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Merck

443786

Tetrachloroethylene

ACS reagent, ≥99.0%

Synonym(s):

PCE, Perchloroethylene

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About This Item

Linear Formula:
CCl2=CCl2
CAS Number:
Molecular Weight:
165.83
UNSPSC Code:
12352101
NACRES:
NA.04
PubChem Substance ID:
EC Number:
204-825-9
Beilstein/REAXYS Number:
1361721
MDL number:
Grade:
ACS reagent
Assay:
≥99.0%
Technique(s):
FTIR: suitable
Bp:
121 °C (lit.)
Vapor pressure:
13 mmHg ( 20 °C)
19 mmHg ( 25 °C)
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Product Name

Tetrachloroethylene, ACS reagent, ≥99.0%

InChI key

CYTYCFOTNPOANT-UHFFFAOYSA-N

InChI

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

SMILES string

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

grade

ACS reagent

vapor density

5.83 (vs air)

vapor pressure

13 mmHg ( 20 °C)
19 mmHg ( 25 °C)

assay

≥99.0%

form

liquid

technique(s)

FTIR: suitable

impurities

≤0.05% water

evapn. residue

≤0.0005%

color

APHA: ≤10

refractive index

n20/D 1.505 (lit.)

bp

121 °C (lit.)

mp

−22 °C (lit.)

solubility

water: soluble 0.15 g/L at 25 °C

density

1.623 g/mL at 25 °C (lit.)

Quality Level

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General description

Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

signalword

Warning

Hazard Classifications

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

target_organs

Central nervous system

Storage Class

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

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available


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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)
Tetrachloroethylene as new film-forming additive to propylene carbonate-based electrolytes for lithium ion batteries with graphitic anode.
Hu Y, et al.
Solid State Ionics, 176(1), 53-56 (2005)
Decomposition of aqueous tetrachloroethylene by Fenton oxidation treatment.
Yoshida M, et al.
Water Science and Technology, 42(1-2), 203-208 (2000)
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.
A History of the Production and Use of Carbon Tetrachloride, Tetrachloroethylene, Trichloroethylene and 1, 1, 1-Trichloroethane in the United States: Part 2--Trichloroethylene and 1, 1, 1-Trichloroethane.
Doherty RE.
Environmental Forensics, 1(2), 83-93 (2000)

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