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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.4885 (lit.)
bp
156-157 °C (lit.)
density
1.07 g/mL at 25 °C (lit.)
functional group
chloro
thioether
storage temp.
2-8°C
SMILES string
CCSCCCl
InChI
1S/C4H9ClS/c1-2-6-4-3-5/h2-4H2,1H3
InChI key
GBNVXYXIRHSYEG-UHFFFAOYSA-N
Related Categories
General description
2-Chloroethyl ethyl sulfide is a monofunctional analog of sulfur mustard (SM; 2,2′-dichloro diethyl sulfide). The mass diffusivity of 2-chloroethyl ethyl sulfide, a chemical warfare agent simulant, was studied.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1A - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
125.6 °F - closed cup
Flash Point(C)
52 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Toxicology and applied pharmacology, 249(2), 178-187 (2010-09-16)
Sulfur mustard is a potent vesicant that induces inflammation, edema and blistering following dermal exposure. To assess molecular mechanisms mediating these responses, we analyzed the effects of the model sulfur mustard vesicant, 2-chloroethyl ethyl sulfide, on EpiDerm-FT™, a commercially available
Free radical biology & medicine, 48(9), 1188-1196 (2010-02-09)
Sulfur mustard (bis-2-(chloroethyl) sulfide; SM) is a highly reactive vesicating and alkylating chemical warfare agent. A SM analog, 2-chloroethyl ethyl sulfide (CEES), has been utilized to elucidate mechanisms of toxicity and as a screen for therapeutics. Previous studies with SM
Archives of toxicology, 93(1), 61-79 (2018-10-17)
Despite its worldwide ban, the warfare agent sulfur mustard (SM) still represents a realistic threat, due to potential release in terroristic attacks and asymmetric conflicts. Therefore, the rigorous and quantitative detection of SM exposure is crucial for diagnosis, health risk
Free radical biology & medicine, 51(12), 2272-2280 (2011-09-17)
Employing mouse skin epidermal JB6 cells and dermal fibroblasts, here we examined the mechanisms of DNA damage by 2-chloroethyl ethyl sulfide (CEES), a monofunctional analog of sulfur mustard (SM). CEES exposure caused H2A.X and p53 phosphorylation as well as p53
Toxicology and applied pharmacology, 247(2), 76-82 (2010-06-22)
Inhalation of vesicants including sulfur mustard can cause significant damage to the upper airways. This is the result of vesicant-induced modifications of proteins important in maintaining the integrity of the lung. Cytochrome P450s are the major enzymes in the lung
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