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48597

Supelco

cis-1,2-Dichloroethene

analytical standard

Sinonimo/i:

cis-1,2-Dichloroethylene, cis-Acetylene dichloride

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About This Item

Formula condensata:
ClCH=CHCl
Numero CAS:
156-59-2
Peso molecolare:
96.94
Beilstein:
1071208
Numero CE:
205-859-7
Numero MDL:
MFCD00000925
Codice UNSPSC:
41116107
ID PubChem:
24872155

Grado

analytical standard

Livello qualitativo

100

CdA

current certificate can be downloaded

Confezionamento

ampule of 1000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.449 (lit.)

P. ebollizione

60 °C (lit.)

Punto di fusione

−80 °C (lit.)

Densità

1.284 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

Cl\C=C/Cl

InChI

1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-
KFUSEUYYWQURPO-UPHRSURJSA-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.

Raccomandato

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H225,H302 + H332,H315,H412

Classi di pericolo

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

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCM8745
MKCH2023
MKCD5041
MKBZ1456V
MKBT0999V

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Biao Jin et al.
Environmental science & technology, 48(11), 6141-6150 (2014-05-09)
Laboratory experiments were performed to investigate and quantify the extent of diffusive isotope fractionation of organic contaminants in aqueous solution. We selected petroleum hydrocarbons (toluene and ethylbenzene, in 1:2 mixtures of labeled (perdeuterated) and nonlabeled isotopologues) and chlorinated solvents (trichloroethene
C Andrew Ramsburg et al.
Environmental science & technology, 44(23), 9105-9111 (2010-11-09)
Abiotic and biotic reductive dechlorination with chlorinated ethene dense non-aqueous-phase liquid (DNAPL) source zones can lead to significant fluxes of complete and incomplete transformation products. Accurate assessment of in situ rates of transformation and the potential for product sequestration requires
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.
He-Ping Zhao et al.
Water research, 44(7), 2276-2282 (2010-01-19)
The presence of other chloroethenes influences aerobic metabolic biodegradation of cis-1,2-dichloroethene (cDCE). A new metabolically cDCE degrading enrichment culture was identified as also being capable of degrading vinyl chloride (VC), but not 1,1-dichloroethene (1,1DCE), trans-1,2-dichloroethene (tDCE), trichloroethene (TCE), or tetrachloroethene
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
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