Tracer library / 16-[18F]fluoro-4-thia-palmitic acid

16-[18F]fluoro-4-thia-palmitic acid

Also written as 16-[18F]fluoro-4-thia-palmitic acid
Radionuclide
F-18 t½ 109.77 min
Modality
PET
Production route
—
Stage
Clinical research
Syntheses indexed
3

What it is

Compound class
fluorothia fatty acid (16-fluoro-4-thia-palmitic acid, a thia-substituted fatty acid analog)
Target / mechanism
—
Clinical application
myocardial fatty acid metabolism imaging for clinical applications (as a fatty acid analog tracer) PMID 31759313
Theranostic pair
—

Published syntheses

ModuleCassettePurificationYield %RCP %Precursor / supplierSource
In-house / custom builtcustom manifoldSPE37.73%
decay-corrected
>96%N-Boc-Tosylpropoxytryptophan methyl ester25136592
2014 Biomed Res Int
We have designed and built an automated module which is compact and easy to use and be maintained. - The radioactivity, radiochemical yield, and end-of-synthesis (EOS) time for 18F-FTP were 0.13 GBq, 37.73% (decay-corrected), and 90 min, respectively.
AllinOne (AiO)
Trasis
vendor cassetteHPLC+SPE11 ± 2
decay-corrected
>97%mesylate precursor of FTP
made in our lab under GLP conditions
29564391
2017 EJNMMI Radiopharm Chem
AllinOne synthesis module - [18F]FTP1211 ± 22500–468060One vessel, one step, HPLC, SPE
TRACERlab FX N Pro—HPLC+SPE7.7±4.5 %
not corrected
95.8%methyl 3-(12-bromododecylthio)propionate31759313
2020 Nucl Med Biol
All the syntheses were optimized in an automated TRACERlab FX-N Pro synthesizer. - [18F]FTP uncorrected yield was 7.7±4.5 %

Precursor

Common precursor
—
Suppliers seen in the literature
—
Cited suppliers in indexed syntheses
made in our lab under GLP conditions
Typical final purification
—

Need this precursor?We can point you to suppliers for 16-[18F]fluoro-4-thia-palmitic acid, or handle the enquiry for you.

Get in touch

Quality control Preliminary - inferred from compound class

Ph. Eur. monograph
not verified No Ph. Eur. check is recorded for this entry.
USP monograph
not verified No USP check is recorded for this entry.
AppearancepHRCP HPLCRCP TLCHPLC UVRadionuclidic (HPGe)Half-lifeActivityEndotoxins (LAL)SterilityFilter integrity
How this set was arrived at. base set per Ph. Eur. general monograph 0125 (rule); organic-phase radiosynthesis assumed from isotope/compound class, no synthesis data confirming it -> GC residual solvents (preliminary); conventional nucleophilic 18F-fluorination assumed from isotope/compound class, no synthesis data confirming K222 use -> Kryptofix test (preliminary)

Tests listed by reference only. Monograph texts are copyrighted and are not reproduced here. How these are derived

Setting up quality control?We can help you scope the equipment needed to release 16-[18F]fluoro-4-thia-palmitic acid.

Get in touch

Notes

Added from reverse module search (stage 6); 1 article(s) with F-18. Stage set/updated at stage 39 from PMID 31759313: 'were used as precursors for the synthesis of [18F]FTHA and [18F]FTP, respectively'.
Ask a question