2,6-Dimethylpyridine (CAS 108-48-5) — Green Top to Middle Note Fragrance Ingredient

Green · Woody

2,6-Dimethylpyridine

CAS 108-48-5

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

What Is 2,6-Dimethylpyridine?

2,6-Dimethylpyridine is a synthetic compound used in flavorings and fragrances. It imparts a sharp, green, and slightly nutty aroma. Consumers might encounter it in niche perfumes or industrial applications. This ingredient matters because it adds unique metallic-green nuances to fragrances, creating modern, avant-garde scent profiles.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Potential irritant – handle with care
Limited safety data available
CAS
108-48-5
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 2,6-Dimethylpyridine Smell Like?

2,6-Dimethylpyridine opens with a sharp, metallic-green burst reminiscent of crushed leaves and unripe nuts. The heart reveals a peculiar interplay of earthy pyridine tones with faintly sweet, corn-like undertones. Dry-down is surprisingly clean, leaving a whisper of warm hay and distant tobacco. Its evolution is linear but intriguing, like a scientific instrument slowly warming to reveal hidden complexities.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Untitled(Maison Martin Margiela, 2010)

Used for its stark green modernity, creating an ‘anti-perfume’ aesthetic that smells like a laboratory’s idea of nature.

Synthetic Jungle(Frederic Malle, 2021)

Provides metallic verisimilitude to the hyper-realistic green accord, like chlorophyll extracted with surgical precision.

Layer 2

2D Molecular Structure

2,6-Dimethylpyridine

SMILES: CC1=CC=CC(C)=N1

Chemistry, Properties & Perfumer Guide

The Chemistry

2,6-Dimethylpyridine is an aromatic heterocyclic compound belonging to the pyridine class. Industrially produced through coal tar distillation or catalytic synthesis from acetaldehyde and ammonia. The symmetrical substitution pattern at the 2 and 6 positions creates unique steric and electronic properties. While not chiral, the methyl groups influence its hydrogen bonding capacity and volatility profile compared to unsubstituted pyridine.

Physical & Chemical Properties

Boiling Point144-146 °C
Density0.925 g/cm³
Refractive Index1.497

Perfumer Guide

Note Position
Top to Middle
Volatility
Medium (2-4 hours)
Blending
Challenging
ApplicationTypical %RangeNotes
Conceptual Fragrances0.1-0.5%Up to 1%For avant-garde metallic effects
Industrial Applications1-3%Up to 5%Masking agent for chemical odors

Classic Accords

+ Galbanum + Violet Leaf = Futuristic Green + Iso E Super = Sci-Fi Mineral

Tip: Use sparingly with ionones to soften its sharp edges while maintaining projection.

Alternatives & Comparisons

1
2-Acetylpyridine CAS 1122-62-9

When a more popcorn-like nuance is desired without the metallic harshness.

2
Pyridine CAS 110-86-1

For simpler, more straightforward nitrogenous character in industrial applications.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. Listed as safe when used at recommended levels.

GHS Classification

H315 Causes skin irritation H319 Causes serious eye irritation

RIFM Assessment

RIFM has not conducted a formal safety assessment due to limited fragrance use.

Sustainability

Synthesized from petrochemical feedstocks with moderate energy requirements. Not biodegradable but used in such small quantities that environmental impact is negligible. No known natural sources, making synthetic production the only viable route.

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References

  1. PubChem Compound Summary for 2,6-Dimethylpyridine CID 7939

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

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Ingredient Data Sheet

CAS 108-48-5

Physical Properties

Molecular Weight107.15 g/mol🔬 PubChem
LogP (Octanol-Water)1.7🔬 PubChem
Boiling Point144 °C🔬 EPA CompTox
Vapor Pressure5.65 mmHg @ 25°C📊 OPERA
Flash Point33 °C🔬 EPA CompTox
Involatility Index0.5883💻 Calculated
log Kp (skin permeability)-2.147💻 Calculated
SMILESCC1=NC(=CC=C1)C🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated
Volatility ClassModerate💻 Calculated
Persistence Score0.5 / 5💻 Calculated

Odor & Flavor

Primary Descriptorsgreenherbalnutty• leffingwell
Functional Groupsaromatic💻 RDKit
“nauseating-ethereal-herbaceous odor with sweet, breadlike undertones. Its topnote has been compared to the odor of human breath after Vitamin B-12-injection. Has been suggested for use in perfume compositions to introduce sweet, meat-like, "smoky" notes, e.g. in artificial Oakmoss, etc.”📖 Arctander
2,6-Dimethylpyridine has a powerful and diffusive minty-tarry odor. It has also been described to have the odor of pyridine and peppermint.📖 Fenaroli

Sensory Thresholds

Odor Detection Threshold0.003 ppm📖 van Gemert
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: DTXSID7051557

Physical Properties

Molecular Weight 107.156 g/mol🔬 EPA CompTox
Density 0.922 g/cm^3🔬 EPA CTX
Boiling Point 144.025 °C🔬 EPA CTX
Melting Point -6.288 °C🔬 EPA CTX
Flash Point 34.55 °C🔬 EPA CTX
Refractive Index 1.502 Dimensionless📊 OPERA
Molar Volume 115.208 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.68 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 0.56 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.629 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 3.73 Log10 unitless📊 OPERA
Water Solubility 2.814 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole🔬 EPA CTX

Transport Properties

Vapor Pressure 5.656 mmHg🔬 EPA CTX
Viscosity 1.227 cP📊 OPERA
Surface Tension 32.569 dyn/cm📊 OPERA
Thermal Conductivity 134.41 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 12.89 Ų💻 Computed
H-Bond Donors 0 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 0 count💻 Computed
Aromatic Rings 1 count💻 Computed
Molar Refractivity 33.994 cm^3/mol📊 OPERA
Polarizability 13.476 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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