≥98.5% 1,2,3,4-Tetrafluorobenzene CAS No.: 551-62-2
C6H2F4
CAS No.: 551-62-2

Synthesis:
一:Using phthalic anhydride as the first ingredient: This procedure typically entails the following actions: Phthalic anhydride first produces chlorophthalic anhydride by a chlorination reaction, and then it interacts with aniline to produce an imine molecule. Following the substitution of potassium fluoride for the chlorine on the benzene ring, 1,2,3,4-tetrafluorobenzene is obtained by hydrolysis and decarboxylation processes.
二:Considering 2,3,4-trifluoroaniline as the initial substance: The following steps are part of this method: 2,3,4-trifluoroaniline first forms a diazonium salt by a diazotization process, and then it combines with fluoroboric acid to generate a diazonium salt of fluoboric acid. Lastly, 1,2,3,4-tetrafluorobenzene is obtained by a high-temperature thermal breakdown reaction.
High-performance battery materials and electrolytes can be made with 1,2,3,4-Tetrafluorobenzene to increase the energy density and cycle stability of batteries.
Physical Properties
|
Boiling point |
95 °C (lit.) |
|
Density |
1.4 g/mL at 25 °C (lit.) |
|
Molecular mass |
150.07 |
|
Assay |
≥98.5% |
|
Flash point |
69 °F |
|
Refractive index |
n20/D 1.408(lit.) |
|
Package |
50kgs or according customer requirement |
|
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Physical And Chemical Properties:
[Density]: 1.4±0.1 g/cm³
[Boiling point]: 92.9±35.0 ℃ at 760 mmHg
[Melting point]: −42 ℃(lit.)
[Molecular formula]: C6H₂F4
[Molecular weight]: 150.074
[Flash point]: 20.6±0.0 ℃
[Exact Mass]: 150.009262
[LogP]: 2.30
[Appearance]: colorless liquid
[Vapor pressure]: 57.4±0.2 mmHg at 25℃
[Refractive Index]: 1.408
[ Storage conditions ]:
Keep away from fire sources, sealed, in a cool, dry and ventilated place
[Stability]:
Stable under normal temperature and pressure
Avoid light, open flame, high temperature, strong oxidants




Packing, Storage, Handling and Transportation
Hexafluorobenzene should be sealed in dry place at room temperature.

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