CHEBI:38854 - perfluorotributylamine

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ChEBI Name perfluorotributylamine
ChEBI ID CHEBI:38854
Definition An organofluorine compound that is tributylamine in which all the hydrogens have been replaced by fluorine atoms.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C12F27N
Net Charge 0
Average Mass 671.09200
Monoisotopic Mass 670.960
InChI InChI=1S/C12F27N/c13-1(14,7(25,26)27)4(19,20)10(34,35)40(11(36,37)5(21,22)2(15,16)8(28,29)30)12(38,39)6(23,24)3(17,18)9(31,32)33
InChIKey RVZRBWKZFJCCIB-UHFFFAOYSA-N
SMILES FC(F)(F)C(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Roles Classification
Chemical Role(s): greenhouse gas
A gas in an atmosphere that absorbs and emits radiation within the thermal infrared range, so contributing to the 'greenhouse effect'.
solvent
A liquid that can dissolve other substances (solutes) without any change in their chemical composition.
Application(s): solvent
A liquid that can dissolve other substances (solutes) without any change in their chemical composition.
blood substitute
A substance that can carry oxygen to and carbon dioxide away from the tissues when introduced into the blood stream. Blood substitutes are used to replace hemoglobin in severe hemorrhage and also to perfuse isolated organs.
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ChEBI Ontology
Outgoing perfluorotributylamine (CHEBI:38854) has functional parent tributylamine (CHEBI:38905)
perfluorotributylamine (CHEBI:38854) has role blood substitute (CHEBI:38849)
perfluorotributylamine (CHEBI:38854) has role greenhouse gas (CHEBI:76413)
perfluorotributylamine (CHEBI:38854) has role solvent (CHEBI:46787)
perfluorotributylamine (CHEBI:38854) is a organofluorine compound (CHEBI:37143)
IUPAC Name
1,1,2,2,3,3,4,4,4-nonafluoro-N,N-bis(nonafluorobutyl)butan-1-amine
Synonyms Sources
FTBA ChEBI
Heptacosafluorotributylamine ChemIDplus
N,N,N-Tris(1,1,2,2,3,3,4,4,4-nonafluorobutyl)amine NIST Chemistry WebBook
Tris(nonafluorobutyl)amine ChemIDplus
Tris(perfluorobutyl)amine ChemIDplus
Manual Xref Database
Perfluorotributylamine Wikipedia
View more database links
Registry Numbers Types Sources
1813883 Reaxys Registry Number Reaxys
1813883 Beilstein Registry Number Beilstein
311-89-7 CAS Registry Number ChemIDplus
311-89-7 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
1397120 PubMed citation Europe PMC
19682704 PubMed citation Europe PMC
2275237 PubMed citation Europe PMC
3799787 PubMed citation Europe PMC
7849929 PubMed citation Europe PMC
7849930 PubMed citation Europe PMC
Last Modified
14 April 2014
General Comment
2014-04-14 Perfluorotributylamine is one of the most potent greenhouse gases yet discovered: see Hong, A.C., et al., Geophys. Res. Lett., 2013, v40(22), 6010-6015.