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3-n-Butyl Phthalide

CAS
EC
Material type
synthetic aroma chemical
Canonical source
arctander
How it behaves

Olfactory profile

Family
Note tendency
Base
Descriptors
balsamic
Intensity
Tenacity
Volatility
chemicals · No. 617

Arctander monograph

Perfume and Flavor Chemicals, page 259.

MW
190.24
BP
300°C
MP
134°C
Sp.Gr.
1.06
Refractive n
Rotation
Appearance

White monoclinic crystals.

Solubility

Soluble 0.04°, in water, 24°, in alcohol. Soluble in oils.

Odor

Very faint honeylike, balsamic odor, easily contaminated from outside odorants.

Uses in perfumery

Finds very little use as such in perfumery.

Uses in flavor

Used in flavor compositions for imitation Cassia, spice blends, Cherry, Honey and various types of Cinnamon flavors, etc.

Production

(many methods) e. g: Benzaldehyde plus Malonic ester with catalyst. Or: Benzaldehyde plus Acetic anhydride plus Sodium acetate (Perkin’s reaction).

Identity
Aliases · 7
Alo-cinnamic acidcis-Cinnamic acidSedanolideTetrahydro-3-n-butyl phthalidetrans-3-Phenylpropenoic acidtrans-beta-Phenylacrylic acidtrans-Cinnamic acid
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).