128252
环硫乙烷
98%
别名:
噻丙烷, 硫化伸乙基
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C2H4S
化学文摘社编号:
分子量:
60.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
102379
Assay:
98%
Form:
liquid
InChI
1S/C2H4S/c1-2-3-1/h1-2H2
SMILES string
C1CS1
InChI key
VOVUARRWDCVURC-UHFFFAOYSA-N
vapor pressure
4.15 psi ( 20 °C)
assay
98%
form
liquid
contains
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.)
functional group
thioether
storage temp.
−20°C
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
- 乙烯硫醚常用于制备有机硫化合物，特别是伯胺和仲胺的巯基化，从而获得氨基硫醇。
- 它用于合成树枝状硫醚配体，用于稳定金纳米粒子（Au NPs）。
- 壳聚糖可以通过环硫乙烷处理进行化学改性，从而获得一种可用于去除水溶液中的二价阳离子的生物聚合物。
乙烯硫醚被用于生物聚合物壳聚糖的化学改性。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
50.0 °F - closed cup
flash_point_c
10 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
法规信息
危险化学品
此项目有
Gold nanoparticles stabilized by thioether dendrimers.
Hermes J P, et al.
Chemistry?A European Journal , 17(48), 13473-13481 (2011)
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
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
Ethylene Sulfide.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2010)
Evangelina Repetto et al.
The Journal of organic chemistry, 77(1), 253-265 (2011-11-19)
Satisfactory procedures are described for the synthesis of 5,6- and 3,4-thiirane derivatives from the respective hexofuranose or hexopyranose epoxide precursors. The controlled ring-opening reaction of thiiranes by 1-thioaldoses was successfully accomplished to afford, regio- and stereoselectively, β-S-(1→4)-3,4-dithiodisaccharides. For instance, the
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持