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The structure of 1,1,1,2,3,3,3-heptafluoropropane
Preferred IUPAC name
Other names
3D model (JSmol)
ECHA InfoCard 100.006.437 Edit this at Wikidata
UN number UN3296
  • InChI=1S/C3HF7/c4-1(2(5,6)7)3(8,9)10/h1H checkY
  • InChI=1/C3HF7/c4-1(2(5,6)7)3(8,9)10/h1H
  • FC(F)(F)C(F)C(F)(F)F
Molar mass 170.03 g/mol
Density 1.46 g/cm3 at -16 °C
Melting point −131 °C (−204 °F; 142 K)
Boiling point −16.4 °C (2.5 °F; 256.8 K)
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1,1,1,2,3,3,3-Heptafluoropropane, also called heptafluoropropane, HFC-227ea (ISO name), HFC-227 or FM-200, as well as apaflurane (INN), is a colourless, odourless gaseous halocarbon commonly used as a gaseous fire suppression agent.


Its chemical formula is CF3-CHF-CF3, or C3HF7. With a boiling point of −16.4 °C, it is a gas at room temperature. It is slightly soluble in water (260 mg/L).


HFC-227ea is used in fire suppression systems that protect data processing and telecommunication facilities, and in fire suppression of many flammable liquids and gases. HFC-227ea is categorized as a Clean Agent and is governed by NFPA 2001 - Standard for Clean Agent Fire Extinguishing Systems. Effective fire suppression requires introducing a concentration of the HFC-227ea agent between 6.25% and 9% depending on the hazard being suppressed. Its NOAEL for cardiac sensitization is 9%. The United States Environmental Protection Agency allows concentration of 9% volume in occupied spaces without mandated egress time, or up to 10.5% for a limited time. Most fire suppression systems are designed to provide concentration of 6.25-9%.

The HFC-227ea fire suppression agent was the first non-ozone-depleting replacement for Halon 1301.[citation needed] In addition, HFC-227ea leaves no residue on valuable equipment after discharge.[2]

HFC-227ea contains no chlorine or bromine atoms, presenting no ozone depletion effect. Its atmospheric lifetime is approximated between 31 and 42 years. It leaves no residue or oily deposits and can be removed by ventilation of the affected space.

As an aerosol propellant, HFC-227ea is used in pharmaceutical metered dose inhalers such as those used for dispensing asthma medication.


At high temperatures, heptafluoropropane will decompose and produce hydrogen fluoride. The decomposition produces a sharp, pungent odour, which can be perceived in concentrations far below a dangerous level. Other decomposition products include carbonyl fluoride, carbon monoxide and carbon dioxide. Prior to re-entry of a room where HFC-227ea system has been activated to suppress a fire, the atmosphere should be tested. An Acid Scavenging Additive added to heptafluoropropane reduces the amount of hydrogen fluoride. Contact with liquid HFC-227ea may cause frostbite.

Climate change considerations[edit]

Heptafluoropropane (HFC-227ea) contributes to climate change. It has a global warming potential (GWP) of 3,220 over 100 years.[3]

Due to its high GWP, the HFC-227ea has been included in the list of controlled substances of the Montreal Protocol (2016 Kigali amendment, in effect in January 2019).[4] Under EU regulations, production, imports and sales of HFC-227ea in spray cans such as freeze sprays or dusters have been prohibited since 2014, as the GWP is over the limit of 150 for these applications.[5][6][7]

Tradenames for HFC-227ea used as fire suppression agent[edit]

See also[edit]

Other fire suppression agents:


  1. ^ NIST datapage for heptafluoropropane
  2. ^ "Fike FE-227 Product Page". Archived from the original on 2007-10-09. Retrieved 2006-12-12.
  3. ^ GOV.UK: Calculate the carbon dioxide equivalent quantity of an F gas. Retrieved on 2018-01-25.
  4. ^ Montreal Protocol Section 1.1. including 2016 Kigali amendment.
  5. ^ "Regulation (EU) No 517/2014 of the European Parliament and of the Council of 16 April 2014 on fluorinated greenhouse gases and repealing Regulation (EC) No 842/2006 — European Environment Agency". www.eea.europa.eu. Retrieved 2021-03-11.
  6. ^ "EU legislation to control F-gases". Climate Action - European Commission. 2016-11-23. Retrieved 2021-03-11.
  7. ^ "ILT onderschept illegale spuitbussen in Rotterdamse haven - Nieuwsbericht - Inspectie Leefomgeving en Transport (ILT)". www.ilent.nl (in Dutch). Ministry of Infrastructure and Water Management. 2020-08-31. Retrieved 2021-03-11.
  8. ^ a b c "Substitutes in Total Flooding Agents". United States Environmental Protection Agency. United States government. 20 November 2014. Retrieved 3 May 2019.

External links[edit]