S,S'-Trimethylene di(p-toluenethiosulfonate)

97%

Reagent Code: #127116
label
Alias s,s'-trimethene (p-toluene thiosulfonate)
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CAS Number 3866-79-3

science Other reagents with same CAS 3866-79-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.6 g/mol
Formula C₁₇H₂₀O₄S₄
badge Registry Numbers
MDL Number MFCD00014918
thermostat Physical Properties
Melting Point 64-67 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a reagent for the formation of thioether bonds. It is particularly effective in the preparation of cyclic sulfides due to its ability to act as a sulfur transfer agent. The compound is also employed in the development of pharmaceuticals and agrochemicals, where it aids in the creation of sulfur-containing molecules that exhibit biological activity. Additionally, it serves as a crosslinking agent in polymer chemistry, enhancing the mechanical properties and stability of various polymeric materials. Its application extends to the field of materials science, where it is used to modify surface properties and improve adhesion in coatings and composites.

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Test Parameter Specification
Melting Point 64-69
Purity (HPLC) 97-100%
Infrared Spectrometry Conforms To Structure

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inventory 5g
10-20 days ฿8,982.00

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S,S'-Trimethylene di(p-toluenethiosulfonate)
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This chemical is primarily utilized in organic synthesis as a reagent for the formation of thioether bonds. It is particularly effective in the preparation of cyclic sulfides due to its ability to act as a sulfur transfer agent. The compound is also employed in the development of pharmaceuticals and agrochemicals, where it aids in the creation of sulfur-containing molecules that exhibit biological activity. Additionally, it serves as a crosslinking agent in polymer chemistry, enhancing the mechanical pro

This chemical is primarily utilized in organic synthesis as a reagent for the formation of thioether bonds. It is particularly effective in the preparation of cyclic sulfides due to its ability to act as a sulfur transfer agent. The compound is also employed in the development of pharmaceuticals and agrochemicals, where it aids in the creation of sulfur-containing molecules that exhibit biological activity. Additionally, it serves as a crosslinking agent in polymer chemistry, enhancing the mechanical properties and stability of various polymeric materials. Its application extends to the field of materials science, where it is used to modify surface properties and improve adhesion in coatings and composites.

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