2'-O-Methyl-5'-O-DMT-pseudouridine 3'-CE phosphoramidite

95%

Reagent Code: #222357
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CAS Number 199737-09-2

science Other reagents with same CAS 199737-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 760.81 g/mol
Formula C₄₀H₄₉N₄O₉P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of modified RNA oligonucleotides, particularly in mRNA vaccine development and therapeutic RNA applications. The 2'-O-methyl pseudouridine modification enhances RNA stability, reduces immunogenicity, and improves translational efficiency when incorporated into mRNA. The DMT (dimethoxytrityl) group enables solid-phase oligonucleotide synthesis by providing reversible protection for the 5'-hydroxyl group, allowing stepwise chain elongation. The CE (cyanoethyl) phosphoramidite group facilitates efficient coupling and is later removed during standard deprotection. This phosphoramidite building block is essential for producing high-quality, modified RNA with improved pharmacological properties for use in vaccines, gene therapies, and functional genomics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿37,000.00
2'-O-Methyl-5'-O-DMT-pseudouridine 3'-CE phosphoramidite
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Used in the synthesis of modified RNA oligonucleotides, particularly in mRNA vaccine development and therapeutic RNA applications. The 2'-O-methyl pseudouridine modification enhances RNA stability, reduces immunogenicity, and improves translational efficiency when incorporated into mRNA. The DMT (dimethoxytrityl) group enables solid-phase oligonucleotide synthesis by providing reversible protection for the 5'-hydroxyl group, allowing stepwise chain elongation. The CE (cyanoethyl) phosphoramidite group fa

Used in the synthesis of modified RNA oligonucleotides, particularly in mRNA vaccine development and therapeutic RNA applications. The 2'-O-methyl pseudouridine modification enhances RNA stability, reduces immunogenicity, and improves translational efficiency when incorporated into mRNA. The DMT (dimethoxytrityl) group enables solid-phase oligonucleotide synthesis by providing reversible protection for the 5'-hydroxyl group, allowing stepwise chain elongation. The CE (cyanoethyl) phosphoramidite group facilitates efficient coupling and is later removed during standard deprotection. This phosphoramidite building block is essential for producing high-quality, modified RNA with improved pharmacological properties for use in vaccines, gene therapies, and functional genomics.

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