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ETHYLENE SULFIDE

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ETHYLENE SULFIDE Basic information

Product Name:
ETHYLENE SULFIDE
Synonyms:
  • 2,3-Dihydrothiirene
  • aethylensulfid
  • Ethylene episulfide
  • Ethylene episulphide
  • Ethylene sulphide
  • ethyleneepisulfide
  • ethyleneepisulphide
  • ethylenesulphide
CAS:
420-12-2
MF:
C2H4S
MW:
60.12
EINECS:
206-993-9
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Simple 3-Membered Ring Compounds
  • Organic Building Blocks
  • Sulfides/Disulfides
  • Sulfur Compounds
  • Thiiranes
Mol File:
420-12-2.mol
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ETHYLENE SULFIDE Chemical Properties

Melting point:
207-209℃
Boiling point:
55-56 °C (lit.)
Density 
1.01 g/mL at 25 °C (lit.)
vapor pressure 
4.15 psi ( 20 °C)
refractive index 
n20/D 1.495(lit.)
Flash point:
50 °F
storage temp. 
-20°C
Water Solubility 
Insoluble in water
solubility 
Chloroform (Soluble), Methanol (Sparingly)
form 
liquid
color 
Colorless to Almost colorless
BRN 
102379
Stability:
Stable at room temperature, but may have butylmercaptan added to enhance stability. Flammable.
LogP
0.556 (est)
CAS DataBase Reference
420-12-2(CAS DataBase Reference)
IARC
3 (Vol. 11, Sup 7) 1987
EPA Substance Registry System
Thiirane (420-12-2)
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Safety Information

Hazard Codes 
F,T
Risk Statements 
11-23/25-41-43
Safety Statements 
16-36/37/39-45-39-26
RIDADR 
UN 1992 3/PG 2
WGK Germany 
3
RTECS 
KX3500000
10-13-23
HazardClass 
6.1(a)
PackingGroup 
I
HS Code 
29349990
Hazardous Substances Data
420-12-2(Hazardous Substances Data)

MSDS

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ETHYLENE SULFIDE Usage And Synthesis

Chemical Properties

clear colourless liquid

Uses

  • Ethylene sulfide is generally used in the preparation of organosulfur compounds, especially for mercaptoethylation of primary and secondary amines to obtain aminothiols.
  • It is used in the synthesis of dendritic thioether ligands to stabilize gold nanoparticles (Au NPs).
  • Chitosan can be chemically modified by treating ethylene sulfide to obtain a biopolymer for the removal of divalent cations from aqueous solutions.

Definition

ChEBI: Thiirane is a saturated organic heteromonocyclic parent and an organosulfur heterocyclic compound.

Safety Profile

Poison by ingestion, intraperitoneal, and subcutaneous routes. Mddly toxic by inhalation. A skin, eye, and mucous membrane irritant. Questionable carcinogen with experimental tumorigenic data. Can react with oxidizing materials. When heated to decomposition, or on contact with acid or acid fumes, it emits highly toxic fumes of SOx. See also SULFIDES.

ETHYLENE SULFIDESupplier

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