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718203

Sigma-Aldrich

Allyl methyl sulfone

greener alternative

96%

Synonym(s):

3-(Methylsulfonyl)-1-propene, MAS

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About This Item

Empirical Formula (Hill Notation):
C4H8O2S
CAS Number:
Molecular Weight:
120.17
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NA.23

Assay

96%

form

liquid

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

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refractive index

n20/D 1.472

bp

244 °C (lit.)

density

1.171 g/mL at 25 °C

application(s)

battery manufacturing

greener alternative category

SMILES string

CS(=O)(=O)CC=C

InChI

1S/C4H8O2S/c1-3-4-7(2,5)6/h3H,1,4H2,2H3

InChI key

WOPDMJYIAAXDMN-UHFFFAOYSA-N

General description

Allyl methyl sulfone is an organosulfur compound. It can be used as a solvent or an additive for electrochemical applications.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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IEEE Sensors Journal, 14(6), 1765-1769 (2014)
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Polymers, 11(7) (2019-07-25)
Hybrid nanocomposites based on electroactive polydiphenylamine-2-carboxylic acid (PDPAC) and single-walled carbon nanotubes (SWCNTs) were obtained for the first time. Polymer-carbon nanomaterials were synthesized via in situ oxidative polymerization of diphenylamine-2-carboxylic acid (DPAC) in the presence of SWCNTs by two different
Attempt to detect garlic allyl sulphides from saliva after consumption of garlic tablets using GC-MS
Watson CJ, et al.
Journal of Microbial & Biochemical Technology, 5, 081-083 (2013)
Joren S Retel et al.
Nature communications, 8(1), 2073-2073 (2017-12-14)
β-barrel proteins mediate nutrient uptake in bacteria and serve vital functions in cell signaling and adhesion. For the 14-strand outer membrane protein G of Escherichia coli, opening and closing is pH-dependent. Different roles of the extracellular loops in this process

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