5- and 6-Decenoic acid (CAS 72881-27-7) — Sweet Heart to base Note Fragrance Ingredient

Sweet · Musky

5- and 6-Decenoic acid

CAS 72881-27-7

Origin
synthetic
Note
Heart to base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 5- and 6-Decenoic acid?

5- and 6-Decenoic acid is a synthetic fragrance ingredient with a distinctive fatty, waxy character. It’s primarily used in perfumery to create creamy, milky, or slightly cheesy nuances. This ingredient matters because it adds unique lactonic and dairy-like facets to fragrances, helping perfumers replicate complex natural aromas that would otherwise be difficult to achieve.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
Approved for fragrance use
Potential skin sensitizer at high concentrations
CAS
72881-27-7
Formula
Mixture
MW
Variable
Odor Family
Sweet · Musky
Layer 1 · Enthusiast

What Does 5- and 6-Decenoic acid Smell Like?

5- and 6-Decenoic acid presents a complex olfactory profile that evolves from sharp, acidic top notes to a creamy, dairy-like heart. The initial impression is reminiscent of aged cheese or sour milk, which soon softens into a waxy, coconut-like aroma. In the dry-down, it reveals subtle animalic undertones that blend beautifully with floral and woody bases. The overall effect is like the transition from fresh goat cheese to sun-warmed coconut flesh, making it invaluable for creating rich, lactonic accords.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Dairy(Demeter Fragrance Library, 1996)

Used to create the photorealistic milk note, contributing creamy-lactonic depth that makes this fragrance so distinctive.

Fils de Dieu du Riz et des Agrumes(Etat Libre d’Orange, 2012)

Provides the subtle coconut-milk nuance that softens the citrus-rice accord, adding creamy sophistication.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

5- and 6-Decenoic acid belongs to the class of medium-chain fatty acids with unsaturated carbon chains. While not found in significant quantities in nature, it’s synthesized through controlled oxidation of decene or via specialized fermentation processes. The mixture typically contains both positional isomers (5- and 6-), with the 5-isomer being slightly more potent olfactively. The double bond position significantly influences the odor character, with 5-decenic acid being more lactonic while 6-decenic acid shows more fatty-waxy characteristics.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
Odor ThresholdVery low (parts per million)

Perfumer Guide

Note Position
Heart to base
Volatility
Medium (2-6 hours)
Blending
Good with lactones, musks, and woody notes
ApplicationTypical %RangeNotes
Fine Fragrance0.1-0.5%Up to 1%Used sparingly for dairy nuances
Functional Fragrances0.01-0.1%Up to 0.3%For creamy body care products

Classic Accords

Tip: Use in trace amounts with lactones to enhance creamy effects without overpowering.

Alternatives & Comparisons

1
Gamma-Nonalactone CAS 104-61-0

For a cleaner coconut-milk effect without the fatty-cheesy aspects.

2
Delta-Decalactone CAS 705-86-2

When a more pronounced peach-like lactonic character is desired.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA. Approved for use within standard fragrance guidelines.

EU Allergen Declaration

Not listed as an EU allergen.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM has reviewed this material and found it safe for use at current industry levels.

Sustainability

As a synthetic material, 5- and 6-Decenoic acid doesn’t rely on agricultural resources. Modern synthesis methods aim to minimize environmental impact through efficient catalysis and reduced solvent use. The carbon footprint is comparable to other specialty fragrance chemicals, with ongoing research into bio-based production routes.

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References

  1. Brenna et al. (2002). Lactones in Flavors and Fragrances. Chemistry & Biodiversity. DOI:10.1002/cbdv.200790001

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

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