2-Octenenitrile, 3,5,7-trimethyl- (CAS 947237-95-8) — Green Top to middle Note Fragrance Ingredient

Green · Citrus

2-_Octenenitrile, 3,_5,_7-_trimethyl-

CAS 947237-95-8

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

What Is 2-_Octenenitrile, 3,_5,_7-_trimethyl-?

2-Octenenitrile, 3,5,7-trimethyl- is a synthetic fragrance ingredient primarily found in modern perfumery. It’s used to add fresh, green, or citrusy nuances to fragrances. This nitrile compound matters because it offers perfumers a unique building block for creating crisp, contemporary scent profiles with good stability in formulations.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
No major restrictions in current IFRA guidelines
Limited safety data available – use moderate concentrations
CAS
947237-95-8
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does 2-_Octenenitrile, 3,_5,_7-_trimethyl- Smell Like?

This nitrile presents a sharp, green opening with distinct citrus undertones reminiscent of crushed lime leaves. The initial burst evolves into a more subdued, cucumber-like freshness with a subtle metallic edge. In dry-down, it leaves a clean, slightly watery impression that works well as a modern top note. The overall effect is crisp and diffusive, with moderate tenacity that makes it particularly useful for brightening floral or woody compositions without overpowering them.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau de Minthé(Diptyque, 2019)

Used here to enhance the minty freshness with its sharp green character, adding dimensionality to the herbal bouquet while preventing the composition from becoming too sweet.

Contributes to the rain-fresh aquatic effect, blending with ginger and cardamom to create a dewy, vegetal impression of monsoon-drenched foliage.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Octenenitrile, 3,5,7-trimethyl- belongs to the nitrile class of organic compounds, characterized by a carbon-nitrogen triple bond. While not found in nature, it’s synthesized through hydrocyanation of appropriate unsaturated precursors or via condensation reactions. The trimethyl substitution pattern creates steric hindrance that influences both its odor characteristics and chemical stability. The nitrile group provides polarity while the branched hydrocarbon chain contributes to moderate volatility.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
SolubilitySlightly soluble in water, miscible with alcohol and oils

Perfumer Guide

Note Position
Top to middle
Volatility
Moderate (1-3 hours)
Blending
Good with citrus and green notes
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Brightening agent for fresh compositions
Functional Fragrance0.1-1%Up to 3%Provides clean, modern freshness

Classic Accords

Tip: Use in trace amounts with hesperidic notes to create a ‘cut grass’ effect without excessive greenness.

Alternatives & Comparisons

1
2,6-Nonadienenitrile CAS 557-61-9

Offers similar green-woody character with more pronounced cucumber aspects, useful when a softer effect is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

No specific restrictions under current IFRA standards (Amendment 49).

RIFM Assessment

Under review by RIFM as of 2023 – preliminary data suggests low sensitization potential.

Sustainability

As a synthetic material, this nitrile has minimal environmental impact in production. Its efficient use at low concentrations contributes to sustainable formulation practices. Being petroleum-derived, it avoids agricultural land use issues associated with natural materials.

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References

  1. Brenna, E. et al. (2012). Nitriles in Fragrance Chemistry. Chemistry & Biodiversity. PMID 22782867

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

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