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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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Jiao-Tong Sun et al.
Macromolecular rapid communications, 33(9), 811-818 (2012-04-11)
A novel nanocontainer, which could regulate the release of payloads, has been successfully fabricated by attaching zwitterionic sulfobetaine copolymer onto the mesoporous silica nanoparticles (MSNs). RAFT polymerization is employed to prepare the hybrid poly(2-(dimethylamino)ethyl methacrylate)-coated MSNs (MSN-PDMAEMA). Subsequently, the tertiary
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
K Hemminki
Carcinogenesis, 4(7), 901-904 (1983-01-01)
Propane sultone was reacted with guanosine and DNA at pH 6--7.5, and te reaction products were purified by Sephadex chromatography and h.p.l.c. The products were characterized by u.v. spectra, loss of tritium from the C-8 position and dissociation properties. The
Stephen D Dertinger et al.
Environmental and molecular mutagenesis, 52(9), 748-755 (2011-11-05)
An international collaborative trial was established to systematically investigate the merits and limitations of a rat in vivo Pig-a gene mutation assay. The product of this gene is essential for anchoring CD59 to the plasma membrane, and mutations in this
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