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About This Item
Linear Formula:
Cl3CCOOH
CAS Number:
Molecular Weight:
163.39
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-927-2
MDL number:
Beilstein/REAXYS Number:
970119
Assay:
≥99.0% (titration)
Form:
powder or crystals
Product Name
Trichloroacetic acid, ≥99.0% (titration)
vapor density
<1 (vs air)
Quality Level
vapor pressure
1 mmHg ( 51 °C)
assay
≥99.0% (titration)
form
powder or crystals
refractive index
n20/D 1.62 (lit.)
pH
1 (at 25 °C, 81,7 g/L)
bp
196 °C (lit.)
mp
54-58 °C (lit.)
solubility
H2O: 1 g/10 mL
density
1.62 g/mL at 25 °C (lit.)
functional group
carboxylic acid, chloro
storage temp.
2-8°C
SMILES string
OC(=O)C(Cl)(Cl)Cl
InChI
1S/C2HCl3O2/c3-2(4,5)1(6)7/h(H,6,7)
InChI key
YNJBWRMUSHSURL-UHFFFAOYSA-N
Application
Traditionally used to precipitate protein. Has been used to determine protein concentration by quantitative precipitation. Used as decalcifier and fixative in microscopy.
Trichloroacetic acid (TCA) can be used as a catalyst to synthesize:
- β-enaminones via condensation reaction of 1,3-dicarbonyl compounds and amines.
- 6-amino-3-methyl-1,4-diphenyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile derivatives via four-component condensation reaction of ethyl acetoacetate, phenylhydrazine, malononitrile, and aromatic aldehydes.
- Tetrahydrobenzo[a]xanthen-11-ones by three-component reaction of aldehydes, 2-naphthol and dimedone.
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1A
wgk
WGK 2
flash_point_f
>235.4 °F - closed cup
flash_point_c
> 113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Storage Class
8A - Combustible corrosive hazardous materials
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Efficient Synthesis of β-Enaminones and β-Enamino Esters Using Tris (Hydrogensulfato) Boron or Trichloroacetic Acid as Catalysts
Karimi-Jaberi Z and Takmilifard Z
European Chemical Bulletin, 2, 211-213 (2013)
Expeditious, four-component synthesis of 1, 4-dihydropyrano [2, 3-c] pyrazole derivatives catalyzed by trichloroacetic acid or ceric sulfate
Jaberi ZK, et al.
Acta Chimica Slovenica, 60(1), 105-108 (2013)
Efficient, one-pot synthesis of tetrahydrobenzo [a] xanthen-11-ones and dibenzo [a, j] xanthenes using trichloroacetic acid as a solid heterogeneous catalyst under solvent-free conditions
Jaber ZK, et al.
E-Journal of Chemistry, 8(4), 1895-1899 (2011)

