Basic information
- Standard SMILES
FC(F)=C(F)F- InChIKey
BFKJFAAPBSQJPD-UHFFFAOYSA-N- Molecular formula
- C2F4
- Average molar mass
- 100.01 g/mol
- Monoisotopic mass
- 99.99361265
Names & identifiers
- Preferred name
- Tetrafluoroethylene
- IUPAC
- 1,1,2,2-tetrafluoroethene
- English name
- Tetrafluoroethylene
- Molecular formula
- C2F4
- Molecular weight
- 100.01
Names & synonyms
Show more names
Database identifiers
- CAS
116-14-3- PubChem CID
- 8301
- DTXSID
DTXSID6021325- ChEMBL
CHEMBL541730- ChEBI
CHEBI:38866- UNII
- OMW63Z518S
- EC Number
- 204-126-9
- Nikkaji
- J1.147.712G、J2.471F
Properties
Computed structural properties
- XLogP
- 1.3
- Topological polar surface area
- 0 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 0
- Heavy atoms
- 6
- Formal charge
- 0
- Complexity
- 55
Physicochemical properties
- Melting point
- -142 °C · -142°C
- Boiling point
- -76.3 °C · -76.3°C
- Density
- 1.1507 · 1.1507
- refractive index
- 1.242 · 1.2420 (estimate)
- Water Solubility
- 110 mg/L · 110mg/L at 28℃
- Specific Heat Capacity
- 0.8 J/ · Cp(gas): 0.8 J/(g·K), at 25℃
- Henry's Law Constant
- 1.6 · 1.6×10-5 mol/(m3Pa) at 25℃, Wilhelm et al. (1977)
- Dielectric constant
- 1.9 · 1.9(Ambient)
- Stability
- Stable. Reactive when heated.
- LogP
- 1.21 at · 1.21 at 20℃
- Toxicology and Carcinogenesis
- Toxicology and Carcinogenesis Studies of Tetrafluoroethylene (CASRN 116-14-3) in F344 Rats and B6C3F1 Mice (Inhalation Studies)
- FDA 21 CFR
- 177.138 · 177.1380; 177.1550; 177.2400;177.2600
- Indirect Additives used in Food Contact Substances
- TETRAFLUOROETHENE
- CAS DataBase Reference
- 116 · 116-14-3(CAS DataBase Reference)
- EWG's Food Scores
- 2 · 2
- FDA UNII
- 63 Z518S · OMW63Z518S
- Proposition 65 List
- Tetrafluoroethylene
- IARC
- 2 A · 2A (Vol. 19, Sup 7, 71, 110) 2017
- NIST Chemistry Reference
- Ethene, tetrafluoro-(116-14-3)
- EPA Substance Registry System
- Tetrafluoroethene (116-14-3)
- ECETOC JACC REPORT
- Tetrafluoroethylene (116-14-3)
- Symbol(GHS)
- 2 · GHS02,GHS04,GHS08
- Signal word
- Danger
- Hazard statements
- 220 · H220-H280-H350-H371
- Hazard Codes
- C,F
- Risk Statements
- 11 · 11
- Safety Statements
- 16 · 16-36/37/39-45
- RIDADR
- 1081 · UN 1081 (TETRAFLUOROETHYLENE, STABILIZED)
- Hazard Note
- Corrosive/Flammable
- TSCA
- TSCA listed
- HazardClass
- 2.1 · 2.1
- Hazardous Substances Data
- 116 · 116-14-3(Hazardous Substances Data)
- Toxicity
- 50 · LC50 (4 hr) in rats, mice, hamsters, guinea pigs (ppm): 37500-45000, 35000, 28500, 28000 (Kennedy)
- REACH Registrations
- Active
Safety & regulation
Safety data
- tsca
- TSCA listed
- ridadr
- UN 1081 (TETRAFLUOROETHYLENE, STABILIZED)
- Toxicity
- LC50 (4 hr) in rats, mice, hamsters, guinea pigs (ppm): 37500-45000, 35000, 28500, 28000 (Kennedy)
- risk_code
- 11
- Signal word
- Danger
- Symbol(GHS)
- GHS02,GHS04,GHS08
- hazard_code
- C,F
- hazard_note
- Corrosive/Flammable
- safety_code
- 16-36/37/39-45
- hazard_class
- 2.1
- Hazard statements
- H220-H280-H350-H371
- REACH Registrations
- Active
- Hazardous Substances Data
- 116-14-3(Hazardous Substances Data)
Chemistry & industry
Applications
DescriptionTetrafluoroethylene is a synthetic, colorless, flammable gas that is insoluble in water. Tetrafluoroethylene is used primarily in the synthesis of polytetrafluoroethylene resins. It is also used as a monomer in the synthesis of copolymers and as a propellant for food product aerosols. When heated to decomposition, tetrafluoroethylene emits highly toxic fluorocarbon fumes. The primary route of human exposure to this compound is inhalation. Acute inhalation exposure to tetrafluoroethylene may result in irritation of the respiratory tract and buildup of fluid in the lungs (pulmonary edema). Contact with this gas can cause eye irritation. This chemical is reasonably anticipated to be a human carcinogen. (NCI05)
UsesIn manufacture of polymers and synthesis of fluorinated refrigerants, dielectric media and solvents. In vinyl polymerization, cycloalkylation and addition reactions.
General DescriptionTetrafluoroethylene, stabilized appears as a colorless odorless gas. Easily ignited. Vapors are heavier than air. May asphyxiate by the displacement of air. May violently polymerize under prolonged exposure to fire or heat, violently rupturing the container. Under prolonged exposure to fire or heat the containers may rupture violently and rocket. Water insoluble.
Preparation methods
PreparationTetrafluoroethylene (TFE) is manufactured from chloroform. Chloroform is fluorinated by reaction with hydrogen fluoride to produce chlorodifluoromethane (R-22). Pyrolysis of chlorodifluoromethane then yields TFE.CHCl3 + 2 HF → CHClF2 + 2 HCl2CHClF2 → C2F4 + 2 HClA laboratory synthesis entails pyrolysis of a PTFE under a vacuum. The PTFE polymer "cracks" and depending on the pressure, produces mainly C2F4.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers24 total
Additional notes
DefinitionTetrafluoroethene is a fluorocarbon. It is a gaseous organic compound (a fluorocarbon and a haloalkene) used to make the plastic polytetrafluoroethene (PTFE).
Related reactions
Linked notes
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