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Merck

291250

Sigma-Aldrich

1,3-Propanesultone

≥99%

Sinónimos:

3-Hydroxypropanesulfonic acid γ-sultone

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About This Item

Fórmula empírica (notación de Hill):
C3H6O3S
Número de CAS:
Peso molecular:
122.14
Beilstein/REAXYS Number:
109782
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥99%

bp

180 °C/30 mmHg (lit.)

mp

30-33 °C (lit.)

density

1.392 g/mL at 25 °C (lit.)

functional group

sulfonic acid

SMILES string

O=S1(OCCC1)=O

InChI

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

InChI key

FSSPGSAQUIYDCN-UHFFFAOYSA-N

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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

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Referencia del producto
Descripción
Precios

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 1B - Eye Dam. 1 - Skin Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

340.7 °F

flash_point_c

171.5 °C

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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
Kang-Ting Huang et al.
Biomacromolecules, 20(9), 3524-3534 (2019-08-06)
This work presents a salt-responsive interpenetrating network (IPN) hydrogel with effective antimicrobial properties and surface regeneration. The hydrogels were engineered using the double network strategy to form loosely cross-linked zwitterionic poly(sulfobetaine vinylimidazole) (pSBVI) networks into the highly cross-linked cationic poly((trimethylamino)ethyl
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
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
Hermann M Bolt et al.
Toxicology letters, 151(1), 251-254 (2004-06-05)
1,3-Propane sultone is directly alkylating, genotoxic and carcinogenic. In rats, it induces local and systemic tumours at multiple target sites. Preponderant systemic tumours occur at the central nervous system, especially gliomas. Other localisations include the mammary gland, the intestine, the

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