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Merck
CN

293113

Sigma-Aldrich

Sulfur monochloride solution

1.0 M in methylene chloride

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About This Item

Empirical Formula (Hill Notation):
Cl2S2
CAS Number:
Molecular Weight:
135.04
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
Form:
liquid
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vapor density

4.7 (vs air)

vapor pressure

25.05 psi ( 55 °C)
7.31 psi ( 20 °C)

form

liquid

autoignition temp.

451 °F

concentration

1.0 M in methylene chloride

SMILES string

ClSSCl

InChI

1S/Cl2S2/c1-3-4-2

InChI key

PXJJSXABGXMUSU-UHFFFAOYSA-N

Packaging

Packaged under nitrogen in Sure/Seal bottles

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Carc. 2 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Supplementary Hazards

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

监管及禁止进口产品

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M J Davies et al.
Free radical research, 33(6), 719-729 (2001-03-10)
Activated phagocytic cells generate hypochlorite (HOCl) via release of hydrogen peroxide and the enzyme myeloperoxidase. HOCl plays an important role in bacterial cell killing, but excessive or misplaced production of HOCI is also known to cause tissue damage. Studies have
[Eye burn caused by sulfur monochloride].
J Peyresblanques et al.
Bulletin des societes d'ophtalmologie de France, 87(3), 429-430 (1987-03-01)
Daniel K W Mok et al.
The Journal of chemical physics, 125(10), 104303-104303 (2006-09-27)
Geometry optimization calculations were carried out on the (approximate)X (1)A(1) state of SCl(2) and the (approximate)X(2)B(1), (approximate)A(2)B(2), (approximate)B(2)A(1), (approximate)C(2)A(1), (approximate)D(2)A(2), and (approximate)E (2)B(2) states of SCl(2) (+) at the restricted-spin coupled-cluster single-double plus perturbative triple excitation [RCCSD(T)] level with basis
F Machetti et al.
Advances in experimental medicine and biology, 483, 399-401 (2002-01-15)
(+/-)trans 2-Aminocyclohexanesulfonic acid and (+/-)trans 2-aminocyclopentanesulfonic acid were prepared from cyclohexene and cyclopentene respectively by sulfur monochloride addition, followed by oxidation to 2-chlorosulfonic acid and substitution of chlorine.

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