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UNDECANOL-1

CAS
—
EC
—
Material type
synthetic aroma chemical
Canonical source
arctander
Formulation

Usage guidance

Suggested min
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Suggested max
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Cost
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Stock
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Compatibility tags
cassiecitruscolognefloralgreenrosetopnoteviolet
How it behaves

Olfactory profile

Family
domestic
Note tendency
Middle
Descriptors
floralfruitygreenherbaceouscitrusysweetfreshoilyrosefatty

A fatty-waxy alcohol with a soft citrus-floral character reminiscent of orange peel and rose petal. Cleaner and less sharp than the corresponding aldehyde (undecanal), with a creamy, slightly soapy undertone that persists into a mild waxy drydown.AI · claude-opus-4-7

Intensity
5 / 10
Tenacity
5 / 10
Volatility
5 / 10
Members

The rest of this material

Composition, IFRA restriction figures, allergen concentrations and where this material is bought are part of Perfume Foundry’s curated library and need an account. Create one or sign in.

chemicals · No. 3031

Arctander monograph

Perfume and Flavor Chemicals, page 1354.

G.R.A.S.FEMA 3097
oilyfruityfloralcitrusyfreshrosy
MW
172.31
BP
241°C
MP
16°C
Sp.Gr.
0.83
Refractive n
—
Rotation
—
Appearance

Colorless oily liquid, solidifying in the cold.

Solubility

Almost insoluble in water, soluble in alcohol and oils.

Odor

Oily-fruity, floral-citrusy odor, slightly fatty, but overall fresh and delicately rosy, in high dilution Mandarin-like.

Flavor

Concentrations below 20 ppm have citrusy, oily-fruity, mildly sweet taste, but higher concentrations tend to produce unpleasantly fatty taste.

Uses in perfumery

This alcohol is frequently, but not very widely used in perfume compositions, often as a companion to the corresponding aldehyde or other aliphatic aldehydes in topnote compositions. It blends well with the floral-citrusy fragrance types, Citrus colognes, Cassie and Violet, green and herbaceous fragrances. It is often used in Rose bases.

Uses in flavor

In imitation Citrus flavors, Lemon, Lime, Mandarin and Orange, and occasionally in Blackcurrant flavor or Rose flavor, it is used in small amounts, equivalent to 3 to 15 ppm in the finished product.

Production

1) by Bouveault-Blanc reduction of Ethyl undecylate. 2) by reduction of Ethyl undecylenate. 3) by Grignard reaction from n-Nonyl magnesiumbromide plus Ethylene oxide.

Identity
Aliases · 5
Alcohol C-11 (saturated)Decyl carbinolHendecanolUndecyl alcoholUndecylic alcohol
Compliance note. Restriction data is sourced directly from IFRA publications and preserved with its document excerpt. Perfume Foundry is a compliance-support tool — not a substitute for a qualified safety assessor (CPSR / PIF).