Decanenitrile (CAS 1975-78-6) — Green Top to Middle Note Fragrance Ingredient

Green · Citrus

Decanenitrile

CAS 1975-78-6

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

What Is Decanenitrile?

Decanenitrile is a synthetic fragrance ingredient rarely encountered by name in consumer products, though it may appear in trace amounts within certain perfumes and functional fragrances. Its subtle presence contributes to the overall complexity of modern scent compositions. This nitrile compound matters to perfumers for its ability to add crisp, slightly metallic green facets to fragrances without overpowering other notes. It’s particularly valued for creating modern interpretations of classic accords where a clean, technical edge is desired.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns at typical usage levels
Limited toxicology data – use prudent concentrations
CAS
1975-78-6
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does Decanenitrile Smell Like?

Decanenitrile presents a sharp, almost clinical opening with distinct green-herbaceous character reminiscent of freshly crushed stems. The initial impression carries a cool metallic edge like stainless steel exposed to morning dew, gradually softening into a waxy, slightly fatty undertone akin to green bell pepper skins. As it dries down, it reveals subtle citrus-rind nuances and a faint almond-like sweetness that never becomes gourmand. The overall effect is clean and modern – a synthetic interpretation of nature’s greenness without earthiness, making it valuable for contemporary fragrances requiring precision-cut freshness.

Scent Profile
Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Decanenitrile belongs to the nitrile family of organic compounds, characterized by a -C≡N functional group attached to a decane chain. Unlike naturally occurring nitriles found in some plants (often as cyanogenic glycosides), this molecule is exclusively synthetic, typically produced through the dehydration of decanamide or by reaction of decanoic acid derivatives with ammonia. The linear carbon chain ensures good volatility while the nitrile group provides dipole interactions that influence both scent characteristics and molecular stability. Being a single isomer compound without chiral centers, it offers consistent performance in formulations.

Physical & Chemical Properties

AppearanceClear liquid
Molecular FormulaC10H19N

Perfumer Guide

Note Position
Top to Middle
Volatility
Medium (2-4 hours)
Blending
Good with citrus and woody notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used as green-modifier in trace amounts
Functional Fragrances0.05-0.2%Up to 0.5%Adds freshness to detergents
Technical Applications1-3%Up to 5%Solvent properties in specialty formulations

Classic Accords

Tip: Use below 0.5% to avoid dominating compositions – works best when barely perceptible as a freshness enhancer.

Alternatives & Comparisons

1
Nonadienenitrile CAS 5585-39-7

Offers similar green character with added floral-cucumber nuances, useful when more pronounced top notes are desired.

2
Octanenitrile CAS 124-12-9

Shorter carbon chain provides brighter, more citrus-leaning green effect with higher volatility.

3
trans-2-Hexenenitrile CAS 14283-62-6

Delivers sharper green-leaf character with grassier aspects for more naturalistic compositions.

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. No specific usage limits established.

RIFM Assessment

No complete RIFM assessment available. Preliminary data suggests low systemic toxicity at fragrance-relevant concentrations.

Sustainability

As a purely synthetic material, Decanenitrile’s production doesn’t impact agricultural resources. Its synthesis typically involves petrochemical feedstocks, though modern routes may incorporate bio-based intermediates. The nitrile group’s stability means it doesn’t readily hydrolyze into more toxic cyanide forms under environmental conditions. Future green chemistry approaches may improve the atom economy of its production processes.

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References

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

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