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774243

Sigma-Aldrich

1,3-Propylene sulfite

greener alternative

99%

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C3H6O3S
Número de CAS:
4176-55-0
Peso molecular:
122.14
Número CE:
224-044-7
Número MDL:
MFCD01682880
Código UNSPSC:
26111700
ID de la sustancia en PubChem:
329767669
NACRES:
NA.23

Ensayo

99%

Formulario

liquid

características de los productos alternativos más sostenibles

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

sustainability

Greener Alternative Product

índice de refracción

n20/D 1.453

bp

73 °C (lit.)

mp

-25 °C (lit.)

densidad

1.347 g/mL at 25 °C

aplicaciones

battery manufacturing

categoría alternativa más sostenible

Enabling,

cadena SMILES

O=S1OCCCO1

InChI

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

Clave InChI

LOURZMYQPMDBSR-UHFFFAOYSA-N

Categorías relacionadas

Descripción general

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.

Aplicación

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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Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palabra de señalización

Danger

Frases de peligro

H315,H317,H318,H335

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

183.0 °F

Punto de inflamabilidad (°C)

83.9 °C

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Certificados de análisis (COA)

Lot/Batch Number
MKCW0687
MKCR8508
MKCP7367
MKCN7185
MKCM2905

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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
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.
Navdeep Kaur et al.
Dalton transactions (Cambridge, England : 2003), 46(4), 1124-1133 (2017-01-04)
A series of dyads and triads using ferrocene (Fc) as the donor and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) as the acceptor, linked either directly or through an N-phenylmethanimine or ethynylbenzene linker have been synthesized. While the former (directly linked) dyads were prepared through
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