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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 – AMINOPOLYHYDROXY RESIN, MP
PRODUCT:
SP-Aminopolyhydroxy Resin, MP, a highly cross-linked polystyrene resin functionalized with a diethanolamine end group

APPLICATIONS:
  • SP-Aminopolyhydroxy Resin is a polymer bound diethanolamine.
  • It is used for scavenging of boronic acids, especially in the purification of Suzuki coupling reactions.
  • Sp-Aminopolyhydroxy resin is a dual-purpose resin, for use as a scavenger to remove excess boronic acids from non aqueous solutions, or to immobilize boronic acids for further functionalization.
  • Sp-Aminopolyhydroxy resin is highly efficient in scavenging oxophilic inorganic and organometallic complexes.
  • This resin also a highly effective scavenger of metals from solution, in particular platinum, titanium and tin species.
PROPERTIES:
Resin Type:  Macro porous poly (styrene-co-divinylbenzene)
Loading:        2.5 – 2.8 mmol/g (Elemental nitrogen analysis)
Bead Size:    330-1225 microns, 15-50 mesh (>90% within)
Typical Tin Scavenging: 3-5 equiv of the resin relative to tin content, 8-12 h at ambient temperature
Compatible Solvents: Polar and non polar solvents, including aqueous solvents
 
REFERENCES:
  1. Thompson, K. A.; Hall, D. G. Chem. Commun. 2000, 2379-2380
  2. Gros, P.; Doudouh, A.; Fort, Y. Tetrahedron Lett. 2004, 45, 6239-6241.
  3. Hall, D. G.; Tailor, J.; Gravel, M. Angew. Chem., Int. Ed. 1999, 38, 3064-3067.
  4. Arimori, S.; James, T. D. Tetrahedron Lett. 2002, 43, 507-509
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