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291250

Sigma-Aldrich

1,3-Propanesultone

≥99%

Synonym(s):

3-Hydroxypropanesulfonic acid γ-sultone

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About This Item

Empirical Formula (Hill Notation):
C3H6O3S
CAS Number:
1120-71-4
Molecular Weight:
122.14
Beilstein:
109782
EC Number:
214-317-9
MDL number:
MFCD00005355
UNSPSC Code:
12352100
PubChem Substance ID:
24857522
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.)

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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Pricing

Signal Word

Danger

Hazard Statements

H301,H312,H315,H318,H350

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (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
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
T G Grasel et al.
Journal of biomedical materials research, 23(3), 311-338 (1989-03-01)
In order to investigate the factors affecting the interaction of polyurethanes and blood, a series of poly(tetramethylene oxide)-based polyurethane block copolymers was synthesized with systematically varying levels of ion incorporation in the hard segment block. A bimolecular nucleophilic substitution reaction
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