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Merck
CN

291250

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24857522
EC Number:
214-317-9
Beilstein/REAXYS Number:
109782
MDL number:
MFCD00005355

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Product Name

1,3-Propanesultone, ≥99%

InChI key

FSSPGSAQUIYDCN-UHFFFAOYSA-N

InChI

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

SMILES string

O=S1(OCCC1)=O

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

Quality Level

200

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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

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

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
BCCN8996
BCCN3435
BCCN5408
BCCG0481
BCCG0482

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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
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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