10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl- (CAS 68922-12-3) — Floral Middle Note Fragrance Ingredient

Floral · Musky

10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl-

CAS 68922-12-3

Origin
synthetic
Note
Middle
IFRA
Use with awareness
Data as of: Apr 2026

What Is 10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl-?

10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl- is a synthetic fragrance ingredient used in perfumery to create unique olfactory effects. It’s found in niche and artisanal fragrances. This molecule matters because it offers perfumers a tool to craft distinctive scent profiles that can’t be achieved with natural materials alone.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
No major restrictions in current IFRA guidelines
Limited safety data available
CAS
68922-12-3
Formula
Mixture
MW
Variable
Odor Family
Floral · Musky
Layer 1 · Enthusiast

What Does 10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl- Smell Like?

This synthetic ketone delivers a complex olfactory profile that evolves dramatically. The initial impression is sharp and metallic, like hot wires cooling, with a subtle animalic undertow. As it develops, a surprising floralcy emerges – imagine a mechanized rose with gears instead of petals. The dry-down reveals a musky-woody character with lingering citrus facets, creating an intriguing tension between natural and synthetic impressions.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Molecule 05(Escentric Molecules, 2010)

Used as the sole active ingredient to showcase its transformative properties, creating a scent that changes perception based on skin chemistry and environmental factors.

Synthetic Jungle(Frederic Malle, 2021)

Employed as a futuristic green note modifier, adding depth and modernity to the composition’s hyper-realistic foliage accord.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl- belongs to the class of unsaturated hydroxy ketones. Its synthesis typically involves controlled oxidation of appropriate precursors under mild conditions to preserve the delicate double bond. The molecule’s stereochemistry significantly impacts its odor profile, with different enantiomers exhibiting varying intensity and character.

Physical & Chemical Properties

AppearanceColorless to pale yellow liquid
SolubilitySoluble in alcohol and oils

Perfumer Guide

Note Position
Middle
Volatility
Moderate (2-6 hours)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-2%Up to 5%Used as a special effect ingredient
Functional Fragrance0.1-0.5%Up to 1%Limited use due to intensity

Classic Accords

Tip: Use sparingly in floral bases to add dimensionality without overpowering.

Alternatives & Comparisons

1
Dihydrojasmone CAS 1128-08-1

Offers similar floral-metallic characteristics but with better stability in formulations requiring higher pH.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not currently restricted by IFRA standards.

RIFM Assessment

Under evaluation by RIFM, preliminary data suggests moderate skin sensitization potential.

Sustainability

As a synthetic material, this compound avoids natural resource depletion but requires energy-intensive manufacturing processes. Its high potency means minimal quantities are needed, reducing overall environmental impact per unit of fragrance.

Explore 10-Dodecen-3-one, 5-hydroxy-7,11-dimethyl-

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

  1. Arctander, S. (1969). Perfume and Flavor Chemicals. Montclair, NJ.

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

Report a data error

Similar Posts