Amino-modified Nucleosides
2-Aminopurine-9-beta-D-(2'-deoxy)riboside
Quick view. A beta-D 2'-deoxyriboside of 2-aminopurine. CAS 3616-24-8. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
2-Aminopurine-9-beta-D-(2'-deoxy)riboside is classified as 2-aminopurine beta-d 2'-deoxyriboside (Formula C10H13N5O3; molecular weight 251.24 g/mol).
2-Aminopurine-9-beta-D-(2'-deoxy)riboside provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For 2-Aminopurine-9-beta-D-(2'-deoxy)riboside, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Names and search terms
Confirmed or normalized name variants
- 2-Aminopurine-2'-deoxyriboside
Useful catalog search terms
- 3616-24-8
- KGCFUCMAUQBXMT-XLPZGREQSA-N
Physicochemical data
| PubChem CID | 10879554 |
|---|---|
| IUPAC name | (2R,3S,5R)-5-(2-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol |
| InChIKey | KGCFUCMAUQBXMT-XLPZGREQSA-N |
| InChI | InChI=1S/C10H13N5O3/c11-10-12-2-5-9(14-10)15(4-13-5)8-1-6(17)7(3-16)18-8/h2,4,6-8,16-17H,1,3H2,(H2,11,12,14)/t6-,7+,8+/m0/s1 |
| SMILES | C1[C@@H]([C@H](O[C@H]1N2C=NC3=CN=C(N=C32)N)CO)O |
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 2-Aminopurine-9-beta-D-(2'-deoxy)riboside 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
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