Skip to Content
Merck
All Photos(1)

Documents

238317

Sigma-Aldrich

Ethyl methyl sulfide

96%

Synonym(s):

(Methylsulfanyl)ethane, (Methylthio)ethane, 1-(Methylthio)ethane, 2-Thiabutane, Ethyl methyl thioether, Ethyl(methyl)sulfane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2SCH3
CAS Number:
Molecular Weight:
76.16
Beilstein:
1696871
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

272 mmHg ( 37.7 °C)

Assay

96%

form

liquid

refractive index

n20/D 1.440 (lit.)

bp

66-67 °C (lit.)

mp

−106 °C (lit.)

density

0.842 g/mL at 25 °C (lit.)

SMILES string

CCSC

InChI

1S/C3H8S/c1-3-4-2/h3H2,1-2H3

InChI key

WXEHBUMAEPOYKP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Microwave spectra of the trans isomer of ethyl methyl sulfide and its 10 isotopic species has been investigated. Chlorination of ethyl methyl sulfide with N-chlorosuccinimide and sulfuryl chloride has been reported.

Pictograms

Flame

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

5.0 °F - closed cup

Flash Point(C)

-15 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Microwave spectrum, structure, dipole moment, and internal rotation of the trans isomer of ethyl methyl sulfide.
Hayashi M, et al.
Journal of Molecular Spectroscopy, 86(1), 129-135 (1981)
Chlorination of unsymmetrical sulfides.
Tuleen DL and Stephens T.
The Journal of Organic Chemistry, 34(1), 31-35 (1969)
Marlize Z Bekker et al.
Journal of agricultural and food chemistry, 66(51), 13483-13491 (2018-12-13)
Diorganopolysulfanes can be generated when hydrogen sulfide (H2S) and thiols are oxidized in the presence of Cu(II) under conditions usually aimed at removing H2S from wine. This work sought to understand if polysulfanes could act as latent sources of H2S
Marlize Z Bekker et al.
Food chemistry, 245, 676-686 (2017-12-31)
Precursors to hydrogen sulfide (H
Ward Said-Ahmad et al.
Analytical chemistry, 89(5), 3199-3207 (2017-02-15)
We describe a simple, sensitive, and robust method for sulfur isotope ratio (

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