PF
← Ingredient library
← prevnext →

BENZYL CAPROATE

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

Usage guidance

Suggested min
—
Suggested max
—
Cost
—
Stock
—
Compatibility tags
gardeniajasminlilymodifiertuberose
How it behaves

Olfactory profile

Family
sweet
Note tendency
Middle
Descriptors
fruitygreensweetjasmin

A soft, oily-fruity ester with a waxy green undercurrent and a mild floral sweetness reminiscent of pineapple skin and unripe apple. Rounder and less sharp than benzyl acetate, with a subtle balsamic-floral facet from the benzyl group.AI · claude-opus-4-7

Intensity
4 / 10
Tenacity
5 / 10
Volatility
6 / 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. 297

Arctander monograph

Perfume and Flavor Chemicals, page 133.

sweetfruitygreenfloral
MW
206.29
BP
—
MP
—
Sp.Gr.
—
Refractive n
—
Rotation
—
Appearance

Colorless liquid.

Solubility

Insoluble in water, soluble in alcohol and oils.

Odor

Sweet, mild-fruity, slightly green odor, reminiscent of Apricot, but with a distinctly floral note.

Flavor

Used in flavor compositions, mainly as a modifier, in imitation Pineapple, Apricot, etc. and in Tutti-frutti flavor.

Uses in perfumery

Occasionally used in perfumes for modifying effect in Jasmin, Gardenia, Tuberose, Lily, etc. usually in combination with lower aliphatic esters of Benzyl alcohol.

Production

Produced by direct esterification of Benzyl alcohol with Hexanoic acid under azeotropic conditions.

Identity
Aliases · 3
Benzy hexanoateBenzy hexoateBenzyl hexylate
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).