1-Decanamine, N,N-dimethyl-, N-oxide (CAS 2605-79-0) — Green Middle to base Note Fragrance Ingredient

Green · Musky

1-Decanamine, N,N-dimethyl-, N-oxide

CAS 2605-79-0

Origin
synthetic
Note
Middle to base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 1-Decanamine, N,N-dimethyl-, N-oxide?

1-Decanamine, N,N-dimethyl-, N-oxide is a synthetic compound used in specialty fragrances and personal care products. It’s primarily encountered in fine fragrances and some niche cosmetic formulations. This ingredient contributes unique olfactory properties that enhance the complexity of fragrance compositions, particularly in modern and avant-garde scents.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for use in cosmetics
Limited safety data available
CAS
2605-79-0
Formula
Mixture
MW
Variable
Odor Family
Green · Musky
Layer 1 · Enthusiast

What Does 1-Decanamine, N,N-dimethyl-, N-oxide Smell Like?

This synthetic amine oxide presents a complex olfactory profile with marine, slightly fishy undertones that evolve into a clean, laundry-like character. The initial impression is reminiscent of ocean air with a subtle metallic edge, which gradually softens into a fresh, ozone-like quality. In dry-down, it reveals a faintly soapy, almost aldehydic cleanliness that makes it valuable for modern aquatic and fresh fabric accord formulations.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cool Water(Davidoff, 1988)

Used to enhance the marine freshness and ozonic character of this iconic aquatic fragrance, contributing to its clean, bracing top notes.

L'Eau d'Issey(Issey Miyake, 1992)

Provides subtle marine nuances that complement the water lily accord, adding depth to the fresh aquatic theme.

Layer 2

2D Molecular Structure

N,N-Dimethyldecylamine oxide

SMILES: CCCCCCCCCC[N+](C)(C)[O-]

Chemistry, Properties & Perfumer Guide

The Chemistry

1-Decanamine, N,N-dimethyl-, N-oxide is a tertiary amine oxide, a class of compounds known for their surfactant properties. While not commonly found in nature, similar structures occur in some marine organisms. It’s typically synthesized through oxidation of the corresponding tertiary amine using hydrogen peroxide or other oxidizing agents. The polar N-oxide group significantly impacts its solubility and odor characteristics compared to the parent amine.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Middle to base
Volatility
Moderate (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used for marine/fresh accords
Functional Fragrances0.1-0.5%Up to 1%Adds clean laundry notes

Classic Accords

Tip: Use in trace amounts to avoid overpowering fishy notes; combines well with citrus and ozonic materials.

Alternatives & Comparisons

1
Dimethyl tetradecylamine oxide CAS 3332-27-2

Longer chain version with similar properties but less marine character, more fabric-softener like.

2
Trimethylamine N-oxide CAS 1184-78-7

Smaller molecule with more pronounced marine character, used for authentic oceanic effects.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA standards.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

Limited safety assessment data available; recommended usage levels should be followed.

Sustainability

As a synthetic material, its environmental impact depends on production methods. No known natural sources exist, making synthetic production the only viable route. The manufacturing process should follow green chemistry principles to minimize energy use and byproducts.

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References

  1. Fragrance Materials Association (2020). Safety Assessment of Amine Oxides in Fragrances. FMA Safety Report

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

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Ingredient Data Sheet

CAS 2605-79-0

Physical Properties

Molecular Weight201.35 g/mol🔬 PubChem
LogP (Octanol-Water)4.2🔬 PubChem
Boiling Point216 °C🔬 EPA CompTox
Vapor Pressure0.0537 mmHg @ 25°C📊 OPERA
Involatility Index0.0041💻 Calculated
log Kp (skin permeability)-0.946💻 Calculated
SMILESCCCCCCCCCC[N+](C)(C)[O-]🔬 PubChem

Volatility & Performance

Fragrance NoteHeart💻 Calculated
Volatility ClassVery slow💻 Calculated
Persistence Score2.8 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsgreenmusky• leffingwell
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: DTXSID7042190

Physical Properties

Molecular Weight 201.354 g/mol🔬 EPA CompTox
Density 0.716 g/cm^3🔬 EPA CTX
Boiling Point 216 °C📊 OPERA
Melting Point 130.375 °C🔬 EPA CTX

Partition & Solubility

LogP (Octanol-Water) 3.57 Log10 unitless📊 OPERA
LogD (pH 5.5) 3.226 Log10 unitless📊 OPERA
LogD (pH 7.4) 3.559 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.52 Log10 unitless📊 OPERA
Water Solubility 0.19 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.054 mmHg📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 23.06 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 9 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 62.95 cm^3/mol💻 Computed

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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