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Thank you very much for your interest in our products. All prices listed on our website are ex-works, Germany, and may attract customs duties when imported.
You may/will be contacted by the shipping company for additional documentation that may be required by the US Customs for clearance.
We offer you the convenience of buying through a local partner, Peptide Solutions LLC who can import the shipment as well as prepay the customs duties and brokerage on your behalf and provide the convenience of a domestic sale.
Continue to Iris Biotech GmbHSend request to US distributorChemischer Name: Fmoc-L-Aspartate alpha-amide-beta-(2-chlorotrityl resin) ester // Synonyme: Fmoc-Asp(2CT resin)-NH2
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Very acid labile resin, which enables synthesis of peptide amides without the use of amide linkers (Rink, Ramage, Sieber, etc.)
Peptides can be cleaved as protected fragments, which enables very easy in-process control of the success and completion of any coupling step.
K. Barlos et all. WO 2013/098802 A2.
K. Barlos, D. Gatos et all., Int. J. Peptide and Protein Res. 1991; 38: 555-561.
K. Barlos and D. Gatos, in Fmoc solid phase peptide synthesis, edit. W.C. Chan and P. D. White, Oxford University Press, 2000.
Attachment of Histidine, Histamine and Urocanic acid to Resins of the Trityl-Type. Eleftheriou, S.; Gatos, D.; Panagopoulos, A.; Stathopoulos, S.; Barlos, K.; Tetrahedron Letters 1999; 40(14): 2825-2828.
G. Sabatino et all, Tetrahedron Letters 1999; 40: 809-812.
E. Atherton et. all. US 7,691,968 B2.
F. Albericio et. all WO 2008/040536 A1.
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