1,3-Nonanediol acetate (mixed esters) (CAS 1322-17-4) — Green Middle Note Fragrance Ingredient

Green · Woody

1,3-Nonanediol acetate (mixed esters)

CAS 1322-17-4

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

What Is 1,3-Nonanediol acetate (mixed esters)?

1,3-Nonanediol acetate is a synthetic fragrance ingredient used in perfumes and personal care products. It contributes fresh, green, and slightly fruity nuances to formulations. This molecule helps create modern, clean scent profiles in body washes, deodorants, and fabric softeners where a long-lasting freshness is desired.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No major safety concerns
Not classified as an allergen
CAS
1322-17-4
Formula
Mixture
MW
Variable
Odor Family
Green · Woody
Layer 1 · Enthusiast

What Does 1,3-Nonanediol acetate (mixed esters) Smell Like?

1,3-Nonanediol acetate presents a crisp, dewy green character with subtle melon-like undertones. The opening is fresh and slightly aqueous, reminiscent of cucumber skin or young bamboo shoots. As it develops, a soft muskiness emerges, lending body without heaviness. The dry-down reveals a clean, almost laundry-like quality with exceptional tenacity on fabric. Its odor profile bridges fruity freshness with woody-musky depth, making it versatile for modern green-floral compositions.

Scent Profile
Layer 2

2D Molecular Structure

1,3-Nonanediol monoacetate

SMILES: CCCCCCC(CCOC(=O)C)O

Chemistry, Properties & Perfumer Guide

The Chemistry

1,3-Nonanediol acetate belongs to the ester class, synthesized through esterification of 1,3-nonanediol with acetic acid. The mixed esters form a complex of positional isomers that influence its odor profile. While purely synthetic in commercial use, related structures occur naturally in some fruits and vegetables. The acetate group enhances volatility compared to the parent diol, while the nine-carbon chain provides optimal hydrophobicity for fabric substantivity.

Physical & Chemical Properties

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

Perfumer Guide

Note Position
Middle
Volatility
Medium (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fabric Care0.5-2%Up to 3%Provides lasting freshness
Personal Care0.1-1%Up to 1.5%Clean green modifier

Classic Accords

Tip: Use with citrus top notes to prevent harshness in green compositions.

Alternatives & Comparisons

1
Hexyl acetate CAS 142-92-7

For brighter fruity-green effects with higher volatility

2
Verdox CAS 88-41-5

When more woody-green character is needed

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.

RIFM Assessment

Not currently evaluated by RIFM but structurally similar compounds show low toxicity.

Sustainability

As a synthetic material, 1,3-Nonanediol acetate production avoids agricultural land use. Modern manufacturing processes typically employ green chemistry principles to minimize waste. The material’s substantivity reduces wash-off in laundry applications, potentially lowering overall fragrance load requirements.

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References

  1. Bauer et al. (2001). Common Fragrance and Flavor Materials.
  2. Arctander (1969). Perfume and Flavor Chemicals.

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

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Ingredient Data Sheet

CAS 1322-17-4

Physical Properties

Molecular Weight202.29 g/mol🔬 PubChem
LogP (Octanol-Water)2.7🔬 PubChem
log Kp (skin permeability)-2.017💻 Calculated
SMILESCCCCCCC(CCOC(=O)C)O🔬 PubChem

Odor & Flavor

Functional Groupsesteralcoholether💻 RDKit
“The title material is intended to be a Jasmin base material. It can introduce the oily-herbaceous undertones, characteristic of Jasmin absolute, but not available from one single chemical. It is used very widely for that purpose at concentrations from 1% up to 5% or in exceptional cases higher. It is very popular in soap perfumes where its stability and diffusive power increase the "odor value" of the soap fragrance.”📖 Arctander
1,3-Nonanediol acetate, mixed esters has an intense, floral odor reminiscent of jasmine. -📖 Fenaroli

Flavor Notes (Arctander)

“This material is also used in flavor composi- tions, and its effect in berry complexes or fruit blends is quite interesting. The concentration is usually very low, because it is a powerful flavor, perceptible well below 1 ppm. From 0.3 to 1.5 ppm is normal in finished products.”📖 Arctander

Regulatory Status

FEMA NumberFEMA 2783⚖️ FEMA GRAS
GRAS StatusGenerally Recognized as Safe⚖️ FEMA GRAS
IOFI ClassificationArtificial📖 Fenaroli
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: DTXSID1047657

Physical Properties

Molecular Weight 202.29 g/mol🔬 PubChem

Partition & Solubility

LogP (Octanol-Water) 2.7 Log10 unitless🔬 PubChem

Molecular Descriptors

Topological Polar Surface Area 46.53 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 3 count💻 Computed
Rotatable Bonds 8 count💻 Computed
Molar Refractivity 56.02 cm^3/mol💻 Computed

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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