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Trifluoroethylene

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Identification
Molecular formula
C2H3F3
CAS number
359-11-5
IUPAC name
1,1,2-trifluoroethylene
State
State

Trifluoroethylene is in a gaseous state at room temperature.

Melting point (Celsius)
-100.00
Melting point (Kelvin)
173.15
Boiling point (Celsius)
2.20
Boiling point (Kelvin)
275.35
General information
Molecular weight
78.04g/mol
Molar mass
78.0410g/mol
Density
1.1166g/cm3
Appearence

Trifluoroethylene is a colorless gaseous compound.

Comment on solubility

Solubility of 1,1,2-Trifluoroethylene

1,1,2-Trifluoroethylene (C2F3H2) exhibits unique solubility characteristics that are influenced by its molecular structure and the presence of fluorine atoms. Its solubility behavior is notable due to the following reasons:

  • Water Solubility: 1,1,2-Trifluoroethylene is sparingly soluble in water. The high electronegativity of fluorine contributes to a relatively low interaction with water molecules, resulting in limited solubility.
  • Organic Solvents: This compound is far more soluble in organic solvents such as acetone, ethanol, and other non-polar solvents. This greater solubility is attributed to its non-polar characteristics, which allow for better interaction with similar organic molecules.
  • Environmental Impact: The solubility behavior of 1,1,2-trifluoroethylene is important for environmental assessments, particularly regarding its potential to migrate in soil and groundwater.

In summary, the solubility of 1,1,2-trifluoroethylene is a crucial factor in its application and environmental interaction. Its limited solubility in water, contrasted with its higher solubility in organic solvents, emphasizes the need for careful handling and consideration in both industrial and research settings.

Interesting facts

Interesting Facts about 1,1,2-Trifluoroethylene

1,1,2-Trifluoroethylene is a fascinating chemical compound, particularly known for its unique properties and applications in various industries. Below are some intriguing aspects of this fluorinated alkene:

  • Innovative Applications: This compound is primarily used in the production of fluoropolymers, which are notable for their non-stick and high-temperature resistant qualities. These materials have extensive use in coatings and sealants.
  • Environmental Considerations: While 1,1,2-trifluoroethylene itself is less hazardous compared to other fluorinated compounds, the environmental impact of its production and degradation needs careful consideration, emphasizing the need for sustainable practices in chemical manufacturing.
  • Fluorine's Role: Adding fluorine atoms can significantly enhance molecular stability and resistance to chemical reactions. This characteristic is particularly valued in applications that require durability.
  • Under Study: Research is ongoing to explore the potential health effects and mechanisms of action of 1,1,2-trifluoroethylene, highlighting the importance of continual assessment in chemical safety.

In summary, 1,1,2-trifluoroethylene stands out as a compound with significant industrial and research value. As the chemical field evolves, maintaining a keen focus on both its benefits and potential environmental concerns will be crucial.

Synonyms
Trifluoroethylene
359-11-5
1,1,2-trifluoroethene
TRIFLUOROETHENE
Ethene, trifluoro-
Ethylene, trifluoro-
1,1,2-Trifluoroethylene
Ethylene trifluoride
HSDB 6260
EINECS 206-626-2
Ethene, 1,1,2-trifluoro-
Z2866M3Z1A
TRIFLUOROETHENE [HSDB]
DTXSID4059887
HFC 1123
C2HF3
UNII-Z2866M3Z1A
TriFE
Ethene, trifluoro
Ethylene, trifluoro
MFCD00039275
Ethene, 1,1,2trifluoro
1,1,2-Trifluoroethylene #
DTXCID4039108
MIZLGWKEZAPEFJ-UHFFFAOYSA-
DTXSID10196701
Trifluoroethylene, >=97.5% (GC)
DB-222266
InChI=1/C2HF3/c3-1-2(4)5/h1H
NS00042026
R1123
1,1,2-Trifluoroethene, 1,1,2-Trifluoroethylene
Q27294901
206-626-2