163023
1,1-Dichloroethylene
contains 200 ppm MEHQ as inhibitor, 99%
Synonym(s):
Vinylidene chloride
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About This Item
Linear Formula:
CH2=CCl2
CAS Number:
Molecular Weight:
96.94
Beilstein:
1733365
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
vapor density
3.46 (vs air)
vapor pressure
9.68 psi ( 20 °C)
Assay
99%
form
liquid
autoignition temp.
968 °F
contains
200 ppm MEHQ as inhibitor
expl. lim.
15.5 %
bp
30-32 °C (lit.)
mp
−122 °C (lit.)
density
1.213 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
ClC(Cl)=C
InChI
1S/C2H2Cl2/c1-2(3)4/h1H2
InChI key
LGXVIGDEPROXKC-UHFFFAOYSA-N
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Application
1,1-Dichloroethylene can be used as a monomer to synthesize polymercomposite latexes by emulsion polymerization.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 1 - Skin Irrit. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-2.2 °F
Flash Point(C)
-19 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Fan Chen et al.
Frontiers in microbiology, 9, 2306-2306 (2018-10-17)
Bioelectrochemical systems (BESs) are regarded as a promising approach for the enhanced dechlorination of chlorinated aliphatic hydrocarbons (CAHs). However, the electron distribution and transfer considering dechlorination, methanogenesis, and other bioprocesses in these systems are little understood. This study investigated the
Erik J Martin et al.
The Journal of pharmacology and experimental therapeutics, 304(1), 121-129 (2002-12-20)
Hepatotoxicity induced by 1,1-dichloroethylene (DCE) is mediated by cytochrome P450-dependent metabolism to reactive intermediates, including the epoxide. We have tested the hypothesis that mitochondria are a primary target of toxicity by investigating dose- and time-dependent effects of DCE on mitochondrial
Juliet A Jones et al.
Chemical research in toxicology, 16(10), 1306-1317 (2003-10-21)
A proteome profiling approach was used to compare effects of two toxicants, 1,1-dicloroethylene (DCE) and diclofenac, which covalently adduct hepatic proteins. Bile was examined as a potential source of protein alterations since both toxicants target the hepatic biliary canaliculus. Bile
Kimberly N Heck et al.
Journal of the American Chemical Society, 130(49), 16592-16600 (2009-06-26)
Insight into the nature of transient reaction intermediates and mechanistic pathways involved in heterogeneously catalyzed chemical reactions is obtainable from a number of surface spectroscopic techniques. Carrying out these investigations under actual reaction conditions is preferred but remains challenging, especially
1,1-Dichloroethylene.
Reviews of environmental contamination and toxicology, 106, 81-91 (1988-01-01)
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