Sulfuryl chloride solution

1.0 M in methylene chloride

Reagent Code: #122790
label
Alias Dichloromethanesulfonyl chloride preparation solution
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CAS Number 7791-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.97 g/mol
Formula SO₂Cl₂
badge Registry Numbers
EC Number 232-245-6
MDL Number MFCD00011451
thermostat Physical Properties
Boiling Point 39.8-40 °C
inventory_2 Storage & Handling
Density 1.352 g/mL at 25 °C
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Sulfuryl chloride solution is widely used in organic synthesis as a chlorinating and sulfonating agent. It is particularly effective in converting alcohols to alkyl chlorides and carboxylic acids to acyl chlorides, which are key intermediates in the production of pharmaceuticals, agrochemicals, and dyes. In the polymer industry, it serves as a cross-linking agent for modifying the properties of polymers, enhancing their thermal stability and mechanical strength. Additionally, it is employed in the synthesis of sulfonamides, which are important in the development of antibacterial drugs. Its ability to introduce chlorine or sulfonyl groups makes it a versatile reagent in various chemical transformations.

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Test Parameter Specification
Appearance Liquid
Concentration 1.0M

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100ml
10-20 days $232.81
inventory 500ml
10-20 days $698.88
Sulfuryl chloride solution
Sulfuryl chloride solution is widely used in organic synthesis as a chlorinating and sulfonating agent. It is particularly effective in converting alcohols to alkyl chlorides and carboxylic acids to acyl chlorides, which are key intermediates in the production of pharmaceuticals, agrochemicals, and dyes. In the polymer industry, it serves as a cross-linking agent for modifying the properties of polymers, enhancing their thermal stability and mechanical strength. Additionally, it is employed in the synthesis of sulfonamides, which are important in the development of antibacterial drugs. Its ability to introduce chlorine or sulfonyl groups makes it a versatile reagent in various chemical transformations.
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