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Catalogue Number |
Product | Order number / Unit |
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| 102 | Mannose Triflate, ultra pure |
102.0020: 20 mg per vial 102.0030: 30 mg per vial Please inquire for customized filling and bulk quantities.
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Precursor for [18F]FDG
(2-[18F]Fluoro-2-deoxy-D-glucose) |
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| packing for FDG MicroLab (GE) | ||
| Molar Mass: 480.37 | ||
| C15H19F3O12S | ||
| [92051-23-5] | ||
| Colourless or nearly colourless crystals packaged in 2 ml dark glass vials ( for GE Microlab) with teflon-faced rubber stoppers, tear-off crimp caps, argon flushed. | ||
| Melting range 119 - 122 degC | ||
| Soluble in acetonitrile, DMSO, methanol, acetone; insoluble in aqueous media. | ||
| Purity: > 99 % | ||
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Certificates:
CoA; melting point, 1H and 19F NMR spectra, IR spectrum, HPLC |
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Chemical Name: CA index name: beta-D-mannopyranose, 1,3,4,6-tetraacetate 2-(trifluoromethane-sulfonate) |
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Synonymes: TATM; mannose triflate; 1,3,4,6-tetra-O-acetyl-2-O-trifluoro-methanesulfonyl-beta-D-mannopyranose |
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Literature: 1. Hamacher K. et al. Efficient stereospecific synthesis of no-carrier-added 2-[18F]fluoro-2-deoxy-D-glucose using amino-polyether supported nucleophilic substitution. J. Nucl. Med. 1986, 27, 235-238. |
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| 2. Padgett H. et al. Computer-controlled radiochemical synthesis: a chemistry process control unit for the automated production of radiochemicals. Appl. Radiat. Isot. 1989, 40, 433-445. | ||
| 3. Pavliak V. et al. A short synthesis of 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-beta-D-glucopyranose and the corresponding alpha-glucosyl chloride from D-mannose. Carbohydr. Res. 1991, 210, 333-337. | ||
| 4. Chirakal R. Traces of fluorine containing impurities in the mannose triflate and their adverse effect on the radiochemical yield of 2-18FDG. XIIth ISRC; Uppsala, Sweden 1997, 214-216. | ||
| date of product catalogue issue: 21 Decmber 2012 | ||
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