| Trichloroacetic acid
|
Trichloroacetic-acid-3D-vdW.pngTrichloroacetic-acid-elpot.png
| General
|
| Systematic name
| Trichloroethanoic acid
|
| Other names
| Trichloroacetic acid
|
| Molecular formula
| CCl3COOH
|
| SMILES
| ClC(Cl)(Cl)C(O)=O
|
| Molar mass
| 163.4 g/mol
|
| Appearance
| white solid
|
| CAS number
| *
|
| Properties
|
| Density and phase
| 1.63 g/cm3, solid
|
| Solubility in water
| very good
|
| Melting point
| 57 °C
|
| Boiling point
| 196 °C
|
| Acidity (pKa)
| 0.77
|
| Dipole moment
| ? D
|
| Hazards
|
| MSDS
| External MSDS
|
| EU classification
| Corrosive C)
Dangerous for
the environment (N)
|
| NFPA 704
|
|
| R-phrases
| ,
|
| S-phrases
| , , ,
, ,
|
| Flash point
| ? °C
|
| RTECS number
| AJ7875000
|
| Supplementary data page
|
Structure and
properties
| n, εr, etc.
|
Thermodynamic
data
| Phase behaviour
Solid, liquid, gas
|
| Spectral data
| UV, IR, NMR, MS
|
| Related compounds
|
| Related chloroacetic acids
| Chloroacetic acid
Dichloroacetic acid
|
| Related compounds
| Acetic acid
Trifluoroacetic acid
Tribromoacetic acid
|
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
Chemical infobox
|
Trichloroacetic acid (also known as trichloroethanoic acid) is an analogue of acetic acid in which the three hydrogen atoms of the methyl group have all been replaced by chlorine atoms.
It is prepared by the reaction of chlorine with acetic acid in the presence of a suitable catalyst.
- CH3COOH + 3Cl2 → CCl3COOH + 3HCl
It is widely used in biochemistry for the precipitation of macromolecules such as proteins, DNA and RNA. Its sodium salt is used as a weedkiller.
Salts of trichloroacetic acid are called trichloroacetates.
See also
External links
Carboxylic acids | Organochlorides
Trichloressigsäure | トリクロロ酢酸 | Kwas trichlorooctowy | Трихлоруксусная кислота
"Trichloroacetic acid"
