Modified Nucleotides
UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt
Quick view. A disodium azido-functionalized UDP-GalNAc analog for research-use enzymatic glycan remodeling and subsequent click-conjugation workflows. CAS 1202854-87-2. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Product profile
UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt is classified as azido-functionalized udp-sugar disodium salt (Formula C17H24N6Na2O16P2; molecular weight 676.33 g/mol).
UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt — Published studies use UDP-6-N3-GalNAc in enzymatic glycan-remodeling research followed by azide-based click conjugation.
For UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium 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-N3-GalNAc.2Na
- UDP-6-azido-6-deoxy-GalNAc disodium salt
Useful catalog search terms
- 1202854-87-2
Physicochemical data
| Calculated molecular weight | 676.33 g/mol |
|---|---|
| CAS context | 1202854-87-2 identifies the parent/free-acid identity and is reused commercially for the disodium form |
| Short name | UDP-6-N3-GalNAc.2Na |
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
- 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.
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.
These points describe UDP-6-azido-6-deoxy-N-acetyl-D-galactosamine disodium salt or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Product-relevant literature
The publications below discuss named chemistry or a structural feature represented by this product. They provide scientific context only and are not an OROGO lot specification or product-performance claim.
Feature and workflow background
These publications discuss a broader chemistry feature or workflow identified from the catalog name or product family. They are background reading only, not evidence for the exact OROGO 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.