Nicotinamide Adenine Dinucleotide (reduced) (NADH)

CAS Number443892-10-2
Molecular FormulaC21H29N7O14P2
Molecular Weight665.4
InChI KeyBOPGDPNILDQYTO-NNYOXOHSSA-N
LogP-5.7
Synonyms
  • NADH
  • DPNH
  • beta-NADH
  • beta-DPNH
  • Dihydrocozymase
  • Coenzyme I, reduced
  • Cozymase I, reduced
  • NADH2
  • 1,4-Dihydronicotinamide adenine dinucleotide
  • Dihydrocodehydrogenase I
  • 58-68-4
  • Reduced codehydrogenase I
  • dihydronicotinamide adenine dinucleotide
  • Codehydrase I, reduced
  • Dihydronicotinamide-adenine dinucleotide
  • Reduced nicotinamide adenine diphosphate
  • Dihydronicotinamide mononucleotide
  • Codehydrogenase I, reduced
  • Reduced diphosphopyridine nucleotide
  • Reduced nicotinamide-adenine dinucleotide
  • UNII-4J24DQ0916
  • Reduced Nicotinamide Adenine Dinucleotide
  • CHEBI:16908
  • 4J24DQ0916
  • nicotinamide adenine dinucleotide (reduced)

Applications:

Uv-Vis Spectrum of Nicotinamide Adenine Dinucleotide (reduced)

January 22, 2026
Access the UV-Vis Spectrum SIELC Library
UV-Vis Spectrum of Nicotinamide Adenine Dinucleotide (reduced) (NADH).

If you are looking for optimized HPLC method to analyze Nicotinamide Adenine Dinucleotide (reduced) (NADH) check our HPLC Applications library

For optimal results in HPLC analysis, it is recommended to measure absorbance at a wavelength that matches the absorption maximum of the compound(s) being analyzed. The UV spectrum shown can assist in selecting an appropriate wavelength for your analysis. Please note that certain mobile phases and buffers may block wavelengths below 230 nm, rendering absorbance measurement at these wavelengths ineffective. If detection below 230 nm is required, it is recommended to use acetonitrile and water as low UV-transparent mobile phases, with phosphoric acid and its salts, sulfuric acid, and TFA as buffers.
For some compounds, the UV-Vis Spectrum is affected by the pH of the mobile phase. The spectra presented here are measured with an acidic mobile phase that has a pH of 3 or lower.

 

 

Application Analytes:
Nicotinamide Adenine Dinucleotide (reduced) (NADH)
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.

HPLC UV Method for Separation of NAD and NADH on PEI Column

January 20, 2026

HPLC Method for Nicotinamide Adenine Dinucleotide (NAD), Nicotinamide Adenine Dinucleotide (reduced) (NADH) on PEI by SIELC Technologies

High Performance Liquid Chromatography (HPLC) Method for Analysis of SNAD and NADH

Nicotinamide adenine dinucleotide (NAD), is a coenzyme found in every single living cell. NAD can exist in two forms: NAD+ and NADH. The conversion of NAD from its oxidized form (NAD+) to its reduced form (NADH), and back, provides the cell with a mechanism for accepting and donating electrons.

NAD and NADH can be retained, separated and UV detected at 264 nm using the PEI column with a simple mobile phase of acetonitrile (ACN) and water with sulfuric acid buffer and detected by UV.

ColumnPEI, 4.6 x 50 mm, 5 µm, 100 A,
Mobile PhaseMeCN/H2O – 60/40%
BufferH2SO4 – 0.2%
Flow Rate1.0 ml/m
DetectionUV 264 nm
Class of Compounds
 Drug
Analyzing CompoundsNicotinamide Adenine Dinucleotide (NAD), Nicotinamide Adenine Dinucleotide (reduced) (NADH)

Application Column

PEI

Column Diameter: 4.6 mm
Column Length: 50 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options:

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Application Analytes:
Nicotinamide Adenine Dinucleotide (NAD)
Nicotinamide Adenine Dinucleotide (reduced) (NADH)

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.

HPLC Separation of NAD and NADH on PEI Column

July 22, 2021

HPLC Method for Nicotinamide Adenine Dinucleotide (NAD), Nicotinamide Adenine Dinucleotide (reduced) (NADH) on PEI by SIELC Technologies

High Performance Liquid Chromatography (HPLC) Method for Analysis of SNAD and NADH

Nicotinamide adenine dinucleotide (NAD), is a coenzyme found in every single living cell. NAD can exist in two forms: NAD+ and NADH. The conversion of NAD from its oxidized form (NAD+) to its reduced form (NADH), and back, provides the cell with a mechanism for accepting and donating electrons.

NAD and NADH can be retained, separated and UV detected at 260 nm using the PEI column with a simple MS-compatible mobile phase of acetonitrile (ACN) and water with Ammonium Acetate (AmAc) buffer and detected by UV, ELSD, CAD or LC/MS.

Condition

Column PEI, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O
Buffer Ammonium Acetate pH 6.8 – 60 mM
Flow Rate 2.0 ml/min
Detection UV 260 nm

Description

Class of Compounds
 Drug
Analyzing Compounds Nicotinamide Adenine Dinucleotide (NAD), Nicotinamide Adenine Dinucleotide (reduced) (NADH)

Application Column

PEI

SIELC Technologies offers custom phases for customers who require specific separations not achievable with commercially available HPLC phases. Considering the vast array of compounds and mixtures requiring analysis, tailored LC phases can significantly enhance separation results for unique and challenging applications. To learn more about our special custom LC phases designed for your specific separation needs, please contact SIELC Technologies at research@sielc.com. Our team of experts is ready to guide you through the process and create a custom solution that addresses your particular chromatographic challenges.

Select options
Application Analytes:
Nicotinamide Adenine Dinucleotide (NAD)
Nicotinamide Adenine Dinucleotide (reduced) (NADH)

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.