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774243

Sigma-Aldrich

1,3-Propylene sulfite

greener alternative

99%

Synonym(s):

2-Oxo-1,3,2-dioxathiane, PS, TMS, Trimethylene sulfite

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About This Item

Empirical Formula (Hill Notation):
C3H6O3S
CAS Number:
4176-55-0
Molecular Weight:
122.14
EC Number:
224-044-7
MDL number:
MFCD01682880
UNSPSC Code:
26111700
PubChem Substance ID:
329767669
NACRES:
NA.23

assay

99%

form

liquid

greener alternative product characteristics

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

sustainability

Greener Alternative Product

refractive index

n20/D 1.453

bp

73 °C (lit.)

mp

-25 °C (lit.)

density

1.347 g/mL at 25 °C

application(s)

battery manufacturing

greener alternative category

Enabling,

SMILES string

O=S1OCCCO1

InChI

1S/C3H6O3S/c4-7-5-2-1-3-6-7/h1-3H2

InChI key

LOURZMYQPMDBSR-UHFFFAOYSA-N

Related Categories

General description

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.

Application

Trimethylene sulfite is used as high temperature additive for electrolytes in Lithium ion batteries. It improves the decomposition resistance of the electrolyte.

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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

183.0 °F

flash_point_c

83.9 °C

Certificates of Analysis (COA)

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Colin Hawco et al.
Frontiers in human neuroscience, 11, 404-404 (2017-09-01)
There has been a distinct shift in neuroimaging from localization of function into a more network based approach focused on connectivity. While fMRI has proven very fruitful for this, the hemodynamic signal is inherently slow which limits the temporal resolution
Zahra Rezaei et al.
Bioorganic chemistry, 90, 103055-103055 (2019-06-21)
Structure activity correlation revealed that the quinoxaline ring is a satisfactory backbone for anticancer activity and a specific functional group at position 1 and 2 can improve the activity. In this basis, besides quinoxaline, imidazoles as potential anticancer agents were
Kang He et al.
Natural product research, 33(20), 2982-2987 (2018-11-30)
A new xanthone glycoside, 3,5,7,8-tetramethoxyxanthone-1-O-β-D-glucopyranoside (1), along with five known compounds, mangiferin (2), kaempferol (3), quercetin (4), chlorogenic acid (5) and diploptene (6), was isolated from the whole plants of Pyrrosia sheareri (Bak.) Ching. The structure of compound 1 was
Feng Bao et al.
Polymers, 11(5) (2019-05-08)
The application of poly(phthalazinone ether ketone)s (PPEKs) resin containing phthalazinone moiety is limited, due to its poor thermoforming processability. To investigate the effects of the phthalazinone's side-group on the thermal stability and processability of the resin, a series of PPEKs
Sheng-Cai Zheng et al.
Nature communications, 8, 15238-15238 (2017-05-04)
Axially chiral compounds are widespread in biologically active compounds and are useful chiral ligands or organocatalysts in asymmetric catalysis. It is well-known that styrenes are one of the most abundant and principal feedstocks and thus represent excellent prospective building blocks
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