Ethyl Maltol (CAS 4940-11-8) — sweet base Note Fragrance Ingredient




sweet caramel

Ethyl Maltol

CAS 4940-11-8

Origin
synthetic
Note
base
IFRA
Generally safe
Data as of: Mar 2026

What Is Ethyl Maltol?

Ethyl Maltol is a synthetic compound used to enhance sweet, caramel-like notes in perfumes and flavored products. You’ll encounter it in gourmand fragrances, candies, and some baked goods. This ingredient matters because it can dramatically amplify sweetness perception at very low concentrations, acting like a ‘volume knob’ for sugary accords without adding actual sugar.

Safety Profile

GENERALLY SAFE

Generally safeUse with awarenessProfessional use
Approved for food and fragrance use
Avoid excessive inhalation of pure powder
CAS
4940-11-8
Formula
C18H22ClNO
MW
303.8
Odor Family
sweet caramel
Ethyl Maltol 2D structure

Ethyl Maltol
C18H22ClNO
Layer 1 · Enthusiast

What Does Ethyl Maltol Smell Like?

Ethyl Maltol delivers an intense, jammy sweetness reminiscent of freshly spun cotton candy dissolving on the tongue. At 10% dilution, it evokes warm caramel drizzled over ripe strawberries. The molecule’s pyramidal shape allows perfect fit into sweetness receptors, creating a lingering effect that amplifies surrounding vanilla and fruit notes. Unlike sugar, it maintains this character even in drydown, subtly rounding rough edges in woody bases.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Angel(Mugler, 1992)

Ethyl Maltol forms the sugary backbone of this groundbreaking gourmand, amplifying patchouli’s chocolatey facets and creating the illusion of melted pralines.

La Vie Est Belle(Lancôme, 2012)

Here it boosts the candied iris accord, making the fragrance smell like a powdered sugar-dusted version of itself.

Layer 2

2D Molecular Structure

2-Ethyl-3-hydroxy-4-pyrone

SMILES: CCC1=C(O)C(=O)C=CO1

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethyl Maltol (C7H8O3) is a heterocyclic compound derived from maltol through ethylation. As a pyranone derivative, its planar structure allows excellent volatility despite moderate molecular weight. Industrial synthesis typically starts from kojic acid or through condensation of ethyl acetoacetate with formaldehyde. The molecule’s key feature is an α,β-unsaturated ketone system adjacent to a hydroxyl group, creating strong hydrogen bonding capacity. This structure is chiral but usually used racemically in fragrance applications.

Physical & Chemical Properties

Molecular Weight 140.14 g/mol
Melting Point 89-93 °C
Boiling Point 161 °C (10 mmHg)
XLogP -0.1

Perfumer Guide

Note Position
Base
Volatility
Low (6+ hours)
Blending
Excellent
Application Typical % Range Notes
Fine Fragrance 0.1-0.5% Up to 1% Sweetness booster
Candles 0.05-0.2% Up to 0.5% Prevents waxy off-notes

Classic Accords

+ Vanilla = Cupcake
+ Raspberry = Jam
+ Tonka = Caramel

Tip: Use sparingly – above 1% it can dominate compositions with cloying sweetness.

Alternatives & Comparisons

1
Maltol CAS 118-71-8

The parent compound, less sweet but with more baked bread character. Use when needing subtlety.

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

Not restricted by IFRA. Listed as generally recognized as safe (GRAS) by FEMA.

RIFM Assessment

RIFM-reviewed with no significant safety concerns at typical use levels.

Sustainability

Synthesized from petrochemical precursors, Ethyl Maltol has moderate environmental impact. Production requires careful solvent management. Some manufacturers now offer bio-based routes using fermented sugars as starting materials, reducing carbon footprint by ~40% compared to traditional synthesis.

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Industry & Science Data

Odor Detection Threshold
70 ppb
in air (orthonasal)
Ref: van Gemert, Odour Thresholds (2011)
Commercial Price
$20–$45/kg
synthetic grade, bulk market
Indicative 2024 pricing. Varies by purity & volume.
Global Usage Rank
#30 most used
by global fragrance volume
Source: IFRA Usage Survey 2015
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References

  1. PubChem Compound Summary for CID 22674 PubChem

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

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Ingredient Data Sheet

CAS 4940-11-8

Physical Properties

Molecular Weight140.14 g/mol🔬 PubChem
LogP (Octanol-Water)0.8🔬 PubChem
Boiling Point289 °C🔬 EPA CompTox
Vapor Pressure0.0015 mmHg @ 25°C📊 OPERA
Flash Point124.8 °C🔬 EPA CompTox
Involatility Index0.0001💻 Calculated
log Kp (skin permeability)-2.987💻 Calculated
SMILESCCC1=C(C(=O)C=CO1)O🔬 PubChem

Volatility & Performance

Fragrance NoteBase💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score3.4 / 5💻 Calculated

Odor & Flavor

Primary Descriptorscaramelfruitysweet• leffingwell
Functional Groupsphenolaromatic💻 RDKit
“stronger or rather, it is 4 times more tenacious and has a similar, but more delicate and uniform odor performance. One of its greatest assets is that of being an enhancer of sweetness, indirectly reducing the need for sugar in the flavored product. This effect is obviously of considerable interest to the beverage manufacturers in our days of "diet-soda" drinking.”📖 Arctander
Ethyl maltol has a very sweet, caramel-like odor of immense tenacity and sweet, fruity taste with initial bitter-tart flavor; rapid loss of flavor per se. It is four to six times more potent than maltol.📖 Fenaroli

Flavor Notes (Arctander)

“Sweet, fruity-jamlike taste, reminiscent of Pineapple, Strawberry, Vanilla and heavy fruit-preserve or syrup, depending upon the concentration. Although its flavor is somewhat similar to that of Palatone (the lower - Methyl - homologue), the subject material is more breadlike, less caramellic, softe”📖 Arctander

Regulatory Status

GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationArtificial📖 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: DTXSID5041516

Physical Properties

Molecular Weight 140.138 g/mol🔬 EPA CompTox
Density 1.39 g/cm^3🔬 EPA CTX
Boiling Point 253.15 °C🔬 EPA CTX
Melting Point 132.58 °C🔬 EPA CTX
Flash Point 124.85 °C🔬 EPA CTX
Refractive Index 1.541 Dimensionless📊 OPERA
Molar Volume 111.126 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 0.914 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 0.567 Log10 unitless📊 OPERA
LogD (pH 7.4) 0.546 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.61 Log10 unitless📊 OPERA
Water Solubility 0.087 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.002 mmHg🔬 EPA CTX
Surface Tension 41.882 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 50.44 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 1 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 34.911 cm^3/mol📊 OPERA
Polarizability 13.84 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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