Butyl anthranilate (CAS 7756-96-9) — Sweet Middle Note Fragrance Ingredient

Sweet · Floral

Butyl anthranilate

CAS 7756-96-9

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

What Is Butyl anthranilate?

Butyl anthranilate is a synthetic fragrance ingredient with a sweet, grape-like aroma. You’ll encounter it in fruity perfumes, body care products, and occasionally in food flavorings. This versatile material bridges fruity and floral accords, adding a subtle sparkle that enhances berry and tropical fruit compositions while providing excellent diffusion.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions in perfumery
Potential mild skin sensitivity
CAS
7756-96-9
Formula
Mixture
MW
Variable
Odor Family
Sweet · Floral
Layer 1 · Enthusiast

What Does Butyl anthranilate Smell Like?

Butyl anthranilate bursts with an initial juicy concord grape impression, like biting into ripe purple grapes warmed by sunlight. The top note carries a faint metallic edge that quickly mellows into a candied floralcy reminiscent of orange blossom honey. As it dries, it reveals a smooth, almost creamy base with whispers of vanilla and a clean muskiness. Its moderate tenacity (4-6 hours) makes it ideal for brightening floral bouquets without overwhelming delicate notes.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Angel(Mugler, 1992)

Used as a fruity-floral bridge between the ethyl maltol caramel and patchouli base, contributing to the scent’s legendary ‘dark berries’ accord.

Light Blue(Dolce & Gabbana, 2001)

Provides subtle grapefruit enhancement in the citrus top while supporting the apple-pear heart notes with juicy realism.

Black Opium(YSL, 2014)

Works synergistically with vanilla and coffee notes to create a narcotic berry-like effect in the fragrance’s addictive drydown.

Layer 2

2D Molecular Structure

Butyl anthranilate

SMILES: CCCCOC(=O)C1=CC=CC=C1N

Chemistry, Properties & Perfumer Guide

The Chemistry

Butyl anthranilate is an ester formed from anthranilic acid and butanol. As a synthetic material, it’s typically produced via Fischer esterification under acidic conditions. The molecule’s planar aromatic ring contributes to its diffusion properties, while the butyl chain provides excellent solubility in both oil and alcohol bases. Unlike some fruity esters, it exhibits remarkable stability across pH ranges, making it suitable for soap and detergent applications.

Physical & Chemical Properties

Boiling Point~300 °C (estimated)
Density~1.05 g/cm³ (estimated)
Vapor PressureLow (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Excellent
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Fruity-floral modifier
Soap/Detergent0.1-0.5%Up to 1%Stable in alkaline systems
Candles1-3%Up to 4%Good heat stability

Classic Accords

+ Bergamot + Hedione = Sparkling citrus + Vanillin + Ethyl Maltol = Gourmand berries + Rose Oxide + Galaxolide = Dewy floral

Tip: Use at 0.2-0.8% to add naturalistic fruitiness without the harshness of cheaper berry bases.

Alternatives & Comparisons

1
Methyl anthranilate CAS 134-20-3

More floral (orange blossom) with less fruity character. Higher vapor pressure makes it more volatile.

2
Ethyl anthranilate CAS 87-25-2

Intermediate between methyl and butyl versions. Offers better citrus compatibility for cologne types.

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 51). Classified as a non-regulated material.

RIFM Assessment

RIFM assessment confirms safe use at current industry levels. No significant toxicity concerns.

Sustainability

As a synthetic material, butyl anthranilate offers consistent quality without agricultural land use. Modern production methods achieve >90% atom efficiency, minimizing waste. Being petroleum-derived, its carbon footprint is offset by requiring lower usage levels than natural alternatives to achieve equivalent effects.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press. ISBN 9781420090866

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

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Physicochemical Properties

DTXSID: DTXSID5024683

Physical Properties

Molecular Weight 193.246 g/mol🔬 EPA CompTox
Density 1.068 g/cm^3🔬 EPA CTX
Boiling Point 255.074 °C🔬 EPA CTX
Melting Point -5 °C🔬 EPA CTX
Flash Point 156.533 °C🔬 EPA CTX
Refractive Index 1.54 Dimensionless📊 OPERA
Molar Volume 179.127 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.66 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 2.892 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.912 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.24 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.001 mmHg📊 OPERA
Viscosity 10.866 cP📊 OPERA
Surface Tension 42.482 dyn/cm📊 OPERA
Thermal Conductivity 154.253 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 52.32 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 56.161 cm^3/mol📊 OPERA
Polarizability 22.264 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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