L-Uridine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- MF
- C9H12N2O6
- MW
- 244.20
- Purity
- 98.45%
L-Uridine is the L-enantiomer, or mirror-image form, of natural D-uridine. CH64038 is identified by CAS 26287-69-4, molecular formula C9H12N2O6, molecular weight 244.20, and PubChem CID 466466.
The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64038 provides the L-uridine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.
Synonyms
L-Uridine; β-L-uridine
Identity and specifications
| Catalog No. | CH64038 |
| CAS No. | 26287-69-4 |
| Molecular Formula | C9H12N2O6 |
| Molecular Weight | 244.20 |
| PubChem CID | 466466 |
| InChIKey | DRTQHJPVMGBUCF-PSQAKQOGSA-N |
| Purity | 98.45% |
Storage conditions
-20 C as powder; -80 C in solvent
Technical attributes
- Nucleobase
- Uracil
- Sugar
- L-Ribose
- Nucleoside class
- Pyrimidine L-ribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- 100 mg; 250 mg; 1 g; 5 g; 25 g; Custom packaging on request
- Physical form
- Solid; white
- Stability
- 3 years as powder; 1 year in solvent
Application context
- Mirror-image / Spiegelmer research: CH64038 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
- Enantiomeric nucleoside studies: L-uridine provides the uridine mirror-image identity for stereochemistry and biostability comparisons.
- L-nucleoside reference: CH64038 provides the L-uridine identity for nucleoside chemistry research.
Related technical resources
Oligonucleotide Modification
Sugar, base, backbone, terminal, and conjugation modifications for ASO, siRNA, guide RNA, aptamer, and research or labeling oligo projects.
Oligonucleotide Synthesis
Support for modified monomers, supports, sulfurizing reagents, cap analogs, and related oligo synthesis inputs.
Public references
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- PubChem Compound 466466
PubChem · CID 466466
Frequently Asked Questions
How is L-uridine different from uridine?
L-Uridine is the L-enantiomer, or mirror-image form, of natural D-uridine. They share molecular formula and mass but have opposite chirality; natural uridine is cataloged separately.
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