Page last updated: 2024-11-05

perfluorotributylamine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Perfluorotributylamine (PFTBA) is a synthetic, highly fluorinated compound with a unique combination of properties that makes it a valuable tool in research and industry. It is highly inert and stable, with a very low dielectric constant, making it an excellent dielectric fluid. It is also characterized by its exceptional chemical and thermal stability. PFTBA is synthesized by the electrochemical fluorination of tributylamine, a process that replaces all hydrogen atoms with fluorine atoms. Due to its inertness and low reactivity, PFTBA is used as a dielectric fluid in high-voltage equipment, as a heat transfer medium in electronic devices, and as a solvent in certain chemical reactions. It is also studied for its potential use as a blood substitute due to its ability to carry oxygen. However, its high persistence and potential environmental impact are concerns, leading to ongoing research on its environmental fate and toxicity.'

perfluorotributylamine: perfluorochemical (3M Co) artificial O(2) carrier [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

perfluorotributylamine : An organofluorine compound that is tributylamine in which all the hydrogens have been replaced by fluorine atoms. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID9397
CHEBI ID38854
SCHEMBL ID36219
MeSH IDM0052985

Synonyms (66)

Synonym
c12f27n
fc 47
311-89-7
perfluorotributylamine
fc 43(47)
fluosol 43
1-butanamine,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)-
tri(nonafluorobutyl)amine
tri(perfluorobutyl)amine
nsc-3501
nsc3501
tributylamine, heptacosafluoro-
heptacosafluorotributylamine
butylamine,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)-
fc 43
fluorocarbon fc 43
tris(nonafluorobutyl)amine
pftba
1-butanamine, 1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)-
heptacosafluorotributylamine, liquid
CHEBI:38854
tris(perfluorobutyl)amine
1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)butan-1-amine
n,n,n-tris(1,1,2,2,3,3,4,4,4-nonafluorobutyl)amine
ftba
ai3-16951
einecs 206-223-1
mediflor fc 43
hsdb 7103
nsc 3501
1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)-1-butanamine
fluorinert fc 43
brn 1813883
1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(1,1,2,2,3,3,4,4,4-nonafluorobutyl)butan-1-amine
AKOS005258126
fluorinert
A820753
P0074
1-butanamine, 1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(1,1,2,2,3,3,4,4,4-nonafluorobutyl)-
3702y1hq6o ,
unii-3702y1hq6o
FT-0631933
perfluorotributylamine [hsdb]
perfluorotri-n-butylamine
SCHEMBL36219
fluorinert fc-43
n,n,n-tris(1,1,2,2,3,3,4,4,4-nonafluorobutyl)amine #
(n-c4f9)3n
butylamine, 1,1,2,2,3,3,4,4,4-nonafluoro-n,n-bis(nonafluorobutyl)-
medifluor fc 47
heptacosafluorotri-n-butylamine
Q-201546
DTXSID0027141
fluorinert (tm) (fc-43) (reg)
heptacosafluorotributylamine, analytical standard, for mass spectrometry
mfcd00000436
perfluorotri-n-butylamine, mass spec std
perfluorotributylamine (pftba), analytical standard
perfluorotributylamine (pftba) ms tuning compound 1000 microg/ml in methanol
E75915
perfluorotributylamine/3mfc40
Q15296722
fluorinert (fc-43)
BS-49211
perfluorotributylamine, 80%
CS-0121618

Research Excerpts

Treatment

ExcerptReferenceRelevance
"The perfluorotributylamine treatment groups had histologic scores indicative of less severe injury between 1 and 4 hours."( Treatment of intestinal ischemia with oxygenated intraluminal perfluorocarbons.
Gore, D; Gourley, WK; Guice, KS; Lobe, TE; Oldham, KT, 1987
)
0.75

Toxicity

ExcerptReferenceRelevance
" is caused by toxic contaminants and not the perfluorochemicals."( Reversal of the endocrine toxicity of commercially produced perfluorochemical emulsion.
Chubb, C, 1985
)
0.27

Compound-Compound Interactions

ExcerptReferenceRelevance
" In this study, the mechanical signal transduction pathway of LIPUS promoting iPSCs-NCSCs proliferation and differentiation was further explored, and the effects of LIPUS combined with iPSCs-NCSCs, perfluorotributylamine (PFTBA), and growth differentiation factor 5 (GDF5) on the repair of peripheral nerve injury were evaluated."( Low-intensity pulsed ultrasound combination with induced pluripotent stem cells-derived neural crest stem cells and growth differentiation factor 5 promotes sciatic nerve regeneration and functional recovery.
Chen, G; Lv, Y; Pan, J; Xia, B; Yang, L; Zou, Y, 2019
)
0.7

Dosage Studied

ExcerptRelevanceReference
" Although differences in vapor pressure and molecular structure may account for varying optimal dosing strategies, several different perfluorocarbons were shown to be principally suitable for aerosol treatment."( Comparison of aerosol therapy with different perfluorocarbons in surfactant-depleted animals.
Brenn, G; Dötsch, J; Kandler, MA; Rascher, W; Scheuerer, K; Schoof, E; von der Hardt, K, 2004
)
0.32
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
greenhouse gasA gas in an atmosphere that absorbs and emits radiation within the thermal infrared range, so contributing to the 'greenhouse effect'.
solventA liquid that can dissolve other substances (solutes) without any change in their chemical composition.
blood substituteA 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.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
organofluorine compoundAn organofluorine compound is a compound containing at least one carbon-fluorine bond.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (222)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990118 (53.15)18.7374
1990's77 (34.68)18.2507
2000's10 (4.50)29.6817
2010's14 (6.31)24.3611
2020's3 (1.35)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 36.98

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index36.98 (24.57)
Research Supply Index5.51 (2.92)
Research Growth Index4.54 (4.65)
Search Engine Demand Index52.87 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (36.98)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews6 (2.45%)6.00%
Case Studies3 (1.22%)4.05%
Observational0 (0.00%)0.25%
Other236 (96.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]