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Merck
모든 사진(1)

문서

128252

Sigma-Aldrich

Ethylene sulfide

98%

동의어(들):

Dimethylene sulfide, Thiirane

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About This Item

실험식(Hill 표기법):
C2H4S
CAS Number:
Molecular Weight:
60.12
Beilstein:
102379
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

4.15 psi ( 20 °C)

분석

98%

형태

liquid

포함

0.5-1.4% n-butyl mercaptan as stabilizer

refractive index

n20/D 1.495 (lit.)

bp

55-56 °C (lit.)

density

1.01 g/mL at 25 °C (lit.)

저장 온도

−20°C

SMILES string

C1CS1

InChI

1S/C2H4S/c1-2-3-1/h1-2H2

InChI key

VOVUARRWDCVURC-UHFFFAOYSA-N

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관련 카테고리

애플리케이션

  • 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.

Ethylene sulfide was used in the chemical modificatoion of biopolymer chitosan.

픽토그램

FlameSkull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

50.0 °F - closed cup

Flash Point (°C)

10 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

Gold nanoparticles stabilized by thioether dendrimers.
Hermes J P, et al.
Chemistry?A European Journal , 17(48), 13473-13481 (2011)
Ethylene Sulfide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2010)
Sulfur-bridged binuclear iron (II) complexes. Effect of ligand constraints on their physical properties; reactions with carbon monoxide and alkyl isocyanides.
Karlin K D and Lippard S J
Journal of the American Chemical Society, 98(22), 6951-6957 (1976)
Adriana P Vieira et al.
International journal of biological macromolecules, 52, 107-115 (2012-09-27)
The biopolymer chitosan was chemically modified in two sequences of reactions: (i) immobilization of methyl acrylate followed by cysteamine and (ii) the sequence of immobilization reactions involving ethylene sulfide, methyl acrylate and finally cysteamine. In both cases the pendant chains
W C Stolte et al.
The Journal of chemical physics, 133(1), 014306-014306 (2010-07-10)
We have investigated the photofragmentation properties of the three-membered ring heterocyclic molecule ethylene sulfide or thiirane, C(2)H(4)S, by time-of-flight mass spectroscopy. Positive ions have been collected as a function of photon energy around the S K ionization threshold. Branching ratios

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