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48597

Supelco

cis-1,2-Dichloroethene

analytical standard

Sinônimo(s):

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

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About This Item

Fórmula linear:
ClCH=CHCl
Número CAS:
156-59-2
Peso molecular:
96.94
Beilstein:
1071208
Número CE:
205-859-7
Número MDL:
MFCD00000925
Código UNSPSC:
41116107
ID de substância PubChem:
24872155

grau

analytical standard

Nível de qualidade

100

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 1000 mg

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.449 (lit.)

p.e.

60 °C (lit.)

pf

−80 °C (lit.)

densidade

1.284 g/mL at 25 °C (lit.)

aplicação(ões)

environmental

Formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Cl\C=C/Cl

InChI

1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-

chave InChI

KFUSEUYYWQURPO-UPHRSURJSA-N

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Aplicação

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

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Nº do produto
Descrição
Preços

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

42.8 °F - closed cup

Ponto de fulgor (°C)

6.0 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (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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