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48597

Supelco

cis-1,2-Dichloroethene

analytical standard

Synonyme(s) :

cis-1,2-dichloroéthylène

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About This Item

Formule linéaire :
ClCH=CHCl
Numéro CAS:
156-59-2
Poids moléculaire :
96.94
Numéro Beilstein :
1071208
Numéro CE :
205-859-7
Numéro MDL:
MFCD00000925
Code UNSPSC :
41116107
ID de substance PubChem :
24872155

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 1000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.449 (lit.)

Point d'ébullition

60 °C (lit.)

Pf

−80 °C (lit.)

Densité

1.284 g/mL at 25 °C (lit.)

Application(s)

environmental

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

Cl\C=C/Cl

InChI

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

Clé InChI

KFUSEUYYWQURPO-UPHRSURJSA-N

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Catégories apparentées

Application

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

En option

Réf. du produit
Description
Tarif

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Danger

Mentions de danger

H225,H302 + H332,H315,H412

Classification des risques

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

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

42.8 °F - closed cup

Point d'éclair (°C)

6.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
MKCR7369
MKCM8745
MKCH2023
MKCD5041
MKBZ1456V

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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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
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
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.
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