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163023

Sigma-Aldrich

1,1-Dichloroethylene

contains 200 ppm MEHQ as inhibitor, 99%

Sinonimo/i:

Vinylidene chloride

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About This Item

Formula condensata:
CH2=CCl2
Numero CAS:
75-35-4
Peso molecolare:
96.94
Beilstein:
1733365
Numero CE:
200-864-0
Numero MDL:
MFCD00011653
Codice UNSPSC:
12162002
ID PubChem:
24850019
NACRES:
NA.23

Densità del vapore

3.46 (vs air)

Tensione di vapore

9.68 psi ( 20 °C)

Saggio

99%

Forma fisica

liquid

Temp. autoaccensione

968 °F

contiene

200 ppm MEHQ as inhibitor

Limite di esplosione

15.5 %

P. eboll.

30-32 °C (lit.)

Punto di fusione

−122 °C (lit.)

Densità

1.213 g/mL at 20 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

ClC(Cl)=C

InChI

1S/C2H2Cl2/c1-2(3)4/h1H2
LGXVIGDEPROXKC-UHFFFAOYSA-N

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Applicazioni

1,1-Dichloroethylene can be used as a monomer to synthesize polymercomposite latexes by emulsion polymerization.

Avvertenze

Danger

Indicazioni di pericolo

H224,H301,H315,H319,H332,H351

Classi di pericolo

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 1 - Skin Irrit. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

-2.2 °F

Punto d’infiammabilità (°C)

-19 °C

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
SHBM2704
SHBL4758
SHBK2437
SHBJ1636
SHBH4288V

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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
Xin Ma et al.
Water research, 40(6), 1155-1166 (2006-02-28)
Column experiments were performed to investigate a technology for remediating aquifers contaminated with chlorinated solvents. The technology involves installation of hollow-fiber membranes in the subsurface to supply hydrogen gas (H2) to groundwater to support biological reductive dechlorination in situ. Three
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
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
Masarin Ban et al.
Toxicology, 184(1), 41-50 (2002-12-31)
Using immunotoxic functional tests, namely IgM response to sheep red blood cells (SRBCs) and interferon-gamma (IFN-gamma) production, this study simultaneously evaluated the effects of inhaled chloroform (10, 20, and 50 ppm), carbon tetrachloride (100, 200, and 300 ppm), 1,1-dichloroethylene (5
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