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Some important organofluorine compounds. A: fluoromethane B: isoflurane C: a CFC D: an HFC E: triflic acid F: Teflon G: PFOS H: fluorouracil I: fluoxetine Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond.
This is the list of extremely hazardous substances defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. § 11002). The list can be found as an appendix to 40 CFR 355. [1] Updates as of 2006 can be seen on the Federal Register, 71 FR 47121 (August 16, 2006). [2]
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IUPAC chemical name; molecular formula; CAS registry number / blend name; Atmospheric lifetime in years; Semi-empirical ozone depletion potential, ODP (normalized to be 1 for R-11) Net global warming potential, GWP, over a 100-year time horizon (normalized to be 1 for R-744, carbon dioxide)
This list is sorted by boiling point of gases in ascending order, but can be sorted on different values. "sub" and "triple" refer to the sublimation point and the triple point, which are given in the case of a substance that sublimes at 1 atm; "dec" refers to decomposition. "~" means approximately. Blue type items have an article available by ...
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Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...
The brand name "Halon" is frequently used interchangeably for BFCs. owever, not all Halons are technically BFCs (some contain chlorine also). BFCs attack the ozone layer even more aggressively than chlorofluorocarbons (CFCs), [ 2 ] and are powerful greenhouse gases , although due to shorter atmospheric lifetimes not as powerful as equivalent ...