Open main menu

1,1-Dichloroethene, commonly called 1,1-dichloroethylene or vinylidene chloride or 1,1-DCE, is an organochloride with the molecular formula C2H2Cl2. It is a colorless liquid with a sharp odor. Like most chlorocarbons, it is poorly soluble in water, but soluble in organic solvents. 1,1-DCE was the precursor to the original cling-wrap, Saran, for food, but this application has been phased out.

1,1-Dichloroethene
Structural formula
Ball-and-stick model
Names
Preferred IUPAC name
1,1-Dichloroethene
Other names
1,1-Dichloroethylene
1,1-DCE
Vinylidene chloride
Vinylidene dichloride
Geminal dichloroethene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.000.786
KEGG
UNII
Properties
C2H2Cl2
Molar mass 96.94 g/mol
Density 1.213 g/cm3
Melting point −122 °C (−188 °F; 151 K)
Boiling point 32 °C (90 °F; 305 K)
0.04% (20°C)[1]
Vapor pressure 500 mmHg (20°C)[1]
-49.2·10−6 cm3/mol
1.3 D
Structure
C2v
Planar
Hazards
NFPA 704
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g., propaneHealth code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroformReactivity code 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g., phosphorusSpecial hazards (white): no codeNFPA 704 four-colored diamond
4
2
2
Flash point −22.8 °C (−9.0 °F; 250.3 K)
Explosive limits 6.5%-15.5%[1]
Lethal dose or concentration (LD, LC):
16,000 ppm (rat, 4 hr)
17,300 ppm (mouse, 2 hr)
16,000 ppm (rat, 8 hr)[2]
US health exposure limits (NIOSH):
PEL (Permissible)
none[1]
REL (Recommended)
Ca[1]
IDLH (Immediate danger)
Ca [N.D.][1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is ☑Y☒N ?)
Infobox references

Contents

ProductionEdit

1,1-DCE is produced by dehydrochlorination of 1,1,2-trichloroethane, a relatively unwanted byproduct in the production of 1,1,1-trichloroethane and 1,2-dichloroethane. The conversion is a base-catalyzed reaction which uses either NaOH or Ca(OH)2 with temperature ca. 100 °C.[3]

Cl2CHCH2Cl + NaOH → Cl2C=CH2 + NaCl + H2O

The gas phase reaction, without the base, would be more desirable but is less selective.[4]

ApplicationsEdit

1,1-DCE is mainly used as a comonomer in the polymerization of vinyl chloride, acrylonitrile, and acrylates. It is also used in semiconductor device fabrication for growing high purity silicon dioxide (SiO2) films.

Polyvinylidene chlorideEdit

As with many other alkenes, 1,1-DCE can be polymerised to form polyvinylidene chloride. A very widely used product, cling wrap, or Saran was made from this polymer. During the 1990s research suggested that, in common with many chlorinated carbon compounds, Saran posed a possible danger to health by leaching, especially on exposure to food in microwave ovens. Since 2004, therefore cling wrap's formulation has changed to a form of polyethylene.

SafetyEdit

The health effects from exposure to 1,1-DCE are primarily on the central nervous system, including symptoms of sedation, inebriation, convulsions, spasms, and unconsciousness at high concentrations.[5] 1,1-DCE is considered a potential occupational carcinogen by the National Institute for Occupational Safety and Health .[6] It is also listed as a chemical known to the state of California to cause cancer and birth defects.[7]

See alsoEdit

ReferencesEdit

  1. ^ a b c d e f NIOSH Pocket Guide to Chemical Hazards. "#0661". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ "1,1-Dichloroethane". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Course CEIC2004 Industrial Chemistry for Engineers. Chemistry Lecture Notes, UNSW
  4. ^ Manfred Rossberg, Wilhelm Lendle, Gerhard Pfleiderer, Adolf Tögel, Eberhard-Ludwig Dreher, Ernst Langer, Heinz Rassaerts, Peter Kleinschmidt, Heinz Strack, Richard Cook, Uwe Beck, Karl-August Lipper, Theodore R. Torkelson, Eckhard Löser, Klaus K. Beutel, Trevor Mann "Chlorinated Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2006, Wiley-VCH, Weinheim. doi:10.1002/14356007.a06_233.pub2.
  5. ^ epa.gov
  6. ^ CDC - NIOSH Pocket Guide to Chemical Hazards
  7. ^ https://oehha.ca.gov/proposition-65/crnr/chemical-listed-effective-december-29-2017-known-state-california-cause-cancer

External linksEdit