Prenyl thioacetate
prenyl thioacetate, S-prenyl thioacetate
pronounced: PREN-il thy-oh-ASS-uh-tate
A close relative of the main skunk molecule, with a gassy, fuel-like twist.
S-(3-Methylbut-2-en-1-yl) ethanethioate · 144.24 g/mol
The molecule
Chemical structure
This is the accurate skeletal structure of Prenyl thioacetate, 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 Prenyl thioacetate?
Prenyl thioacetate is a close chemical cousin of the main skunk molecule. It carries the same prenyl building block, with a small acetate group added. It was described as part of the prenylated sulphur family found in cannabis.
Its smell leans gassy and fuel-like. It is one of the compounds thought to sit behind the "diesel" or "gas" character that some cultivars are known for.
What the research says
The Science
Like the other members of this family, it appears in very small amounts and needs sensitive sulphur-detecting equipment to measure. It tends to rise and fall alongside the main skunk molecule as the plant matures and is cured.
Because it is so new to science, most of what is known is about its smell rather than any effect in the body.
Aroma snapshot
How Prenyl thioacetate Smells
Skunk & diesel familyStrong even in small amounts, with a gassy, fuel-like edge.
Its role in the smell
Part of the Whole
Adds a gassy, savoury layer on top of the pure skunk note. Blended with terpenes, it helps build the 'gas' profiles many people look for.
Good to know
A Note on Safety
Prenyl thioacetate 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
Prenyl thioacetate: Common Questions
What does 'gassy' or 'diesel' cannabis mean?
Is it the same as the main skunk molecule?
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.
- 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).