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48527

Supelco

trans-1,2-Dichloroethene

analytical standard

Sinonimo/i:

trans-1,2-Dichloroethylene, trans-1,2-Dichloroethene, trans-Acetylene dichloride

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About This Item

Formula condensata:
ClCH=CHCl
Numero CAS:
156-60-5
Peso molecolare:
96.94
Beilstein:
1420761
Numero CE:
205-860-2
Numero MDL:
MFCD00062942
Codice UNSPSC:
12000000
ID PubChem:
24872050

Grado

analytical standard

Tensione di vapore

5.16 psi ( 20 °C)

Limite di esplosione

12.8 %

Confezionamento

ampule of 5000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.446 (lit.)

P. eboll.

48 °C (lit.)

Punto di fusione

−50 °C (lit.)

Densità

1.257 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

Cl\C=C\Cl

InChI

1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1+
KFUSEUYYWQURPO-OWOJBTEDSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H225,H332,H412

Classi di pericolo

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Flam. Liq. 2

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

42.8 °F - closed cup

Punto d’infiammabilità (°C)

6.0 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
LB97670V
LB85359V
LB83747V
LB82021V
LB79619

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Darlene D Wagner et al.
BMC genomics, 13, 200-200 (2012-05-24)
Geobacter lovleyi is a unique member of the Geobacteraceae because strains of this species share the ability to couple tetrachloroethene (PCE) reductive dechlorination to cis-1,2-dichloroethene (cis-DCE) with energy conservation and growth (i.e., organohalide respiration). Strain SZ also reduces U(VI) to
Timothy E Mattes et al.
FEMS microbiology reviews, 34(4), 445-475 (2010-02-12)
Extensive use and inadequate disposal of chloroethenes have led to prevalent groundwater contamination worldwide. The occurrence of the lesser chlorinated ethenes [i.e. vinyl chloride (VC) and cis-1,2-dichloroethene (cDCE)] in groundwater is primarily a consequence of incomplete anaerobic reductive dechlorination of
Florian Schevenels et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(13), 4335-4343 (2013-01-22)
Highly functionalised benzofurans have been prepared from ortho-hydroxyphenones and 1,1-dichloroethylene. The key intermediate, a chloromethylene furan, smoothly rearranged into the corresponding benzofuran carbaldehyde under acidic conditions. Some mechanistic investigations have been performed and several biologically active benzofurans have been synthesised.
Federico Aulenta et al.
Bioresource technology, 101(24), 9728-9733 (2010-08-17)
Quinone moieties in humic substances have previously been shown to serve as extracellular electron acceptors in different metabolic pathways. Here we show that the humic acid analogue antraquinone-2,6-disulfonate (AQDS) can also serve as an electron donor in the microbial reductive
M Rovira-Esteva et al.
The Journal of chemical physics, 136(12), 124514-124514 (2012-04-03)
Trans-1,2-dichloroethene (HClC=CClH) has several structural and dynamic anomalies between its low- and high-density liquid, previously found through neutron scattering experiments. To explain the microscopic origin of the differences found in those experiments, a series of molecular dynamics simulations were performed.
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