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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/REAXYS Number:
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.)

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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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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG0481
BCCG0482
BCCG0488
BCCG0487
BCCG0486

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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
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
C Singh et al.
Mutation research, 144(4), 239-242 (1985-12-01)
Pre- and post-treatments with caffeine enhanced propane sultone (PS)-induced growth damage in barley. The caffeine post-treatments were, however, more effective in potentiating PS-induced growth damage and caused an additive effect on the frequency of chlorophyll mutations.
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
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