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901588

Sigma-Aldrich

1,3-Propanesultone solution

1 M in THF

Sinónimos:

1,2-Oxathiolane 2,2-dioxide, 3-Hydroxypropanesulfonic acid γ-sultone

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About This Item

Fórmula lineal:
C3H6O3S
Número de CAS:
1120-71-4
MDL number:
MFCD00005355
UNSPSC Code:
12352200
NACRES:
NA.22

form

liquid

concentration

1 M in THF

refractive index

n/D 1.4144

density

0.9266 g/mL

InChI

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

InChI key

FSSPGSAQUIYDCN-UHFFFAOYSA-N

Application

1,3-Propanesultone has been used in:
  • preparation of poly[2-ethynyl-N-(propylsulfonate)pyridinium betaine], a new ionic conjugated polymer
  • preparation of novel poly(4-vinylpyridine) supported acidic ionic liquid catalyst
  • preparation of poly((2-(dimethylamino)ethyl methacrylate)-co-3-dimethyl(methacryloyloxyethyl)ammonium propanesulfonate)-coated mesoporous silica nanoparticles
  • sulfonation of surface of self-assembled nanoporous silica colloidal crystalline films comprised of 184nm-diameter silica spheres
Valuable building block or solvent offered as a solution in tetrahydrofuran for more convenient handling.

Related product

Referencia del producto
Descripción
Precios

P50706

1,3-Propanesultone, 98%

291250

1,3-Propanesultone, ≥99%

809985

1,3-Propanesultone, battery grade, ≥99%, acid <200 ppm, H2O <100 ppm

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Central nervous system, Respiratory system

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-2.0 °F

flash_point_c

-18.88 °C

Certificados de análisis (COA)

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Junke Wang et al.
Ultrasonics sonochemistry, 21(1), 29-34 (2013-06-12)
A novel poly(4-vinylpyridine) supported acidic ionic liquid catalyst was synthesized by the reaction of 4-vinylpyridine with 1,3-propanesultone, followed by the polymerization and the addition of the heteropolyacid. Due to the combination of polymer features and ionic liquid, it acted as
Yeong-Soon Gal et al.
Journal of nanoscience and nanotechnology, 14(7), 5480-5484 (2014-04-25)
A new ionic conjugated polymer was prepared by the activated polymerization of 2-ethynylpyridine with the ring-opening of 1,3-propanesultone without any additional initiator or catalyst. This polymer was characterized by various instrumental methods to have conjugated polymer backbone system with pendant
G E Milo et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(11), 5229-5234 (1996-05-28)
Two structurally unrelated chemicals, aflatoxin B1 and propane sultone, transformed human foreskin cells to a stage of anchorage-independent growth. Isolation from agar and repopulation in monolayer culture of these transformed cells was followed by transfection with a cDNA library, which
Joanna J Smith et al.
Langmuir : the ACS journal of surfaces and colloids, 24(6), 2650-2654 (2008-02-16)
The surface of self-assembled nanoporous silica colloidal crystalline films comprised of 184-nm-diameter silica spheres has been sulfonated using 1,3-propanesultone. The transport of ions through the sulfonated films has been studied using cyclic voltammetry in water as a function of ion
Y Oshiro et al.
Toxicology letters, 9(4), 301-306 (1981-12-01)
The standard method of the C3H/10T1/2 cell transformation assay cannot adequately detect alkylating agents. A modification of the standard procedure as described by Bertram and Heidelberger using a large number of synchronized cells and high levels of toxicity was evaluated
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