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
EC Number
  • 684-527-7
324535
KEGG
UNII
  • InChI=1S/C4H8Cl2S/c5-1-3-7-4-2-6/h1-4H2 checkY
    Key: QKSKPIVNLNLAAV-UHFFFAOYSA-N checkY
  • InChI=1/C4H8Cl2S/c5-1-3-7-4-2-6/h1-4H2
    Key: QKSKPIVNLNLAAV-UHFFFAOYAK
  • ClCCSCCCl
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.[1]
Density 1.27 g/mL, liquid
Melting point 14.4 °C (57.9 °F; 287.5 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[2]
Solubility Alcohols, ethers, hydrocarbons, lipids, THF
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Flammable, toxic, vesicant, carcinogenic, mutagenic
GHS labelling:[3]
GHS06: ToxicGHS07: Exclamation mark
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)
NFPA 704 four-colored diamond
4
1
1
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).
☒N verify (what is checkY☒N ?)
Infobox references

Bis(2-chloroethyl)sulfide is the organosulfur compound with the formula (ClCH2CH2)2S. It is a prominent member of a family of cytotoxic and blister agents known as mustard agents. Sometimes referred to as mustard gas, the term is technically incorrect: bis(2-chloroethyl)sulfide is a liquid at room temperature. In warfare it was dispersed in the form of a fine mist of liquid droplets.[4][5]

Synthesis

Bis(2-chloroethyl)sulfide has been prepared in a variety of ways. In the Depretz method, sulfur dichloride is treated with ethylene:

SCl2 + 2 C2H4 → (ClC2H4)2S

In the Levinstein process, disulfur dichloride is used instead:[6][7]

S2Cl2 + 2 C2H4 → (ClC2H4)2S + 1⁄8 S8

In the Meyer method, thiodiglycol is produced from chloroethanol and potassium sulfide, and the resulting diol is then treated with phosphorus trichloride:[8][9]

3 (HOC2H4)2S + 2 PCl3 → 3 (ClC2H4)2S + 2 P(OH)3

In the Meyer–Clarke method, concentrated hydrochloric acid (HCl) is used instead of PCl3:

(HOC2H4)2S + 2 HCl → (ClC2H4)2S + 2 H2O

Thionyl chloride and phosgene, the latter of which is also a choking agent, have also been used as chlorinating agents. These compounds have the added advantage in that if they are used in excess, they remain as impurities in the finished product and can therefore produce additional mechanisms of toxicity.

Reactions

The idealized combustion of mustard gas in oxygen produces hydrochloric acid and sulfuric acid, in addition to carbon dioxide and water:

(ClC2H4)2S + 7 O2 → 4 CO2 + 2 H2O + 2 HCl + H2SO4

Bis(2-chloroethyl)sulfide reacts with sodium hydroxide, giving divinyl sulfide:

(ClC2H4)2S + 2 NaOH → (CH2=CH)2S + 2 H2O + 2 NaCl

Sodium ethoxide acts similarly.

Safety

Upon skin contact or inhalation, bis(2-chloroethyl)sulfide is a nonspecific toxin. It is a strong alkylating agent, which affects DNA, RNA, and proteins.[10]

See also

References

  1. ↑ FM 3–8 Chemical Reference handbook, US Army, 1967
  2. ↑ Mustard agents: description, physical and chemical properties, mechanism of action, symptoms, antidotes and methods of treatment. Organisation for the Prohibition of Chemical Weapons. Accessed June 8, 2010.
  3. ↑ "Pubchem".
  4. ↑ "Sulfur Mustard: Blister Agent". Centers for Disease Control and Prevention. Archived from the original on 2023-11-01. Retrieved 2023-12-28.
  5. ↑ Ghabili, Kamyar; Agutter, Paul S.; Ghanei, Mostafa; Ansarin, Khalil; Panahi, Yunes; Shoja, Mohammadali M. (2011). "Sulfur mustard toxicity: History, chemistry, pharmacokinetics, and pharmacodynamics". Critical Reviews in Toxicology. 41 (5): 384–403. doi:10.3109/10408444.2010.541224. PMID 21329486. S2CID 28491672.
  6. ↑ Stewart, Charles D. (2006). Weapons of mass casualties and terrorism response handbook. Boston: Jones and Bartlett. p. 47. ISBN 0-7637-2425-4.
  7. ↑ "Chemical Weapons Production and Storage". Federation of American Scientists. Archived from the original on August 11, 2014.
  8. ↑ E. M. Faber and G. E. Miller (1932). "β-Thiodiglycol". Organic Syntheses. 12: 68. doi:10.15227/orgsyn.012.0068.
  9. ↑ Institute of Medicine (1993). Chapter 5: Chemistry of Sulfur Mustard and Lewisite. The National Academies Press. ISBN 0-309-04832-X. {{cite book}}: |work= ignored (help)
  10. ↑ Kehe, Kai; Szinicz, Ladislaus (2005). "Medical aspects of sulphur mustard poisoning". Toxicology. 214 (3): 198–209. doi:10.1016/j.tox.2005.06.014. PMID 16084004.
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