Skip to Content
Merck
CN

32530

Diethyl sulfide

puriss., ≥99.0% (GC)

Synonym(s):

1,1′-Thiobisethane, Ethyl sulfide, NSC 75157

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(C2H5)2S
CAS Number:
352-93-2
Molecular Weight:
90.19
EC Number:
206-526-9
UNSPSC Code:
12352100
PubChem Substance ID:
329754011
Beilstein/REAXYS Number:
1696909
MDL number:
MFCD00009270

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 pressure

105 mmHg ( 37.7 °C)

grade

puriss.

assay

≥99.0% (GC)

refractive index

n20/D 1.442

bp

90-92 °C (lit.)

mp

−100 °C (lit.)

density

0.837 g/mL at 25 °C (lit.)

SMILES string

CCSCC

InChI

1S/C4H10S/c1-3-5-4-2/h3-4H2,1-2H3

InChI key

LJSQFQKUNVCTIA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Diethyl sulfide is a simulant for chemical agent mustard gas. Photooxidation of gaseous diethyl sulfide over TiO2 in a flow reactor was investigated.

Application

Diethyl sulfide was employed as ancillary ligand in the preparation of brightly luminescent Pt(II) pincer complexes.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

15.8 °F - closed cup

flash_point_c

-9 °C - closed cup

ppe

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

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Anton M Prokhorov et al.
Journal of the American Chemical Society, 136(27), 9637-9642 (2014-06-18)
A series of three Pt(II) complexes with a doubly cyclometalating terdentate ligand L1, L1H2 = 3,6-bis(p-anizolyl)-2-carboranyl-pyridine, and diethyl sulfide (1), triphenylphosphine (2), and t-butylisonitrile (3) as ancillary ligands were synthesized. X-ray diffraction studies of 1 and 2 show a coordination
Gas-phase photocatalytic oxidation of diethyl sulfide over TiO< sub> 2</sub>: kinetic investigations and catalyst deactivation.
Kozlov DV, et al.
Applied Catalysis. B, Environmental, 42(1), 77-87 (2003)
R Singh et al.
Chemical research in toxicology, 10(1), 70-77 (1997-01-01)
Postlabeling can be one of the most sensitive methods for the measurement of DNA adducts. However, for the determination of alkylated adducts, essential requirements are standards which must be fully chemically characterized. In order to develop a postlabeling assay for
Beer Singh et al.
Journal of hazardous materials, 139(1), 38-43 (2006-08-26)
Breakthrough behavior of diethyl sulphide vapors on carbon systems such as active carbon, NaOH/CrO3/C, NaOH/CrO3/EDA/C and RuCl3/C has been studied by using modified Wheeler equation and the same was used to calculate the pseudo-first-order rate constant (kv) and kinetic saturation
V Vodyanoy et al.
Neuroscience letters, 73(3), 253-258 (1987-01-27)
The steady-state conductance of planar bimolecular lipid membranes (BLMs) modified with rat olfactory epithelial homogenate (ROH) becomes sensitive to very low concentrations of odorant in the presence of adenosine triphosphate (ATP) and guanosine triphosphate (GTP). The chemosensitivity is not observed
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