291250
1,3-Propanesultone
≥99%
Sinónimos:
3-Hydroxypropanesulfonic acid γ-sultone
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Fórmula empírica (notación de Hill):
C3H6O3S
Número CAS:
Peso molecular:
122.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-317-9
Beilstein/REAXYS Number:
109782
MDL number:
Assay:
≥99%
Servicio técnico
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≥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
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 1B - Eye Dam. 1 - Skin Irrit. 2
Clase de almacenamiento
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
340.7 °F
flash_point_c
171.5 °C
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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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