Deoxyuridine

Deoxyuridine

CAS Number951-78-0
Molecular FormulaC9H12N2O5
Molecular Weight228.204
InChI KeyMXHRCPNRJAMMIM-SHYZEUOFSA-N
LogP-1.6
Synonyms
  • 2'-DEOXYURIDINE
  • deoxyuridine
  • 951-78-0
  • Uracil deoxyriboside
  • 2-Deoxyuridine
  • 1-((2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
  • Deoxyribose uracil
  • Uridine, 2'-deoxy-
  • 2'-Desoxyuridine
  • UNII-W78I7AY22C
  • CCRIS 2832
  • dURD
  • EINECS 213-455-7
  • BRN 0024433
  • 2 -Deoxyuridine
  • CHEBI:16450
  • 1-(2-Deoxy-beta-D-erythro-pentofuranoxyl)uracil
  • MFCD00006527
  • 1-(2-Deoxy-beta-D-ribofuranosyl)uracil
  • AK-54658

Applications:

HPLC Method for Analysis of Deoxyuridine on Chromite™ Column on Alltesta™

November 4, 2025

HPLC Method for Deoxyuridine on Chromni™ by SIELC Technologies


High Performance Liquid Chromatography (HPLC) Method for Analysis of Deoxyuridine

Deoxyuridine (dU) is an nucleoside with the C9H12N2O5 molecular formula. While in living organisms it exists primarily to occasionally become a part of DNA, it’s variants, Idoxuridine and Trifluoride, work as antiviral drugs. If consumed, Deoxyuridine can be toxic.

Deoxyuridine can be retained and analyzed using the Chromni™ stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water and acetonitrile (MeCN) with phosphoric acid as a buffer. Detection is performed using UV.

ColumnChromni™, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseMeCN – 90%
BufferAmFm pH 3.0 – 30 mM
Flow Rate1.0 ml/min
DetectionUV 275 nm

Class of CompoundsNucleotide Base
Analyzing CompoundsDeoxyuridine

Application Column

Chromni™

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

Add to cart
Application Analytes:
Deoxyuridine

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

Separation of Deoxyribo Nucleosides

September 24, 2003

Primesep 200 separates with baseline resolution the nucleosides (deoxyuridine, deoxyguanosine, deoxycytidine, deoxyadenozine) by a combination of cation exchange and reversed phase. These compounds are not retained on a traditional C18 column. Primesep 200 has an embedded anionic functional group which helps retain polar compounds by polar and ion-exchange mechanisms. Excellent peak shape results with a mass spec compatible mobile phase of water, acetonitrile (MeCN, ACN) and trifluoracetic acid (TFA) with UV detection at 270 nm.

Application Column

Primesep 200

Column Diameter: 4.6 mm
Column Length: 250 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

Add to cart
Application Analytes:
Deoxyadenosine
Deoxycytidine
Deoxyguanosine
Deoxyuridine

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.