2′-F-U Phosphoramidite
It is a 2′-fluorouridine phosphoramidite monomer with high purity, strong fluorination modification stability, good solubility in common organic solvents, stable coupling activity, and suitable for 2′-fluorinated RNA synthesis systems.
2′-MOE-Bz-A Phosphoramidite
It is a 2′-methoxyethoxybenzoyl-protected adenosine phosphoramidite monomer with high purity, excellent MOE modification stability, good solubility in organic solvents, and suitable for 2′-MOE modified RNA synthesis systems.
2′-MOE-iBu-G Phosphoramidite
It is a 2′-methoxyethoxyisobutyryl-protected guanosine phosphoramidite monomer with high purity, stable MOE modified structure, good solubility in organic solvents, strong selectivity of protecting groups, and suitable for 2′-MOE modified RNA synthesis scenarios.
2′-MOE-T Phosphoramidite
It is a 2′-methoxyethoxythymidine phosphoramidite monomer with high purity, excellent MOE modification stability, good solubility in common organic solvents, stable coupling activity, and suitable for 2′-MOE modified nucleic acid preparation systems.
2′-MOE-5mC Phosphoramidite
It is a 2′-methoxyethoxy-5-methylcytidine phosphoramidite monomer with high purity, excellent stability of MOE and methyl double modification, good solubility in organic solvents, and suitable for 2′-MOE modified nucleic acid synthesis systems.
2′-O-4′-C-Locked-Bz-A Phosphoramidite
It is a benzoyl-protected locked adenosine phosphoramidite monomer with high purity, strong locked structure rigidity, excellent chemical stability, good solubility in organic solvents, and suitable for LNA (locked nucleic acid) synthesis systems.
2′-O-4′-C-Locked-T Phosphoramidite
It is a locked thymidine phosphoramidite monomer with high purity, stable locked structure, good solubility in common organic solvents, stable coupling activity, and suitable for LNA preparation and modification scenarios.
2′-O-4′-C-Locked-iBu-G Phosphoramidite
It is an isobutyryl-protected locked guanosine phosphoramidite monomer with high purity, strong locked structure rigidity, high selectivity of protecting groups, excellent solubility in organic solvents, and suitable for LNA synthesis systems.
2′-O-4′-C-Locked-5-Me-Bz-C Phosphoramidite
It is a 5-methylbenzoyl-protected locked cytidine phosphoramidite monomer with high purity, strong stability of locked and methyl double modification, good solubility in organic solvents, and suitable for LNA synthesis scenarios.
2′-O-4′-C-Locked-Bz-A-Me Phosphoramidite
It is a methylated benzoyl-protected locked adenosine phosphoramidite monomer with high purity, stable structure of locked and methyl double modification, good solubility in organic solvents, and suitable for methylated LNA synthesis systems.
2′-O-4′-C-Locked-iBu-G-Me Phosphoramidite
It is a methylated isobutyryl-protected locked guanosine phosphoramidite monomer with high purity, excellent stability of locked and methyl double modification, easily removable protecting groups, and suitable for methylated LNA synthesis scenarios.
2′-O-4′-C-Locked-T-Me Phosphoramidite
It is a methylated locked thymidine phosphoramidite monomer with high purity, stable structure of locked and methyl double modification, good solubility in common organic solvents, stable coupling activity, and suitable for methylated LNA preparation systems.
2′-O-4′-C-Locked-5-Me-Bz-C-Me Phosphoramidite
It is a double methylated benzoyl-protected locked cytidine phosphoramidite monomer with high purity, extremely strong stability of multiple modifications, excellent solubility in organic solvents, and suitable for high stability LNA synthesis systems.
3′-NH-Tr-2′,3′-dT-5′-CE Phosphoramidite
It is a 3′-amino trityl-protected deoxythymidine phosphoramidite monomer with high purity, clear amino modification site, good solubility in organic solvents, and suitable for amino modified oligonucleotide synthesis systems.
3′-NH-Tr-2′,3′-Bz-ddC-5′-CE Phosphoramidite
It is a 3′-amino trityl-protected benzoyl dideoxycytidine phosphoramidite monomer with high purity, clear amino and dideoxy double modification sites, good solubility in organic solvents, and suitable for amino modified ddC oligonucleotide synthesis scenarios.
3′-NH-Tr-2′,3′-iBu-ddG-5′-CE Phosphoramidite
It is a 3′-amino trityl-protected isobutyryl dideoxyguanosine phosphoramidite monomer with high purity, strong stability of amino and dideoxy modification, good solubility in organic solvents, and suitable for amino modified ddG oligonucleotide synthesis systems.
3′-NH-Tr-2′,3′-DMF-ddA-5′-CE Phosphoramidite
It is a 3′-amino trityl-protected dimethylformamide dideoxyadenosine phosphoramidite monomer with high purity, clear amino and dideoxy modification sites, excellent solubility in organic solvents, and suitable for amino modified ddA oligonucleotide synthesis scenarios.
2′-O-C16-Bz-A Phosphoramidite
It is a 2′-O-hexadecyl benzoyl-protected adenosine phosphoramidite monomer with high purity, strong lipophilicity of long-chain alkyl modification, good solubility in organic solvents, and suitable for lipid modified RNA synthesis systems.
2′-O-C16-Ac-C Phosphoramidite
It is a 2′-O-hexadecyl acetyl-protected cytidine phosphoramidite monomer with high purity, excellent lipophilicity of long-chain alkyl modification, good solubility in organic solvents, and suitable for lipid modified RNA synthesis scenarios.
2′-O-C16-iBu-G Phosphoramidite
It is a 2′-O-hexadecyl isobutyryl-protected guanosine phosphoramidite monomer with high purity, strong lipophilicity of long-chain alkyl modification, high selectivity of protecting groups, and suitable for lipid modified RNA synthesis systems.