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PRODUCTS
SP - Sulfonic Acid Resin, MP
SP - Triethylamine Resin, MP
SP - Carbonate Resin, MP
SP - Borohydride Resin, MP
SP - Cyanoborohydride Resin, MP
SP - Thiophenol Resin, MP
SP - Thiourea Resin, MP
SP - Sulfonyl Chloride Resin, MP
SP - Aminopolyhydroxy Resin, MP
SP - Diisopropylethylamine Resin, MP
SP - Trisamine Resin, MP
SP - Hydrazide Resin, MP
SP - Tribromide Resin, MP
SP - Merrifield High Loaded Resin, MP
SP - Thiophenol Resin, MP Fine
SP - Thiourea Resin, MP - Fine
SP - Trisamine Resin, MP - Fine
SP - Thio - Silica
SP - Trisamine - Silica
SP - Thiourea - Silica
SP - TMT - Silica
SP - Aminopolyhydroxy Resin, MP - Fine
SP - Piperazine - Silica
SP - Piperazine Resin, MP
SP - TMT Resin, MP
SP - THIOUREA RESIN, MP
PRODUCT:
SP-Thiourea Resin, MP, a highly cross-linked polystyrene resin functionalized with a Thiourea end group
 
APPLICATIONS:
  • SP-Thiourea Resin is a polymer bound thoiurea.
  • It is designed to provide strong interactions with a variety of heavy metal species.
  • It is highly effective in scavenging of all forms of palladium.
  • It can be also used for scavenging of metals like platinum, ruthenium, tin, mercury, nickel, copper.
  • Other uses for these compounds have also been reported, including hydrogenolysis of endoperoxides.
  • There also remains the possibility of using these polymer supported reagents as co-catalysts in some metal mediated reactions.
  • Polymer supported Thiourea bound transition metals have been reported as effective catalysts for organic synthesis.
  • It is compatible in both aqueous and non aqueous solutions.
PROPERTIES:
Resin Type:  Macroporous poly (styrene-co-divinylbenzene)
Loading:        3.6 - 3.4 mmol/g (Elemental nitrogen, sulphur analysis)
Bead Size:    330-1225 microns, 15-50 mesh (>90% within)
Typical Scavenging: 3-5 equivalent of resin relative to the metal content, for a period of 12-16 hours, room temperature.
Compatible Solvents: Polar and non polar solvents, including aqueous solvents.
   
REFERENCES:
  1. Vickerstaffe, E.; Warrington, B. H.; Ladlow, M. J. Comb. Chem. 2005, 7, 385-397.
  2. Bicak, N.; Sherrington, D. C.; Sungur, S.; Tan, N. React. Funct. Polym. 2003, 54, 141-147
  3. Warmus, J. S.; Ryder, T. R.; Hodges, J. C.; Kennedy, R. M.; Brady, K. D. Bioorg. Med. Chem. Lett. 1998, 8, 2309-2314.
  4. Zuo, G.; Muhammed, M. React. Polym. 1995, 24, 165-181.
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