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B85501

Sigma-Aldrich

1,4-Butane sultone

≥99%

Synonym(s):

4-Hydroxybutane-1-sulfonic acid δ-sultone

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About This Item

Empirical Formula (Hill Notation):
C4H8O3S
CAS Number:
1633-83-6
Molecular Weight:
136.17
Beilstein:
110588
EC Number:
216-647-9
MDL number:
MFCD00006584
UNSPSC Code:
12352100
PubChem Substance ID:
24892078
NACRES:
NA.22

Quality Level

200

Assay

≥99%

form

liquid

refractive index

n20/D 1.464 (lit.)

bp

>165 °C/25 mmHg (lit.)

mp

12-15 °C (lit.)

density

1.331 g/mL at 25 °C (lit.)

SMILES string

O=S1(=O)CCCCO1

InChI

1S/C4H8O3S/c5-8(6)4-2-1-3-7-8/h1-4H2

InChI key

MHYFEEDKONKGEB-UHFFFAOYSA-N

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Application

1,4-Butane sultone can be employed as a reactant in the preparation of conjugated polymers which include polybetaine, poly[2-ethynyl-N-(4-sulfobutyl)pyridinium betaine] (PESPB).
It can also be used in the preparation of Bronsted acid catalysts such as 4-(succinimido)-1-butane sulfonic acid and poly(4-vinylpyridinium butane sulfonic acid) hydrogen sulfate. These catalysts facilitate the synthesis of 1-amidoalkyl-2-naphthols, substituted quinolines, and pyrano[4,3-b]pyran derivatives.

Pictograms

Exclamation markHealth hazard
GHS07,GHS08

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

309.2 °F

Flash Point(C)

154 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Vajihe Nejadshafiee et al.
Materials science & engineering. C, Materials for biological applications, 101, 42-52 (2019-04-29)
A novel magnetic bio-adsorbent has been prepared by the loading of Fe3O4 NPs and immobilization of 1,4-butane sultone on the surface of activated carbon. The activated carbon was synthesized from pistachio shell as a carbon material of biogenic, bio-resources and
Li-Hang Hsu et al.
Scientific reports, 10(1), 2911-2911 (2020-02-23)
Quaternary ammonium compounds (QACs) are classified as cationic surfactants, and are known for their biocidal activity. However, their modes of action are thus far not completely understood. In this study, we synthesized a gemini QAC, PMT12-BF4 and found that it
Meihong Liu et al.
Journal of hazardous materials, 396, 122582-122582 (2020-04-26)
In this work, a novel method of carbodiimide-assisted zwitterionic modification was proposed and implemented to incorporate zwitterionic moieties onto poly(piperazine amide) membrane for improved water permeability and anti-depositing property, which are crucial for highly efficient nanofiltration of dye-contained effluents. Carboxyl
Synthesis and electro-optical properties of self-doped ionic conjugated polymers: poly [2-ethynyl-N-(4-sulfobutyl) pyridinium betaine]
Gal Y-S, et al.
Current Applied Physics, 5(1), 38-42 (2005)
4-(Succinimido)-1-butane sulfonic acid as a Bronsted acid catalyst for synthesis of pyrano [4, 3-b] pyran derivatives under solvent-free conditions
Khaligh NG, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 26(1), 26-30 (2015)
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