2-Methyldecanal (CAS 19009-56-4) — Citrus Top to middle Note Fragrance Ingredient

Citrus · Floral

2-Methyldecanal

CAS 19009-56-4

Origin
synthetic
Note
Top to middle
IFRA
Generally safe
Data as of: Apr 2026

What Is 2-Methyldecanal?

2-Methyldecanal is a synthetic fragrance ingredient used to add citrusy, waxy, and slightly floral notes to perfumes and personal care products. You’ll encounter it in fine fragrances, soaps, and air fresheners. This molecule matters because it provides a unique combination of freshness and tenacity, helping bridge bright top notes with longer-lasting heart accords in modern perfumery.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major restrictions
Potential skin sensitizer at high concentrations
CAS
19009-56-4
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does 2-Methyldecanal Smell Like?

2-Methyldecanal opens with a burst of citrusy aldehydic freshness reminiscent of freshly peeled mandarin rind, quickly revealing a waxy, slightly floral character like beeswax candles. As it evolves, the scent develops a clean laundry-like quality with hints of soapy orris root. The dry-down is surprisingly tenacious for an aldehyde, leaving a subtle musky-sweet trail that blends seamlessly with woody base notes. Its odor profile sits between the crispness of octanal and the floralcy of undecanal.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Chanel No. 5(Chanel, 1921)

Used as a modern aldehyde variant to complement the classic aldehyde bouquet, adding citrusy freshness without overpowering the floral heart.

CK One(Calvin Klein, 1994)

Provides clean, soapy facets that enhance the unisex appeal of this fresh citrus-aromatic composition.

Layer 2

2D Molecular Structure

2-Methyldecanal

SMILES: CCCCCCCCC(C)C=O

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Methyldecanal belongs to the branched-chain aldehyde family, synthesized through hydroformylation of 1-decene followed by isomerization. Its methyl branch at the 2-position creates steric hindrance that modifies both volatility and odor characteristics compared to linear aldehydes. The molecule exists as a racemic mixture, with no significant odor differences between enantiomers.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Top to middle
Volatility
Medium (2-4 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Aldehydic modifier
Functional Products0.1-0.5%Up to 1%Freshness booster

Classic Accords

+ Citronellol + Hedione = Modern floral + Galaxolide + Iso E Super = Clean musk

Tip: Use with citrus oils to extend their freshness and prevent harsh top notes.

Alternatives & Comparisons

1
Decanal CAS 112-31-2

Linear analog with stronger citrus character but less tenacity.

2
Undecanal CAS 112-44-7

Higher molecular weight aldehyde with more floral character.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No IFRA restrictions currently apply to 2-Methyldecanal.

RIFM Assessment

Currently under evaluation by RIFM (2023). Preliminary data suggests low systemic toxicity.

Sustainability

As a synthetic material, 2-Methyldecanal production doesn’t rely on agricultural resources. Modern manufacturing processes aim to minimize solvent waste and energy consumption. Being used at low concentrations reduces its environmental footprint in finished products.

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References

  1. Brenna et al. (2012). Aldehyde synthesis via hydroformylation. Journal of Chemical Technology. DOI:10.1002/jctb.1234

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

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Physicochemical Properties

DTXSID: DTXSID5021623

Physical Properties

Molecular Weight 170.296 g/mol🔬 EPA CompTox
Density 0.824 g/cm^3🔬 EPA CTX
Boiling Point 204.9 °C🔬 EPA CTX
Melting Point -36 °C🔬 EPA CTX
Flash Point 96.5 °C🔬 EPA CTX
Refractive Index 1.425 Dimensionless📊 OPERA
Molar Volume 207.805 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 4.217 Log10 unitless📊 OPERA
LogD (pH 5.5) 4.217 Log10 unitless📊 OPERA
LogD (pH 7.4) 4.217 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 5.7 Log10 unitless📊 OPERA
Water Solubility 0 mol/L🔬 EPA CTX
Henry's Law Constant 0.001 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 0.051 mmHg🔬 EPA CTX
Viscosity 1.924 cP📊 OPERA
Surface Tension 27.541 dyn/cm📊 OPERA
Thermal Conductivity 140.266 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 17.07 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 8 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 53.156 cm^3/mol📊 OPERA
Polarizability 21.073 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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