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Merck
CN

T7209

1,1,1,2-Tetrachloroethane

ReagentPlus®, 99%

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About This Item

Linear Formula:
ClCH2CCl3
CAS Number:
630-20-6
Molecular Weight:
167.85
EC Number:
211-135-1
UNSPSC Code:
12352101
NACRES:
NA.04
PubChem Substance ID:
329826862
Beilstein/REAXYS Number:
1733216
MDL number:
MFCD00000807
Assay:
99%
Bp:
138 °C (lit.)
Vapor pressure:
12.0 mmHg

Key Documents

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InChI key

QVLAWKAXOMEXPM-UHFFFAOYSA-N

InChI

1S/C2H2Cl4/c3-1-2(4,5)6/h1H2

SMILES string

ClCC(Cl)(Cl)Cl

vapor pressure

12.0 mmHg

product line

ReagentPlus®

assay

99%

form

liquid

dilution

(for general lab use)

refractive index

n20/D 1.481 (lit.)

bp

138 °C (lit.)

mp

-70.2 °C

density

1.598 g/mL at 25 °C (lit.)

Quality Level

100

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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1

Storage Class

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

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR9728
MKCK6604
MKBS3769V
MKBF2316
MKBF2316V

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M Paolini et al.
Mutagenesis, 5(1), 51-54 (1990-01-01)
The synergistic effect of NADPH and NADH on P450 functions upon pre-mutagens requiring metabolism during the incubation conditions used in the liver microsomal assay (LMA) was studied. The mean specific activity (Asp) during 1 h of pre-incubation (LMA) of some
D L Story et al.
Toxicology and industrial health, 2(4), 351-362 (1986-12-01)
Nine chlorinated aliphatics (CAs)--1,1-dichloroethane, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2-trichloroethane, trichloroethylene, tetrachloroethylene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, and hexachloroethane--were examined in a rat liver foci assay for evidence of initiating and promoting potential. Young adult male Osborne-Mendel rats (ten/group) were given partial hepatectomies, followed 24 hr
L O Svaasand et al.
Lasers in surgery and medicine, 32(2), 137-142 (2003-02-01)
Cryogen spray cooling (CSC) is used extensively for epidermal protection during laser-induced photothermolysis of port wine stains and other vascular skin lesions. The efficacy of CSC depends critically on the heat transfer coefficient (H) at the skin surface for which
J A Thompson et al.
Chemico-biological interactions, 51(3), 321-333 (1984-10-01)
The susceptibility of polychlorinated ethanes to reductive metabolism was evaluated by measuring the amount of each compound consumed during anaerobic incubations with rat live microsomes; 1,1,1,2-tetrachloroethane, pentachloroethane and hexachloroethane were metabolized extensively, 1,1,1,2-tetrachloroethane and the trichloroethanes were metabolized very slowly
Federico Aulenta et al.
Biodegradation, 17(3), 193-206 (2006-05-23)
This study investigated the biotransformation pathways of 1,1,2,2-tetrachloroethane (1,1,2,2-TeCA) in the presence of chloroethenes (i.e. tetrachloroethene, PCE; trichloroethene, TCE) in anaerobic microcosms constructed with subsurface soil and groundwater from a contaminated site. When amended with yeast extract, lactate, butyrate, or
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