VINYL CHLORIDE (75-01-4, 9002-86-2)

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Suppliers

• Sigma-Aldrich - Search for VINYL CHLORIDE
• Fisher Scientific - Search for VINYL CHLORIDE
• TCI - Search for VINYL CHLORIDE

Most-cited Publications

• Ultrafast synthesis of ultrahigh molar mass polymers by metal-catalyzed living radical polymerization of acrylates, methacrylates, and vinyl chloride mediated by SET at 25 degrees C. (Journal of the American Chemical Society, 2006)
• Dual-Mode Sorption of Low-Polarity Compounds in Glassy Poly(Vinyl Chloride) and Soil Organic Matter (Environmental Science & Technology, 1997)
• Biotransformation of tetrachloroethylene to trichloroethylene, dichloroethylene, vinyl chloride, and carbon dioxide under methanogenic conditions (Applied and Environmental Microbiology, 1985)
• Detoxification of vinyl chloride to ethene coupled to growth of an anaerobic bacterium (Nature, 2003)
• Aqueous room temperature metal-catalyzed living radical polymerization of vinyl chloride. (Journal of the American Chemical Society, 2002)
• A calcium-sensitive electrode based on a liquid ion exchanger in a poly(vinyl chloride) matrix (Analyst, 1970)

Areas of Application

Safety

• Request a Demo
  Predict GHS Hazards for Any Chemical in silico.
  Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more.
• H220: Extremely flammable gas
  Danger Flammable gases - Category 1
• H315: Causes skin irritation
  Warning Skin corrosion/irritation - Category 2
• H350: May cause cancer
  Danger Carcinogenicity - Category 1A, 1B
• H370: Causes damage to organs
  Danger Specific target organ toxicity, single exposure - Category 1
• H402: Harmful to aquatic life
  Hazardous to the aquatic environment, acute hazard - Category 3

Trends

Alternate Names

• Chloroethylene
• SMILES
  C=CCl
• InChIKey
  BZHJMEDXRYGGRV-UHFFFAOYSA-N

Estimated Properties

External Links

• Pubchem - VINYL CHLORIDE
• Wikipedia - vinyl chloride
  Vinyl chloride is an organochloride with the formula H2C=CHCl that is also called vinyl chloride monomer (VCM) or chloroethene. This colorless compound is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). About 13 billion kilograms are produced annually.

Synthesis

Reactant  +  1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (Nicolaou IBX dehydrogenation)

Synthesis of VINYL CHLORIDE ›

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