Nucleotides
Uridine 5'-diphosphate trisodium salt
Quick view. The three-sodium salt of uridine 5'-diphosphate, with beta-D-ribofuranose and a 5'-diphosphate group, CAS 123334-08-7. CAS 123334-08-7. Catalog target purity: By inquiry. Availability: Inquiry only — contact OROGO to confirm current availability.
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Structure
Structure form boundary. The displayed drawing omits catalog counterions and does not establish the complete supplied form, counterion stoichiometry or hydration state.
Product profile
Uridine 5'-diphosphate trisodium salt is classified as nucleotides (Formula C9H11N2Na3O12P2; molecular weight 470.11).
Uridine 5'-diphosphate trisodium salt is associated with uridine-containing substrates for U-position incorporation in RNA or modified RNA studies.
For Uridine 5'-diphosphate trisodium salt, confirm the current specification, storage conditions and downstream-method compatibility before routine use.
Names and search terms
Confirmed or normalized name variants
- 5'-UDP . 3Na
- Uridine-5'-diphosphoric acid trisodium salt
- R52013
Useful catalog search terms
- CAS 123334-08-7
Physicochemical data
| Parent PubChem CID | 6031 |
|---|---|
| MDL number | MFCD00006524 |
| Nucleoside | Uridine |
| Phosphate state | 5'-Diphosphate |
| Counterions | 3 sodium ions |
| Representative parent PubChem CID | 6031 |
| Representative parent InChIKey | XCCTYIAWTASOJW-XVFCMESISA-N |
| Representative parent InChI | InChI=1S/C9H14N2O12P2/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1 |
| Representative parent SMILES | C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)O)O)O |
| Representative parent canonical SMILES | C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)(O)O)O)O |
| Structure scope | The displayed structure and database identifiers describe the counterion-free parent, not the complete trisodium supplied form. |
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.
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