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Product
Fmoc-His(Trt)-OH Fmoc-His(Trt)-OH. Group: Biochemicals. Alternative Names: Na-Fmoc-N(im)-trityl-L-histidine. Grades: Highly Purified. CAS No. 109425-51-6. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C40H33N3O4. US Biological Life Sciences. USBiological 7
Worldwide
Fmoc-His(Trt)-OH Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH 2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation [1]. Uses: Scientific research. Group: Peptides. CAS No. 109425-51-6. Pack Sizes: 25 g; 100 g; 500 g. Product ID: HY-W010712. MedChemExpress MCE
Fmoc-His(Trt)-OH High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of histidine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-His(Trt)-OH, N-α-Fmoc-N-im-trityl-L-histidine. Product Category: Amino Acids. CAS No. 109425-51-6. Molecular formula: C40H33N3O4. Mole weight: 619.71. Product ID: ACM109425516. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
Fmoc-His(Clt)-OH A useful derivative for the convergent synthesis of peptide due to the enhanced stability of Clt group compared to Trt group to mildy acidic reagents. Fmoc-His-(Clt)-OH gives approximately a third less racemization when compared to Fmoc-His(Trt)-OH during slow coupling reactions. Uses: Peptide synthesis. Additional or Alternative Names: Fmoc-His(Clt)-OH, N-α-Fmoc-N-im-2-chlorotrityl-L-histidine. Product Category: Amino Acids. CAS No. 224032-19-3. Mole weight: 654.15. Product ID: ACM224032193-1. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry.
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.

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