Pyridine, 5-hexyl-2-methyl- (CAS 710-40-7) — Balsamic Middle Note Fragrance Ingredient

Balsamic · Woody

Pyridine, 5-hexyl-2-methyl-

CAS 710-40-7

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

What Is Pyridine, 5-hexyl-2-methyl-?

Pyridine, 5-hexyl-2-methyl- is a synthetic aroma chemical used in niche fragrances to add leathery, smoky nuances. It’s found in avant-garde perfumes seeking unconventional effects. This molecule matters because it provides perfumers with a unique tool to create modern, edgy accords that push beyond traditional fragrance boundaries.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Used in controlled concentrations
Requires careful handling
CAS
710-40-7
Formula
Mixture
MW
Variable
Odor Family
Balsamic · Woody
Layer 1 · Enthusiast

What Does Pyridine, 5-hexyl-2-methyl- Smell Like?

A sharp, pungent opening evolves into a complex leathery-smoky heart with animalic undertones. The dry-down reveals a persistent, slightly medicinal character reminiscent of aged tobacco and cured hides. Its metallic edge cuts through sweeter notes like a knife through butter, making it ideal for modern leather accords.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Cuir de Russie(Chanel, 1927)

Used sparingly to enhance the authentic birch tar leather accord, adding depth and modernity to this classic composition.

Tuscan Leather(Tom Ford, 2007)

Provides the raw, unfinished leather character that makes this fragrance so distinctive and contemporary.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

This pyridine derivative belongs to the heterocyclic nitrogen-containing compounds class. Synthesized through alkylation reactions of pyridine precursors, its structure features a hexyl side chain that contributes to its hydrophobic character. The methyl group at position 2 influences its volatility and odor profile. The nitrogen atom creates a dipole moment that affects its interaction with olfactory receptors.

Physical & Chemical Properties

Boiling PointNot available
DensityNot available

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good with woody notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used sparingly for leather effects
Functional Fragrance0.01-0.1%Up to 0.2%Masking agent in industrial applications

Classic Accords

Tip: Use in trace amounts and balance with softer materials to avoid overwhelming compositions.

Alternatives & Comparisons

1
Isobutyl quinoline CAS 93-19-6

Less aggressive alternative for leather accords with similar functionality but smoother profile.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions currently apply to this material.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

Currently under review by RIFM for comprehensive safety assessment.

Sustainability

As a synthetic material, production involves petrochemical feedstocks but requires relatively low energy inputs compared to natural alternatives. Its potency means small quantities suffice, reducing overall environmental impact per kilogram of fragrance produced.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Allured Publishing.

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

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