Butyl salicylate (CAS 2052-14-4) — Balsamic Middle Note Fragrance Ingredient

Balsamic · Woody

Butyl salicylate

CAS 2052-14-4

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

What Is Butyl salicylate?

Butyl salicylate is a synthetic fragrance ingredient commonly found in perfumes, soaps, and lotions. It contributes a warm, balsamic scent reminiscent of wintergreen with floral undertones. This versatile material helps create long-lasting fragrance bases and is valued for its ability to blend well with both floral and woody accords.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
IFRA compliant at standard usage levels
Potential skin sensitizer at high concentrations
CAS
2052-14-4
Formula
Mixture
MW
Variable
Odor Family
Balsamic · Woody
Layer 1 · Enthusiast

What Does Butyl salicylate Smell Like?

Butyl salicylate opens with a crisp, medicinal wintergreen top note that quickly mellows into a rounded balsamic heart. The drydown reveals a surprisingly floral character – imagine antique roses preserved in a cedar chest. Unlike methyl salicylate’s sharpness, butyl salicylate has a softer, more diffusive quality that lingers close to the skin like the memory of sun-warmed leather.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Shalimar(Guerlain, 1925)

Used as a balsamic bridge between citrus top notes and vanilla/tonka base. Provides warmth without overpowering the delicate bergamot.

Opium(YSL, 1977)

Amplifies the spice accord while tempering the clove’s sharpness. Creates a velvety texture in the oriental base.

Layer 2

2D Molecular Structure

Butyl salicylate

SMILES: CCCCOC(=O)C1=CC=CC=C1O

Chemistry, Properties & Perfumer Guide

The Chemistry

Butyl salicylate is an ester formed from salicylic acid and butanol. As a synthetic material, it’s typically produced via Fischer esterification. The butyl chain increases lipophilicity compared to methyl salicylate (XLogP ~3.5 vs ~2.5), contributing to its longer-lasting scent profile. While not found in nature, it shares structural similarities with plant-derived salicylates.

Physical & Chemical Properties

Boiling Point260-262 °C
Density1.07 g/cm³
Refractive Index1.510-1.513

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance1-3%Up to 5%Base modifier for oriental and fougère accords
Soap0.5-1%Up to 2%Provides lasting balsamic character

Classic Accords

+ Vanilla + Tonka = Oriental + Oakmoss + Coumarin = Fougère

Tip: Use to smooth harsh woody notes and add diffusion to heavy bases.

Alternatives & Comparisons

1
Benzyl salicylate CAS 118-58-1

More floral and less balsamic. Preferred when a softer, powdery effect is desired.

2
Isobutyl salicylate CAS 87-19-4

Brighter top note with similar longevity. Useful in citrus colognes.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No restrictions under IFRA 49th Amendment. Category 4 usage limit 3.8%.

EU Allergen Declaration

Not listed in EU allergen regulations.

GHS Classification

H315 Causes skin irritation H319 Causes serious eye irritation

RIFM Assessment

RIFM assessment complete. Safe at current usage levels.

Sustainability

Synthetic production avoids plant harvesting pressures. Esterification process has moderate environmental impact. Readily biodegradable (OECD 301D).

Explore Butyl salicylate

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. PubChem Compound Summary for Butyl salicylate CID 7184

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

Report a data error

Ingredient Data Sheet

CAS 2052-14-4

Physical Properties

Molecular Weight194.23 g/mol🔬 PubChem
LogP (Octanol-Water)4.6🔬 PubChem
Boiling Point271 °C🔬 EPA CompTox
Flash Point107 °C🔬 EPA CompTox
log Kp (skin permeability)-0.619💻 Calculated
SMILESCCCCOC(=O)C1=CC=CC=C1O🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated

Odor & Flavor

Primary Descriptorsbalsamicwoody• leffingwell
Functional Groupsesterphenoletheraromatic💻 RDKit
“odor, resembling Ethyl benzoate (but weaker) with a trace of Wintergreen note. Not as floral as iso-Butyl salicylate (next monograph). Not nearly as versatile as that ester, but quite powerful in compositions.”📖 Arctander
Butyl salicylate has a rough herbaceous chemical odor.📖 Fenaroli

Sensory Thresholds

Odor Detection Threshold0.007 ppm (n=3)📖 van Gemert
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: DTXSID8062153

Physical Properties

Molecular Weight 194.23 g/mol🔬 EPA CompTox
Density 1.075 g/cm^3🔬 EPA CTX
Boiling Point 271 °C🔬 EPA CTX
Melting Point -3.52 °C🔬 EPA CTX
Flash Point 107.05 °C🔬 EPA CTX
Refractive Index 1.526 Dimensionless📊 OPERA
Molar Volume 175.276 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.63 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 4.191 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.141 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 8.5 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.002 mmHg📊 OPERA
Viscosity 13.945 cP📊 OPERA
Surface Tension 39.876 dyn/cm📊 OPERA
Thermal Conductivity 146.175 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 46.53 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 4 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 53.806 cm^3/mol📊 OPERA
Polarizability 21.33 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