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Fmoc-Nalpha-methyl-N-im-trityl-L-histidine Fmoc-nalpha-methyl-n-im-trityl-l-histidine (FMOC-His(Trt)-OH) is a derivative of the amino acid Histidine. It is used as a building block for the synthesis of peptides and proteins. Histidine is a non-polar, essential amino acid involved in many biological processes such as the biosynthesis of proteins, metal ion binding, and catalysis in enzyme reactions. FMOC-His(Trt)-OH contains a 9-fluorenylmethyloxycarbonyl (Fmoc) protecting group on the amino terminus and a trityl (Trt) protecting group on the imidazole nitrogen. Uses: Fmoc-his(trt)-oh is mainly used as a starting material for the synthesis of peptides and proteins. it is used in spps for the incorporation of histidine residues in the peptide sequence. the resulting peptides and proteins have various applications in scientific experiments, including drug discovery and development, vaccine development, and biological research. Additional or Alternative Names: FMOC-His(Trt)-OH. Product Category: Amino Acids. CAS No. 1217840-61-3. Molecular formula: C41H35N3O4. Mole weight: 633.7. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-(1-tritylimidazol-4-yl)propanoic acid. Canonical SMILES: CN(C(CC1=CN(C=N1)C(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)O)C(=O)OCC5C6=CC=CC=C6C7=CC=CC=C57. Density: 1.2±0.1 g/cm3. Product ID: ACM1217840613. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Fmoc-N-Me-His(Trt)-OH Building block for introduction of N-α-methyl-histidine amino-acid residues by Fmoc SPPS. Product has poor solubility but does dissolve upon activation in NMP with HBTU/DIPEA. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-N-Me-His(Trt)-OH, N-α-Fmoc-N-α-methyl-im-trityl-L-histidine. Product Category: Amino Acids. CAS No. 1217840-61-3. Mole weight: 633.73. Product ID: ACM1217840613-1. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Fmoc-N-Me-His(Trt)-OH Fmoc-N-Me-His(Trt)-OH (Fmoc-MeHis(Trt)-OH) is a is an amino acid derivative containing amino and carboxyl groups. Fmoc-N-Me-His(Trt)-OH for the synthesis of Fmoc-MeHis (Trt) -Leu-OH [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Fmoc-MeHis(Trt)-OH. CAS No. 1217840-61-3. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W142161. MedChemExpress MCE

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