Skip to Content
Merck
CN
All Photos(1)

Documents

B85501

Sigma-Aldrich

1,4-Butane sultone

≥99%

Synonym(s):

4-Hydroxybutane-1-sulfonic acid δ-sultone

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H8O3S
CAS Number:
Molecular Weight:
136.17
Beilstein:
110588
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Looking for similar products? Visit Product Comparison Guide

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

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

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service