Tracers / [18F]RSO2CF2H

[18F]RSO2CF2H

Also written as [18F]difluoromethyl heteroaryl sulfones; [18F]RSO2CF2H; [F-18]RSO2CF2H
Radionuclide
F-18 t½ 109.7 min
Modality
PET
Production route
Cyclotron liquid target
Stage
Research
Syntheses indexed
0

What it is

Compound class
Target / mechanism
Not a target-directed tracer - a reagent/prosthetic class ([18F]difluoromethyl aryl/heteroaryl sulfones) enabling direct 18F-difluoromethylation / [18F]difluorocarbene transfer for PET tracer synthesis PMID 40660014
Clinical application
None - radiochemistry methodology / building block, not a clinical imaging agent PMID 40660014
Theranostic pair

Regulatory status

FDA
No Drugs@FDA / openFDA drug registry — no approved application found; search: https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=BasicSearch.process&searchTerm=difluoromethyl+sulfone+F-18
EMA (centralised)
Other approvals
Brand names

Clinical use

Typical injected activity
Uptake time

Reported in the literature. Not a dosing recommendation.

Published syntheses

No synthesis has been parsed for this agent yet.

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Quality control Preliminary — inferred from compound class

Ph. Eur. monograph
USP monograph
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

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Notes

Target and application not filled - to be taken from the publication.