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重要文件

443786

Sigma-Aldrich

四氯乙烯

ACS reagent, ≥99.0%

同義詞:

PCE, 全氯乙烯

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About This Item

線性公式:
CCl2=CCl2
CAS號碼:
分子量::
165.83
Beilstein:
1361721
EC號碼:
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.04
bp:
121 °C (lit.)
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等級

ACS reagent

品質等級

蒸汽密度

5.83 (vs air)

蒸汽壓力

13 mmHg ( 20 °C)
19 mmHg ( 25 °C)

化驗

≥99.0%

形狀

liquid

技術

FTIR: suitable

雜質

≤0.05% water

蒸發殘留物

≤0.0005%

顏色

APHA: ≤10

折射率

n20/D 1.505 (lit.)

bp

121 °C (lit.)

mp

−22 °C (lit.)

溶解度

water: soluble 0.15 g/L at 25 °C

密度

1.623 g/mL at 25 °C (lit.)

SMILES 字串

Cl\C(Cl)=C(\Cl)Cl

InChI

1S/C2Cl4/c3-1(4)2(5)6

InChI 密鑰

CYTYCFOTNPOANT-UHFFFAOYSA-N

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一般說明

Tetrachloroethylene (perchloroethylene, PCE), is a chlorinated ethylene compound commonly used as a dry cleaning and degreasing solvent.[1] It shows IR transparency as it has no C–H bonds making it an ideal solvent for IR spectroscopy.[2][3] PCE is a man-made pollutant which is difficult to degrade.[4] It is a ground water contaminant[5] which has adverse effect on human health due to its potential toxicity and carcinogenicity.[6] Some of the methods proposed for its degradation are Fenton oxidation treatment,[7] reductive dehalogenation under methanogenic condition,[6] and reduction using zero valent metal ions.[5] One of the methods reported for its synthesis is by reacting ethylene dichloride and chlorine.[8]

應用

Tetrachloroethylene may be used as a film-forming electrolyte additive in the manufacture of lithium ion batteries.[9] It may also be used as an extractant for the estimation of oil and grease in water by Fourier transform infrared spectroscopy (FT-IR).[2]

訊號詞

Warning

危險分類

Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

標靶器官

Central nervous system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available


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Jenn-Shing Chen et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(10), 2287-2293 (2004-07-14)
The dimerization of 2,2-dimethyl-3-ethyl-3-pentanol in tetrachloroethylene in the diluted region has been studied at four temperatures by IR spectroscopy. The aforementioned solute compound is chosen because self-association beyond dimerization is hampered by the steric hindrance generated by the bulky sidechains.
D Ryoo et al.
Nature biotechnology, 18(7), 775-778 (2000-07-11)
Tetrachloroethylene (PCE) is thought to have no natural source, so it is one of the most difficult contaminants to degrade biologically. This common groundwater pollutant was thought completely nonbiodegradable in the presence of oxygen. Here we report that the wastewater
Validation of a FT-IR method for the determination of oils and grease in water using tetrachloroethylene as the extraction solvent.
Farmaki E, et al.
Desalination, 210(1), 52-60 (2007)
Robert DM and Murphy B.
Chlorinated Solvents: A Forensic Evaluation, 84-85 (2013)
Sorption of trichloroethylene and tetrachloroethylene in a batch reactive metallic iron-water system.
D R Burris et al.
Environmental science & technology, 29(11), 2850-2855 (1995-11-01)

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