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Tetrafluoroethylene

Tetrafluoroethylene structure

Tetrafluoroethylene 

structure
  • CAS No:

    116-14-3

  • Formula:

    C2F4

  • Chemical Name:

    Tetrafluoroethylene

  • Synonyms:

    Ethene,1,1,2,2-tetrafluoro-;Ethylene,tetrafluoro-;Ethene,tetrafluoro-;1,1,2,2-Tetrafluoroethene;Tetrafluoroethylene;Tetrafluoroethene;Perfluoroethene;Perfluoroethylene;TFE;1,1,2,2-Tetrafluoroethylene;Ethylene tetrafluoride;R 1114;Teflon 851K02730;PFC 1114;BYK 990;FO 1114;9014-83-9;1449755-53-6

  • Categories:

    Organic Chemistry  >  Hydrocarbons and Derivatives

Description

Colorless, odorless gas.

Tetrafluoroethylene Basic Attributes

100.02

100.01

204-126-9

2903399090

Characteristics

0

1.21 (est)

Tetrafluoroethylene, 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.

1.519 g/cm3 @ Temp: -76 °C

-142.5 °C

-75.9 °C

<32 deg F (<0 deg C) (closed cup) /Tetrafluoroethylene, inhibited/

1.241

In water, 1.59X10+2 mg/L at 25 deg C

Store in a cool, dry, well-ventilated location. Separate from oxidizing materials, air, sulfur trioxide, halogen compounds. Outside or detached storage is preferred. /Tetrafluoroethylene, inhibited/

22800 mmHg at 70°F

3.87

Inhalation-rat LC50: 40000PPM/4 hours; inhalation-mouse LC50: 143000 mg/m3/4 hours

Flammable; decomposes toxic hydrogen fluoride gas when exposed to heat; prevents burns

Explodes when heated. /Tetrafluoroethylene, inhibited/

Odorless

Safety Information

2.1

1081

11

16-36/37/39-45

C,F

Treasury is ventilated, low temperature and dry; stored separately from oxidant

Corrosive/Flammable

Explosive when mixed with air

Stable. Reactive when heated.

P201, P202, P281, P308+P313, P405, P501

H350I

Toxicity

practically nontoxic

Tetrafluoroethylene Use and Manufacturing

Methods of Manufacturing

The preparation of tetrafluoroethylene is obtained by thermal cracking of difluorochloromethane at high temperature. Reaction equation: 2CHClF2→CF2=CF2+2HCl adopts platinum-lined tube as the cracking reaction tube and superheated steam as the diluent, and is cracked at a temperature of 600-900 ℃ to obtain tetrafluoroethylene. After cooling and separation, and then washed with water and alkali to remove hydrogen chloride, and then pressurized and rectified at -20 ℃, 2.02 MPa, the polymer grade pure product with a content of 99.9% or more can be obtained.

Uses

In manufacture of polymers and synthesis of fluorinated refrigerants, dielectric media and solvents.In vinyl polymerization, cycloalkylation and addition reactions.

Computed Properties

Molecular Weight:100.01
XLogP3:1.3
Hydrogen Bond Acceptor Count:4
Exact Mass:99.99361265
Monoisotopic Mass:99.99361265
Heavy Atom Count:6
Complexity:55.6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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