A ribonucleotide
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Uridine-5'-monophosphate

Item No. 35382

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
5′-uridylic acid
CAS Number
58-97-9
Synonyms
  • UMP
  • 5′-UMP
Molecular Formula
C9H13N2O9P
Formula Weight
324.2
Purity
≥95%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
DMF: 5 mg/mlDMSO: 10 mg/mlEthanol: 15 mg/mlPBS (pH 7.2): 5 mg/ml
λmax
262 nm
SMILES
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@@]([H])(N2C(NC(C=C2)=O)=O)[C@@H]1O
InChi Code
InChI=1S/C9H13N2O9P/c12-5-1-2-11(9(15)10-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,10,12,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChi Key
DJJCXFVJDGTHFX-XVFCMESISA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    500 mg

    $103

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    1 g

    $194

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    5 g

    $601

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    Product Description

    Uridine-5'-monophosphate is a ribonucleotide.1 It is formed via decarboxylation of orotidine-5'-monophosphate (5'-OMP) by OMP decarboxylase. Uridine-5’-monophosphate is further phosphorylated by uridine-5’-monophosphate-CMP kinase to form UDP (Item No. 18137) and UTP (Item No. 9003530) during nucleic acid biosynthesis. Formulations containing uridine-5’-monophosphate have been used as dietary supplements.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Berg, J.M., Tymoczko, J.L., and Stryer, L. Nucleotide biosynthesis. Biochemistry (2002).