Amino-modified Nucleosides
6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
Quick view. 6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is listed for research-use inquiry under Amino-modified Nucleosides. Its identity is controlled by the retained exact structure and product-form evidence because no public CAS Registry Number is assigned. A public CAS number is not assigned for this exact form. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
![Chemical structure of 6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine](/structures/56c425c8050bdd4f.svg)
Product profile
6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine is classified as amino-modified nucleosides (Formula C10H14N6O4; molecular weight 282.26).
6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine provides a reactive functional group for conjugation, immobilization or linker-extension studies.
For 6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine, functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
Physicochemical data
| CAS status | No public CAS assigned |
|---|---|
| Identity control | Reviewed exact name, structure, and product form |
| InChIKey | MSFNJQTVYAIIRF-RRKCRQDMSA-N |
| InChI | InChI=1S/C10H14N6O4/c11-10-13-8(15-19)4-2-12-16(9(4)14-10)7-1-5(18)6(3-17)20-7/h2,5-7,17-19H,1,3H2,(H3,11,13,14,15)/t5-,6+,7+/m0/s1 |
| SMILES | C1[C@@H]([C@H](O[C@H]1N2C3=NC(=NC(=C3C=N2)NO)N)CO)O |
| Canonical SMILES | C1[C@@H]([C@H](O[C@H]1N2C3=NC(=NC(=C3C=N2)NO)N)CO)O |
| PubChem CID | 175676304 |
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 6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Frequently asked questions
Can the package size for 6-Amino-4-hydroxyamino-1-(2-deoxy-beta-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine be customized?
Yes. Share the initial quantity, expected future scale, delivery timeline and packaging preference for review.
What information should be included in a quote request?
Quote catalog number BX-AMN-0099, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
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.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.