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Merck
CN

80521

三氯乙酰氯

for GC derivatization, derivatization grade (GC derivatization), ≥98.5%

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线性分子式:
Cl3CCOCl
化学文摘社编号:
分子量:
181.83
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-926-7
Beilstein/REAXYS Number:
774120
MDL number:
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产品名称

三氯乙酰氯, for GC derivatization, derivatization grade (GC derivatization), ≥98.5%

InChI

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

InChI key

PVFOMCVHYWHZJE-UHFFFAOYSA-N

SMILES string

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

grade

derivatization grade (GC derivatization)

vapor pressure

16 mmHg ( 20 °C)

assay

≥98.5%
98.5-101.5% (AT)

form

liquid

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations

refractive index

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

bp

114-116 °C (lit.)

mp

−57 °C (lit.)

density

1.629 g/mL at 25 °C (lit.)

Quality Level

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pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

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

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

213.8 °F - open cup

flash_point_c

101 °C - open cup

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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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