Skip to Content
MilliporeSigma
All Photos(1)

Documents

471690

Sigma-Aldrich

1,3,2-Dioxathiolane 2,2-dioxide

98%

Synonym(s):

1,2-Ethylene sulfate, 1,3,2λ6-Dioxathiolane-2,2-dione, 1,3,2-Dioxathiolan-2,2-dioxide, Ethylene sulfate

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C2H4O4S
CAS Number:
1072-53-3
Molecular Weight:
124.12
MDL number:
MFCD00221769
UNSPSC Code:
12352100
PubChem Substance ID:
24870755
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

95-97 °C (lit.)

storage temp.

2-8°C

SMILES string

O=S1(=O)OCCO1

InChI

1S/C2H4O4S/c3-7(4)5-1-2-6-7/h1-2H2

InChI key

ZPFAVCIQZKRBGF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

1,3,2-Dioxathiolane 2,2-dioxide may be employed in the preparation of imidazolidinium salts.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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

Customers Also Viewed

Slide 1 of 4

1 of 4

1,3-BUTYLENE GLYCOL SULFITE AldrichCPR

S359173

1,3-BUTYLENE GLYCOL SULFITE

1,3-Propanesultone ≥99%

Sigma-Aldrich

291250

1,3-Propanesultone

Tris(trimethylsilyl) phosphite ≥95.0% (GC)

Sigma-Aldrich

93412

Tris(trimethylsilyl) phosphite

Dimethyl sulfite 99%

Sigma-Aldrich

108618

Dimethyl sulfite

Computational Study of Ring Strain in 1, 3, 2-Dioxathiolane, its 2-Oxide and its 2, 2-Dioxide.
Petersenb KN and Skanckeb PN.
Acta Chemica Scandinavica, 53, 1003-1008 (1999)
1, 3, 2-Dioxathiolane 2, 2-Dioxide.
Lynch NJ, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2009)
Rodolphe Jazzar et al.
Journal of organometallic chemistry, 691(14), 3201-3205 (2006-01-01)
Protonated versions of N-heterocyclic carbenes (NHC,H(+)) are classically prepared by closing the ring through the introduction of the CH+ fragment. He we report a totally different synthetic approach, which can be viewed as the addition of a 1,3-diazaallyl anion to
Eric Schönemann et al.
Polymers, 11(6) (2019-06-12)
Films of zwitterionic polymers are increasingly explored for conferring fouling resistance to materials. Yet, the structural diversity of polyzwitterions is rather limited so far, and clear structure-property relationships are missing. Therefore, we synthesized a series of new polyzwitterions combining ammonium
Fuqiang An et al.
Scientific reports, 9(1), 14108-14108 (2019-10-03)
Recently, high-energy density cells containing nickel-rich cathodes and silicon-based anodes have become a practical solution for increasing the driving range of electric vehicles. However, their long-term durability and storage performance is comparatively poor because of the unstable cathode-electrolyte-interphase (CEI) of

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