Modified Nucleotides
UDP-6-azido-6-deoxy-D-Gal.2Na
Quick view. We supply UDP-6-azido-6-deoxy-D-Gal.2Na as a functionalized nucleotide analog for enzymatic labeling, click chemistry, affinity capture or fluorescence-based nucleic acid workflows. CAS 868208-96-2. Catalog target purity: Specification on request.
Structure and identity
The structure drawing for this item is being finalized. Use the CAS number and machine-readable identifiers below to confirm the requested protecting groups, stereochemistry, salt or counterion and hydration state before ordering.
CAS, molecular formula, SMILES or InChI data are shown below when available.
We withhold a drawing when a related compound, alternate salt or incompletely specified stereoisomer could be mistaken for the requested material.
Agreed identity and purity criteria are documented in the quotation, specification and lot-specific data package.
Product profile
UDP-6-azido-6-deoxy-D-Gal.2Na is classified as nucleotide or nucleotide analog (Formula C15H23N5O16P2; molecular weight 591.32).
UDP-6-azido-6-deoxy-D-Gal.2Na can support enzyme-substrate, in-vitro transcription, polymerase-screening or analytical-reference studies as appropriate to its phosphate state.
For UDP-6-azido-6-deoxy-D-Gal.2Na, 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
Useful catalog search terms
- CAS 868208-96-2
- Nucleotide or nucleotide analog
- azide click handle
- Modified Nucleotides
Physicochemical data
| Key chemistry motifs | azide click handle |
|---|---|
| SMILES | O[C@@H]1[C@@H]([C@@H](COP(O)(=O)OP(O)(=O)O[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CN=[N+]=[N-])O2)O)O[C@H]1N1C=CC(=O)NC1=O)O |&1:1,2,3,14,15,16,18,20,28,r| |
| InChIKey | YLSUUMDTTUVTGP-MLLUUDRENA-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.
Additional application examples
- UDP-6-azido-6-deoxy-D-Gal.2Na is a nucleotide analog, can be used in the synthesis of azido-sugars and labeling experiments to scrutinize the capabilities of glycosyltransferases.
- 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.
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.
These points describe UDP-6-azido-6-deoxy-D-Gal.2Na 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 UDP-6-azido-6-deoxy-D-Gal.2Na 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-MODN-0220 and CAS 868208-96-2, 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-6-deoxy-D-Gal.2Na or the named structural feature represented by this product.