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Documenti fondamentali

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46262

Supelco

1,1,2-Trichloroethane

analytical standard

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About This Item

Formula condensata:
ClCH2CHCl2
Numero CAS:
79-00-5
Peso molecolare:
133.40
Beilstein:
1731726
Numero CE:
201-166-9
Numero MDL:
MFCD00000852
Codice UNSPSC:
41116107
ID PubChem:
329757112
NACRES:
NA.24

Grado

analytical standard

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.471 (lit.)

P. ebollizione

110-115 °C (lit.)

Densità

1.435 g/mL at 25 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

ClCC(Cl)Cl

InChI

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

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Applicazioni

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

Pittogrammi

Skull and crossbonesHealth hazard
GHS06,GHS08

Avvertenze

Danger

Indicazioni di pericolo

H302 + H312,H331,H351,H412

Classi di pericolo

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

Rischi supp

EUH066

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCB7564
BCBS3646V

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1,1,2,2-Tetrachloroethane reagent grade, ≥98%

Sigma-Aldrich

185434

1,1,2,2-Tetrachloroethane

1,1-Dichloroethylene analytical standard

Supelco

02574

1,1-Dichloroethylene

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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