HPLC Method for 2'-Deoxycytidine 5'-Monophosphate, Cytidine Monophosphate on Newcrom B by SIELC Technologies

High Performance Liquid Chromatography (HPLC) Method for Analysis of 2'-Deoxycytidine 5'-Monophosphate, Cytidine Monophosphate .

Cytidine-5′-monophosphate is a nucleoside monophosphate with C9H14N3O8P chemical formula. It is a fundamental building block for RNA and DNA as well as an intermediate in phospholipid synthesis.

2′-Deoxycytidine 5′-Monophosphate is a deoxyribonucleotide with C9H14N3O7P chemical formula. It is crucial when it comes to DNA synthesis. dCMP is often used in genetic research, biotechnology, and development of pharmaceuticals with a focus on antiviral and anticancer drugs.

2'-Deoxycytidine 5'-Monophosphate, Cytidine Monophosphate can be retained and analyzed using the Newcrom B stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water and acetonitrile (MeCN) with a phosphoric acid buffer. Detection is performed using UV.

Nucleotides are the monomers of DNA and RNA, composed of a five-carbon sugar, a nitrogenous base, and at least one phosphate group. Primesep SB is a good column for separating these highly polar compounds. Primesep SB is a reverse-phase column with strong embedded basic ion-pairing groups. Retention can me manipulated by adjusting acetonitrile, and the baseline separation can be achieved in under 6 minutes using a gradient. 

Nucleotides are important biological molecules which serve as subunits of nucleic acids. They are composed of a five-carbon sugar, a nitrogenous base, and at least one phosphate group. Nucleotides cannot be retained by reverse-phase chromatography without an ion-pairing reagent due to their highly polar nature. Primesep SB is capable of retaining and separating nine nucleotides. Primesep SB is a reverse-phase column with strong embedded basic ion-pairing groups.

Cytidine phosphates are nucleotides. Nucleotides contain a nucleobase, five-carbon sugar and one or three phosphate groups. All three cytidines are very polar and cannot be retained by reversed-phase chromatography without a ion-pairing reagent. Mixed-mode Primesep SB column easily allows to retain and separate mono-, di-, and tri-phospates by anion-exchange mechanism. Other nucleotides can be separated as well by this approach. Nucleotides in biofluids can be analyzed directly on this column without any significant sample preparation. Most of the proteins from biological fluids will be repelled from the surface of silica gel. Method is compatible with UV, ELSD, CAD and LC/MS.