Modified Nucleotides
UDP-6-Azido-N-Acetylgalactosamine Sodium Salt
Quick view. We supply UDP-6-Azido-N-Acetylgalactosamine Sodium Salt as a functionalized nucleotide analog for enzymatic labeling, click chemistry, affinity capture or fluorescence-based nucleic acid workflows. CAS 1202854-87-2. Catalog target purity: ≥98%.
Product profile
UDP-6-Azido-N-Acetylgalactosamine Sodium Salt is classified as nucleotide or nucleotide analog (Formula C17H26N6O16P2; molecular weight 632.37).
UDP-6-Azido-N-Acetylgalactosamine Sodium Salt can support enzyme-substrate, in-vitro transcription, polymerase-screening or analytical-reference studies as appropriate to its phosphate state.
For UDP-6-Azido-N-Acetylgalactosamine Sodium Salt, copper-catalyzed, copper-free or inverse-electron-demand click conditions can affect sensitive oligonucleotides differently; residual metal, solvent and purification strategy should be controlled.
Names and search terms
Confirmed or normalized name variants
- UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine
Useful catalog search terms
- CAS 1202854-87-2
- Nucleotide or nucleotide analog
- azide click handle
- amine functionality
- Modified Nucleotides
Physicochemical data
| Key chemistry motifs | azide click handle; amine functionality |
|---|---|
| CAS context | The listed CAS refers to the parent/free-acid identity; confirm the supplied salt or counterion in the current specification. |
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.
Additional application examples
- Typical qualification includes identity, salt/counterion, assay basis, water content and enzyme compatibility.
- Related uses include LC-MS/HPLC method development and comparison with native or modified nucleotide controls.
Product-specific evaluation notes
Potential advantages
- Click-compatible handles separate oligonucleotide synthesis from late-stage labeling, which helps screen multiple payloads from a common intermediate.
- Reactive handles make the product adaptable across dye-labeling, surface-coupling and ligand-conjugation workflows.
- A defined GalNAc intermediate helps decouple ligand-linker optimization from sequence optimization.
Method limitations
- Copper-catalyzed, copper-free or inverse-electron-demand click conditions can affect sensitive oligonucleotides differently; residual metal, solvent and purification strategy should be controlled.
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
- In-vitro affinity and in-vivo delivery behavior may diverge; valency, linker length and conjugation site need empirical confirmation.
These points describe UDP-6-Azido-N-Acetylgalactosamine Sodium Salt or its named chemical feature. Broader product-family guidance is maintained on the category page.
Related products
3'-OMe-GDP Disodium Salt
Modified Nucleotides · CAS: 78771-34-3
BX-INTE-00143'-OMe-GMP
Modified Nucleotides · CAS: 400806-41-9
BX-INTE-00153'-OMe-GMP TEA Salt
Modified Nucleotides · CAS: 860605-85-2
BX-INTE-0021Im-3'-OMe-GMP
Modified Nucleotides · CAS: 1005791-93-4
BX-INTE-0023Im-GDP
Modified Nucleotides · CAS: 1199264-75-9
BX-MN-0025(-)-Emtricitabine Triphosphate Tetrasodium Salt
Modified Nucleotides · CAS: 1188407-46-6
Frequently asked questions
Can the package size for UDP-6-Azido-N-Acetylgalactosamine Sodium Salt 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-MN-0139 and CAS 1202854-87-2, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-relevant literature
The publications below discuss UDP-6-Azido-N-Acetylgalactosamine Sodium Salt or the named structural feature represented by this product.