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Bis-(2-chloroethyl)sulfide

HCID 10461
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GrundinformationenNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
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Grundinformationen

CAS
505-60-2
Standard-SMILES
ClCCSCCCl
InChIKey
QKSKPIVNLNLAAV-UHFFFAOYSA-N
Summenformel
C4H8Cl2S
Durchschnittliche Molmasse
159,081 g/mol
Monoisotopische Masse
157,97237662

Namen und Bezeichner

Bevorzugter Name
Bis-(2-chloroethyl)sulfide
IUPAC
1-Chloro-2-[(2-chloroethyl)sulfanyl]ethane
Englischer Name
Mustard gas
Summenformel
C4H8Cl2S
Molmasse
159.08

Namen und Synonyme

YPERITEMustard gasSULFURMUSTARDSULPHURMUSTARDDichlorodiethyl sulfidebis-β-chloroethyl sulfideBIS(2-CHLORETHYL)SULPHIDEβ,β'-dichloroethyl sulfideBIS(2-CHLOROETHYL)SULPHIDEQKSKPIVNLNLAAV-UHFFFAOYSA-N

Datenbank-Bezeichner

CAS
505-60-2
PubChem CID
10461
DTXSID
DTXSID0037100
ChEMBL
CHEMBL455341
ChEBI
CHEBI:25434
UNII
T8KEC9FH9P
EC Number
684-527-7
Nikkaji
J1.571G

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
13 · 13-14°
Siedepunkt
760 · bp760 215-217°; bp10 98°
Dichte
13 · d13 1.338 (solid); d420 1.2741 (liq)
Dampfdichte
5.4 · 5.4
Brechungsindex
20 · nD20 1.53125
Flammpunkt
221 °F · 221°F
Aggregatzustand
liquid
Farbe
Colorless (if pure), to light-yellow, oily liquid
Wasserlöslichkeit
0.69 g/L · 0.69g/L(25 ºC)
Henry's Law Constant
3 · 3.0×10-1 mol/(m3Pa) at 25℃, Hine and Mookerjee (1975)
EPA chemische Informationen
Mustard gas (505-60-2)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

tsca
TSCA listed
ridadr
2927
Toxizität
LD50 in rats, mice (mg/kg): 3.3, 8.6 i.v. (Anslow)
hazard_class
6.1(a)
packing_group
I
Giftige Stoffe Daten
505-60-2(Hazardous Substances Data)

Chemie und Industrie

Anwendungen · 2 Einträge

BeschreibungMustard gas/sulphur mustard is an organic chemical substance synthesised by treating sulphur dichloride with ethylene. Mustard gas is a chemical substance closely related to chemical warfare class agents. It is a cytotoxic and vesicant chemical substance, and exposures are known to cause blisters on the exposed skin. Pure mustard gas/sulphur mustards are colourless, viscous liquids at room temperature. However, when used in impure form, such as warfare agents, they appear as yellow brown in colour. As the name indicates, mustard gas has an odour resembling the garlic, horseradish, or mustard plants. Mustard gas is the common name given to 1,1-thiobis(2-chloroethane), a chemical warfare agent that is believed to have first been used near Ypres in Flanders on 12 July 1917. Mustard gas is a thick liquid at ambient temperature. It is heavier than water as a liquid and heavier than air as a vapour. It does not occur naturally in the environment. Pure liquid mustard gas is colourless and odourless. It is stable, combustible, and incompatible with strong oxidising agents. Mustard gas on mixing with other chemical substances appears brown in colour and gives off a garlic-like smell. When heated, it decomposes and emits highly toxic, corrosive fumes and fumes of oxides of sulphur and chlorine-containing compounds. It is soluble in fats and oils, gasoline, kerosene, acetone, carbon tetrachloride, alcohol, tetrachloroethane, ethylbenzoate, and ether, and solubility in water is negligible. It is miscible with the OP nerve agents. During earlier years, mustard gas was in use as an important chemical warfare agent. In fact, it was used in large amounts during World Wars I and II. Mustard gas was first used by the German army in 1917. It was one of the most lethal of all the poisonous chemicals used during the war. It was reportedly used in the Iran–Iraq war in 1980–1988. It is not presently used in the United States, except for research purposes.

VerwendenFormerly in chemical warfare. In biological studies of alkylating agents.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

2,2'-Thiodiethyldiacetatcyanoformyl chlorideBIS(2-CHLOROETHYL)TRISULPHIDE

Zugehörige Reaktionen

2
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 1085127
HRID 1085127als Eduktuspto-grants-1991_04
Reaktionsgleichung von HRID 1480985
HRID 1480985als Eduktuspto-grants-2016_08

Notizen zur Verbindung

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Auf dieser SeiteGrundinformationenNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
Carbonocyanidic fluoride
BIS(2-CHLOROETHYL)DISULPHIDE
Acetylchlorid
Ethylen

Nachgelagerte Produkte

2-Chloroethyl vinyl sulfideethenylsulfanylethene2-chloroethanethiol1,1,1,2-Tetrachlorethan

Ergänzende Hinweise

DefinitionChEBI: An ethyl sulfide that is diethyl sulfide in which a hydrogen from each of the terminal methyl groups is replaced by a chlorine. It is a powerful vesicant regulated under the Chemical Weapons Convention.