TRiethylene glycol dimethanesulfonate

95%

Reagent Code: #238201
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CAS Number 80322-82-3

science Other reagents with same CAS 80322-82-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.35 g/mol
Formula C₈H₁₈O₈S₂
badge Registry Numbers
MDL Number MFCD01677750
thermostat Physical Properties
Boiling Point 508.9±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.343±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as a crosslinking agent in polymer chemistry, particularly in the production of specialty resins and functional polymers. It enables the formation of stable networks in polymeric materials, enhancing thermal and mechanical properties. Commonly applied in the development of ion-exchange membranes and hydrogels for controlled release systems. Also utilized in organic synthesis as a bifunctional alkylating agent due to its reactive sulfonate ester groups. Its ability to bridge molecular chains makes it valuable in creating tailored macromolecular architectures for advanced material applications.

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inventory 1g
10-20 days ฿7,500.00

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TRiethylene glycol dimethanesulfonate
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Used primarily as a crosslinking agent in polymer chemistry, particularly in the production of specialty resins and functional polymers. It enables the formation of stable networks in polymeric materials, enhancing thermal and mechanical properties. Commonly applied in the development of ion-exchange membranes and hydrogels for controlled release systems. Also utilized in organic synthesis as a bifunctional alkylating agent due to its reactive sulfonate ester groups. Its ability to bridge molecular chain

Used primarily as a crosslinking agent in polymer chemistry, particularly in the production of specialty resins and functional polymers. It enables the formation of stable networks in polymeric materials, enhancing thermal and mechanical properties. Commonly applied in the development of ion-exchange membranes and hydrogels for controlled release systems. Also utilized in organic synthesis as a bifunctional alkylating agent due to its reactive sulfonate ester groups. Its ability to bridge molecular chains makes it valuable in creating tailored macromolecular architectures for advanced material applications.

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