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466212

Sigma-Aldrich

1,1,2-Trichloroethane

contains ≤3% 2-propanol as stabilizer, 97%

Synonym(s):

β-Trichloroethane, Vinyltrichloride

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About This Item

Linear Formula:
ClCH2CHCl2
CAS Number:
Molecular Weight:
133.40
Beilstein/REAXYS Number:
1731726
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

contains

≤3% 2-propanol as stabilizer

refractive index

n20/D 1.471 (lit.)

bp

110-115 °C (lit.)

density

1.435 g/mL at 25 °C (lit.)

SMILES string

ClCC(Cl)Cl

InChI

1S/C2H3Cl3/c3-1-2(4)5/h2H,1H2

InChI key

UBOXGVDOUJQMTN-UHFFFAOYSA-N

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General description

1,1,2-Trichloroethane (1,1,2-TCA), a chlorinated aliphatic hydrocarbon, is a common groundwater pollutant. Microbial detoxification of 1,1,2-TCA has been studied. Ni supported on mesoporous silica (SBA-16) catalyzed hydrodechlorination of 1,1,2-trichloroethane has been reported. Rotational isomers of 1,1,2-trichloroethane in the gaseous and liquid states have been investigated by the infrared absorption spectra.

Application

  • Advanced Material Development: Research into the synthesis of UiO-66 3D photonic crystals highlights the use of 1,1,2-Trichloroethane in the creation of new materials for efficient vapor detection, supporting advancements in sensor technology (Wang et al., 2022).

pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2

supp_hazards

wgk_germany

WGK 3


Certificates of Analysis (COA)

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Trichloroethylene anhydrous, contains 40 ppm diisopropylamine as stabilizer, ≥99%

Sigma-Aldrich

372145

Trichloroethylene

Tetrachloroethylene anhydrous, ≥99%

Sigma-Aldrich

371696

Tetrachloroethylene

Single-step preparation of Ni catalysts supported on mesoporous silicas (SBA-15 and SBA-16) and the effect of pore structure on the selective hydrodechlorination of 1, 1, 2-trichloroethane to VCM.
Park Y, et al.
Catalysis Today, 97(2), 195-203 (2004)
Infrared Absorption Investigation on the Rotational Isomerism of 1, 1, 2-Trichloroethane.
Kuratani K and Mizushima S-I.
J. Chem. Phys. , 22(8), 1403-1405 (1954)
Siyan Zhao et al.
PloS one, 10(3), e0119507-e0119507 (2015-04-04)
1,1,2-trichloroethane (1,1,2-TCA) has become a common groundwater pollutant due to historically extensive utilization, improper disposal, as well as from incomplete dechlorination of 1,1,2,2-tetrachloroethane. Currently, limited information is available on microbial detoxification of 1,1,2-TCA. Desulfitobacterium sp. strain PR, which was isolated
Michio M Matsushita et al.
Journal of the American Chemical Society, 127(36), 12450-12451 (2005-09-08)
A bromide salt of a TTF-based cross-cyclophane-type donor displayed characteristic nonlinear voltage-biased conductivity. As the applied voltage was increased, the passing current was enhanced abruptly at 54 kV.cm-1, exhibiting hysteretic behavior. X-ray analysis of the current-induced low-resistance state of the
Robert Zaleśny et al.
Journal of molecular modeling, 13(6-7), 785-791 (2007-04-18)
The UV-Vis spectra of series of polymethylmethacrylate (PMMA) copolymers with attached trans-azobenzene derivatives were measured in 1,1,2-trichloroethane. In order to gain some insight into the recorded spectra, the quantum chemical calculations were performed for the substituted azobenzenes using both configuration

Protocols

US EPA Method TO-17: GC Analysis of Volatiles on VOCOL® after Collection/Desorption using Air Toxics Tube

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