Abstract
A facile synthesis method for the preparation of [1–11C]butanol, a regional cerebral blood flow imaging agent, was developed. Using a solid phase extraction method, the highly polar and volatile molecule [1–11C]butanol was quickly concentrated, purified, and released as final product; boasting high radiochemical and chemical purities as well as high radiochemical yields. The final drug product was obtained as a sterile, pyrogen-free solution that conforms United States Pharmacopeia (USP) <823> requirements.
| Original language | English |
|---|---|
| Article number | 109078 |
| Journal | Applied Radiation and Isotopes |
| Volume | 159 |
| DOIs | |
| State | Published - May 2020 |
Keywords
- Cerebral blood flow
- Grignard reagent
- Solid phase extraction
- [1–C]Butanol
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