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Merck

B85501

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892078
EC Number:
216-647-9
Beilstein/REAXYS Number:
110588
MDL number:
MFCD00006584
Assay:
≥99%
Form:
liquid

Key Documents

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InChI key

MHYFEEDKONKGEB-UHFFFAOYSA-N

InChI

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

SMILES string

O=S1(=O)CCCCO1

assay

≥99%

form

liquid

Quality Level

200

bp

>165 °C/25 mmHg (lit.)

mp

12-15 °C (lit.)

density

1.331 g/mL at 25 °C (lit.)

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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

Health hazardExclamation mark
GHS08,GHS07

signalword

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

309.2 °F

flash_point_c

154 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB4493
STBL3228
STBK9334
STBK4254
STBJ6978

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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)
Poly (4-vinylpyridinium butane sulfonic acid) hydrogen sulfate: An efficient, heterogeneous poly (ionic liquid), solid acid catalyst for the one-pot preparation of 1-amidoalkyl-2-naphthols and substituted quinolines under solvent-free conditions
Kiasat AR, et al.
Chinese Journal of Catalysis, 34(10), 1861-1868 (2013)
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
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)
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
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