Dimethyl sulfide

Chemical compound From Wikipedia, the free encyclopedia

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 smell 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.

Quick facts Names, Identifiers ...
Dimethyl sulfide
Skeletal formula of dimethyl sulfide with all implicit hydrogens shown
Skeletal formula of dimethyl sulfide with all implicit hydrogens shown
Spacefill model of dimethyl sulfide
Spacefill model of dimethyl sulfide
Names
Preferred IUPAC name
(Methylsulfanyl)methane[3]
Other names
  • (Methylthio)methane[3]
  • Dimethyl sulfide[3]
  • Dimethyl thioether[4]
Identifiers
3D model (JSmol)
1696847
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.770 Edit this at Wikidata
EC Number
  • 200-846-2
KEGG
MeSH dimethyl+sulfide
RTECS number
  • PV5075000
UNII
UN number 1164
  • InChI=1S/C2H6S/c1-3-2/h1-2H3 checkY
    Key: QMMFVYPAHWMCMS-UHFFFAOYSA-N checkY
  • Key: QMMFVYPAHWMCMS-UHFFFAOYAH
  • CSC
Properties
(CH3)2S
Molar mass 62.13 g·mol−1
Appearance Colourless liquid
Odor Stench: cabbage, sulfurous, unpleasant
Density 0.846 g·cm−3
Melting point −98 °C; −145 °F; 175 K
Boiling point 35 to 41 °C; 95 to 106 °F; 308 to 314 K
log P 0.977
Vapor pressure 53.7 kPa (at 20 °C)
−44.9×10−6 cm3/mol
1.435
Thermochemistry
−63.9 to −66.9 kJ⋅mol−1
−2.1812 to −2.1818 MJ⋅mol−1
Hazards
GHS labelling:
GHS02: Flammable GHS05: Corrosive GHS07: Exclamation mark
Danger
H225, H315, H318, H335
P210, P261, P280, P305+P351+P338
Flash point −36 °C (−33 °F; 237 K)
206 °C (403 °F; 479 K)
Explosive limits 19.7%[clarification needed]
Safety data sheet (SDS) osha.gov
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Occurrence and production

DMS originates primarily from DMSP, a major secondary metabolite in some marine algae.[5] DMS is the most abundant biological sulfur compound emitted to the atmosphere.[6][7] Emission occurs over the oceans by phytoplankton.

DMS is also produced naturally by bacterial transformation of dimethyl sulfoxide (DMSO).[8]

Marine phytoplankton also produce dimethyl sulfide,[9] and DMS is also produced by bacterial cleavage of extracellular DMSP.[10] This may be an adaptive trait, as the algae can use the resulting clouds to disperse themselves around the world.[11] DMS has been characterized as the "smell of the sea",[12] though it would be more accurate to say that DMS is a component of the smell of the sea, others being chemical derivatives of DMS, such as oxides, and yet others being algal pheromones such as dictyopterenes.[13]

Dimethyl sulfide, dimethyl disulfide, and dimethyl trisulfide have been found among the volatiles given off by the fly-attracting plant known as dead-horse arum (Helicodiceros muscivorus). Those compounds are components of an odor like rotting meat, which attracts various pollinators that feed on carrion, such as many species of flies.[14]

Brewing

DMS can occur in beer as a product from either S-Methylmethionine (SMM) or dimethyl sulfoxide (DMSO). Most SSM and DMSO stem from the malt, formed during the malting process (germination and kilning), and converted to DSM during the brewing process. SMM is converted to DSM when heated, both during kilning and during boiling of the wort. DMSO may form during kilning, from oxidation of DSM. It is heat stable and may remain in the wort into fermentation, where bacteria (or yeast) can reduce it to DSM.[15]

Astronomical detection

Dimethyl sulfide has been detected in comets, which indicates non-living sources are available.[16] For comet 67P/Churyumov-Gerasimenko, the European Space Agency sampled the cloud of dust and gas shed from the comet.[17][18][19]

Industrial production

In industry dimethyl sulfide is produced by treating hydrogen sulfide with methanol over an aluminium oxide catalyst:[20]

2 CH3OH + H2S → (CH3)2S + 2 H2O

Dimethyl sulfide is emitted by kraft pulping mills as a side product from delignification.

Odor

Dimethyl sulfide has a characteristic odor commonly described as cabbage-like. It becomes highly disagreeable at even quite low concentrations. Some reports claim that DMS has a low olfactory threshold that varies from 0.02 to 0.1 ppm[clarification needed] between persons, but it has been suggested that the odor attributed to dimethyl sulfide may in fact be due to disulfides, polysulfides and thiol impurities, since the odor of dimethyl sulfide is much less disagreeable after it is freshly washed with saturated aqueous mercuric chloride.[21] Dimethyl sulfide is also available as a food additive to impart a savory flavor; in such use, its concentration is low. Beetroot,[22] asparagus,[23] cabbage, maize and seafoods produce dimethyl sulfide when cooked.

Dimethyl sulfide is also produced by marine planktonic microorganisms such as the coccolithophores. It contributes to the characteristic odor of sea air. In the Victorian era, before DMS was discovered, the origin of sea air's 'bracing' aroma was misattributed to ozone.[24]

Dimethyl sulfide is the main volatile product various of truffles. It is the compound that animals trained to uncover the fungus (such as pigs and detection dogs) sniff out when searching for them.[25]

Chemical reactions

Lewis basicity

As a Lewis base. It is classified as a soft ligand (see also ECW model). It forms complexes with many transition metals. For example, it serves a displaceable ligand in chloro(dimethyl sulfide)gold(I).[26] It is used is for the production of borane dimethyl sulfide from diborane:[20]

B2H6 + 2 (CH3)2S → 2 BH3·S(CH3)2

Other reactions

With chlorinating agents such as sulfuryl chloride, dimethyl sulfide converts to chloromethyl methyl sulfide:

SO2Cl2 + (CH3)2S → SO2 + HCl + ClCH2SCH3

Like other methylthio compounds, DMS is deprotonated by butyl lithium:[27]

CH3CH2CH2CH2Li + (CH3)2S → CH3CH2CH2CH3 + LiCH2SCH3

Oxidation and reduction

Oxidation of dimethyl sulfide gives the solvent dimethyl sulfoxide. Further oxidation affords dimethyl sulfone. Dimethyl sulfide is used in the workup of the ozonolysis of alkenes, where it reduces the intermediate trioxolane.

The Swern oxidation produces dimethyl sulfide by reduction of dimethylsulfoxide.[26]

DMS is oxidized in the marine atmosphere to various sulfur-containing compounds, such as sulfur dioxide, dimethyl sulfoxide (DMSO), dimethyl sulfone, methanesulfonic acid and sulfuric acid.[28] Among these compounds, sulfuric acid has the potential to create new aerosols which act as cloud condensation nuclei. It usually results in the formation of sulfate particles in the troposphere. Through this interaction with cloud formation, the massive production of atmospheric DMS over the oceans may have a significant impact on the Earth's climate.[29][30] The CLAW hypothesis suggests that in this manner DMS may play a role in planetary homeostasis.[31]

DMS is oxidized by atmospheric NO3 radical to give atmospheric nitric acid.[32]

Safety

Dimethyl sulfide is highly flammable;[33] its flash point is −38 °C (−36 °F)[34] or −49 °C (−56 °F).[35] Its self-ignition temperature is 205 °C (401 °F).[35] It is an eye and skin irritant and is harmful if swallowed. It has an unpleasant odor at even extremely low concentrations.[36]

Dimethyl sulfide is normally present at very low levels in healthy people, namely less than 7 nM in blood, less than 3 nM in urine and 0.13 to 0.65 nM on expired breath.[37][38]

At pathologically dangerous concentrations, this is known as dimethylsulfidemia. This condition is associated with blood borne halitosis and dimethylsulfiduria.[39][40][41]

See also

References

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