Amino-modified Nucleosides
3'-N-Acetyl-3'-amino-3'-deoxyuridine
Quick view. Uridine derivative bearing a 3'-acetamido group in place of the 3'-hydroxyl. CAS 2305415-89-6. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
3'-N-Acetyl-3'-amino-3'-deoxyuridine is classified as amino-modified nucleosides (Formula C11H15N3O6; molecular weight 285.25 g/mol).
3'-N-Acetyl-3'-amino-3'-deoxyuridine provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For 3'-N-Acetyl-3'-amino-3'-deoxyuridine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Names and search terms
Useful catalog search terms
- 2305415-89-6
Physicochemical data
| Nucleoside | Uridine |
|---|---|
| Substitution pattern | 3'-N-acetyl-3'-amino-3'-deoxy |
| InChIKey | BUUSLPRPRSICHU-PEBGCTIMSA-N |
Release documentation
The current specification defines the analytical method and acceptance criteria; the released lot result is reported on the CoA.
Additional HPLC, MS or NMR documentation can be agreed during technical review where available.
Product-specific evaluation notes
Potential advantages
- Reactive handles make the product adaptable across dye-labeling, surface-coupling and ligand-conjugation workflows.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
These points describe 3'-N-Acetyl-3'-amino-3'-deoxyuridine or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Product-family literature
These publications provide peer-reviewed context for the Amino-modified Nucleosides product family and its named chemistry. They are background reading only, not evidence for the exact product, supplied form, lot specification, availability or performance.
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Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.