Atomfair 1,4-Butane sultone C4H8O3S

Description 1,4-Butane Sultone (CAS 1633-83-6) is a high-purity cyclic sulfonate ester with the molecular formula C4H8O3S . Also known as oxathiane 2,2-dioxide , this versatile organosulfur compound is widely utilized in organic synthesis, polymer chemistry, and electrolyte formulations. Its cyclic structure and reactive sulfone group make it an excellent precursor for sulfonic acid derivatives, surfactants, and specialty polymers. This product is rigorously tested for purity and consistency, ensuring optimal performance in research and industrial applications. Available in various quantities, it is supplied with comprehensive analytical documentation including GC/MS, NMR, and HPLC data.

Description

1,4-Butane Sultone (CAS 1633-83-6) is a high-purity cyclic sulfonate ester with the molecular formula C₄H₈O₃S. Also known as oxathiane 2,2-dioxide, this versatile organosulfur compound is widely utilized in organic synthesis, polymer chemistry, and electrolyte formulations. Its cyclic structure and reactive sulfone group make it an excellent precursor for sulfonic acid derivatives, surfactants, and specialty polymers. This product is rigorously tested for purity and consistency, ensuring optimal performance in research and industrial applications. Available in various quantities, it is supplied with comprehensive analytical documentation including GC/MS, NMR, and HPLC data.

CAS No: 1633-83-6
Molecular Formula: C4H8O3S
Molecular Weight: 136.17
Exact Mass: 136.01941529
Monoisotopic Mass: 136.01941529
IUPAC Name: oxathiane 2,2-dioxide
SMILES: C1CCS(=O)(=O)OC1
Synonyms: 1,4-BUTANE SULTONE, 1,4-Butanesultone, Butane sultone, 1,2-Oxathiane, 2,2-dioxide, 1,2-Oxathiane 2,2-dioxide

Application

1,4-Butane sultone is primarily used as a key intermediate in the synthesis of sulfonated polymers and surfactants. It serves as a precursor for lithium-ion battery electrolytes, enhancing thermal stability and conductivity. Researchers also employ it in the preparation of zwitterionic compounds and as a sulfonation agent in organic transformations.

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