Dimethyl disulfide

Dimethyl disulfide
Dimethyl disulfide
Identifiers
Abbreviations DMDS
CAS number 624-92-0 YesY
PubChem 12232
ChemSpider 11731 YesY
ChEBI CHEBI:4608 YesY
Jmol-3D images Image 1
Properties
Molecular formula C2H6S2
Molar mass 94.2 g mol−1
Appearance Colorless to yellowish liquid[1]
Density 1.06 g/cm3[1]
Melting point

-85 °C, 188 K, -121 °F ([1])

Boiling point

110 °C, 383 K, 230 °F ([1])

Solubility in water 2.5 g/L (20 °C)[1]
Hazards
Flash point 15 °C (59 °F)[1]
Autoignition
temperature
370 °C (698 °F)[1]
LD50 190 mg/kg (oral, rat)[2]
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Dimethyl disulfide (DMDS) is an organic chemical compound with the molecular formula CH3SSCH3 which is the simplest disulfide. It is a flammable liquid with an unpleasant odor.

DMDS can be produced by the reaction of methanethiol with sulfur:

2 CH3SH + S → CH3SSCH3 + H2S

Uses

DMDS is used as a food additive in onion, garlic, cheese, meats, soups, savory flavors, and fruit flavors.[2]

Industrially, DMDS is used in oil refineries as a sulfiding agent.[3]

References

  1. ^ a b c d e f g Record in the GESTIS Substance Database from the IFA
  2. ^ a b Dimethyl disulfide, Good Scents Company
  3. ^ Dimethyl Disulfide (DMDS), Arkema, Inc.

Wikimedia Foundation. 2010.

Игры ⚽ Нужно сделать НИР?

Look at other dictionaries:

  • Disulfide bond — In chemistry, a disulfide bond (Br.E. disulphide bond) is a covalent bond, usually derived by the coupling of two thiol groups. The linkage is also called an SS bond or disulfide bridge. The overall connectivity is therefore R S S R. The… …   Wikipedia

  • tetramethylthiuram disulfide — | ̷ ̷ ̷ ̷| ̷ ̷ ̷ ̷ ̷ ̷| ̷ ̷ ̷ ̷ noun Etymology: tetramethyl + thiuram : a crystalline irritating compound [(CH3)2NCS]2S2 made by oxidation of a salt of dimethyl dithiocarbamic acid and used chiefly as an accelerator of rubber vulcanization and as …   Useful english dictionary

  • Functional group — For other uses, see Functional group (disambiguation) and Moiety (disambiguation). Benzyl acetate has an ester functional group (in red), an acetyl moiety (circled with green) and a benzyloxy moiety (circled with orange). Other divisions can be… …   Wikipedia

  • Wine fault — A wine fault or defect is an unpleasant characteristic of a wine often resulting from poor winemaking practices or storage conditions, and leading to wine spoilage. Many of the compounds that cause wine faults are already naturally present in… …   Wikipedia

  • climate — /kluy mit/, n. 1. the composite or generally prevailing weather conditions of a region, as temperature, air pressure, humidity, precipitation, sunshine, cloudiness, and winds, throughout the year, averaged over a series of years. 2. a region or… …   Universalium

  • Dimethyldisulfid — Strukturformel Allgemeines Name Dimethyldisulfid Andere Namen …   Deutsch Wikipedia

  • Kraft process — The Kraft process (also known as Kraft pulping or sulfate process) describes a technology for conversion of wood into wood pulp consisting of almost pure cellulose fibers. The process entails treatment of wood chips with a mixture of sodium… …   Wikipedia

  • Paper pollution — The production, use and recycling of paper has a number of adverse effects on the environment which are known collectively as paper pollution. Pulp mills contribute to air, water and land pollution. Discarded paper is a major component of many… …   Wikipedia

  • Huntsman (chemical plant) — Huntsman Chemical Company of Australia Pty Ltd (HCCA)operate a complex chemical manufacturing plant in Somerville Rd Brooklyn in Melbourne. The site is approximately 40 hectares in size and is located in the City of Brimbank. HCCA is partially… …   Wikipedia

  • Pulp (paper) — Fibres in wood pulp Pulp is a lignocellulosic fibrous material prepared by chemically or mechanically separating cellulose fibres from wood, fibre crops or waste paper. Wood pulp is the most common raw material in papermaking. Contents …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”