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Contents

   



(Top)
 


1 Production  





2 Applications  



2.1  Polyvinylidene chloride  







3 Safety  





4 See also  





5 References  





6 External links  














1,1-Dichloroethylene






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From Wikipedia, the free encyclopedia
 

(Redirected from Vinylidene chloride)

1,1-Dichloroethylene
Structural formula
Structural formula
Ball-and-stick model
Ball-and-stick model
Names
Preferred IUPAC name

1,1-Dichloroethene

Other names

1,1-Dichloroethylene
1,1-DCE
Vinylidene chloride
Vinylidene dichloride
Asymmetrical dichloroethene

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChemSpider
ECHA InfoCard 100.000.786 Edit this at Wikidata
KEGG

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C2H2Cl2/c1-2(3)4/h1H2 ☒N

    Key: LGXVIGDEPROXKC-UHFFFAOYSA-N ☒N

  • ClC(Cl)=C

Properties

Chemical formula

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)

Solubility in water

2,240mg/L (25°C)
Vapor pressure 500 mmHg (20°C)[1]

Magnetic susceptibility (χ)

-49.2·10−6cm3/mol

Dipole moment

1.3 D
Structure

Point group

C2v

Molecular shape

Planar
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 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. propaneInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
2
4
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):

LDLo (lowest published)

1500 mg/kg (rat)
194 mg/kg (mouse)[2]

LCLo (lowest published)

200 ppm (rat, 4.1 hr)
98 ppm (mouse, 22–23 hr)
1,000 ppm (rat, 2.4 hr)[2]
NIOSH (US health exposure limits):

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 checkY☒N ?)

Infobox references

1,1-Dichloroethylene, commonly called vinylidene chlorideor1,1-DCE, is an organochloride with the molecular formula CHCl2CH3. 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 clingwrap, Saran, for food, but this application has been phased out.

Production[edit]

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]

Applications[edit]

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 chloride[edit]

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.

Safety[edit]

The health effects from exposure to vinylidene chloride are primarily on the central nervous system, including symptoms of sedation, inebriation, convulsions, spasms, and unconsciousness at high concentrations.[5]

International Agency for Research on Cancer has put vinylidene chloride in Class 2B, meaning possibly carcinogenic to humans. National Institute for Occupational Safety and Health considers vinylidene chloride a potential occupational carcinogen.[6]

See also[edit]

References[edit]

  1. ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0661". National Institute for Occupational Safety and Health (NIOSH).
  • ^ a b "Toxicological Review of 1,1-Dichloroethylene" (PDF). United States Environmental Protection Agency. Washington, D.C. June 2002.
  • ^ Course CEIC2004 Industrial Chemistry for Engineers. Chemistry Lecture Notes, UNSW
  • ^ 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.
  • ^ epa.gov
  • ^ CDC - NIOSH Pocket Guide to Chemical Hazards
  • External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=1,1-Dichloroethylene&oldid=1226575127"

    Categories: 
    Chloroalkenes
    Halogenated solvents
    Vinylidene compounds
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    This page was last edited on 31 May 2024, at 14:39 (UTC).

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