Sulfuryl chloride

97%

  • Product Code: 123048
  Alias:    Sulfonyl chloride; sulfuryl chloride, sulfuryl dichloride, sulfuryl chloride, sulfuryl dichloride, sulfone dichloride
  CAS:    7791-25-5
Molecular Weight: 134.97 g./mol Molecular Formula: SO₂Cl₂
EC Number: 232-245-6 MDL Number: MFCD00011451
Melting Point: −54 °C(lit.) Boiling Point: 68-70 °C(lit.)
Density: 1.665 g/mL at 20 °C(lit.) Storage Condition: room temperature, dry
Product Description: Sulfuryl chloride is widely used in organic synthesis as a chlorinating agent, particularly for converting alcohols, carboxylic acids, and amines into their corresponding chlorides. It is also employed in the production of pharmaceuticals, agrochemicals, and dyes, where precise chlorination is required. In the polymer industry, it serves as a cross-linking agent for modifying the properties of certain plastics and rubbers. Additionally, it is utilized in the preparation of sulfur-containing compounds and as a reagent in chemical reactions like the Friedel-Crafts acylation. Its strong reactivity makes it valuable in laboratory settings for specialized synthetic processes.
Product Specification:
Test Specification
Free Chlorine 0-0.5
Purity (Titration By Agno3) 96.5-103.5
Sulfur Dioxide (So2) 0-0.5
Appearance Colorless To Yellow To Green Liquid
Infrared Spectrometry Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
500.000 10-20 days $26.58
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2500.000 10-20 days $83.06
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10000.000 10-20 days $252.91
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Sulfuryl chloride
Sulfuryl chloride is widely used in organic synthesis as a chlorinating agent, particularly for converting alcohols, carboxylic acids, and amines into their corresponding chlorides. It is also employed in the production of pharmaceuticals, agrochemicals, and dyes, where precise chlorination is required. In the polymer industry, it serves as a cross-linking agent for modifying the properties of certain plastics and rubbers. Additionally, it is utilized in the preparation of sulfur-containing compounds and as a reagent in chemical reactions like the Friedel-Crafts acylation. Its strong reactivity makes it valuable in laboratory settings for specialized synthetic processes.
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