Nucleotides
UDP-N-trifluoroacetylglucosamine disodium salt
Quick view. The disodium salt of UDP-N-trifluoroacetylglucosamine (UDP-GlcNTFA), CAS 1355005-47-8. CAS 1355005-47-8. Catalog target purity: ≥98%. Availability: Inquiry only; contact BX Lab to confirm current availability.
Structure confirmation
This item requires structure confirmation before quotation. Send the target structure, CAS number, SMILES, InChI or drawing for our technical review.
Canonical name plus a structure drawing, SMILES, InChI or unambiguous CAS number.
Protecting groups, stereochemistry, salt or counterion, hydration and requested form.
Agreed identity and purity criteria are documented in the quotation, specification and lot-specific data package.
Product profile
UDP-N-trifluoroacetylglucosamine disodium salt is classified as nucleotides.
UDP-N-trifluoroacetylglucosamine disodium salt — Reported in the literature as a nucleotide-sugar donor for chemoenzymatic oligosaccharide synthesis.
For UDP-N-trifluoroacetylglucosamine disodium salt, 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
- UDP-GlcNTFA.2Na
- Uridine 5'-diphospho-N-trifluoroacetylglucosamine disodium salt
- UDP-N-trifluoroacetylglucosamine (disodium)
Useful catalog search terms
- CAS 1355005-47-8
- PMID 27220687
- DOI 10.1080/10826068.2016.1188315
Physicochemical data
| Compound class | Nucleotide sugar |
|---|---|
| Sugar substituent | N-Trifluoroacetylglucosamine |
| Nucleotide moiety | Uridine 5'-diphosphate |
| Salt form | Disodium |
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.
- 2′-fluoro motifs can improve nuclease resistance while preserving RNA-like geometry in many sequence contexts.
Method limitations
- Functional handles may require orthogonal protection, pH control and rapid purification to avoid hydrolysis, oxidation or cross-reaction.
- Coupling, deprotection and biological performance remain sequence- and position-dependent.
These points describe UDP-N-trifluoroacetylglucosamine disodium salt 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-N-trifluoroacetylglucosamine disodium 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-NUCL-0168 and CAS 1355005-47-8, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
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 a BX Lab lot specification or product-performance claim.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.