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46262

Supelco

1,1,2-Trichloroethane

analytical standard

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About This Item

Linear Formula:
ClCH2CHCl2
CAS Number:
79-00-5
Molecular Weight:
133.40
Beilstein:
1731726
EC Number:
201-166-9
MDL number:
MFCD00000852
UNSPSC Code:
41116107
PubChem Substance ID:
329757112
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.471 (lit.)

bp

110-115 °C (lit.)

density

1.435 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

ClCC(Cl)Cl

InChI

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

InChI key

UBOXGVDOUJQMTN-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

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

Supplementary Hazards

EUH066

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB7564
BCBS3646V
SZBE157XV
SZBA207XV
SZBA207X

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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
Maciej Bujak et al.
Chemical communications (Cambridge, England), (37)(37), 4439-4441 (2008-09-20)
Pressure-induced transformations between gauche-, gauche+ and transoid conformations have been evidenced by X-ray single-crystal diffraction for 1,1,2-trichloroethane, and the energies of intermolecular interactions, conformational conversion, and the latent heat have been determined.
Chuanjie Cheng et al.
The Journal of organic chemistry, 74(15), 5671-5674 (2009-06-19)
In the presence of 1,1,2-trichloroethane, a novel procedure for the Pd-C catalytic N-debenzylation of benzylamines was established. The method proceeded in a synergistic catalytic system and directly gave the products as crystal amine hydrochlorides in practically quantitative yields.
Kenneth Y Lee et al.
Journal of hazardous materials, 128(2-3), 218-226 (2005-10-06)
This paper presents the results from a well-defined, circular-shaped, multicomponent dense nonaqueous phase liquid (DNAPL) pool dissolution experiment conducted in a three-dimensional, bench scale model aquifer. The multicomponent pool is a mixture of tetrachloroethylene (PCE) and 1,1,2-trichloroethane (1,1,2-TCA); PCE was
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Protocols

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

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