7-Nonen-2-ol, 4,8-dimethyl-, (4S)- (CAS 379693-55-7) — Green Top to middle Note Fragrance Ingredient

Green · Citrus

7-_Nonen-_2-_ol, 4,_8-_dimethyl-_, (4S)_-

CAS 379693-55-7

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

What Is 7-_Nonen-_2-_ol, 4,_8-_dimethyl-_, (4S)_-?

This synthetic fragrance ingredient is a specialized molecule used by perfumers to create unique scent profiles. While not commonly encountered in everyday products, it appears in niche and artistic fragrances. Its importance lies in its ability to contribute distinctive green, marine, or ozonic nuances that are difficult to achieve with natural materials alone.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
No major restrictions reported
Limited safety data available
CAS
379693-55-7
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does 7-_Nonen-_2-_ol, 4,_8-_dimethyl-_, (4S)_- Smell Like?

This molecule delivers a crisp, aquatic freshness reminiscent of sea breeze meeting coastal vegetation. The initial burst carries a slightly metallic edge that quickly softens into a dewy green character, like crushed stems after rain. As it evolves, subtle fruity undertones emerge – imagine unripe melon rind with a whisper of citrus zest. The dry-down reveals a clean, almost mineralic quality that lingers close to the skin.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Sel Marin(Heeley, 2008)

Used to enhance the marine accord, contributing a realistic seaweed-like greenness that complements the salt and mineral notes.

Erolfa(Creed, 1992)

Provides a crisp top note that bridges the citrus opening to the ambergris base, creating a seamless aquatic transition.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

This chiral molecule belongs to the unsaturated alcohol class, featuring a nine-carbon chain with hydroxyl and methyl groups at specific positions. The (4S) stereochemistry influences its odor profile and strength. Synthesized through controlled oxidation of corresponding alkenes or via Grignard reactions, its production requires careful control to maintain optical purity. The molecular structure suggests moderate polarity and volatility, making it useful as a top-to-middle note modifier.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
SolubilitySoluble in alcohol, insoluble in water

Perfumer Guide

Note Position
Top to middle
Volatility
Moderate (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Marine and green accords
Functional Fragrance0.1-0.5%Up to 1%Clean and fresh applications

Classic Accords

Tip: Stabilize in ethanol before adding to aqueous systems to prevent cloudiness.

Alternatives & Comparisons

1
Undecavertol CAS 81782-77-6

Offers similar green-fruity aspects but with greater tenacity and less marine character.

2
Melonal CAS 106-72-9

Provides stronger melon-like fruity notes when a sweeter profile is desired.

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.

RIFM Assessment

Under evaluation by RIFM; preliminary data suggests low sensitization potential.

Sustainability

As a synthetic material, its production avoids natural resource depletion. However, the multi-step synthesis requires energy input and generates byproducts that must be properly managed. Future green chemistry approaches may improve its environmental profile.

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References

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

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