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Product Line: Life Science

5-O-DMT-2-O-Me-rU-3-CEDPA

CAS 110764-79-9

Molecular structure of 5-O-DMT-2-O-Me-rU-3-CEDPA

CAS · 110764-79-9

01

Product Overview

5-O-DMT-2-O-Me-rU-3-CEDPA is a high-purity nucleosides-nucleotides supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance: White to off-white powder
Solubility Clarity (in acetonitrile and 20% DMF): 0.2 M solution is free from undissolved particulate
Solubility Clarity (in dichloromethane:acetonitrile 50:50): 0.2 M solution is free from undissolved particulate
Identity (by HNMR): To conform structure
Purity (HPLC): 99.0% min
Single critical impurity: 0.3% max
Non-critical single impurity: 0.5% max
Unknown single impurity: 0.3% max
31P NMR Purity: 98.0% min
POI Impurities (100–170 ppm): 0.5% max
Residual Solvent: 3.0% max
Moisture: 0.5% max
03

Applications

 

 

1. Synthetic RNA Oligonucleotide Production

Used in solid-phase oligonucleotide synthesis (SPOS) for generating RNAs containing 2′-O-methyluridine.

Commonly applied in:

siRNA duplexes

mRNA vaccines

RNA aptamers

antisense oligonucleotides (ASOs)

2. RNA Therapeutics

Facilitates the production of chemically stabilized RNAs with improved biological activity.

2′-O-methyl modifications help:

Increase resistance to ribonucleases

Enhance binding specificity

Minimize off-target effects

Reduce immunogenicity in vivo

3. Epitranscriptomic and Molecular Biology Research

Used in modified RNA synthesis to investigate the biological roles of 2′-O-methylation, particularly in rRNA, tRNA, and snRNA.

Helps model natural RNA modifications for structure-function studies.

4. Diagnostics and Probing Tools

Incorporated into RNA probes and biosensors to improve target recognition and stability in biological assays.

04

Benefits

 

1. Enhanced RNA Stability

The 2′-O-methyl group significantly increases resistance to enzymatic degradation by RNases.

2. Reduced Immune Activation

Modified nucleosides like 2′-O-Me-rU help synthetic RNA evade innate immune detection, important for therapeutic safety.

3. Improved Hybridization Specificity

2′-O-methyl modifications enhance duplex stability and improve target discrimination in antisense and siRNA applications.

4. Reliable Synthetic Performance

DMT and CEDPA protecting groups ensure high coupling efficiency and clean deprotection, enabling high-fidelity RNA synthesis.

05

Conclusion

5-O-DMT-2-O-Me-rU-3-CEDPA (CAS 110764-79-9) is a phosphoramidite reagent designed for precise incorporation of 2′-O-methyluridine into synthetic RNA strands. It is essential in the creation of stable, low-immunogenic, high-performance RNA oligonucleotides used in therapeutics, molecular research, and diagnostic tools. With high stability and synthesis efficiency, it plays a critical role in advancing RNA technology and epitranscriptomics.

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