-3-Hexen-1-yl Methyl Carbonate ●
TL;DR. This ingredient is used as a fragrance material, adding fresh green, fruity, leafy odor notes to perfumes, hair care, skin care, and wash-off products. It can also help round or mask the base odor of a formula.
What does -3-Hexen-1-yl Methyl Carbonate do in a cosmetic formula?
This ingredient is used as a fragrance material, adding fresh green, fruity, leafy odor notes to perfumes, hair care, skin care, and wash-off products. It can also help round or mask the base odor of a formula.
Is -3-Hexen-1-yl Methyl Carbonate clean?
From a clean-beauty perspective, its main friction is that it functions within fragrance, where transparency and sensitization assessment matter. It is not typically treated as a headline restricted-list material, but use should follow IFRA limits and brand fragrance disclosure standards.
Is -3-Hexen-1-yl Methyl Carbonate sustainable?
This material is commonly made by chemical synthesis from an unsaturated alcohol feedstock and a it-forming reagent, with either petrochemical or bio-based inputs depending on the supplier. It is a small ester-like molecule and is expected to break down more readily than highly persistent fragrance materials, though the overall footprint depends on the manufacturing route.
Is -3-Hexen-1-yl Methyl Carbonate COSMOS-approved?
It fits COSMOS only when supplied as part of a compliant natural-origin fragrance system that meets the standard’s aromatic-material rules and IFRA requirements. Fully synthetic supply is a weaker fit with COSMOS-organic or COSMOS-natural and has mixed Green Chemistry alignment, mainly due to feedstock and reagent choices.
How does -3-Hexen-1-yl Methyl Carbonate work chemically?
This compound is an unsaturated aliphatic it ester, so the it linkage supports fruity diffusion while the six-carbon unsaturated chain contributes a fresh green odor profile. The double bond can oxidize during storage, so formulators typically use fragrance-level dosing, limit exposure to air, heat, and light, and check compatibility with strongly acidic or alkaline systems that can cleave it esters.
Last updated 2026-05-13