Phenethyl tiglate (CAS 55719-85-2) — Floral Top to middle Note Fragrance Ingredient

Floral · Sweet

Phenethyl tiglate

CAS 55719-85-2

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

What Is Phenethyl tiglate?

Phenethyl tiglate is a synthetic fragrance ingredient used in perfumes and personal care products. It adds a fruity, floral character reminiscent of roses with a hint of tropical fruit. You’ll encounter it in floral bouquets and fruity fragrances. This molecule matters because it bridges floral and fruity accords, offering perfumers a versatile tool for creating modern, complex scents. Its stability makes it valuable in formulations where longevity is desired.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Limited safety data available
CAS
55719-85-2
Formula
Mixture
MW
Variable
Odor Family
Floral · Sweet
Layer 1 · Enthusiast

What Does Phenethyl tiglate Smell Like?

Phenethyl tiglate unfolds with an initial burst of ripe pear and tropical fruit, quickly revealing a lush rose heart with hints of honeyed sweetness. As it evolves, the scent develops a velvety texture reminiscent of peach skin, settling into a soft floral-woody drydown. The fruity top notes persist longer than expected, creating an unusual bridge between fresh and voluptuous accords. Imagine biting into a perfectly ripe Bartlett pear while smelling a bouquet of dew-covered tea roses.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chance Eau Tendre(Chanel, 2010)

Used here to enhance the fruity-floral duality, adding pear-like freshness to the jasmine heart while maintaining Chanel’s signature polish.

La Vie Est Belle(Lancôme, 2012)

Contributes to the candied fruit opening, blending seamlessly with the iris and patchouli base for a modern gourmand-floral effect.

Layer 2

2D Molecular Structure

Phenethyl 2-methylcrotonate

SMILES: C\C=C(/C)C(=O)OCCC1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Phenethyl tiglate is an ester formed by the reaction of phenethyl alcohol with tiglic acid. This unsaturated ester belongs to the class of phenylpropanoids, though it’s produced synthetically. The trans-configuration of the tiglate moiety contributes to its distinctive fruity character. Industrial synthesis typically involves acid-catalyzed esterification under controlled conditions to prevent isomerization.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor Threshold0.01 ppm (estimated)

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Fruity-floral modifier
Body Care0.1-0.5%Up to 1%Adds sophistication to fruity notes

Classic Accords

+ Rose Absolute = Enhanced floralcy + Bergamot + Pear Ethyl Acetate = Sparkling fruity bouquet

Tip: Use with ionones to create pear-rose effects that transition smoothly into woody bases.

Alternatives & Comparisons

1
Phenethyl acetate CAS 103-45-7

For simpler rose-honey effects without the fruity complexity, though less tenacious.

2
Ethyl tiglate CAS 5837-78-5

When more pronounced fruity character is desired without the floral aspect.

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

Under evaluation by RIFM as of 2023.

Sustainability

As a synthetic material, phenethyl tiglate doesn’t require agricultural resources. Production typically uses petrochemical feedstocks, though bio-based routes are being explored. Its potency means relatively small quantities are needed in formulations.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials.

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

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Physicochemical Properties

DTXSID: DTXSID8047684

Physical Properties

Molecular Weight 204.269 g/mol🔬 EPA CompTox
Density 1.154 g/cm^3🔬 EPA CTX
Boiling Point 289.032 °C📊 OPERA
Melting Point 12.556 °C📊 OPERA
Flash Point 156.482 °C📊 OPERA
Refractive Index 1.513 Dimensionless📊 OPERA
Molar Volume 201.683 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.682 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.682 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.682 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 6.9 Log10 unitless📊 OPERA
Water Solubility 0.001 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.01 mmHg📊 OPERA
Surface Tension 35.487 dyn/cm📊 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 4 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 60.642 cm^3/mol📊 OPERA
Polarizability 24.04 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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