Skip to Content
Merck
All Photos(4)

Key Documents

U6375

Sigma-Aldrich

Uridine 5′-monophosphate disodium salt

≥99%

Synonym(s):

5′-UMP-Na2, U 5′-P, UMP, Uridylic acid disodium salt

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C9H11N2Na2O9P
CAS Number:
Molecular Weight:
368.15
Beilstein:
3582885
EC Number:
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.26

biological source

(chemical)

Quality Level

Assay

≥99%

form

powder

storage temp.

−20°C

SMILES string

[Na+].[Na+].O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP([O-])([O-])=O)N2C=CC(=O)NC2=O

InChI

1S/C9H13N2O9P.2Na/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);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1

InChI key

KURVIXMFFSNONZ-WFIJOQBCSA-L

Looking for similar products? Visit Product Comparison Guide

General description

Uridine 5′-monophosphate is a pyrimidine mononucleotide. It is formed by decarboxylation of orotidine 5′-monophosphate. UMP is further converted to UTP (uridine 5′-triphosphate) using kinases.

Application

Uridine 5′-monophosphate disodium salt has been used to study the effect of pyrimidine synthesis inhibitor, 5-azacytidine, on cholesterol and lipid metabolism. It has been used to study the effect of nucleotides on growth of specific intestinal bacteria.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Adams RLP, et al.
The Biochemistry of the Nucleic Acids (2013)
Nucleotides modify growth of selected intestinal bacteria in vitro.
Sauer N, et al.
Livestock Science, 133, 161-163 (2010)
The epigenetic drug 5-azacytidine interferes with cholesterol and lipid metabolism.
Poirier S, et al.
The Journal of Biological Chemistry, 289, 18736-18751 (2014)
Willem Kasper Spoelstra et al.
Langmuir : the ACS journal of surfaces and colloids, 36(8), 1956-1964 (2020-01-30)
Coacervates are polymer-rich droplets that form through liquid-liquid phase separation in polymer solutions. Liquid-liquid phase separation and coacervation have recently been shown to play an important role in the organization of biological systems. Such systems are highly dynamic and under
Stefanie Bäurer et al.
Journal of chromatography. A, 1560, 45-54 (2018-05-24)
Herein, we present a novel silica-based stationary phase modified with N-propyl-N'-2-pyridylurea selector. Due to the weakly basic properties of the pyridine selector and the presence of residual silanols after selector immobilization, a zwitterionic surface with a pI observed at approximately

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service