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774243

Sigma-Aldrich

1,3-Propylene sulfite

greener alternative

99%

Synonyme(s) :

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

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About This Item

Formule empirique (notation de Hill):
C3H6O3S
Numéro CAS:
4176-55-0
Poids moléculaire :
122.14
Numéro CE :
224-044-7
Numéro MDL:
MFCD01682880
Code UNSPSC :
26111700
ID de substance PubChem :
329767669
Nomenclature NACRES :
NA.23

Niveau de qualité

100

Essai

99%

Forme

liquid

Caractéristiques du produit alternatif plus écologique

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

sustainability

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Indice de réfraction

n20/D 1.453

pb

73 °C (lit.)

Pf

-25 °C (lit.)

Densité

1.347 g/mL at 25 °C

Application(s)

battery manufacturing

Autre catégorie plus écologique

Enabling,

Chaîne SMILES 

O=S1OCCCO1

InChI

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

Clé InChI

LOURZMYQPMDBSR-UHFFFAOYSA-N

Catégories apparentées

Description générale

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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809977

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900018

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Fluoroethylene carbonate, battery grade, ≥99%, acid <200 ppm, anhydrous

Pictogrammes

CorrosionExclamation mark
GHS05,GHS07

Mention d'avertissement

Danger

Mentions de danger

H315,H317,H318,H335

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

183.0 °F

Point d'éclair (°C)

83.9 °C

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Certificats d'analyse (COA)

Lot/Batch Number
MKCW0687
MKCR8508
MKCP7367
MKCN7185
MKCM2905

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
Taek Lee et al.
Nanomaterials (Basel, Switzerland), 9(7) (2019-08-03)
In the present study, we fabricated a dual-mode cardiac troponin I (cTnI) biosensor comprised of multi-functional DNA (MF-DNA) on Au nanocrystal (AuNC) using an electrochemical method (EC) and a localized surface plasmon resonance (LSPR) method. To construct a cTnI bioprobe
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
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
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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