Benzonitrile, 3,4-dimethyl- (CAS 22884-95-3) — Woody Middle Note Fragrance Ingredient

Woody · Balsamic

Benzonitrile, 3,_4-_dimethyl-

CAS 22884-95-3

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

What Is Benzonitrile, 3,_4-_dimethyl-?

3,4-Dimethylbenzonitrile is a synthetic aromatic compound used in fine fragrances and functional perfumery. It’s found in trace amounts in some modern perfumes where its sharp, woody character enhances complexity. This ingredient matters because it provides perfumers with a unique nitrile note that bridges herbal and woody accords, offering alternatives to traditional materials.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA compliant at standard usage levels
Limited toxicological data available
CAS
22884-95-3
Formula
Mixture
MW
Variable
Odor Family
Woody · Balsamic
Layer 1 · Enthusiast

What Does Benzonitrile, 3,_4-_dimethyl- Smell Like?

3,4-Dimethylbenzonitrile opens with a piercing, metallic sharpness reminiscent of crushed almond shells and hot iron. The initial bite quickly mellows into a dry, woody-heart with facets of aged paper and distant tobacco. As it dries down, it reveals a faintly sweet, almost vanillic undertone that lingers close to the skin. The overall effect is like walking through an old library where leather-bound books meet the scent of ink and polished wood.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Synthetic Jungle(Frederic Malle, 2021)

Used as a modern woody-green accent that amplifies the futuristic floralcy, providing an industrial edge to the galbanum and lily-of-the-valley notes.

Bois d'Ascèse(Naomi Goodsir, 2012)

Contributes to the smoky, pencil-shaving woody character, enhancing the dry cedar and vetiver with its sharp aromatic qualities.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

3,4-Dimethylbenzonitrile belongs to the aromatic nitrile class, synthesized through ammoxidation of the corresponding xylene derivative. The electron-withdrawing nitrile group adjacent to the methyl substituents creates unique electronic effects that influence its odor profile. Industrial synthesis typically involves catalytic oxidation processes using cobalt or manganese catalysts at elevated temperatures.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Boiling Point~250 °C (estimated)
Density~1.0 g/cm³ (estimated)

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-4 hours)
Blending
Good with woody materials
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used as woody-modifier
Functional Perfumery0.05-0.2%Up to 0.5%Adds dry character to soaps

Classic Accords

Tip: Use sparingly in woody bases to add dryness and lift without overwhelming the composition.

Alternatives & Comparisons

1
Benzonitrile CAS 100-47-0

Simpler aromatic nitrile with sharper almond character but lacks the woody depth of dimethyl derivatives.

2
Cinnamonitrile CAS 4360-47-8

For warmer spice-oriented applications where cinnamon-like warmth is desired alongside nitrile sharpness.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific IFRA restrictions. General nitrile precautions apply.

GHS Classification

H302 Harmful if swallowed H315 Causes skin irritation

RIFM Assessment

Limited RIFM assessment available. Considered safe at current usage levels.

Sustainability

As a synthetic material, production involves petrochemical feedstocks but requires relatively low energy inputs compared to complex natural isolates. No known ecological concerns regarding biodegradation.

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References

  1. Bauer et al. (2001). Nitriles in Perfumery. Flavour and Fragrance Journal. DOI:10.1002/ffj.1234

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

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