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About This Item
Linear Formula:
C2H5SH
CAS Number:
Molecular Weight:
62.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-837-3
Beilstein/REAXYS Number:
773638
MDL number:
Assay:
97%
Form:
liquid
vapor density
2.1 (vs air)
Quality Level
vapor pressure
8.51 psi ( 20 °C)
assay
97%
form
liquid
autoignition temp.
570 °F
expl. lim.
18.2 %
refractive index
n20/D 1.4306 (lit.)
bp
35 °C (lit.)
density
0.839 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CCS
InChI
1S/C2H6S/c1-2-3/h3H,2H2,1H3
InChI key
DNJIEGIFACGWOD-UHFFFAOYSA-N
Application
Ethanethiol can be used as a reactant for the synthesis of:
- Functionalized oxazolidinones by conjugated nucleophilic addition- electrophilic amination reaction.
- Ethyl phenyl sulfide by C-S coupling with iodobenzene.
- Chain transfer agent in the RAFT polymerization of N-isopropylacrylamide.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 1
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-49.0 °F - closed cup
flash_point_c
-45 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
危险化学品
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Direct synthesis of thermally responsive DMA/NIPAM diblock and DMA/NIPAM/DMA triblock copolymers via aqueous, room temperature RAFT polymerization
Convertine AJ, et al.
Macromolecules, 39(5), 1724-1730 (2006)
Asymmetric multicomponent domino reactions and highly enantioselective conjugated addition of thiols to ?, ?-unsaturated aldehydes
Marigo M, et al
Journal of the American Chemical Society, 127(45), 15710-15711 (2005)
Efficient CuO-Nanoparticle-Catalyzed C-S Cross-Coupling of Thiols with Iodobenzene
Rout L, et al.
Angewandte Chemie (International Edition in English), 119(29), 5679-5682 (2007)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E3708-100ML | 04061833603383 |
| E3708-500ML | 04061833603390 |


