Cis-3-Hexenyl Benzoate

TL;DR. This ingredient is used as a fragrance material, adding a green, leafy, fruity nuance to perfumes, hair care, body care, and fragranced skin care. It can also help round out floral and fresh scent profiles in a formula.

What does Cis-3-Hexenyl Benzoate do in a cosmetic formula?

This ingredient is used as a fragrance material, adding a green, leafy, fruity nuance to perfumes, hair care, body care, and fragranced skin care. It can also help round out floral and fresh scent profiles in a formula.

Is Cis-3-Hexenyl Benzoate clean?

From a clean-beauty perspective, this is mainly flagged because it is a fragrance component, a category that can be associated with sensitivity for some users and with disclosure concerns. It is not a headline restricted preservative or UV filter, but responsible use depends on fragrance safety assessment and IFRA-style concentration limits.

Is Cis-3-Hexenyl Benzoate sustainable?

This material can be made synthetically or from nature-derived feedstocks, so its sustainability profile depends heavily on sourcing and manufacturing route. As a small ester, it is expected to break down through ester hydrolysis and microbial metabolism, with lower persistence concerns than many long-lived film-formers or silicones.

Is Cis-3-Hexenyl Benzoate COSMOS-approved?

It is only aligned with COSMOS when it is part of a compliant natural fragrance system and made through permitted sourcing and processing routes. It fits Green Chemistry better when produced from renewable feedstocks by direct esterification, while petroleum-derived inputs and solvent-heavy purification weaken the profile.

How does Cis-3-Hexenyl Benzoate work chemically?

The molecule is a hydrophobic unsaturated alkenyl ester with an aromatic carboxylate group, which is why it partitions into oil phases and fragrance concentrates rather than water. It is typically used at trace fragrance levels, often well below 1% in finished products, and it should be protected from strong acid or alkaline conditions and high heat because esters can hydrolyze and unsaturated chains can oxidize.

Last updated 2026-05-13