1,3-Propanesultone丨CAS 1120-71-4

1,3-Propanesultone丨CAS 1120-71-4
Product Introduction:
Catalog No.: SS128651
CAS No.: 1120-71-4
Purity (GC)/Grade: 99.9%min/Battery Grade
Product Name: 1,3-Propanesultone
Molecular Formula: C3H6O3S
Molecular Weight: 122.14
Synonym(s): 1,2-Oxathiolane 2,2-dioxide; 3-Hydroxy-1-propanesulfonic acid gamma-sultone; Propane sultone
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Technical Parameters
Description

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Specifications of 1,3-Propanesultone丨CAS 1120-71-4

 

Property

Specification

Grade

Battery grade

Appearance (35°C)

Colorless to light yellow liquid or crystals, no solid impurity

Purity (GC)

99.9% min

Water (K.F)

80 ppm max

Acid (HF)

30 ppm max

Colority (Pt-Co)

30 max

Single impurity (K, Na, Fe, Ni, Cr, Mn, Al, Mg, Ca, Ba, Cd, Cu, Pb, Zn)

1 ppm max

 

Transport Information of 1,3-Propanesultone丨CAS 1120-71-4

 

Parameter

Specification

UN Number

2810

Class

 

Packing Group

 

H.S. Code

 

Stability & Reactivity

The product is chemically stable under standard ambient conditions (room temperature).

Storage

Tightly closed. Store in a closed, dry, ventilated place

Condition to Avoid

 

Package

 

 

Manufacturing Information of 1,3-Propanesultone丨CAS 1120-71-4

 

Parameter

Specification

Capacity

20MT/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

 

Stock

 

1,3-Propanesultone丨CAS 1120-71-4 is a cyclic sulfonic ester with the molecular formula C3H6O3S. It is a highly reactive lactone of 1-hydroxypropanesulfonic acid and exists as a colorless liquid or crystalline solid under standard conditions. Due to its strained ring structure, it readily undergoes ring-opening reactions, making it a valuable intermediate in both organic synthesis and industrial applications.

 

Applications of 1,3-Propanesultone丨CAS 1120-71-4

 

1. Electrolyte Additive in Lithium-ion Batteries
1,3-Propanesultone丨CAS 1120-71-4 is widely used as a film-forming additive in electrolytes for lithium-ion batteries (LIBs):
● Solid Electrolyte Interphase (SEI) formation: It decomposes at the electrode surface during the initial charge cycle to form a stable SEI layer, which protects the anode and enhances battery lifespan.
● Improved cycling stability: The SEI formed by 1,3-propanesultone contributes to lower impedance and enhanced capacity retention during repeated charge/discharge cycles.
● Thermal stability: It helps improve the thermal performance of LIBs, supporting safety and efficiency at elevated temperatures.
2. Synthesis of Zwitterionic Surfactants and Polymers
1,3-Propanesultone丨CAS 1120-71-4 is a key precursor in the synthesis of zwitterionic compounds, especially sulfobetaines, which are used in:
● Surfactants: These compounds are non-ionic and pH-stable, ideal for applications in cosmetics, detergents, and antifouling coatings.
● Biocompatible polymers: Sulfobetaine-functionalized polymers resist protein adsorption and biofouling, making them ideal for medical devices, biosensors, and drug delivery systems.
3. Pharmaceutical Intermediates
Due to its reactivity with amines and alcohols, 1,3-propanesultone is employed in the modification of active pharmaceutical ingredients (APIs) or intermediates:
● Quaternization agent: It introduces sulfonate functional groups to enhance water solubility or modify the pharmacokinetics of compounds.
● Biofunctional molecules: Useful in preparing molecules with ionic tags for bioanalytical and diagnostic purposes.
4. Ion-exchange Resin and Membrane Modification
In the field of materials science, 1,3-propanesultone is used to modify membranes and resins:
● Ion-exchange resins: Incorporation of sulfonic acid groups through 1,3-propanesultone allows the creation of cation-exchange materials.
● Fuel cell membranes: It is used to introduce sulfonic acid functionalities in polymeric membranes, improving proton conductivity.

 

Benefits of 1,3-Propanesultone丨CAS 1120-71-4

 

1. High Reactivity for Functionalization
1,3-Propanesultone's strained ring structure enables efficient ring-opening reactions with various nucleophiles, allowing for rapid and selective modification of target molecules.
2. Versatile Precursor for Functional Materials
It serves as a key building block for a wide range of materials, from ionic liquids to functional monomers, supporting innovations in energy storage, coatings, and biotechnology.
3. Enhanced Electrochemical Performance in LIBs
In lithium-ion battery applications, its use helps to extend battery life, improve safety, and maintain capacity over time by contributing to a robust SEI layer.
4. Wide Industrial Applicability
Its ability to introduce sulfonate groups makes it suitable across sectors, including electronics, cosmetics, environmental engineering, and healthcare.

 

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