3-Mercaptohexyl acetate
3-mercaptohexyl acetate, 3-sulfanylhexyl acetate, 3-MHA
pronounced: three mer-KAP-toh-HEX-il ASS-uh-tate
The passion-fruit molecule. The acetate cousin of 3-MH, even more tropical.
3-Sulfanylhexyl acetate · 176.28 g/mol
The molecule
Chemical structure
This is the accurate skeletal structure of 3-Mercaptohexyl acetate, drawn from PubChem data. Each corner and line-end is a carbon atom. The yellow S marks sulphur, the atom that gives this whole family its powerful smell.
About
What is 3-Mercaptohexyl acetate?
3-Mercaptohexyl acetate, or 3-MHA, is the acetate cousin of 3-MH. Adding the acetate group pushes the smell even further towards passion fruit and tropical punch.
Like 3-MH, it is a star of flavour chemistry in wine and beer, and it was reported among the compounds behind fruity, exotic cannabis.
What the research says
The Science
The 2023 study grouped 3-MHA with 3-MH as key drivers of tropical, fruity aromas in certain cultivars. The two often appear together.
It is another extremely powerful smell, active at tiny concentrations.
Aroma snapshot
How 3-Mercaptohexyl acetate Smells
Tropical & fruity familyAn even punchier passion-fruit smell, powerful at trace levels.
Its role in the smell
Part of the Whole
Layers a ripe passion-fruit punch over the top of fruity cultivars, deepening their tropical character.
Good to know
A Note on Safety
3-Mercaptohexyl acetate is an aroma compound, present in cannabis in trace amounts. It is not a medicine and has no dose of its own. What matters for you is the whole product and how it is prescribed.
Always choose and adjust your medicine with your prescriber and pharmacist, never by smell alone.
Questions
3-Mercaptohexyl acetate: Common Questions
What is the difference between 3-MH and 3-MHA?
Do these tropical smells mean the cannabis is stronger?
References
- Oswald, I.W.H., Ojeda, M.A., Pobanz, R.J., Koby, K.A., Buchanan, A.J., Del Rosso, J., Guzman, M.A. and Martin, T.J. (2021) 'Identification of a new family of prenylated volatile sulfur compounds in cannabis revealed by comprehensive two-dimensional gas chromatography', ACS Omega, 6(47), pp. 31667-31676. doi: 10.1021/acsomega.1c04196.
- Oswald, I.W.H. et al. (2023) 'Minor, nonterpenoid volatile compounds drive the aroma differences of exotic cannabis', ACS Omega, 8(36), pp. 39203-39216.
- Russo, E.B. (2011) 'Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects', British Journal of Pharmacology, 163(7), pp. 1344-1364. doi: 10.1111/j.1476-5381.2011.01238.x.
- National Center for Biotechnology Information (2025) PubChem Compound Database. Bethesda: U.S. National Library of Medicine. Available at: https://pubchem.ncbi.nlm.nih.gov (Accessed: 3 August 2026).