Butyric acid (CAS 107-92-6) — Musky Base Note Fragrance Ingredient

Musky · Balsamic

Butyric acid

CAS 107-92-6

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

What Is Butyric acid?

Butyric acid is a short-chain fatty acid found naturally in rancid butter, parmesan cheese, and human sweat. It’s also synthesized for use in food flavorings and some perfumes. While its pure form smells intensely unpleasant (like vomit), carefully controlled amounts can add dairy-like depth to fragrances, especially when blended with sweeter ingredients.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Strong odor – requires precise dosing
Can cause skin irritation at high concentrations
CAS
107-92-6
Formula
Mixture
MW
Variable
Odor Family
Musky · Balsamic
Layer 1 · Enthusiast

What Does Butyric acid Smell Like?

Pure butyric acid assaults the nose with a piercing, acrid sourness reminiscent of spoiled milk, vomit, and locker room sweat. Yet when diluted below 0.1%, it transforms – adding a creamy, slightly cheesy nuance that enhances dairy accords. In perfumery, it behaves like a volatile chemical chameleon: initially repulsive, then evolving into a warm, animalic base that boosts the richness of vanilla, coconut, and tropical fruit notes. The dry-down leaves a faint fermented butter sensation, making it invaluable for creating authentic dairy or body-odor realism in niche compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Protection(Etat Libre d’Orange, 2006)

Uses butyric acid’s sweaty edge to amplify the blood-iron accord, creating a visceral, corporeal fragrance that walks the line between repulsion and fascination.

Layer 2

2D Molecular Structure

Butanoic acid

SMILES: CCCC(O)=O

Chemistry, Properties & Perfumer Guide

The Chemistry

Butyric acid (C4H8O2) is the simplest fatty acid that retains enough carbon atoms to exhibit both hydrophilic and hydrophobic properties. Industrially produced via oxidation of butyraldehyde or fermentation by anaerobic bacteria like Clostridium butyricum. Its volatility stems from the short 4-carbon chain, while the carboxyl group gives it water solubility. Exists as two enantiomers, though most commercial forms are racemic mixtures. Key to its olfactory impact is the molecule’s ability to bind strongly to human olfactory receptors tuned to detect rancidity.

Physical & Chemical Properties

Boiling Point163.5 °C
Density0.96 g/cm³
Vapor Pressure0.43 mmHg at 25°C
SolubilityMiscible in water, ethanol, ether

Perfumer Guide

Note Position
Base
Volatility
Low (hours-days)
Blending
Challenging
ApplicationTypical %RangeNotes
Fine Fragrance0.01-0.1%Up to 0.5%For animalic/milky effects
Flavorings5-50 ppmUp to 100 ppmDairy flavor enhancement
Functional Fragrances0.001-0.01%Up to 0.05%Masking malodors

Classic Accords

Tip: Always pre-dilute to 1% or lower before blending – direct use will contaminate equipment.

Alternatives & Comparisons

1
Isobutyric acid CAS 79-31-2

Less aggressive sibling with similar dairy character but reduced vomit nuance. Preferable for mainstream applications.

2
Valeric acid CAS 109-52-4

Longer carbon chain produces a more cheesy, less acidic odor profile for sustained dairy effects.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions. Classified as a weak sensitizer at high concentrations.

GHS Classification

H314 Causes severe skin burns and eye damage

RIFM Assessment

RIFM evaluation concludes safe use at current industry levels with proper handling precautions.

Sustainability

Most butyric acid is synthesized from petrochemical feedstocks, though some is produced via bacterial fermentation of plant biomass. The synthetic route has higher carbon footprint but avoids agricultural land use. Emerging bio-based production methods using genetically modified E. coli show promise for greener synthesis.

Explore Butyric acid

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References

  1. PubChem Compound Summary for Butyric Acid CID 264

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

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Ingredient Data Sheet

CAS 107-92-6

Physical Properties

Molecular Weight88.11 g/mol🔬 PubChem
LogP (Octanol-Water)0.8🔬 PubChem
Boiling Point163.5 °C🔬 EPA CompTox
Vapor Pressure0.43 mmHg @ 25°C📊 OPERA
Flash Point76.7 °C🔬 EPA CompTox
Involatility Index0.0494💻 Calculated
log Kp (skin permeability)-2.669💻 Calculated
SMILESCCCC(=O)O🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassSlow💻 Calculated
Persistence Score0.5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsbuttery• leffingwell
“Powerful, penetrating, diffusive sour odor, reminiscent of rancid butter. However, being water-soluble, the odor "airs out" easier from a room than one should expect, also it can be washed off the skin easily with water, leaving little or no odor if washing is performed im-”📖 Arctander
n-Butyric acid has a persistent, penetrating, rancid, butter-like odor and burning, acid taste.📖 Fenaroli

Flavor Notes (Arctander)

“Used in flavor compositions, primarily in Butter flavor. Also in imitation Cheese, Nut, Fruit, in Butterscotch and Caramel, Rum, etc.”📖 Arctander

Sensory Thresholds

Odor Detection Threshold1.7412 ppm (n=24)📖 van Gemert

Regulatory Status

FEMA NumberFEMA 2221⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationNature Identical📖 Fenaroli
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: DTXSID8021515

Physical Properties

Molecular Weight 88.106 g/mol🔬 EPA CompTox
Density 0.958 g/cm^3🔬 EPA CTX
Boiling Point 163.7 °C🔬 EPA CTX
Melting Point -6.708 °C🔬 EPA CTX
Flash Point 72.192 °C🔬 EPA CTX
Refractive Index 1.411 Dimensionless📊 OPERA
Molar Volume 89.188 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.598 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 0.06 Log10 unitless📊 OPERA
LogD (pH 7.4) -1.744 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.23 Log10 unitless📊 OPERA
Water Solubility 0.663 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 1.175 mmHg🔬 EPA CTX
Viscosity 1.82 cP📊 OPERA
Surface Tension 29.578 dyn/cm📊 OPERA
Thermal Conductivity 147.456 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 37.3 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 2 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 22.145 cm^3/mol📊 OPERA
Polarizability 8.779 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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