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Supelco

1,1,2-Trichloroethane

analytical standard

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About This Item

Fórmula linear:
ClCH2CHCl2
Número CAS:
79-00-5
Peso molecular:
133.40
Beilstein:
1731726
Número CE:
201-166-9
Número MDL:
MFCD00000852
Código UNSPSC:
41116107
ID de substância PubChem:
329757112
NACRES:
NA.24

grau

analytical standard

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.471 (lit.)

p.e.

110-115 °C (lit.)

densidade

1.435 g/mL at 25 °C (lit.)

aplicação(ões)

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

cadeia de caracteres SMILES

ClCC(Cl)Cl

InChI

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

chave InChI

UBOXGVDOUJQMTN-UHFFFAOYSA-N

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Aplicação

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

Pictogramas

Skull and crossbonesHealth hazard
GHS06,GHS08

Palavra indicadora

Danger

Classificações de perigo

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

Perigos de suplementos

EUH066

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
BCCB7564
BCBS3646V

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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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