Trifluorotoluene

Trifluorotoluene
Names
Preferred IUPAC name
(Trifluoromethyl)benzene
Other names
Benzotrifluoride (BTF)
α,α,α-Trifluorotoluene
CF3Ph
PhCF3
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.396 Edit this at Wikidata
EC Number
  • 202-635-0
UNII
  • InChI=1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H
    Key: GETTZEONDQJALK-UHFFFAOYSA-N
  • C1=CC=C(C=C1)C(F)(F)F
Properties
C6H5CF3
Molar mass 146.11 g/mol
Appearance colorless liquid
Odor aromatic
Density 1.19 g/mL at 20 °C
Melting point −29.05 °C (−20.29 °F; 244.10 K)
Boiling point 103.46 °C (218.23 °F; 376.61 K)
<0.1 g/100 mL at 21 °C
Solubility soluble in ether, benzene, ethanol, acetone
miscible in n-heptane, CCl4
1.41486 (13 °C)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
3
0
Flash point 12 °C (54 °F; 285 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Trifluorotoluene is an organic compound with the formula of C6H5CF3. This colorless fluorocarbon is used as a specialty solvent in organic synthesis and an intermediate in the production of pesticides and pharmaceuticals.[1]

  1. ^ Banks, R.E. Organofluorine Chemicals and their Industrial Applications, Ellis Horwood LTD, Chichester, 1979.

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