ester version with slightly more candied character, preferred when brighter top notes are needed.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions (as of Amendment 49).

GHS Classification

H315 Skin irritation

RIFM Assessment

RIFM assessment confirms safe use at current industry levels.

Sustainability

As a synthetic material, production avoids agricultural land use. Modern manufacturing routes minimize solvent waste through catalytic processes. Being highly potent reduces transportation footprint per odor unit compared to natural extracts.

Explore Methyl beta-phenylglycidate

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 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: DTXSID80865851

Physical Properties

Molecular Weight 178.187 g/mol🔬 EPA CompTox
Density 1.187 g/cm^3📊 OPERA
Boiling Point 239.992 °C📊 OPERA
Melting Point 25.569 °C📊 OPERA
Flash Point 106.579 °C📊 OPERA
Refractive Index 1.546 Dimensionless📊 OPERA
Molar Volume 146.079 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.703 Log10 unitless📊 OPERA
LogD (pH 5.5) 1.703 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.703 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.86 Log10 unitless📊 OPERA
Water Solubility 0.029 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.009 mmHg📊 OPERA
Viscosity 5.215 cP📊 OPERA
Surface Tension 43.966 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 38.83 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 46.223 cm^3/mol📊 OPERA
Polarizability 18.324 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