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C1006

Sigma-Aldrich

Cytidine 5′-monophosphate disodium salt

Sigma Grade, ≥99%, crystalline

Synonym(s):

C-5′-P, CMP

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About This Item

Linear Formula:
C9H12N3O8PNa2
CAS Number:
Molecular Weight:
367.16
EC Number:
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.51

biological source

synthetic

Quality Level

grade

Sigma Grade

assay

≥99%

form

crystalline

solubility

water: 100 mg/mL, clear to very slightly hazy, colorless to very faintly yellow

storage temp.

2-8°C

SMILES string

[Na].NC1=NC(=O)N(C=C1)C2OC(COP(O)(O)=O)C(O)C2O

InChI

1S/C9H14N3O8P.Na.H/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18);;

InChI key

RCIPNLSOCXMZDD-UHFFFAOYSA-N

Application

Cytidine 5′-monophosphate disodium salt has been used:
  • in nucleotide stock solution
  • as an ectonucleotidase (ENTase) inhibitor to probe 5′-ENTase activity in cortical neurons
  • in in vitro studies to estimate its effect on growth response of selected bacteria strains that dominate the piglets′ small intestine

Biochem/physiol Actions

Cytidine 5′-monophosphate (CMP) is used as a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) to form CDP which upon phosphorylation to CTP supports DNA and RNA biosynthesis.
Cytidine monophosphate (CMP) serve as a nucleotide carrier for sugars.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Carbohydrate Metabolism III: Glycoproteins, Glycolipids, GPI Anchors, Proteoglycans, and Peptidoglycans
Medical Biochemistry, 307-330 (2002)
Charuni A Amarasekara et al.
Journal of chromatography. A, 1638, 461892-461892 (2021-01-22)
With advances in the design and fabrication of nanofluidic devices during the last decade, there have been a few reports on nucleic acid analysis using nanoscale electrophoresis. The attractive nature of nanofluidics is the unique phenomena associated with this length
Nicotinamide riboside, a form of vitamin B3, protects against excitotoxicity-induced axonal degeneration
Vaur P, et al.
Faseb Journal (2017)
Thomas Doneux et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 10(9-10), 1649-1655 (2009-04-07)
The interaction of cytidine 5'-monophosphate (CMP) with gold surfaces is studied by means of in situ infrared spectroscopy and cyclic voltammetry at the Au(111)|aqueous solution interface. Similar to other nucleic acid components, cytidine 5'-monophosphate is chemisorbed on the surface at
P Briozzo et al.
Structure (London, England : 1993), 6(12), 1517-1527 (1998-12-24)
. Nucleoside monophosphate kinases (NMP kinases) catalyze the reversible transfer of a phosphoryl group from a nucleoside triphosphate to a nucleoside monophosphate. Among them, cytidine monophosphate kinase from Escherichia coli has a striking particularity: it is specific for CMP, whereas

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