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| Names | |||
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IUPAC name
Thietane
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| Other names
Thiacyclobutane
Trimethylene sulfide |
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| Identifiers | |||
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287-27-4 |
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| 3D model (Jmol) | Interactive image | ||
| 102383 | |||
| ChemSpider |
8895 |
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| ECHA InfoCard | 100.005.469 | ||
| EC Number | 206-015-0 | ||
| PubChem | 9251 | ||
| UN number | 1993 | ||
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| Properties | |||
| C3H6S | |||
| Molar mass | 74.14 g·mol−1 | ||
| Appearance | Colourless liquid | ||
| Odor | Sulfurous | ||
| Density | 1.028 g cm−3 | ||
| Boiling point | 94 to 95 °C (201 to 203 °F; 367 to 368 K) | ||
| Hazards | |||
| GHS pictograms |
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| GHS signal word | DANGER | ||
| H225, H302 | |||
| P210 | |||
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EU classification (DSD)
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| R-phrases | R11, R22 | ||
| S-phrases | S16 | ||
| NFPA 704 | |||
| Flash point | -11(9) °C | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |||
Thietane is a heterocyclic compound containing a saturated four-membered ring with three carbon atoms and one sulfur atom.
Thietane, and its derivative 2-propylthietane, are strong-smelling mouse alarm pheromones and predator scent analogues. Both the mouse and human olfactory receptors MOR244-3 and OR2T11, respectively, were found to respond to thietane in the presence of copper.