Ethylene dodecanedioate (CAS 54982-83-1) — Musky Base Note Fragrance Ingredient

Musky · Balsamic

Ethylene dodecanedioate

CAS 54982-83-1

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

What Is Ethylene dodecanedioate?

Ethylene dodecanedioate is a synthetic fragrance ingredient primarily used as a musk-like fixative in perfumery. It appears in high-end fragrances, particularly those aiming for a clean, powdery dry-down. This molecule matters because it provides long-lasting warmth without animalic qualities, making it valuable for modern musks that need to comply with ethical sourcing standards.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No known skin sensitization
Limited toxicology data available
CAS
54982-83-1
Formula
Mixture
MW
Variable
Odor Family
Musky · Balsamic
Layer 1 · Enthusiast

What Does Ethylene dodecanedioate Smell Like?

Ethylene dodecanedioate unfolds as a diaphanous musk with the texture of powdered vanilla beans and the cleanliness of sun-dried linen. Initially muted, it develops into a radiant warmth reminiscent of skin musk after a summer shower. The dry-down exhibits remarkable tenacity, leaving a faintly sweet, almost talcum-like trail that lingers for hours without overwhelming.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Molecule 04(Escentric Molecules, 2019)

This minimalist fragrance showcases ethylene dodecanedioate as the sole active ingredient, demonstrating its capacity to create a subtle yet persistent skin-hugging musk.

Glow(Jennifer Lopez, 2002)

Used here to amplify the clean musk accord, providing a synthetic alternative to traditional animalic musks while maintaining warmth.

Layer 2

2D Molecular Structure

1,4-Dioxacyclohexadecane-5,16-dione

SMILES: O=C1CCCCCCCCCCC(=O)OCCO1

Chemistry, Properties & Perfumer Guide

The Chemistry

Ethylene dodecanedioate belongs to the ester class, synthesized through esterification of dodecanedioic acid with ethylene glycol. The linear C12 structure contributes to its musk-like character while the diester configuration enhances stability. Unlike macrocyclic musks, this compound lacks ring strain, making it more synthetically accessible. The absence of chiral centers simplifies production.

Physical & Chemical Properties

StateWhite crystalline solid
Melting Point78-82°C (literature)

Perfumer Guide

Note Position
Base
Volatility
Very low (12+ hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Musk foundation
Detergents0.1-0.3%Up to 1%Fabric substantivity

Classic Accords

Tip: Best added during the alcohol phase for complete dissolution before incorporating volatile top notes.

Alternatives & Comparisons

1
Ethylene brassylate CAS 105-95-3

A more floral-leaning synthetic musk with similar substantivity but brighter tonal qualities.

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 49 (2022).

RIFM Assessment

Under evaluation by RIFM’s Novel Materials program (2023).

Sustainability

As a fully synthetic material, production avoids animal-derived ingredients and doesn’t deplete natural resources. The manufacturing process employs standard petrochemical feedstocks with moderate energy requirements.

Explore Ethylene dodecanedioate

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. IFRA Standards Library (2022). Amendment 49. IFRA

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

Report a data error

Ingredient Data Sheet

CAS 54982-83-1

Physical Properties

Molecular Weight256.34 g/mol🔬 PubChem
LogP (Octanol-Water)3.6🔬 PubChem
Boiling Point337.3 °C🔬 EPA CompTox
Vapor Pressure0.0002 mmHg @ 25°C📊 OPERA
Flash Point166 °C🔬 EPA CompTox
log Kp (skin permeability)-1.708💻 Calculated
SMILESC1CCCCCC(=O)OCCOC(=O)CCCC1🔬 PubChem

Volatility & Performance

Fragrance NoteBase💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score8 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsbalsamicmusky• leffingwell
Functional Groupsesterether💻 RDKit

Sensory Thresholds

Odor Detection Threshold0.01 ppm📖 van Gemert

Trade Names

MC-4 (Soda Aromatic), Zenolide (IFF), Musk YH (Yinghai).📖 Surburg
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: DTXSID1044568

Physical Properties

Molecular Weight 256.342 g/mol🔬 EPA CompTox
Density 1.059 g/cm^3🔬 EPA CTX
Boiling Point 337.3 °C🔬 EPA CTX
Melting Point 17.573 °C🔬 EPA CTX
Flash Point 166 °C🔬 EPA CTX
Refractive Index 1.439 Dimensionless📊 OPERA
Molar Volume 258.918 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 3.65 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 3.182 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.182 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 9.45 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0 mmHg🔬 EPA CTX
Viscosity 6.59 cP📊 OPERA
Surface Tension 31.277 dyn/cm📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 52.6 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 4 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 68.036 cm^3/mol📊 OPERA
Polarizability 26.972 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