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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 | |||
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 | |||
EU classification (DSD)
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R-phrases | R11, R22 | ||
S-phrases | S16 | ||
NFPA 704 | |||
Flash point | -11(9) °C | ||
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.