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D55008

Sigma-Aldrich

Dichloroacetyl chloride

98%

Synonym(s):

α,α-Dichloroacetyl chloride, 2,2-Dichloroacetyl chloride, Dichloracetyl chloride, Dichloroacetic acid chloride, Dichloroethanoyl chloride

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About This Item

Linear Formula:
Cl2CHCOCl
CAS Number:
79-36-7
Molecular Weight:
147.39
Beilstein:
1209426
EC Number:
201-199-9
MDL number:
MFCD00000840
UNSPSC Code:
12352100
PubChem Substance ID:
24893840
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.46 (lit.)

bp

107-108 °C (lit.)

density

1.532 g/mL at 25 °C (lit.)

SMILES string

ClC(Cl)C(Cl)=O

InChI

1S/C2HCl3O/c3-1(4)2(5)6/h1H

InChI key

FBCCMZVIWNDFMO-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

H314,H350,H400

Hazard Classifications

Aquatic Acute 1 - Carc. 1B - Eye Dam. 1 - Skin Corr. 1A

Supplementary Hazards

EUH071

Storage Class Code

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

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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A R Sellakumar et al.
Journal of the National Cancer Institute, 79(2), 285-289 (1987-08-01)
A series of earlier studies showed that inhalation exposures of rats to three water-reactive electrophilic compounds produced brisk yields of nasal cancer even when the animals were exposed for only 30 days (6 hr/day X 5 day/wk). In addition, carcinogenic
Rolf König et al.
Chemical research in toxicology, 21(3), 572-582 (2008-02-26)
Dichloroacetyl chloride (DCAC) is a reactive metabolite of trichloroethene (TCE). TCE and its metabolites have been implicated in the induction of organ-specific and systemic autoimmunity, in the acceleration of autoimmune responses, and in the development of liver toxicity and hepatocellular
M F Khan et al.
Immunopharmacology and immunotoxicology, 19(2), 265-277 (1997-05-01)
Welders are exposed to dichloroacetyl chloride (DCAC) when trichloroethene (TCE) is used as a degreasing agent. Human exposure to TCE and tetrachloroethane can also lead to formation of DCAC in situ through metabolism. Due to its strong acylating property, it
Hsin-Hung Ou et al.
Journal of hazardous materials, 146(1-2), 302-308 (2007-01-24)
Batch photocatalytic degradation of 80+/-2.5 ppm V trichloroethylene (TCE) was conducted to investigate the effect of the oxygen and relative humidity (RH) on the formation of the dichloroacetyl chloride (DCAC) and phosgene. Based on the simultaneous ordinary differential equations (ODEs)
Ping Cai et al.
Toxicology and applied pharmacology, 216(2), 248-255 (2006-06-30)
Dichloroacetyl chloride (DCAC) is formed from trichloroethene (TCE), which is implicated in inducing/accelerating autoimmune response. Due to its potent acylating activity, DCAC may convert proteins to neo-antigens and thus could induce autoimmune responses. Dichloroacetic anhydride (DCAA), which is a similar
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