Mannose triflate

• Description :

  Mannose triflate is a glucose analog. Mannose triflate is a precursor for 18F-FDG synthesis for PET applications. Mannose triflate binds to 18F via SN2 nucleophilic substitution reaction. Mannose triflate can be used for an imaging technique in detection of cancer[1][2][3].

• Product Name Alternative :

  TATM

• UNSPSC :

  12352200

• Hazard Statement :

  H302, H315, H319, H335

• Target :

  Biochemical Assay Reagents

• Type :

  Biochemical Assay Reagents

• Related Pathways :

  Others

• Applications :

  Cancer-programmed cell death

• Field of Research :

  Cancer

• Assay Protocol :

  https://www.medchemexpress.com/mannose-triflate.html

• Purity :

  99.79

• Solubility :

  DMSO : ≥ 100 mg/mL

• Smiles :

  CC(O[C@@H]1[C@@H]([C@@H](O[C@@H]([C@H]1OC(C)=O)COC(C)=O)OC(C)=O)OS(C(F)(F)F)(=O)=O)=O

• Molecular Formula :

  C15H19F3O12S

• Molecular Weight :

  480.36

• Precautions :

  H302, H315, H319, H335

• References & Citations :

  [1]Yu S.Review of F-FDG Synthesis and Quality Control. Biomed Imaging Interv J. 2006 Oct;2 (4) :e57|[2]Chirakal R, et al. Base-mediated decomposition of a Mannose triflate during the synthesis of 2-deoxy-2-18F-fluoro-D-glucose[J]. Applied radiation and isotopes, 1995, 46 (3) : 149-155.|[3]Claggett SB, et al. Simplified programming and control of automated radiosynthesizers through unit operations. EJNMMI Res. 2013 Jul 15;3 (1) :53.

• Shipping Conditions :

  Room Temperature

• Storage Conditions :

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category :

  Biochemical Assay Reagents

• Clinical Information :

  No Development Reported

• CAS Number :

  [92051-23-5]