48597
cis-1,2-Dichloroethene
analytical standard
Synonym(s):
cis-1,2-Dichloroethylene, cis-Acetylene dichloride
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About This Item
Linear Formula:
ClCH=CHCl
CAS Number:
Molecular Weight:
96.94
EC Number:
205-859-7
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1071208
MDL number:
NACRES:
NA.24
grade
analytical standard
CofA
current certificate can be downloaded
packaging
ampule of 1000 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.449 (lit.)
bp
60 °C (lit.)
mp
−80 °C (lit.)
density
1.284 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
storage temp.
2-8°C
SMILES string
Cl\C=C/Cl
InChI
1S/C2H2Cl2/c3-1-2-4/h1-2H/b2-1-
InChI key
KFUSEUYYWQURPO-UPHRSURJSA-N
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
flash_point_f
42.8 °F - closed cup
flash_point_c
6.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Regulatory Information
危险化学品
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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.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 48597 | 04061836953911 |