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30-0610

Sigma-Aldrich

1,1,2,2-Tetrachloroethane

JIS special grade, ≥97.0%

Synonym(s):

Acetylene tetrachloride

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About This Item

Linear Formula:
CHCl2CHCl2
CAS Number:
Molecular Weight:
167.85
Beilstein:
969206
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:

grade

JIS special grade

vapor density

5.8 (vs air)

vapor pressure

8 mmHg ( 20 °C)

Assay

≥97.0%

form

liquid

availability

available only in Japan

refractive index

n20/D 1.494 (lit.)

bp

147 °C (lit.)

mp

−43 °C (lit.)

density

1.586 g/mL at 25 °C (lit.)

SMILES string

ClC(Cl)C(Cl)Cl

InChI

1S/C2H2Cl4/c3-1(4)2(5)6/h1-2H

InChI key

QPFMBZIOSGYJDE-UHFFFAOYSA-N

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Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Aquatic Chronic 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Wan-Chun Tsai et al.
Journal of chromatography. A, 1216(45), 7846-7850 (2009-10-07)
A novel sample preparation method "Dispersive liquid-liquid-liquid microextraction" (DLLLME) was developed in this study. DLLLME was combined with liquid chromatography system to determine chlorophenoxy acid herbicide in aqueous samples. DLLLME is a rapid and environmentally friendly sample pretreatment method. In
Marcos Caroli Rezende et al.
Magnetic resonance in chemistry : MRC, 47(6), 505-510 (2009-04-01)
Spectra of the N-phenyl-5,6-dihydro-2,4-diphenylbenzo[h]quinolinium tetrafluoroborate (1) and of the N-phenyl-5,6,8,9-tetrahydro-7-phenyldibenzo[c,h]acridinium tetrafluoroborate (2) were recorded in various solvents and temperatures. The analysis of the (1)H-NMR spectra of the tetrafluoroborate salt 1, recorded in acetone, acetonitrile, 1,1,2,2-tetrachloroethane and chloroform, revealed the existence
Srigokul Upadhyayula et al.
The journal of physical chemistry. B, 115(30), 9473-9490 (2011-06-21)
Electrostatic properties of proteins are crucial for their functionality. Carboxyamides are small polar groups that, as peptide bonds, are principal structural components of proteins that govern their electrostatic properties. We investigated the medium dependence of the molar polarization and of
Martin Elsner et al.
Environmental science & technology, 41(11), 4111-4117 (2007-07-07)
Despite widespread implementation of zero-valent iron remediation schemes, the manner and order of chemical bond cleavage in iron-mediated organohalide transformations remains imperfectly understood. We present insights from carbon isotope fractionation for the dehalogenation of 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA) and 1,1,1-trichloroethane (1,1,1-TCA) by
William A Arnold et al.
Environmental science & technology, 36(16), 3536-3541 (2002-09-07)
Products of the transformation of organic pollutants in the environment are often predicted based on the structure of the parent compounds. In some cases, however, multiple products may result from the same reaction pathway. In this study, the reduction of

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