4-Hexen-1-ol, (4Z)- (CAS 928-91-6) — Green Top Note Fragrance Ingredient

Green · Citrus

4-Hexen-1-ol, (4Z)-

CAS 928-91-6

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

What Is 4-Hexen-1-ol, (4Z)-?

4-Hexen-1-ol, (4Z)- is a synthetic fragrance ingredient often used to add fresh, green notes to perfumes and scented products. You’ll encounter it in body washes, air fresheners, and some light floral perfumes. This molecule matters because it provides a crisp, dewy-leaf effect that helps create naturalistic green accords without relying on expensive botanicals.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
IFRA compliant at standard usage levels
Monitor for skin sensitivity in leave-on products
CAS
928-91-6
Formula
Mixture
MW
Variable
Odor Family
Green · Citrus
Layer 1 · Enthusiast

What Does 4-Hexen-1-ol, (4Z)- Smell Like?

A vibrant green burst reminiscent of freshly crushed tomato leaves or snapped pea stems, with a slightly waxy undertone that recalls cucumber skin. The initial sharpness softens into a dewy vegetal sweetness, like morning grass after rain, before fading cleanly without woody residue. In dilution, it gains an almost melon-like juiciness that works beautifully in modern citrus compositions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Vent Vert(Balmain, 1947)

Used here to amplify the hyper-realistic galbanum effect, creating that iconic ‘green lightning’ effect that made this fragrance revolutionary.

Un Jardin Sur Le Nil(Hermès, 2005)

Provides the juicy green mango facet that makes this tropical composition feel simultaneously ripe and refreshing.

Layer 2

2D Molecular Structure

4-Hexen-1-ol, (4Z)-

SMILES: C\C=C/CCCO

Chemistry, Properties & Perfumer Guide

The Chemistry

A six-carbon unsaturated alcohol with a cis double bond at position 4. Industrially produced via hydroformylation of butadiene followed by selective reduction. The Z-configuration is critical for odor quality – the E-isomer smells markedly harsher and more metallic. This stereospecificity makes industrial synthesis challenging, with typical commercial material being 85-92% Z-isomer.

Physical & Chemical Properties

Boiling Point157-158 °C
Density0.845 g/cm³
Refractive Index1.438
Flash Point46 °C

Perfumer Guide

Note Position
Top
Volatility
Medium (1-3 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Green note enhancer
Functional Products0.1-0.5%Up to 1%Freshness booster
Home Care0.05-0.2%Up to 0.5%Cut-grass effect

Classic Accords

Tip: Stabilize in ethanol before adding to water-based systems to prevent clouding.

Alternatives & Comparisons

1
cis-3-Hexenol CAS 928-96-1

When a brighter, more intensely grassy effect is needed, though it lacks the waxy nuance of the 4-isomer.

2
Stemone CAS 63868-78-6

For more floral-green effects with better persistence, though at higher cost.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards (as of Amendment 49).

RIFM Assessment

RIFM assessment completed in 2013 – no significant safety concerns at current use levels.

Sustainability

Synthesized from petrochemical feedstocks with moderate energy requirements. No known ecological toxicity at environmental concentrations from fragrance use. Preferred over natural extracts for consistent quality and reduced agricultural impact.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials. Wiley-VCH. ISBN 978-3-527-30364-6
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Steffen Arctander. OCLC 9131

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

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Ingredient Data Sheet

CAS 928-91-6

Physical Properties

Molecular Weight100.16 g/mol🔬 PubChem
LogP (Octanol-Water)1.2🔬 PubChem
Boiling Point159 °C🔬 EPA CompTox
log Kp (skin permeability)-2.459💻 Calculated
SMILESCC=CCCCO🔬 PubChem

Volatility & Performance

Fragrance NoteTop💻 Calculated

Odor & Flavor

Primary Descriptorsfruitygreen• leffingwell
Functional Groupsalcoholalkene💻 RDKit

Sensory Thresholds

Odor Detection Threshold0.1 ppm📖 van Gemert
Data Sources & Attribution
Physical data: PubChem (NIH/NLM), U.S. EPA CompTox Dashboard, EPA OPERA models, RDKit. Odor & flavor: Arctander (Perfume & Flavor Chemicals), Fenaroli's Handbook of Flavor Ingredients, Leffingwell. Thresholds: van Gemert (Compilations of Odour Threshold Values). Regulatory: IFRA Standards 51st, FEMA GRAS. Trade names: Surburg (Common Fragrance & Flavor Materials). All data compiled and cross-referenced for perfumertools.com.

Physicochemical Properties

DTXSID: DTXSID10883609

Physical Properties

Molecular Weight 100.161 g/mol🔬 EPA CompTox
Density 0.862 g/cm^3📊 OPERA
Boiling Point 158.369 °C📊 OPERA
Melting Point -34.345 °C📊 OPERA
Flash Point 60.302 °C📊 OPERA
Refractive Index 1.443 Dimensionless📊 OPERA
Molar Volume 118.697 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 1.304 Log10 unitless📊 OPERA
LogD (pH 5.5) 1.304 Log10 unitless📊 OPERA
LogD (pH 7.4) 1.304 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.65 Log10 unitless📊 OPERA
Water Solubility 0.124 mol/L📊 OPERA
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 1.32 mmHg📊 OPERA
Viscosity 2.298 cP📊 OPERA
Surface Tension 27.068 dyn/cm📊 OPERA
Thermal Conductivity 151.846 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 20.23 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 3 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 31.439 cm^3/mol📊 OPERA
Polarizability 12.463 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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