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1,4-Butane sultone / 100 G

Purity: 99 %
Synonym: Butane sultone; 1,4-Butanesultone; 1,2-Oxathiane, 2,2-dioxide; 4-Hydroxybutane-1-sulfonic acid δ-sultone
Molecular Formula: C4H8O3S
Molecular Weight: 136.17
SKU: MND-43508
CAS Number: 1633-83-6
MDL number: MFCD00006584
EC Number: 216-647-9
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100 G  
115.50 EUR



Safety Information


Hazard Statements

H302
H315
H319
H335
H317
H351

Precautionary Statements

P202
P280
P301 + P312
P305 + P351 + P338
P308 + P313
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)154 °C
Flash Point (F)309.2 °F
Density1.331 g/mL at 25 °C (lit.)
Boiling Point>165 °C/25 mmHg (lit.)
Melting Point12-15 °C (lit.)

 Product Description

1,4-Butane sultone is a chemical compound utilized as a versatile alkylating agent in organic synthesis, known for its ability to introduce sulfonate groups into various organic molecules.

 

Application:

It is commonly employed in the synthesis of specialty chemicals, including surfactants, pharmaceutical intermediates, and polymer additives, due to its alkylating and sulfonating properties.

 

 

Articles:

- Determination of Low-ppm Levels of 1,4-Butane Sultone in Sulfobutyl Ether β-Cyclodextrin Using Liquid–Liquid Extraction and GC–MS

Publication Date: 05 July 2012

Meng Wang, Hongmei Wen, Sheng Yu & Zhengyu Yan

https://doi.org/10.1007/s10337-012-2275-8

 

- Modification of poly(butylene terephthalate) by reaction with 1,4-butane sultone; synthesis and thermal characterization of new telechelic PBT ionomers

Publication Date: August 31, 2013

Corrado Berti , Annamaria Celli , Elisabetta Marianucci EMAIL logo and Micaela Vannini

https://doi.org/10.1515/epoly.2008.8.1.865

 

- Simple hydrothermal synthesis of sphere-like TiO2 nanoparticles and their functionalization with 1,4-butane sultone as a new heterogeneous catalyst

Publication Date: 12 June 2017

Maliheh M. Hosseini, Eskandar Kolvari, Somayeh Zolfagharinia & Mina Hamzeh

https://doi.org/10.1007/s13738-017-1118-9