Saltar al contenido
MilliporeSigma

E3708

Sigma-Aldrich

Ethanethiol

97%

Sinónimos:

Ethyl mercaptan, Mercaptan C2

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
C2H5SH
Número de CAS:
Peso molecular:
62.13
Beilstein/REAXYS Number:
773638
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

¿Está buscando productos similares? Visita Guía de comparación de productos

Categorías relacionadas

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.

signalword

Danger

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_germany

WGK 3

flash_point_f

-49.0 °F - closed cup

flash_point_c

-45 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

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)
R Hanczkó et al.
Journal of chromatography. A, 1163(1-2), 25-42 (2007-07-04)
The main aims of this work were (a) to present the characteristics and stability of the o-phthalaldehyde (OPA)-ethanethiol (ET) derivatives of 22 amino acids, including the believed-to-be less stable OPA derivatives providing glycine, gamma-aminobutyric acid, beta-alanine, histidine, ornithine, lysine and
Taicheng An et al.
Journal of hazardous materials, 183(1-3), 372-380 (2010-08-10)
This study aims to compare the biological degradation performance of ethanethiol using strain RG-1 and B350 commercial mixed microorganisms, which were inoculated and immobilized on ceramic particles in twin-biotrickling filter columns. The parameters affecting the removal efficiency, such as empty

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico