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Principaux documents

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:
Poids moléculaire :
122.14
Numéro CE :
Numéro MDL:
Code UNSPSC :
26111700
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Niveau de qualité

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

Chaîne SMILES 

O=S1OCCCO1

InChI

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

Clé InChI

LOURZMYQPMDBSR-UHFFFAOYSA-N

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.

Pictogrammes

CorrosionExclamation mark

Mention d'avertissement

Danger

Mentions de danger

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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Consulter la Bibliothèque de documents

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
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
Stephen P Bailey et al.
International journal of sports physiology and performance, 14(7), 927-933 (2019-01-25)
The purpose of this investigation is to determine the effects of different forms of a CHO MR on quadriceps muscle performance and corticospinal motor excitability. Ten subjects (5 females, 5 males; 25±1 years; 1.71±0.03 m 73±5 kg) completed 4 trials.
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
Dalila Rocco et al.
Polymers, 11(7) (2019-07-26)
The synthesis and characterization of 4'-(4-methoxyphenyl)-3,2':6',3″-terpyridine (2) (IUPAC PIN 24-(4-methoxyphenyl)-12,22:26,32-terpyridine) are described, and its coordination behaviour with cobalt(II) thiocyanate has been investigated. In a series of experiments, crystals were grown at room temperature by layering a MeOH solution of Co(NCS)2

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