cis-3-Hexenyl Benzoate

Aroma chemical · Green / Floral

green, balsamic, floral — heart to base note.

Aroma illustration for cis-3-Hexenyl Benzoate: green leaves, drops of golden resin and pink flowers, for its green, balsamic and floral notes. It illustrates smell associations, not the material or its source.Skeletal formula of cis-3-Hexenyl Benzoate, C13H16O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what cis-3-Hexenyl Benzoate smells like (green, balsamic, floral), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 5367706). Stereochemistry is not shown; the coloured background is decoration.
Images

By the RUŌOD Lab TeamRevision 1Updated

In short

cis-3-Hexenyl benzoate is the benzoate ester of leaf alcohol. It joins a soft green note to a balsamic floral one and lasts far longer than leaf alcohol itself.

What cis-3-Hexenyl Benzoate smells like

Cis-3-hexenyl benzoate is a mild, green-herbaceous material with a woody, balsamic undertone. Arctander describes it as mild but tenacious, green-herbaceous and woody, and notes that as a green material it is much weaker than the esters of the lower aliphatic acids. Bedoukian lists green, herbaceous, floral and woody; other sources add a gentle floral, orchid-like note, and IFF describes it as only slightly green with a mild herbaceous quality.

Leading note
Mild green-herbaceous
Supporting facets
Woody, balsamic
Faint facets
Orchid-like floral
Character
Mild, soft, green, tenacious
  • green
  • balsamic
  • floral

What makes cis-3-Hexenyl Benzoate distinctive

It is a green that lasts rather than one that strikes: mild, woody and balsamic where the light leaf esters are sharp and fleeting, so it carries a soft greenness into the heart and base.

Where the descriptions disagree: Bedoukian and others call it floral; IFF describes only a slight green, mild herbaceous quality.

How cis-3-Hexenyl Benzoate is used

Used as a soft, tenacious green modifier and blender in floral and fresh compositions, where it extends greenness without the sharpness of the lighter esters.

Typical role: blender (smooths the joins between other materials).

How cis-3-Hexenyl Benzoate differs from similar materials

cis-3-Hexenyl Acetate
Arctander notes the benzoate is much weaker than the lower-acid esters such as the acetate; it is mild and tenacious, where the acetate is sharp, fruity and brief. (compared directly by a cited source)
cis-3-Hexenyl Salicylate
The salicylate is fresher and more floral, with a lily-of-the-valley note; the benzoate is milder, more herbaceous and woody.
Hexyl Benzoate
Hexyl benzoate is woodier and sappier, like cut cypress twigs; the cis-3-hexenyl ester is green-herbaceous with an orchid-like floral note.

An asterisk marks a difference that a cited source states directly. The others compare the published descriptions of each material. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

Stable in most bases.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Green / Floral
Note position
Heart to base note
Physical form at room temperature
Liquid
CAS number
25152-85-6
Molecular formula
C13H16O2
Molecular weight
204.26 g/mol
IUPAC name
[(Z)-hex-3-enyl] benzoate

The CAS number, formula and molecular weight are taken from PubChem compound 5367706, whose own record lists this CAS number; checked 19 October 2026.

Safety and compliance

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. Companies notifying the ECHA C&L Inventory report it as not meeting the GHS hazard criteria (1,593 of 1,661 reports). Unless it is harmonised, this is the notifiers' own classification, not a binding one.

This page is general information, not a safety assessment or a specification. Confirm identity, composition, IFRA status and allergen content from your supplier's documents for the lot you hold.

Materials it works with

Used in formulas and accords

Used in 3 published formulas

cis-3-Hexenyl Benzoate is an ingredient in 2 perfume formulas and 1 base in the Formula & Accord Library.

Community formulas

RUŌOD House Originals

Original compositions by RUŌOD House.

Further reading

Questions about cis-3-Hexenyl Benzoate

Is cis-3-Hexenyl Benzoate natural or synthetic?

The molecule occurs in nature. Commercial cis-3-Hexenyl Benzoate may be made by synthesis or obtained from natural sources, so check the supplier's specification if the distinction matters to you.

What is the CAS number of cis-3-Hexenyl Benzoate?

25152-85-6. It was checked against PubChem on 19 October 2026.

Which published formulas use cis-3-Hexenyl Benzoate?

cis-3-Hexenyl Benzoate is used in 3 published formulas in the RUŌOD Lab Formula & Accord Library: Cut Stem Atelier, Honeysuckle Base and Linden Afternoon. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

Keep your own record of cis-3-Hexenyl Benzoate — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.