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Documenti fondamentali

80521

Supelco

Trichloroacetyl chloride

for GC derivatization, ≥98.5%

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About This Item

Formula condensata:
Cl3CCOCl
Numero CAS:
Peso molecolare:
181.83
Beilstein:
774120
Numero CE:
Numero MDL:
Codice UNSPSC:
12000000
ID PubChem:
NACRES:
NA.22

Grado

for GC derivatization

Livello qualitativo

Tensione di vapore

16 mmHg ( 20 °C)

Saggio

≥98.5%
98.5-101.5% (AT)

Forma fisica

liquid

Impiego in reazioni chimiche

reagent type: derivatization reagent
reaction type: Acylations

Indice di rifrazione

n20/D 1.470 (lit.)
n20/D 1.470-1.472

P. eboll.

114-116 °C (lit.)

Punto di fusione

−57 °C (lit.)

Densità

1.629 g/mL at 25 °C (lit.)

Stringa SMILE

ClC(=O)C(Cl)(Cl)Cl

InChI

1S/C2Cl4O/c3-1(7)2(4,5)6
PVFOMCVHYWHZJE-UHFFFAOYSA-N

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Pittogrammi

CorrosionExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

213.8 °F - open cup

Punto d’infiammabilità (°C)

101 °C - open cup


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Hülya Senöz et al.
Chemical & pharmaceutical bulletin, 51(4), 444-447 (2003-04-04)
The pyrrolidine and morpholine enamines of cyclic ketones such as cyclohexanone and cyclopentanone were successfully diacetylated at alpha- and alpha'-positions with trichloroacetyl chloride using zinc catalyst. Morpholine enamines of the cyclic ketones gave acetylated morpholine in good yields besides the
Taigo Kashiwabara et al.
The Journal of organic chemistry, 74(24), 9433-9439 (2009-11-20)
Chlorinative dimerization of terminal alkynes with trichloroacetyl chloride as chlorine donor proceeds in the presence of rhodium catalysts to give (Z,Z)-1,4-dichloro-1,3-butadienes stereoselectively. Ligand screening has revealed that reactions using sterically bulky and electron-donating ligands like trimesitylphosphine are high yielding. The
D Reichert et al.
Mutation research, 117(1-2), 21-29 (1983-04-01)
Dichloroacetylene (DCA) is a highly reactive compound that decomposes rapidly in contact with air into a series of chlorinated aliphatic hydrocarbons (e.g., phosgene, trichloroacetyl chloride, trichloroacryloyl chloride and hexachlorobutadiene). Experiments were performed to compare the mutagenic properties of DCA and
A M Saillenfait et al.
Archives of toxicology, 70(2), 71-82 (1995-01-01)
The embryotoxicity of trichloroethylene (TRI), tetrachloroethylene (PER), and of four of their oxidative metabolites i.e. trichloroacetic acid, dichloroacetic acid, chloral hydrate, and trichloroacetyl chloride, was studied in vitro, using the rat whole embryo culture system. Embryos from Sprague-Dawley rats were
E Eliasson et al.
Chemico-biological interactions, 116(1-2), 123-141 (1999-01-07)
Halothane hepatitis occurs because susceptible patients mount immune responses to trifluoroacetylated protein antigens, formed following cytochrome P450-mediated bioactivation of halothane to trifluoroacetyl chloride. In the present study, an in vitro approach has been used to investigate the cytochrome P450 isozyme(s)

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