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HYDROXYCITRONELLAL

RESTRICTIONConflicted evidence
CAS
107-75-5
EC
—
Material type
other
Canonical source
document derived

Hydroxycitronellal, with the CAS number 107-75-5, is a synthetic fragrance compound commonly used in perfumery for its floral and citrus-like scent profile. It is often employed to impart a fresh, green, and slightly sweet character to fragrances, making it a popular choice in floral and fruity compositions. Hydroxycitronellal typically sits in the heart or base of a formula, where it can enhance the overall olfactory experience by adding depth and complexity. In terms of safety and regulatory considerations, Hydroxycitronellal is recognized as a potential allergen and is subject to certain restrictions under IFRA guidelines. Perfumers should be mindful of its usage levels in formulations, particularly in products intended for leave-on applications, to ensure compliance with safety standards and to minimize the risk of allergic reactions in sensitive individuals. Its versatility and pleasant scent make it a valuable ingredient in a wide range of fragrance types. — AI-generated summary, 2026-09-02.

Formulation

Usage guidance

Suggested min
—
Suggested max
—
Cost
£240/kg
Stock
—
Compatibility tags
muguetwhite-floralfougerefloral-aldehydicchypre
How it behaves

Olfactory profile

Family
sweet
Note tendency
Base
Descriptors
sweetfloral

A classic muguet (lily-of-the-valley) aromachemical — soft, sweet, watery floral with a fresh green-linden facet. Rounded and creamy rather than sharp, it lends a dewy floral transparency but can read as slightly waxy and old-fashioned on its own.AI · claude-opus-4-7

Intensity
6 / 10
Tenacity
7 / 10
Volatility
4 / 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.

Reverse-composition

Contained in

Other ingredients whose composition declares this material as a constituent. The percentage shown is the supplier-declared concentration in that parent.

Ingredient%Range
INDOLENE60%—
POIVRE FORT—10–20%
MIMOSA DE PROVENCE—5–10%
ORRISODORE—5–10%
FLEUR DE TABAC—3–5%
OCEAN BREEZE FRAGRANCE OIL—1–5%
PRUNOL SP—1–5%
MILK F-TEC1.9802%—
GARDENIA1%—
LILAC0.85%—
VIOLET OIL0.4%—
OEILLET 2080.03%—
chemicals · No. 1728

Arctander monograph

Perfume and Flavor Chemicals, page 717.

TOPtenacity · highpower · strongFEMA 2583
sweetfloral
MW
170.27
BP
241°C
MP
—
Sp.Gr.
0.93
Refractive n
—
Rotation
—
Appearance

Colorless oily or viscous liquid.

Solubility

Very slightly soluble in water, soluble in alcohol and oils. Poorly soluble in mineral oil and glycerin or propylene glycol.

Odor

Sweet-floral, at first delicate and refreshingly mild, but often increasing in odor strength after short olfactory study. The floral notes are mild, light and resemble Lily of the Valley.

Flavor

Hydroxycitronellal has a sweet-floral taste, but shows a bitter aftertaste at concentrations higher than 20 ppm, sometimes even much lower than that.

Uses in perfumery

This aldehyde is one of the most frequently used floralizing perfume materials. Originally introduced as a 'Muguet' material, it finds its way into almost every type of floral fragrance, and a great many nonfloral ones. Its concentration in perfumes may vary from about 1% (which rarely gives effect unless supported by parallel materials) up to 30 or 40%, in straight floral types.

Uses in flavor

High-grade Hydroxycitronellal is used sparingly in flavor compositions as a floralizer in many types of flavor: Berry complexes, Citrus, Violet, Cherry, etc. and in general, a discrete touch of floral note in a flavor tends to give impression of 'richness' or 'body' which are highly desirable virtues.

Production

Produced from (many methods) e. g. from Myrcene, via Myrcene dihydrochloride to Dichloro dimethyloctene. This is converted to Chloro dihydrogeranyl acetate (and -neryl acetate) with Sodium Acetate in Benzene in presence of Triethylamine. The acetates are saponified with Calcium hydroxide to yield Hydroxycitronellol, from which the aldehyde is prepared by oxidation. Older methods start from Citronellal via the Bisulfite which is hydrated to yield Hydroxycitronellal.

Identity
Aliases · 29
Hydroxycitronellal — custom:56a1113,7-Dimethyl-7-hydroxyoctanalHydroxycitronellalOctanal, 7-hydroxy-3,7-dimethyl-7-Hydroxy-3,7-dimethyloctanalAnthosalCentaflorCitronellalhydrateCyclaliaCycliaCyclodorCyclohydronalCyclosia baseFixolFixonalHyceleaHyleaLaurinalLaurinal (commercial name)LaurineLaurine (commercial name)LilyaldehydeMajalMuguet synthetiqueMuguettine principeOxydihydrocitronellalPhixiaStorineTilleul
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).