Dimethyl trisulphide
dimethyl trisulphide, DMTS
pronounced: dy-METH-il try-SUL-fide
Three sulphur atoms in a row. A savoury, oniony smell found in cooked foods.
Dimethyl trisulphide · 126.31 g/mol
The molecule
Chemical structure
This is the accurate skeletal structure of Dimethyl trisulphide, 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 Dimethyl trisulphide?
Dimethyl trisulphide, or DMTS, has three sulphur atoms joined in a row. That gives it a strong, savoury, oniony smell.
It is common in cooked foods, from fried onions to aged cheese. In cannabis it adds a savoury, cooked depth to the overall aroma.
What the research says
The Science
Like DMS, DMTS is found widely in food, so its smell is well known. It is far more powerful than DMS thanks to those extra sulphur atoms.
In cannabis it is one of several savoury sulphur notes that sit beneath the brighter skunk and fruit smells.
Aroma snapshot
How Dimethyl trisulphide Smells
Everyday sulphur familyPowerful and savoury; a little reads as onion or cooked meat.
Its role in the smell
Part of the Whole
Deepens the savoury base of the aroma, adding a cooked, oniony richness under the sharper top-notes.
Good to know
A Note on Safety
Dimethyl trisulphide 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
Dimethyl trisulphide: Common Questions
Why does some cannabis smell savoury or oniony?
Is DMTS stronger than DMS?
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).