Skip to Content
Merck

E3708

Ethanethiol

97%

Synonym(s):

Ethyl mercaptan, Mercaptan C2

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
C2H5SH
CAS Number:
75-08-1
Molecular Weight:
62.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894342
EC Number:
200-837-3
Beilstein/REAXYS Number:
773638
MDL number:
MFCD00004887
Assay:
97%
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

vapor density

2.1 (vs air)

Quality Level

200

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

WGK 3

flash_point_f

-49.0 °F - closed cup

flash_point_c

-45 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBS6135
SHBL0318
SHBJ3066
STBG8296
STBG6629

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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)
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)
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
Nariyasu Mano et al.
Analytical chemistry, 81(22), 9395-9401 (2009-10-23)
The analysis of post-translational phosphorylation is a crucial step in understanding the mechanisms of many physiological events. Numerous approaches for the development of analytical methods aimed at the detection and quantification of phosphorylated proteins by mass spectrometry have been reported
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service