Dimethyl sulfide
| Names | |
|---|---|
| Preferred IUPAC name
(Methylsulfanyl)methane | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| Abbreviations | DMS Me2S |
| 1696847 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.770 |
| EC Number |
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| KEGG | |
| MeSH | dimethyl+sulfide |
PubChem CID |
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| RTECS number |
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| UNII | |
| UN number | 1164 |
CompTox Dashboard (EPA) |
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| Properties | |
| C2H6S | |
| Molar mass | 62.13 g·mol−1 |
| Appearance | Colourless liquid |
| Odor | Stench: cabbage, sulfurous, unpleasant |
| Density | 0.846 g/cm3 |
| Melting point | −98 °C; −145 °F; 175 K |
| Boiling point | 38 °C (decomposes at 450 °C) |
| 2 g/L (at 20 °C) | |
| log P | 0.977 |
| Vapor pressure | 50.5 kPa (at 20 °C) |
| −44.9×10−6 cm3/mol | |
Refractive index (nD) |
1.435 |
| Thermochemistry | |
Std enthalpy of formation (ΔfH⦵298) |
−63.9 to −66.9 kJ⋅mol−1 |
Std enthalpy of combustion (ΔcH⦵298) |
−2.1812 to −2.1818 MJ⋅mol−1 |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H225, H319 | |
| P210, P261, P280, P305+P351+P338 | |
| NFPA 704 (fire diamond) | |
| Flash point | −48 °C (−54 °F; 225 K) |
| 205 °C (401 °F; 478 K) | |
| Explosive limits | Upper: 19.7% v/v Lower: 2.2% v/v |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
> 2000 mg/kg (oral, rat) > 5000 mg/kg (dermal, rabbit) |
LC50 (median concentration) |
40250 ppm (rat, 4 h) |
| Safety data sheet (SDS) | Fisher Scientific |
| Related compounds | |
Related chalcogenides |
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Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Dimethyl sulfide (DMS) or methylthiomethane is an organosulfur compound with the formula (CH3)2S. It is the simplest thioether and has a characteristic disagreeable odor. It is a flammable liquid that boils at 37 °C (99 °F). It is a component of the odor produced from cooking of certain vegetables (notably maize, cabbage, and beetroot) and seafoods. It is also an indication of bacterial contamination in brewing. It is a breakdown product of dimethylsulfoniopropionate (DMSP), and is also produced by the bacterial metabolism of methanethiol.