|Systematic IUPAC name
Dimeric sulfenic chloride
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||135.04 g/mol|
|Appearance||Light-amber to yellow-red, oily liquid|
|Odor||pungent, nauseating, irritating|
|Melting point||-80 °C (-112 °F; 193 K)|
|Boiling point||137.1 °C (278.8 °F; 410.2 K)|
|decomposes, with loss of HCl|
|Solubility||soluble in ethanol, benzene, ether, chloroform, CCl4|
|Vapor pressure||7 mmHg (20 °C)|
Refractive index (nD)
|1.60 D |
|Safety data sheet||ICSC 0958|
Dangerous for the environment (N)
|R-phrases (outdated)||R14, R20, R25, R29, R35, R50|
|S-phrases (outdated)||(S1/2), S26, S36/37/39, S45, S61|
|NFPA 704 (fire diamond)|
|Flash point||118.5 °C (245.3 °F; 391.6 K)|
|234 °C (453 °F; 507 K)|
|Lethal dose or concentration (LD, LC):|
LCLo (lowest published)
|150 ppm (mouse, 1 min)|
|NIOSH (US health exposure limits):|
|TWA 1 ppm (6 mg/m3)|
|C 1 ppm (6 mg/m3)|
IDLH (Immediate danger)
Related sulfur chlorides
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Some alternative names for this compound are sulfur monochloride (the name implied by its empirical formula, SCl), disulphur dichloride (British English Spelling) and sulphur monochloride (British English Spelling). S2Cl2 has the structure implied by the formula Cl-S-S-Cl, wherein the angle between the Cla-S-S and S-S-Clb planes is 90°. This structure is referred to as gauche, and is akin to that for H2O2. A rare isomer of S2Cl2 is S=SCl2; this isomer forms transiently when S2Cl2 is exposed to UV-radiation (see thiosulfoxides).
Pure disulfur dichloride is a yellow liquid that "smokes" in moist air due to reaction with water. An idealized (but complicated) equation is:
It is produced by partial chlorination of elemental sulfur. The reaction proceeds at usable rates at room temperature. In the laboratory, chlorine gas is led into a flask containing elemental sulfur. As disulfur dichloride is formed, the contents become a golden yellow liquid:
Excess chlorine produces sulfur dichloride, which causes the liquid to become less yellow and more orange-red:
The reaction is reversible, and upon standing, SCl2 releases chlorine to revert to the disulfur dichloride. Disulfur dichloride has the ability to dissolve large quantities of sulfur, which reflects in part the formation of polysulfanes:
Disulfur dichloride can be purified by distillation from excess elemental sulfur.
It reacts with ammonia to give heptasulfur imide (S7NH) and related S-N rings S8-x(NH)x (x = 2, 3).
S2Cl2 has been used to introduce C-S bonds. In the presence of aluminium chloride (AlCl3), S2Cl2 reacts with benzene to give diphenyl sulfide:
Anilines (1) react with S2Cl2 in the presence of NaOH to give 1,2,3-benzodithiazolium salts (2) (Herz reaction) which can be transformed into ortho-aminothiophenolates (3), these species are precursors to thioindigo dyes.
It is also used to prepare sulfur mustard, commonly known as "mustard gas", by reaction with ethylene at 60 °C (the Levinstein process):
Other uses of S2Cl2 include the manufacture of sulfur dyes, insecticides, and synthetic rubbers. It is also used in cold vulcanization of rubbers, as polymerization catalyst for vegetable oils and for hardening soft woods.
This substance is listed in Schedule 3 Part B - Precursor Chemicals of the Chemical Weapons Convention (CWC). Facilities that produce and/or process and/or consume Scheduled chemicals may be subject to control, reporting mechanisms and inspection by the OPCW (Organisation for the Prohibition of Chemical Weapons).