Benzyl laurate (CAS 140-25-0) — Floral Base Note Fragrance Ingredient

Floral · Musky

Benzyl laurate

CAS 140-25-0

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

What Is Benzyl laurate?

Benzyl laurate is a synthetic fragrance ingredient often used as a fixative in perfumes and personal care products. It helps other scents last longer on the skin. This ingredient matters because it adds subtle floral undertones while stabilizing more volatile fragrance components, creating longer-lasting scent experiences in everything from fine perfumes to body lotions.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No significant safety concerns
Patch test recommended for sensitive skin
CAS
140-25-0
Formula
Mixture
MW
Variable
Odor Family
Floral · Musky
Layer 1 · Enthusiast

What Does Benzyl laurate Smell Like?

Benzyl laurate offers a delicate, waxy-floral character with faint honeyed undertones. Its odor is subtle rather than dominant—imagine the ghost of a gardenia blossom wrapped in clean laundry musk. The fragrance stays close to the skin, evolving minimally over time but providing remarkable tenacity. As a base note, it acts like invisible scaffolding that helps brighter aromas maintain their structure for hours without calling attention to itself.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used as a stabilizing base that subtly amplifies the floral bouquet while preventing top notes from dissipating too quickly.

Shalimar(Guerlain, 1925)

Helps anchor the vanilla-oriental accord, adding just enough waxy texture to balance the sweetness.

Layer 2

2D Molecular Structure

Dodecanoic acid, phenylmethyl ester

SMILES: CCCCCCCCCCCC(=O)OCC1=CC=CC=C1

Chemistry, Properties & Perfumer Guide

The Chemistry

Benzyl laurate is an ester formed by the condensation of benzyl alcohol and lauric acid. As a synthetic ingredient, it’s typically produced through acid-catalyzed esterification. The molecule lacks chirality, making its synthesis straightforward without stereochemical considerations. Its twelve-carbon laurate chain provides excellent lipid solubility, while the benzyl group contributes mild aromatic character. This combination creates a molecule that’s both stable and effective at modulating fragrance volatility.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~300 °C (estimated)
Density~0.95 g/cm³ (estimated)

Perfumer Guide

Note Position
Base
Volatility
Very low (hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Fixative for floral compositions
Body Lotions0.5-2%Up to 3%Enhances fragrance longevity

Classic Accords

+ Vanilla + Benzoin = Creamy oriental + Rose absolute + Sandalwood = Velvety floral

Tip: Use to extend the life of citrus top notes without weighing them down.

Alternatives & Comparisons

1
Benzyl benzoate CAS 120-51-4

More aromatic with less waxiness; better for amplifying floral character rather than stabilizing.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards.

RIFM Assessment

Considered safe as used in current fragrance practices according to RIFM.

Sustainability

As a synthetic ingredient, benzyl laurate avoids agricultural resource demands. Its production from petrochemical precursors raises some environmental concerns, but its efficiency as a fixative means less material is needed overall compared to some natural alternatives.

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References

  1. Benzyl Laurate – Cosmetic Ingredient Review CIR Assessment

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

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Ingredient Data Sheet

CAS 140-25-0

Physical Properties

Molecular Weight290.4 g/mol🔬 PubChem
LogP (Octanol-Water)6.8🔬 PubChem
Boiling Point352 °C🔬 EPA CompTox
Vapor Pressure0 mmHg @ 25°C📊 OPERA
Flash Point109 °C🔬 EPA CompTox
log Kp (skin permeability)0.357💻 Calculated
SMILESCCCCCCCCCCCC(=O)OCC1=CC=CC=C1🔬 PubChem

Volatility & Performance

Fragrance NoteBase💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score17.4 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsfatty• leffingwell
Functional Groupsesteretheraromatic💻 RDKit
“Very faint, fatty odor. Probably odorless to most people when this ester is absolutely pure.”📖 Arctander
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: DTXSID7059692

Physical Properties

Molecular Weight 290.447 g/mol🔬 EPA CompTox
Density 0.937 g/cm^3📊 OPERA
Boiling Point 369.392 °C📊 OPERA
Melting Point 8.5 °C🔬 EPA CTX
Flash Point 132.713 °C📊 OPERA
Refractive Index 1.488 Dimensionless📊 OPERA
Molar Volume 307.307 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 7.019 Log10 unitless📊 OPERA
LogD (pH 5.5) 7.019 Log10 unitless📊 OPERA
LogD (pH 7.4) 7.019 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.84 Log10 unitless📊 OPERA
Water Solubility 0 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg📊 OPERA
Viscosity 12.395 cP📊 OPERA
Surface Tension 33.58 dyn/cm📊 OPERA
Thermal Conductivity 146.329 mW/(m*K)📊 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 12 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 88.538 cm^3/mol📊 OPERA
Polarizability 35.099 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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