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Reagent Kits
IBA Synthera®
GE TRACERlab
Siemens Explora™ FDG
4
Ancillary Supply Sets
GE TRACERlab
IBA Synthera®
Cassettes
GE TRACERlab MX
IBA Synthera®
Trasis AllinOne
READI-CLING™ Cartridges
GE TRACERlab
Siemens Explora™
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PET Chemicals
Complexation Agents for [
64
Cu]-Labelling
Complexation Agents for [
64
Cu]-Labelling
Complexation Agents for [
68
Ga]-Labelling
DOTA-TOC
DOTA-TATE
DOTA-NOC
PSMA-11
DOTA
DOTAEt
NOTA
18
F/
11
C Labelled Compounds
ABP688
ADIBO
AMD
beta-CFT
beta-CIT
Choline
DAA1106
DASB
Fallypride
FAZA
FDG
FDOPA
FES
FET
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FLB457
FLT
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MET
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MPPF
NNC112
MSTAT
PBR06
PBR111
PBR28
PHNO
PIB
PK11195
Raclopride
THK523
T807
WAY100635
18
F Intermediates
18
F-SFB and Aryl Fluoride
Intermediates for Alkyl Fluoride
Click Chemistry Reagents
18
F Ion Tracers
Oxygen-18 Water (O-18)
Oxygen-18 Water 98 Atom %
Oxygen-18 Water 10 Atom %
Doubly Labelled Water
Oxygen-18 Recycling
SPECT Chemicals
*I-Labelled Compounds
beta-CIT
Hippuran
IBZM
IMZ
MIBG
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99m
Tc
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PET
Technetium-99
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18
F/
11
C Labelled Compounds
/
FES
/
16alpha-Fluoroestradiol (5 mg)
16alpha-Fluoroestradiol (5 mg)
Reference standard for 16alpha-[
18
F]Fluoroestradiol
Product No.:
FES-90-0005
16alpha-Fluoroestradiol
Product No.:FES-90
CAS No.:92817-10-2
Product Name:
16alpha-Fluoroestradiol
Synonyms:
Estra-1,3,5(10)-triene-3,17-diol, 16-fluoro-, (16alpha,17beta); 16alpha-Fluoro-13beta-methyl-1,3,5(10)-gonatriene-3,17beta-diol; 16alpha-Fluoro-17beta-estradiol
CAS No.:
92817-10-2
Molecular Formula:
C
18
H
23
FO
2
Molecular Weight:
290.37
Application:
Reference standard for 16alpha-[
18
F]Fluoroestradiol
Presentation:
Packaged in amber vials or amber screw-cap vials with teflon-coated stoppers under argon atmosphere
Storage and Stability
Store the product at -20 ℃, protected from light.
Short-term storage at higher temperatures does not affect product quality.
Notes
Complete documentation - Certificates of Analysis including testing reports of
1
H-NMR and HPLC spectra for each shipment
Customized dispensing available
Research
Mankoff D.A. et al. [
18
F]Fluoroestradiol Radiation Dosimetry in Human PET Studies.
J. Nucl. Med.
2001, 42, 679-684.
Stalford A.C. et al. The metabolism of 16-fluoroestradiols in vivo: chemical strategies for restricting the oxidative biotransformations of an estrogen-receptor imaging agent.
Steroids.
1997, 62, 750-761.
Roemer J. et al. Further
13
C NMR spectroscopic proof of 16alpha-F configuration in 16-fluoroestradiol derivatives. Forschungszent. Rossendorf, [Ber.] FZR 1997, 165, 192-193.
18
F-Fluoroestradiol Tumor Uptake Is Heterogeneous and Influenced by Site of Metastasis in Breast Cancer Patients