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Atomfair 2-Chloroethanesulphonic acid C2H5ClO3S
Description 2-Chloroethanesulphonic Acid (CAS No. 15484-44-3) is a high-purity organic sulfonic acid derivative with the molecular formula C2H5ClO3S . This compound, also known by its IUPAC name 2-chloroethanesulfonic acid , is widely utilized in chemical synthesis and research applications due to its reactive sulfonic acid and chloro functional groups. It is supplied as a white crystalline solid with excellent solubility in water and polar organic solvents, ensuring versatility in laboratory and industrial processes. Each batch undergoes rigorous quality control, including HPLC and NMR analysis, to guarantee ??98% purity. Ideal for use in organic synthesis, pharmaceuticals, and material science, this reagent…
Description
Description
2-Chloroethanesulphonic Acid (CAS No. 15484-44-3) is a high-purity organic sulfonic acid derivative with the molecular formula C2H5ClO3S. This compound, also known by its IUPAC name 2-chloroethanesulfonic acid, is widely utilized in chemical synthesis and research applications due to its reactive sulfonic acid and chloro functional groups. It is supplied as a white crystalline solid with excellent solubility in water and polar organic solvents, ensuring versatility in laboratory and industrial processes. Each batch undergoes rigorous quality control, including HPLC and NMR analysis, to guarantee ??98% purity. Ideal for use in organic synthesis, pharmaceuticals, and material science, this reagent is packaged under inert conditions to ensure stability and longevity. Store in a cool, dry place away from light and moisture.
- CAS No: 15484-44-3
- Molecular Formula: C2H5ClO3S
- Molecular Weight: 144.58
- Exact Mass: 143.9647929
- Monoisotopic Mass: 143.9647929
- IUPAC Name: 2-chloroethanesulfonic acid
- SMILES: C(CCl)S(=O)(=O)O
- Synonyms: 2-CHLOROETHANESULFONIC ACID, 2-Chloroethanesulphonic acid, 2-chloroethane-1-sulfonic acid, Y8E4MUF2AV, EINECS 241-935-6
Application
2-Chloroethanesulphonic acid is commonly employed as an intermediate in the synthesis of sulfonate esters and other organosulfur compounds. It serves as a key reagent in pharmaceutical research, particularly in the modification of biomolecules and drug candidates. Additionally, its reactive chloro and sulfonic acid groups make it valuable in polymer chemistry for functionalizing materials and creating ion-exchange resins.
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