Skatole (CAS 83-34-1) — fecal base Note Fragrance Ingredient

fecal floral

Skatole

CAS 83-34-1

Origin
synthetic
Note
base
IFRA
Use with awareness
Data as of: Mar 2026

What Is Skatole?

Skatole is a fragrance molecule with a dual personality. At high concentrations, it smells distinctly fecal, but at trace levels it contributes warm, floral nuances. You’ll encounter it in some perfumes and flavorings. This paradoxical ingredient matters because it demonstrates how concentration transforms perception – what’s repulsive at one level becomes desirable at another.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
GRAS at low concentrations
Potentially offensive at high doses
CAS
83-34-1
Formula
C9H9N
MW
131.17
Odor Family
fecal floral
Skatole 2D structure
Skatole
C9H9N
Layer 1 · Enthusiast

What Does Skatole Smell Like?

Skatole presents a fascinating olfactory paradox. Undiluted, it assaults with an intensely fecal, animalic character reminiscent of barnyards. Yet when meticulously diluted below 0.1%, it metamorphoses into a warm, sweet floral with narcotic undertones – like overripe tropical fruit dipped in honey. As a base note, it provides animalic depth that evolves into a velvety floralcy over hours. Master perfumers use it to add carnal complexity to white florals, where it behaves like a shadowy twin to jasmine absolute.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Jungle L'Éléphant(Kenzo, 1996)

Used as a counterpoint to the lush florals, skatole adds animalic warmth that transforms the composition from pretty to primal. It creates tension with the vanilla base.

Muscs Koublai Khan(Serge Lutens, 1998)

Skatole contributes to the legendary animalic musk accord, providing fecal facets that make the scent feel alive and human.

Layer 2

2D Molecular Structure

3-Methylindole

SMILES: CC1=CNC2=C1C=CC=C2

Chemistry, Properties & Perfumer Guide

The Chemistry

Skatole (3-methylindole) is an aromatic heterocyclic compound belonging to the indole class. While found naturally in mammalian feces and some flowers like orange blossoms, commercial skatole is synthesized via Fischer indole synthesis from phenylhydrazine and propionaldehyde. The planar structure allows π-π stacking interactions that influence its odor threshold. Chirality isn’t relevant as the molecule lacks stereocenters.

Physical & Chemical Properties

Boiling Point265-266 °C
Melting Point95 °C
Vapor Pressure0.0055 mmHg
XLogP2.6
SolubilityAlcohol, benzene, chloroform

Perfumer Guide

Note Position
Base
Volatility
Very low (hours-days)
Blending
Expert-level
ApplicationTypical %RangeNotes
Fine Fragrance0.001-0.01%Up to 0.1%Animalic modifier
Flavorings0.0001-0.001 ppmUp to 0.01 ppmFruity nuance

Classic Accords

+ Jasmine + Civet = Animalic floral + Vanilla + Tonka = Dirty gourmand

Tip: Always pre-dilute to 0.1% or below before incorporating to avoid overwhelming fecal character.

Alternatives & Comparisons

1
Indole CAS 120-72-9

Less animalic but similar floral effects at low levels. Prefer when skatole’s fecal notes are too pronounced.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. IFRA, REACH, EU Cosmetics Regulation standards update periodically. Consult current IFRA Standards Library before formulating. Not legal or regulatory advice.

IFRA Status

No IFRA restrictions. FEMA GRAS# 3019.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM evaluation confirms safe use at current levels in fragrances.

Sustainability

Synthetic production avoids animal-derived sources. Manufacturing uses standard petrochemical feedstocks with moderate environmental impact. No known ecological concerns at usage levels.

Explore Skatole

Browse essential oils and aroma compounds.

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References

  1. PubChem Skatole CID 6736

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

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Ingredient Data Sheet

CAS 83-34-1

Physical Properties

Molecular Weight131.17 g/mol🔬 PubChem
LogP (Octanol-Water)2.6🔬 PubChem
Boiling Point265 °C🔬 EPA CompTox
Vapor Pressure0.0055 mmHg @ 25°C📊 OPERA
Flash Point132 °C🔬 EPA CompTox
Involatility Index0.0005💻 Calculated
log Kp (skin permeability)-1.654💻 Calculated
SMILESCC1=CNC2=CC=CC=C12🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score3.5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsanimalicfloralfruity• leffingwell
Functional Groupsaromatic💻 RDKit
“The use of Skatole in flavors may come as a surprise to some perfumers who find it hard to believe that we can "eat" this odor. But minute traces are useful in Grape and Cheese imitation flavor, fruit complexes, Nut flavors, etc., highest in Cheese flavor. Concentrations in the end product vary from 0.01 to 1 ppm.”📖 Arctander
Skatole has a characteristic putrid, fecal odor at high concentrations, becoming pleasant, sweet, warm at very low concentrations. It has a warm overripe fruity flavor below 1 ppm.📖 Fenaroli

Flavor Notes (Arctander)

“The taste of Skatole is warm, overripe fruity at concentrations below 0.1 ppm, while it becomes more animal near 1 ppm. The use of Skatole in flavors may come as a surprise to some perfumers who find it hard to believe that we can "eat" this odor. But minute traces are useful in Grape and Cheese imi”📖 Arctander

Sensory Thresholds

Odor Detection Threshold0.0126 ppm (n=24)📖 van Gemert

Regulatory Status

FEMA NumberFEMA 3019⚖️ 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: DTXSID8021775

Physical Properties

Molecular Weight 131.178 g/mol🔬 EPA CompTox
Density 1.115 g/cm^3📊 OPERA
Boiling Point 265.625 °C🔬 EPA CTX
Melting Point 96.084 °C🔬 EPA CTX
Flash Point 132.05 °C🔬 EPA CTX
Refractive Index 1.655 Dimensionless📊 OPERA
Molar Volume 118.147 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 2.6 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 2.578 Log10 unitless📊 OPERA
LogD (pH 7.4) 2.593 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 7.77 Log10 unitless📊 OPERA
Water Solubility 0.004 mol/L🔬 EPA CTX
Henry's Law Constant 0.17 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 0.006 mmHg🔬 EPA CTX
Viscosity 4.881 cP📊 OPERA
Surface Tension 46.401 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 15.79 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 0 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 2 count💻 Computed
Molar Refractivity 43.353 cm^3/mol📊 OPERA
Polarizability 17.187 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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