Skip to Content
MilliporeSigma
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
All Photos(1)

About This Item

Linear Formula:
CH3CH2SCH3
CAS Number:
624-89-5
Molecular Weight:
76.16
Beilstein/REAXYS Number:
1696871
EC Number:
210-868-4
MDL number:
MFCD00009268
UNSPSC Code:
12352100
PubChem Substance ID:
24854294
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
GHS02

signalword

Danger

hcodes

H225

Hazard Classifications

Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

5.0 °F - closed cup

flash_point_c

-15 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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

Chlorination of unsymmetrical sulfides.
Tuleen DL and Stephens T.
The Journal of Organic Chemistry, 34(1), 31-35 (1969)
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)
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 (
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