Mustard gas
| Names | |
|---|---|
| Preferred IUPAC name
1-Chloro-2-[(2-chloroethyl)sulfanyl]ethane | |
| Other names
Bis(2-chloroethyl) sulfide HD Iprit Schwefel-LOST Lost Sulfur mustard Senfgas Yellow cross liquid Yperite Distilled mustard Mustard T- mixture 1,1'-thiobis[2-chloroethane] Dichlorodiethyl sulfide | |
| Identifiers | |
3D model (JSmol) |
|
| 1733595 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.209.973 |
| EC Number |
|
| 324535 | |
| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C4H8Cl2S | |
| Molar mass | 159.07 g·mol−1 |
| Appearance | Colorless if pure. Normally ranges from pale yellow to dark brown. Slight garlic or horseradish type odor. |
| Density | 1.27 g/mL, liquid |
| Melting point | 14.45 °C (58.01 °F; 287.60 K) |
| Boiling point | 217 °C (423 °F; 490 K) begins to decompose at 217 °C (423 °F) and boils at 218 °C (424 °F) |
| 7.6 mg/L at 20°C | |
| Solubility | Alcohols, ethers, hydrocarbons, lipids, THF |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Flammable, toxic, vesicant, carcinogenic, mutagenic |
| GHS labelling: | |
| Danger | |
| H300, H310, H315, H319, H330, H335 | |
| P260, P261, P262, P264, P270, P271, P280, P284, P301+P310, P302+P350, P302+P352, P304+P340, P305+P351+P338, P310, P312, P320, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 105 °C (221 °F; 378 K) |
| Safety data sheet (SDS) | External MSDS |
| Related compounds | |
Related compounds |
Nitrogen mustard, Bis(chloroethyl) ether, Chloromethyl methyl sulfide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Mustard gas or sulfur mustard are names commonly used for the organosulfur chemical compound bis(2-chloroethyl) sulfide, which has the chemical structure S(CH2CH2Cl)2, as well as other species. In the wider sense, compounds with the substituents −SCH2CH2X or −N(CH2CH2X)2 are known as sulfur mustards or nitrogen mustards, respectively, where X = Cl or Br. Such compounds are potent alkylating agents, making mustard gas acutely and severely toxic. Mustard gas is a carcinogen. There is no preventative agent against mustard gas, with protection depending entirely on skin and airways protection, and no antidote exists for mustard poisoning.
Also known as mustard agents, this family of compounds comprises infamous cytotoxins and blister agents with a long history of use as chemical weapons. The name mustard gas is technically incorrect; the substances, when dispersed, are often not gases but a fine mist of liquid droplets that can be readily absorbed through the skin and by inhalation. The skin can be affected by contact with either the liquid or vapor. The rate of penetration into skin is proportional to dose, temperature and humidity.
Sulfur mustards are viscous liquids at room temperature and have an odor resembling mustard plants, garlic, or horseradish, hence the name. When pure, they are colorless, but when used in impure forms, such as in warfare, they are usually yellow-brown. Mustard gases form blisters on exposed skin and in the lungs, often resulting in prolonged illness ending in death.