|
|
|||||||||||||||||||||||||||||||||||||
|
|
||||||||||||||||||||||||||||||||||||||
%20Phosphoramidite_files/image003.gif)
%20Phosphoramidite_files/image004.gif)
%20Phosphoramidite_files/image002.jpg){kind=small}
%20Phosphoramidite_files/image007.png)
DMT-dC(bz) Phosphoramidite
Catalog NO.: DNA-PM-002 | CAS NO.: 102212-98-6 | Brand: BIOCAXIS
Category
Carbohydrates, Nucleosides & Nucleotides, DNA Phosphoramidites
Synonyms:
Cytidine, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxy-, 3′-[2-cyanoethyl bis(1-methylethyl)phosphoramidite], DMT-dC(bz) amidite, N-benzoyl-5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxycytidine, 3′-[2-cyanoethyl N,N-?bis(1-methylethyl)phosphoramidite], N4-Benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxycytidine-3′-O-[O-(2-cyanoethyl)-N,N′-diisopropylphosphoramidite]
Molecular Formula
C46H52N5O8P
Molecular Weight
833.91
General description
DMT-dC(bz) Phosphoramidite belongs to the group of DNA Phosphoramidites.Its key features include:
Exocyclic amine functions are protected by a benzoyl group (dA(bz) anddC(bz)) or isobutyryl group (dG(ib))
Recommended cleavage and deprotection conditions are 8 hours at 55 °Cor 24 hours at room temperature using concentrated ammonia solution, for standard base-protected oligonucleotides
The high coupling efficiency of Proligo′s DNA phosphoramidites leads to high-yield and high-quality oligonucleotides
Usage
Solid phase synthesis of DNA and RNA oligonucleotides in chemical or enzymatic processes.