*** Welcome to piglix ***

Disulfur dichloride

Disulfur dichloride
Wireframe model of disulfur dichloride
Ball and stick model of disulfur dichloride
Spacefill model of disulfur dichloride
Names
IUPAC name
Disulfur dichloride
Systematic IUPAC name
Dichlorodisulfane
Other names
Bis[chloridosulfur](SS)

Dimeric sulfenic chloride

Sulfur monochloride
Identifiers
10025-67-9 YesY
85408-26-0 (isobutenate) YesY
3D model (Jmol) Interactive image
ChemSpider 23192 YesY
19158348 (isobutenate) N
ECHA InfoCard 100.030.021
EC Number 233-036-2
MeSH Sulfur+monochloride
PubChem 24807
RTECS number WS4300000
UNII NJ7YR2EV0D N
UN number 3390
Properties
S2Cl2
Molar mass 135.04 g/mol
Appearance Light-amber to yellow-red, oily liquid
Odor pungent, nauseating, irritating
Density 1.688 g/cm3
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)
−62.2·10−6 cm3/mol
1.658
Structure
C2, gauche
1.60 D
Hazards
Safety data sheet ICSC 0958
Toxic (T)
Harmful (Xn)
Corrosive (C)
Dangerous for the environment (N)
R-phrases R14, R20, R25, R29, R35, R50
S-phrases (S1/2), S26, S36/37/39, S45, S61
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g., calcium Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 118.5 °C (245.3 °F; 391.6 K)
234 °C (453 °F; 507 K)
Lethal dose or concentration (LD, LC):
150 ppm (mouse, 1 min)
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 1 ppm (6 mg/m3)
REL (Recommended)
C 1 ppm (6 mg/m3)
IDLH (Immediate danger)
5 ppm
Related compounds
Related sulfur chlorides
Sulfur dichloride
Thionyl chloride
Sulfuryl chloride
Related compounds
Disulfur difluoride
Disulfur dibromide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

Dimeric sulfenic chloride

Disulfur dichloride is the chemical compound of sulfur and chlorine with the formula S2Cl2.

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 different isomer of S2Cl2 is S=SCl2; this isomer forms transiently when S2Cl2 is exposed to UV-radiation (see thiosulfoxides).

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).

Pure disulfur dichloride is a yellow liquid that smokes in air due to reaction with water:

It is synthesized by partial chlorination of elemental sulfur. The reaction takes place 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 gives 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:

Pure disulfur dichloride is obtained by distilling the yellow-orange liquid over excess elemental sulfur.

S2Cl2 also arises from the chlorination of CS2 as in the synthesis of thiophosgene.


...
Wikipedia

...